subject:(Chick Embryo cytology mesh )

University of Utah

1. Ravindranathan, Ajay. Glutamate receptors in the developing auditory system of chick;.

Degree: PhD, Neurobiology & Anatomy;, 1999, University of Utah

URL: http://content.lib.utah.edu/cdm/singleitem/collection/etd1/id/967/rec/591

► The main goal of this thesis was to identify differences in AMPA receptor subunit structure and function in auditory and nonauditory neurons. These data could… (more)

▼ The main goal of this thesis was to identify differences in AMPA receptor subunit structure and function in auditory and nonauditory neurons. These data could then serve as a possible explanation for the unique properties possessed by AMPA receptors in the auditory systems. Initially, as the sequence of splice variants of chick AMPA receptors was unavailable, the first step thus involved cloning the flip and flop isoforms of GluRs 1-4. Next, enzymes that cut either the flip or the flop isoform were identified and used ascertain the relative abundances of flip and flop isoforms of AMPA receptor subunit mRNA. The study showed that chick AMPA receptors exist as flip and flop isoforms and are differentially distributed in the CNS chick. Multiple band obtained when GluR4 was amplified from the chick CNS, suggested that additional splice variants may be present. Sequencing confirmed that three additional variants were present, caused by splicing at a c-terminal site. One of these variants had been previously described in rat, whereas the other two were novel. The spatial and temporal distribution of these novel isoforms and their splice variants were examined. Additionally, the distribution of these variants in specific cell-types was examined. AMPA receptors on auditory neurons posses highly specialized physiological properties. We hypothesized that these unique physiological properties were a function of the molecular make-up of the receptor. The study showed that auditory AMPA receptors are enriched in GluRs 3 and 4 flop and deficient in GluR2. Additionally, auditory neurons are highly permeable to calcium and this permeability is not due to lake of expression of GluR2 or a lack of RNA editing at the Q/R site. It is hypothesized that the high calcium permeability may be due to differential incorporation of GluR2 into AMPA receptors on the surface of these neurons. The data in this thesis will be an invaluable tool not only to researchers who study the auditory system but to the neuroscience community at large, given the importance of AMPA receptors in the nervous system.

Subjects/Keywords: Chick Embryo

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APA (6^th Edition):

Ravindranathan, A. (1999). Glutamate receptors in the developing auditory system of chick;. (Doctoral Dissertation). University of Utah. Retrieved from http://content.lib.utah.edu/cdm/singleitem/collection/etd1/id/967/rec/591

Chicago Manual of Style (16^th Edition):

Ravindranathan, Ajay. “Glutamate receptors in the developing auditory system of chick;.” 1999. Doctoral Dissertation, University of Utah. Accessed January 15, 2021. http://content.lib.utah.edu/cdm/singleitem/collection/etd1/id/967/rec/591.

MLA Handbook (7^th Edition):

Ravindranathan, Ajay. “Glutamate receptors in the developing auditory system of chick;.” 1999. Web. 15 Jan 2021.

Vancouver:

Ravindranathan A. Glutamate receptors in the developing auditory system of chick;. [Internet] [Doctoral dissertation]. University of Utah; 1999. [cited 2021 Jan 15]. Available from: http://content.lib.utah.edu/cdm/singleitem/collection/etd1/id/967/rec/591.

Council of Science Editors:

Ravindranathan A. Glutamate receptors in the developing auditory system of chick;. [Doctoral Dissertation]. University of Utah; 1999. Available from: http://content.lib.utah.edu/cdm/singleitem/collection/etd1/id/967/rec/591

2. Bhaskar, Nitu. Teratological evaluation of formulated Dicofol and Deltamethrin in chick embryo.

Degree: Microbiology, 2014, The IIS University

URL: http://shodhganga.inflibnet.ac.in/handle/10603/19957

►

In the present work, teratogenic potential of commercial formulations of two insecticides: dicofol (Colonel-S) and deltamethrin (Decis) were evaluated in developing chick embryo by observing… (more)

▼

In the present work, teratogenic potential of commercial formulations of two insecticides: dicofol (Colonel-S) and deltamethrin (Decis) were evaluated in developing chick embryo by observing certain changes in structural, biochemical and pathological parameters. The study consisted of three experimental plans which were based on exposure of fertilized eggs of Gallus domesticus to each insecticide on three critical periods of their embryogenesis. These eggs were immersed in aqueous emulsions (prepared in distilled water) of each insecticide at 250, 500 and1000 mg L¬-1 of dicofol and 12.5, 25 and 50 mg L¬-1 of deltamethrin which were based on recommended dose (500 mg L-1 of dicofol and 25 mg L-1 of deltamethrin) of each insecticide used for crop protection technique. In first experimental plan, the subjects were exposed with these chemicals on 0 day of incubation and their teratological evaluation was carried out on Embryonic Day (ED) 4, 7 and 10. In second experimental plan, eggs were treated on ED 4 followed by their sampling on ED 7, 10 and 16. Fertilized eggs were exposed on ED 7 in the experimental plan 3, and embryos were sacrificed on ED 16. All recovered embryos on ED 4, 7 and 10 were evaluated for survivability rate, wet body weight, gross morphological malformations and biochemical estimations of whole body, while those sacrificed on ED 16 were examined for above mentioned external teratological parameters, then histopathological (liver) and biochemical studies (brain and liver), and skeleton preparations were done in these treated animals. The result revealed that administration of dicofol and deltamethrin in developing chick embryo caused significant decrease in their survivability success, wet body weight and increase of various external (such as general growth retardation, hematomas, subcutaneous hemorrhage, ectopic viscera, anophthalmia, microphthalmia, microcephaly, anencephaly and exencephaly) and skeletal malformations (poor ossification of axial and appendicular skeleton bones, scoliosis an

Summary p.155-166, References p.167-186

Advisors/Committee Members: Shahani, Lata.

Subjects/Keywords: Dicofol; Deltamethrin; Chick Embryo; Life Sciences

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APA (6^th Edition):

Bhaskar, N. (2014). Teratological evaluation of formulated Dicofol and Deltamethrin in chick embryo. (Thesis). The IIS University. Retrieved from http://shodhganga.inflibnet.ac.in/handle/10603/19957

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16^th Edition):

Bhaskar, Nitu. “Teratological evaluation of formulated Dicofol and Deltamethrin in chick embryo.” 2014. Thesis, The IIS University. Accessed January 15, 2021. http://shodhganga.inflibnet.ac.in/handle/10603/19957.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7^th Edition):

Bhaskar, Nitu. “Teratological evaluation of formulated Dicofol and Deltamethrin in chick embryo.” 2014. Web. 15 Jan 2021.

Vancouver:

Bhaskar N. Teratological evaluation of formulated Dicofol and Deltamethrin in chick embryo. [Internet] [Thesis]. The IIS University; 2014. [cited 2021 Jan 15]. Available from: http://shodhganga.inflibnet.ac.in/handle/10603/19957.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Bhaskar N. Teratological evaluation of formulated Dicofol and Deltamethrin in chick embryo. [Thesis]. The IIS University; 2014. Available from: http://shodhganga.inflibnet.ac.in/handle/10603/19957

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

University of Pretoria

3. Venter, Chantelle. An in ovo investigation of the cellular effects of the heavy metals cadmium and chromium alone and in combination.

Degree: MSc, Anatomy, 2014, University of Pretoria

URL: http://hdl.handle.net/2263/46019

► Many heavy metals are essential for biological functions; however some of these metals, especially at high concentrations, can have serious adverse effects on humans. The… (more)

▼ Many heavy metals are essential for biological functions; however some of these metals, especially at high concentrations, can have serious adverse effects on humans. The main sources of heavy metal exposure are through agriculture, transport, mining and related operations. South Africa has a thriving mining industry and is known for its rich mineral resources, but due to the incorrect method of disposal of the waste from these mines, substances, including heavy metals, get into the water and air supply, affecting the people living in close proximity to these mines. Exposure is through inhalation of contaminated air and consumption of contaminated food and water. The most vulnerable to heavy metals are the developing fetus, because of the high rate of cell division and differentiation. In the current study, two heavy metals cadmium (Cd) and chromium (Cr) were chosen based on the possibility of being exposed to them in South Africa. Thus, the aim of this study was to investigate the possible cellular effects of the heavy metals Cd and Cr alone and in combination, at different concentrations, on brain, liver and kidney tissue by using a chick embryo model. This model was successfully implemented over a 14 day period after which the embryos were terminated and the brains, livers and kidneys removed and processed for light- and transmission electron microscopy (with energy dispersive spectroscopy and electron energyloss spectroscopy). In addition, the effect of Cd and Cr alone and in combination on DNA structure and micronuclei formation was evaluated. The levels of the major antioxidant component, glutathione was determined in the brains of the chick embryos. At low concentration of Cd and Cr alone and in combination, a hormesis effect was observed in the survival rates and weights of the chick embryos, while at x1000 physiological dose (PD) Cr and Cd alone and in combination the effects were toxic. The majority of viable embryos did not have any macro-anatomy abnormalities. Morphological evaluation of the brain, liver and kidney samples revealed that Cd caused severe alterations at its highest concentration with minor alterations at the lower concentrations. Cr and the metal combination groups on the other hand, only caused minimal alterations throughout the concentration ranges evaluated. The presence of Cd and Cr alone and in combination in the liver tissue was confirmed with the electron energy-loss spectroscopy analysis that detected these metals in the nuclei, mitochondria and Golgi complexes of the hepatocytes. This might contribute to the ultrastructural changes observed in this organ. The genotoxicity testing on the red blood cells revealed no substantial differences, as only a few micronuclei were present. Although heavy metals cause DNA damage through an indirect mechanism of oxidative damage, the presence of Cd and Cr in the nucleus and mitochondria indicates that these metals may have a direct effect on DNA structure. With DNA agarose gel electrophoresis it was found that Cd… Advisors/Committee Members: Oberholzer, Hester Magdalena (advisor), Taute, Helena (coadvisor).

Subjects/Keywords: UCTD; Heavy metals; Chromium; Chick embryo; Ultrastructure

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APA (6^th Edition):

Venter, C. (2014). An in ovo investigation of the cellular effects of the heavy metals cadmium and chromium alone and in combination. (Masters Thesis). University of Pretoria. Retrieved from http://hdl.handle.net/2263/46019

Chicago Manual of Style (16^th Edition):

Venter, Chantelle. “An in ovo investigation of the cellular effects of the heavy metals cadmium and chromium alone and in combination.” 2014. Masters Thesis, University of Pretoria. Accessed January 15, 2021. http://hdl.handle.net/2263/46019.

MLA Handbook (7^th Edition):

Venter, Chantelle. “An in ovo investigation of the cellular effects of the heavy metals cadmium and chromium alone and in combination.” 2014. Web. 15 Jan 2021.

Vancouver:

Venter C. An in ovo investigation of the cellular effects of the heavy metals cadmium and chromium alone and in combination. [Internet] [Masters thesis]. University of Pretoria; 2014. [cited 2021 Jan 15]. Available from: http://hdl.handle.net/2263/46019.

Council of Science Editors:

Venter C. An in ovo investigation of the cellular effects of the heavy metals cadmium and chromium alone and in combination. [Masters Thesis]. University of Pretoria; 2014. Available from: http://hdl.handle.net/2263/46019

Penn State University

4. Schilling, Megan. Transcriptional Responses of Innate Immune Genes in the Developing Chick Embryo of Inbred and Outbred Lines to Newcastle Disease Virus Infection.

Degree: 2019, Penn State University

URL: https://submit-etda.libraries.psu.edu/catalog/16639mas985

► Newcastle Disease Virus (NDV) is an important poultry pathogen that has impacts on poultry production, trade, and food security worldwide, but particularly in low- and… (more)

▼ Newcastle Disease Virus (NDV) is an important poultry pathogen that has impacts on poultry production, trade, and food security worldwide, but particularly in low- and middle-income countries where the disease is endemic. There are high mortality rates associated with the introduction of virulent strains of NDV in poultry flocks, which causes severe economic burdens on smallholder poultry farmers. In Africa, and particularly Tanzania, poultry are primarily farmed extensively. This type of production is defined by little to no veterinary care, poor biosecurity, and scavenging conditions. Commonly, these birds are exposed to dangerous pathogens in the field, however, not all birds die or even demonstrate clinical signs, hence there some natural disease resistance in these populations. Since these populations have existed without purposive or artificial selection, genes that are important for disease resistance may be harbored within these backyard poultry populations. These studies have aimed to determine mechanisms contributing to the natural disease resistance in backyard poultry through examining the innate immune response in the chick embryo of both highly inbred and outbred lines. The chick embryo becomes immunocompetent prior to hatching and is within the protective environment of the shell. Through the use of the chick embryo, the costs of experiments will be greatly reduced with larger sample sizes, minimal husbandry and biosecurity is needed, and the effects of confounding variables will be reduced. These studies first validated the chick embryo as a model to examine the innate immune response to NDV in poultry through examining the transcriptional response of innate immune genes throughout chick embryonic immune development in multiple tissues. This determined the optimal infection timepoint of 18 days of development and tissue harvest 72 hours post infection, just prior to hatching. Using this model, the transcriptional response of innate immune genes in highly inbred lines differing in the level of susceptibility to NDV revealed a conserved response, a breed-dependent response, and a subline-dependent response. The breed-dependent genes were also examined in highly outbred populations from Tanzania to determine if the same genes would be differentially expressed in these populations. Through these studies, we were able to propose a panel of genes, including NOS2, CCL4, CAMP, and IL8, associated with the level of susceptibility of different lines to NDV infection. These genes provide candidate genomic regions for future studies to uncover genetic markers for selective breeding strategies that will improve poultry production for smallholder farmers worldwide. Advisors/Committee Members: Vivek Kapur, Dissertation Advisor/Co-Advisor, Vivek Kapur, Committee Chair/Co-Chair, Isabella Cattadori, Committee Member, Suresh Varma Kuchipudi, Committee Member, Bhushan M Jayarao, Outside Member.

Subjects/Keywords: Newcastle disease virus; chick embryo; NDV; Tanzania; innate immunity; ecotypes

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APA (6^th Edition):

Schilling, M. (2019). Transcriptional Responses of Innate Immune Genes in the Developing Chick Embryo of Inbred and Outbred Lines to Newcastle Disease Virus Infection. (Thesis). Penn State University. Retrieved from https://submit-etda.libraries.psu.edu/catalog/16639mas985

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16^th Edition):

Schilling, Megan. “Transcriptional Responses of Innate Immune Genes in the Developing Chick Embryo of Inbred and Outbred Lines to Newcastle Disease Virus Infection.” 2019. Thesis, Penn State University. Accessed January 15, 2021. https://submit-etda.libraries.psu.edu/catalog/16639mas985.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7^th Edition):

Schilling, Megan. “Transcriptional Responses of Innate Immune Genes in the Developing Chick Embryo of Inbred and Outbred Lines to Newcastle Disease Virus Infection.” 2019. Web. 15 Jan 2021.

Vancouver:

Schilling M. Transcriptional Responses of Innate Immune Genes in the Developing Chick Embryo of Inbred and Outbred Lines to Newcastle Disease Virus Infection. [Internet] [Thesis]. Penn State University; 2019. [cited 2021 Jan 15]. Available from: https://submit-etda.libraries.psu.edu/catalog/16639mas985.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Schilling M. Transcriptional Responses of Innate Immune Genes in the Developing Chick Embryo of Inbred and Outbred Lines to Newcastle Disease Virus Infection. [Thesis]. Penn State University; 2019. Available from: https://submit-etda.libraries.psu.edu/catalog/16639mas985

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

University of Cambridge

5. Schaeffer, Julia. The Molecular Regulation of Spinal Nerve Outgrowth.

Degree: PhD, 2018, University of Cambridge

URL: https://www.repository.cam.ac.uk/handle/1810/271632

► During amniote embryogenesis, the segmented pattern characteristic of the vertebral column appears early during development through the sequential formation of multipotent structures called somites. Somites… (more)

▼ During amniote embryogenesis, the segmented pattern characteristic of the vertebral column appears early during development through the sequential formation of multipotent structures called somites. Somites differentiate subsequently into dermomyotome (giving rise later to skin and skeletal muscles) and sclerotome (giving rise to vertebral bone structures and cartilage). In addition, sclerotomes subdivide following their rostro-caudal intrasegmental boundary into an axon growth-permissive region (anterior half) and an axon growth-repulsive region (posterior half). This binary system instructs motor and sensory axon navigation, as well as neural crest cell migration, to ensure that the peripheral nervous system develops without obstruction by the future cartilage and bones of the vertebral column. Repellent cues are expressed in posterior half-sclerotomes in order to exclude navigating axons from “no-go” areas and restrict their growth to specific exit points of the future vertebral column. Interestingly, similar repellent cues (e.g. Eph/Ephrins) are expressed in the adult central nervous system (CNS) and have been shown to control connectivity and plasticity throughout life. Following brain or spinal cord injury, these repellent molecules are upregulated by reactive astrocytes accumulating at the lesion site, and may impede axon regeneration in this region. In this dissertation, I am presenting the results of a differential gene expression analysis of anterior and posterior half-sclerotomes, based on RNA-sequencing data and using the chick embryo as a model organism. This study led to the identification of molecules, previously uncharacterized in this system, that may play a role in adhesive and mechanical properties of somites and in axon guidance and fasciculation. I focused on the functional analysis of one molecule of the posterior half-sclerotome, the extracellular matrix protein Fibulin-2. To look at its role in the segmentation of spinal axons, I used ectopic misexpression in a subset of segments based on somite electroporation. The width of spinal nerve bundle growth was restricted by Fibulin-2 overexpression in posterior and anterior half-sclerotomes, suggesting a role in sharpening/controlling the path of spinal axon growth. In addition, I showed that this could occur via an interaction with the axon growth repellent Semaphorin 3A. Then I looked at the expression of Fibulin-2 in two models of CNS injury: mouse cerebral cortical stab injury and rat dorsal crush spinal cord injury. In both cases, I observed an increase in Fibulin-2 protein level compared to control. I also used primary cultures of rat cortical astrocytes to show that the expression of Fibulin-2 after inflammatory cytokine-induced activation is increased. Finally, I studied a candidate axon growth repellent previously identified in the laboratory. I explored the hypothesis that this repellent molecule is an O-glycosylated, spliced variant form of a known protein. To characterize this repellent molecule, I used RNA-sequencing data from chick…

Subjects/Keywords: development; spinal nerves; chick embryo; segmentation; spinal cord injury; axon guidance

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APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6^th Edition):

Schaeffer, J. (2018). The Molecular Regulation of Spinal Nerve Outgrowth. (Doctoral Dissertation). University of Cambridge. Retrieved from https://www.repository.cam.ac.uk/handle/1810/271632

Chicago Manual of Style (16^th Edition):

Schaeffer, Julia. “The Molecular Regulation of Spinal Nerve Outgrowth.” 2018. Doctoral Dissertation, University of Cambridge. Accessed January 15, 2021. https://www.repository.cam.ac.uk/handle/1810/271632.

MLA Handbook (7^th Edition):

Schaeffer, Julia. “The Molecular Regulation of Spinal Nerve Outgrowth.” 2018. Web. 15 Jan 2021.

Vancouver:

Schaeffer J. The Molecular Regulation of Spinal Nerve Outgrowth. [Internet] [Doctoral dissertation]. University of Cambridge; 2018. [cited 2021 Jan 15]. Available from: https://www.repository.cam.ac.uk/handle/1810/271632.

Council of Science Editors:

Schaeffer J. The Molecular Regulation of Spinal Nerve Outgrowth. [Doctoral Dissertation]. University of Cambridge; 2018. Available from: https://www.repository.cam.ac.uk/handle/1810/271632

University of Waterloo

6. Li, Abby. Examining Cell Movements in the Neurulating Chick Embryo.

Degree: 2008, University of Waterloo

URL: http://hdl.handle.net/10012/3532

► The avian embryo is a popular animal model because it is widely available (Antin et al., 2004), it is easily manipulated, and it can provide… (more)

Subjects/Keywords: Developmental biology; Chick embryo; Neurulation

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APA (6^th Edition):

Li, A. (2008). Examining Cell Movements in the Neurulating Chick Embryo. (Thesis). University of Waterloo. Retrieved from http://hdl.handle.net/10012/3532

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16^th Edition):

Li, Abby. “Examining Cell Movements in the Neurulating Chick Embryo.” 2008. Thesis, University of Waterloo. Accessed January 15, 2021. http://hdl.handle.net/10012/3532.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7^th Edition):

Li, Abby. “Examining Cell Movements in the Neurulating Chick Embryo.” 2008. Web. 15 Jan 2021.

Vancouver:

Li A. Examining Cell Movements in the Neurulating Chick Embryo. [Internet] [Thesis]. University of Waterloo; 2008. [cited 2021 Jan 15]. Available from: http://hdl.handle.net/10012/3532.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Li A. Examining Cell Movements in the Neurulating Chick Embryo. [Thesis]. University of Waterloo; 2008. Available from: http://hdl.handle.net/10012/3532

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

University of Florida

7. Nathaniel, Rajkumar, 1971-. Role of CrmA in regulating inflammation and apoptosis during cowpox virus infection.

Degree: 2003, University of Florida

URL: https://ufdc.ufl.edu/AA00025810

Subjects/Keywords: Apoptosis; Chickens; Cytokines; Enzymes; Infections; Inflammation; Molecules; Receptors; Serpins; Viruses; Apoptosis ( mesh ); Capases ( mesh ); Chick Embryo ( mesh ); Cowpox ( mesh ); Department of Molecular Genetics and Microbiology thesis Ph.D ( mesh ); Immunity ( mesh ); Inflammation ( mesh ); Interleukins ( mesh ); Poxviridae Infections ( mesh ); Research ( mesh ); Serpins ( mesh )

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APA (6^th Edition):

Nathaniel, Rajkumar, 1. (2003). Role of CrmA in regulating inflammation and apoptosis during cowpox virus infection. (Thesis). University of Florida. Retrieved from https://ufdc.ufl.edu/AA00025810

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16^th Edition):

Nathaniel, Rajkumar, 1971-. “Role of CrmA in regulating inflammation and apoptosis during cowpox virus infection.” 2003. Thesis, University of Florida. Accessed January 15, 2021. https://ufdc.ufl.edu/AA00025810.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7^th Edition):

Nathaniel, Rajkumar, 1971-. “Role of CrmA in regulating inflammation and apoptosis during cowpox virus infection.” 2003. Web. 15 Jan 2021.

Vancouver:

Nathaniel, Rajkumar 1. Role of CrmA in regulating inflammation and apoptosis during cowpox virus infection. [Internet] [Thesis]. University of Florida; 2003. [cited 2021 Jan 15]. Available from: https://ufdc.ufl.edu/AA00025810.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Nathaniel, Rajkumar 1. Role of CrmA in regulating inflammation and apoptosis during cowpox virus infection. [Thesis]. University of Florida; 2003. Available from: https://ufdc.ufl.edu/AA00025810

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

University of Florida

8. Poage, Robert Eliot, 1964-. The Effects of repetitive stimulation on synaptic transmission in the chick ciliary ganglion.

Degree: 1995, University of Florida

URL: https://ufdc.ufl.edu/AA00029763

Subjects/Keywords: Action potentials; Calcium; Frogs; Ganglia; Nerves; Neurons; Neurotransmitters; Synapses; Time constants; Transmitters; Action Potentials ( mesh ); Calcium Channels – physiology ( mesh ); Chick Embryo – physiology ( mesh ); Ciliary Body – physiology ( mesh ); Department of Neuroscience thesis Ph.D ( mesh ); Electric Stimulation ( mesh ); Electrophysiology ( mesh ); Ganglia – physiology ( mesh ); Synaptic Transmission – physiology ( mesh )

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APA (6^th Edition):

Poage, Robert Eliot, 1. (1995). The Effects of repetitive stimulation on synaptic transmission in the chick ciliary ganglion. (Thesis). University of Florida. Retrieved from https://ufdc.ufl.edu/AA00029763

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16^th Edition):

Poage, Robert Eliot, 1964-. “The Effects of repetitive stimulation on synaptic transmission in the chick ciliary ganglion.” 1995. Thesis, University of Florida. Accessed January 15, 2021. https://ufdc.ufl.edu/AA00029763.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7^th Edition):

Poage, Robert Eliot, 1964-. “The Effects of repetitive stimulation on synaptic transmission in the chick ciliary ganglion.” 1995. Web. 15 Jan 2021.

Vancouver:

Poage, Robert Eliot 1. The Effects of repetitive stimulation on synaptic transmission in the chick ciliary ganglion. [Internet] [Thesis]. University of Florida; 1995. [cited 2021 Jan 15]. Available from: https://ufdc.ufl.edu/AA00029763.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Poage, Robert Eliot 1. The Effects of repetitive stimulation on synaptic transmission in the chick ciliary ganglion. [Thesis]. University of Florida; 1995. Available from: https://ufdc.ufl.edu/AA00029763

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

University of California – Irvine

9. Tran, Stephanie Thuy-Vy. A Wound Healing Study on Embryonic Chick Corneas using Second Harmonic Generation Imaging.

Degree: Biomedical Engineering, 2015, University of California – Irvine

URL: http://www.escholarship.org/uc/item/3pp9f6x4

► Damage or infection to the adult cornea results in scarring and loss of transparency. Since fetal tissue has been known to regenerate without scarring, we… (more)

Subjects/Keywords: Biomedical engineering; Chick embryo; Collagen; Cornea; nlo-hrmac; Second Harmonic Generation; wound healing

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APA (6^th Edition):

Tran, S. T. (2015). A Wound Healing Study on Embryonic Chick Corneas using Second Harmonic Generation Imaging. (Thesis). University of California – Irvine. Retrieved from http://www.escholarship.org/uc/item/3pp9f6x4

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16^th Edition):

Tran, Stephanie Thuy-Vy. “A Wound Healing Study on Embryonic Chick Corneas using Second Harmonic Generation Imaging.” 2015. Thesis, University of California – Irvine. Accessed January 15, 2021. http://www.escholarship.org/uc/item/3pp9f6x4.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7^th Edition):

Tran, Stephanie Thuy-Vy. “A Wound Healing Study on Embryonic Chick Corneas using Second Harmonic Generation Imaging.” 2015. Web. 15 Jan 2021.

Vancouver:

Tran ST. A Wound Healing Study on Embryonic Chick Corneas using Second Harmonic Generation Imaging. [Internet] [Thesis]. University of California – Irvine; 2015. [cited 2021 Jan 15]. Available from: http://www.escholarship.org/uc/item/3pp9f6x4.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Tran ST. A Wound Healing Study on Embryonic Chick Corneas using Second Harmonic Generation Imaging. [Thesis]. University of California – Irvine; 2015. Available from: http://www.escholarship.org/uc/item/3pp9f6x4

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

University of Utah

10. Dolana, Gary Harward. Effect of temperature on the infectivity and propagation of western equine encephalitis virus;.

Degree: MS;, Pathology;, 1961, University of Utah

URL: http://content.lib.utah.edu/cdm/singleitem/collection/etd1/id/195/rec/392

► The propagation of WEE virus variants L.P.7 and S.P. #6 infected chick embryo cells maintained as monolayer and in suspension was studied at 25° and… (more)

▼ The propagation of WEE virus variants L.P.7 and S.P. #6 infected chick embryo cells maintained as monolayer and in suspension was studied at 25° and 37°C. The results may be summarized as follows: 1. The lag-period of the growth cycle for L.P. #6 and S.P. #7 was found to be 10 hours when the infected cells were maintained as a monolayer or in suspension and incubated at 25°C. The lag period for S.P. #6 infected cells in suspension and as a monolayer incubated at 37° was found to be 2 hours while that for L.P. #7 was 1 ½ hours. 2. The maximum number of PFU in both variants present in the extracellular fluid was reached after 72 hours of incubation of infected monolayers at 25°C. With S.P, #6 infected cells in suspension the maximum titer of S.P. #6 PFU was attained after 48 hours of incubation at 25°C while with L.P. #7 infected cells the maximum PFU was reached after only 36 hours of incubation at 25°C. S.P. #6 infected cell in suspension, however, released a larger number of PFU than did L.P. #7 infected cells. The reverse was true with cells maintained as a monolayer. 3. The maximum number of PFU released into the extracellular fluid by S.P. #6 and L.P. #7 infected cells in suspension or maintained as a monolayer occurred after 10 hours of incubation at 37°C. The highest titer was produced by cell infected with the large plaque variant. 4. On the basis of infective center assay and counts of replicate non-infected monolayers the number of PFU released per infected cell was determined. An experiment was designed to study the cytopathic changes that develop in WEE virus infected chick embryo cells incubated at 25°C and 37°C. the results of this experiment may be summarized as follows: 1. Cytopathogenicity was first observed in L.P. #7 infected cells after 8 hours of incubation at 37°C. S.P. #6 infected cell did not show definite signs of cytopathic changes until after 10 hours of incubation at 37°C. 2. Infected cells incubated at 25°C developed observable cytopathogenicity after 24 hours of incubation. 3. Comparisons were made with the development of cytopathogenicity and the propagation of the two variants at the two experimental temperatures.

Subjects/Keywords: Chick Embryo Cell Culture; Epidemiology; Epizoology

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APA (6^th Edition):

Dolana, G. H. (1961). Effect of temperature on the infectivity and propagation of western equine encephalitis virus;. (Masters Thesis). University of Utah. Retrieved from http://content.lib.utah.edu/cdm/singleitem/collection/etd1/id/195/rec/392

Chicago Manual of Style (16^th Edition):

Dolana, Gary Harward. “Effect of temperature on the infectivity and propagation of western equine encephalitis virus;.” 1961. Masters Thesis, University of Utah. Accessed January 15, 2021. http://content.lib.utah.edu/cdm/singleitem/collection/etd1/id/195/rec/392.

MLA Handbook (7^th Edition):

Dolana, Gary Harward. “Effect of temperature on the infectivity and propagation of western equine encephalitis virus;.” 1961. Web. 15 Jan 2021.

Vancouver:

Dolana GH. Effect of temperature on the infectivity and propagation of western equine encephalitis virus;. [Internet] [Masters thesis]. University of Utah; 1961. [cited 2021 Jan 15]. Available from: http://content.lib.utah.edu/cdm/singleitem/collection/etd1/id/195/rec/392.

Council of Science Editors:

Dolana GH. Effect of temperature on the infectivity and propagation of western equine encephalitis virus;. [Masters Thesis]. University of Utah; 1961. Available from: http://content.lib.utah.edu/cdm/singleitem/collection/etd1/id/195/rec/392

North Carolina State University

11. Ozden, Ozkan. Expression of Claudin Tight Junction Proteins in Response to Varying Environmental and Physiological Conditions.

Degree: PhD, Zoology, 2009, North Carolina State University

URL: http://www.lib.ncsu.edu/resolver/1840.16/3173

► In this study, the localization and possible functions of claudin tight junction proteins in bird and fish gastrointestinal tract were investigated. Claudin expression was detected… (more)

Subjects/Keywords: microarrays; tight junctions; claudin; Tilapia; fish; gastrointestinal tract; intestine; glucocorticoid; embryo; chick

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APA (6^th Edition):

Ozden, O. (2009). Expression of Claudin Tight Junction Proteins in Response to Varying Environmental and Physiological Conditions. (Doctoral Dissertation). North Carolina State University. Retrieved from http://www.lib.ncsu.edu/resolver/1840.16/3173

Chicago Manual of Style (16^th Edition):

Ozden, Ozkan. “Expression of Claudin Tight Junction Proteins in Response to Varying Environmental and Physiological Conditions.” 2009. Doctoral Dissertation, North Carolina State University. Accessed January 15, 2021. http://www.lib.ncsu.edu/resolver/1840.16/3173.

MLA Handbook (7^th Edition):

Ozden, Ozkan. “Expression of Claudin Tight Junction Proteins in Response to Varying Environmental and Physiological Conditions.” 2009. Web. 15 Jan 2021.

Vancouver:

Ozden O. Expression of Claudin Tight Junction Proteins in Response to Varying Environmental and Physiological Conditions. [Internet] [Doctoral dissertation]. North Carolina State University; 2009. [cited 2021 Jan 15]. Available from: http://www.lib.ncsu.edu/resolver/1840.16/3173.

Council of Science Editors:

Ozden O. Expression of Claudin Tight Junction Proteins in Response to Varying Environmental and Physiological Conditions. [Doctoral Dissertation]. North Carolina State University; 2009. Available from: http://www.lib.ncsu.edu/resolver/1840.16/3173

Washington University in St. Louis

12. Oltean, Alina. Mechanics of Early Retina and Lens Development in the Embryo.

Degree: PhD, Biomedical Engineering, 2016, Washington University in St. Louis

URL: https://openscholarship.wustl.edu/eng_etds/171

► Mechanical forces play an essential role in morphogenesis, the shaping of embryonic structures. This research focuses mainly on eye development, a problem that has… (more)

▼ Mechanical forces play an essential role in morphogenesis, the shaping of embryonic structures. This research focuses mainly on eye development, a problem that has been studied for decades using a variety of approaches. However, the mechanics of the early stages of eye formation remain incompletely understood. The embryonic eyes begin as bilateral protrusions called optic vesicles (OVs) that grow outward from the anterior end of the brain tube. The optic vesicles contact and adhere to the overlying surface ectoderm (SE) via extracellular matrix (ECM). Then, both layers thicken in the region of contact to form the retinal and lens placodes, which bend inward (invaginate) to form the roughly spherical optic cup (OC, primitive retina) and lens pit, respectively. These two structures then separate, and the lens pit continues to fold until it closes to create the lens vesicle (LV). The primary aim of this research is to determine the biophysical mechanisms that create the OC and LV in the chick embryo. Throughout, we used a combination of experiments and computational modeling. First, we explored the hypothesis that the ECM locally constrains the OV as it grows, forcing it to thicken and invaginate. The integrity of the matrix was disrupted by removing its major source, the SE, and degrading the matrix chemically at different stages of development. At relatively early stages of invagination, removing the SE caused the curvature of the OV to reverse as it `popped out' and became convex, but the OV remained concave at later stages and invaginated further during subsequent culture. Disrupting the ECM had a similar effect, with the OV popping out at early to mid-stages of invagination. These results suggest that the ECM is required for the early stages but not the late stages of OV invagination. A finite-element model consisting of a growing spherical OV attached to a relatively stiff layer of ECM reproduced the observed behavior, as well as measured changes in OV curvature, wall thickness, and invagination depth reasonably well. These results support the matrix constraint hypothesis for retinal placode formation and invagination. Next, we studied the forces that create the LV. Studies have shown that, like the retinal placode, the lens placode is produced by growth of the SE constrained locally by ECM, while actomyosin contraction at the apical surface of the lens placode plays a major role in its subsequent invagination. Our experiments and modeling support this view but also suggest that apical contraction alone does not generate sufficient force to close the LV. We propose that programmed cell death, or apoptosis, which has been observed near the opening in the lens pit, supplies the required force for closure by causing tissue surrounding the opening to shorten circumferentially. Finite-element modeling and experiments involving apoptosis inhibitors support this idea. Finally, we investigated the possible role of mechanical feedback in regulating the contractile behavior of neuroepithelia… Advisors/Committee Members: Larry A. Taber, Steven Bassnett, Philip V. Bayly, Spencer P. Lake, Ruth J. Okamoto.

Subjects/Keywords: biomechanics; chick embryo; computational modeling; eye development; lens; retina; Biomechanics; Biomedical; Developmental Biology

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APA (6^th Edition):

Oltean, A. (2016). Mechanics of Early Retina and Lens Development in the Embryo. (Doctoral Dissertation). Washington University in St. Louis. Retrieved from https://openscholarship.wustl.edu/eng_etds/171

Chicago Manual of Style (16^th Edition):

Oltean, Alina. “Mechanics of Early Retina and Lens Development in the Embryo.” 2016. Doctoral Dissertation, Washington University in St. Louis. Accessed January 15, 2021. https://openscholarship.wustl.edu/eng_etds/171.

MLA Handbook (7^th Edition):

Oltean, Alina. “Mechanics of Early Retina and Lens Development in the Embryo.” 2016. Web. 15 Jan 2021.

Vancouver:

Oltean A. Mechanics of Early Retina and Lens Development in the Embryo. [Internet] [Doctoral dissertation]. Washington University in St. Louis; 2016. [cited 2021 Jan 15]. Available from: https://openscholarship.wustl.edu/eng_etds/171.

Council of Science Editors:

Oltean A. Mechanics of Early Retina and Lens Development in the Embryo. [Doctoral Dissertation]. Washington University in St. Louis; 2016. Available from: https://openscholarship.wustl.edu/eng_etds/171

University of Cambridge

13. Schaeffer, Julia. The molecular regulation of spinal nerve outgrowth.

Degree: PhD, 2018, University of Cambridge

URL: https://doi.org/10.17863/CAM.18626 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.744495

► During amniote embryogenesis, the segmented pattern characteristic of the vertebral column appears early during development through the sequential formation of multipotent structures called somites. Somites… (more)

▼ During amniote embryogenesis, the segmented pattern characteristic of the vertebral column appears early during development through the sequential formation of multipotent structures called somites. Somites differentiate subsequently into dermomyotome (giving rise later to skin and skeletal muscles) and sclerotome (giving rise to vertebral bone structures and cartilage). In addition, sclerotomes subdivide following their rostro-caudal intrasegmental boundary into an axon growth-permissive region (anterior half) and an axon growth-repulsive region (posterior half). This binary system instructs motor and sensory axon navigation, as well as neural crest cell migration, to ensure that the peripheral nervous system develops without obstruction by the future cartilage and bones of the vertebral column. Repellent cues are expressed in posterior half-sclerotomes in order to exclude navigating axons from “no-go” areas and restrict their growth to specific exit points of the future vertebral column. Interestingly, similar repellent cues (e.g. Eph/Ephrins) are expressed in the adult central nervous system (CNS) and have been shown to control connectivity and plasticity throughout life. Following brain or spinal cord injury, these repellent molecules are upregulated by reactive astrocytes accumulating at the lesion site, and may impede axon regeneration in this region. In this dissertation, I am presenting the results of a differential gene expression analysis of anterior and posterior half-sclerotomes, based on RNA-sequencing data and using the chick embryo as a model organism. This study led to the identification of molecules, previously uncharacterized in this system, that may play a role in adhesive and mechanical properties of somites and in axon guidance and fasciculation. I focused on the functional analysis of one molecule of the posterior half-sclerotome, the extracellular matrix protein Fibulin-2. To look at its role in the segmentation of spinal axons, I used ectopic misexpression in a subset of segments based on somite electroporation. The width of spinal nerve bundle growth was restricted by Fibulin-2 overexpression in posterior and anterior half-sclerotomes, suggesting a role in sharpening/controlling the path of spinal axon growth. In addition, I showed that this could occur via an interaction with the axon growth repellent Semaphorin 3A. Then I looked at the expression of Fibulin-2 in two models of CNS injury: mouse cerebral cortical stab injury and rat dorsal crush spinal cord injury. In both cases, I observed an increase in Fibulin-2 protein level compared to control. I also used primary cultures of rat cortical astrocytes to show that the expression of Fibulin-2 after inflammatory cytokine-induced activation is increased. Finally, I studied a candidate axon growth repellent previously identified in the laboratory. I explored the hypothesis that this repellent molecule is an O-glycosylated, spliced variant form of a known protein. To characterize this repellent molecule, I used RNA-sequencing data from chick…

Subjects/Keywords: 612.8; development; spinal nerves; chick embryo; segmentation; spinal cord injury; axon guidance

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APA (6^th Edition):

Schaeffer, J. (2018). The molecular regulation of spinal nerve outgrowth. (Doctoral Dissertation). University of Cambridge. Retrieved from https://doi.org/10.17863/CAM.18626 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.744495

Chicago Manual of Style (16^th Edition):

Schaeffer, Julia. “The molecular regulation of spinal nerve outgrowth.” 2018. Doctoral Dissertation, University of Cambridge. Accessed January 15, 2021. https://doi.org/10.17863/CAM.18626 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.744495.

MLA Handbook (7^th Edition):

Schaeffer, Julia. “The molecular regulation of spinal nerve outgrowth.” 2018. Web. 15 Jan 2021.

Vancouver:

Schaeffer J. The molecular regulation of spinal nerve outgrowth. [Internet] [Doctoral dissertation]. University of Cambridge; 2018. [cited 2021 Jan 15]. Available from: https://doi.org/10.17863/CAM.18626 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.744495.

Council of Science Editors:

Schaeffer J. The molecular regulation of spinal nerve outgrowth. [Doctoral Dissertation]. University of Cambridge; 2018. Available from: https://doi.org/10.17863/CAM.18626 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.744495

University of Florida

14. Swanson, Douglas James, 1964-. The Effects of chronic prenatal ethanol exposure on CNS cholinergic development.

Degree: 1994, University of Florida

URL: https://ufdc.ufl.edu/AA00067426

Subjects/Keywords: Research ( mesh ); Disease Models, Animal ( mesh ); Fetal Alcohol Syndrome – etiology ( mesh ); Fetal Alcohol Syndrome – chemically induced ( mesh ); Ethanol – toxicity ( mesh ); Ethanol – pharmacology ( mesh ); Prenatal Exposure Delayed Effects ( mesh ); Purkinje Cells – drug effects ( mesh ); Purkinje Cells – growth and development ( mesh ); Cholinergic Fibers – drug effects ( mesh ); Cholinergic Fibers – growth and development ( mesh ); Rats ( mesh ); Chick Embryo ( mesh ); Department of Neuroscience thesis Ph.D ( mesh )

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APA (6^th Edition):

Swanson, Douglas James, 1. (1994). The Effects of chronic prenatal ethanol exposure on CNS cholinergic development. (Thesis). University of Florida. Retrieved from https://ufdc.ufl.edu/AA00067426

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16^th Edition):

Swanson, Douglas James, 1964-. “The Effects of chronic prenatal ethanol exposure on CNS cholinergic development.” 1994. Thesis, University of Florida. Accessed January 15, 2021. https://ufdc.ufl.edu/AA00067426.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7^th Edition):

Swanson, Douglas James, 1964-. “The Effects of chronic prenatal ethanol exposure on CNS cholinergic development.” 1994. Web. 15 Jan 2021.

Vancouver:

Swanson, Douglas James 1. The Effects of chronic prenatal ethanol exposure on CNS cholinergic development. [Internet] [Thesis]. University of Florida; 1994. [cited 2021 Jan 15]. Available from: https://ufdc.ufl.edu/AA00067426.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Swanson, Douglas James 1. The Effects of chronic prenatal ethanol exposure on CNS cholinergic development. [Thesis]. University of Florida; 1994. Available from: https://ufdc.ufl.edu/AA00067426

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

15. Beck, Kylie. VITRIFICATION AND CHORIOALLANTOIC MEMBRANE (CAM) CULTURE OF BOVINE OVARIAN TISSUE.

Degree: 2015, University of Saskatchewan

URL: http://hdl.handle.net/10388/ETD-2015-05-2051

► The overall objectives of this thesis were to develop a short-term culture system and to examine the effects of vitrification and short-term culture on the… (more)

▼ The overall objectives of this thesis were to develop a short-term culture system and to examine the effects of vitrification and short-term culture on the viability of fresh and vitrified bovine ovarian tissue and the follicles within. The first objective was to compare the health and development of preantral follicles in bovine ovarian tissue, as well as the neovascularization of these tissues, subjected to avian chorioallantoic membrane (CAM) culture with the traditional in vitro culture system. We hypothesized that the chorioallantoic membrane (CAM) of the chicken embryo is a  more suitable culture system than traditional in vitro culture. Bovine ovaries were retrieved from a local abattoir and cortical pieces (1-2mm3) were randomly assigned to one of the following groups; control (fixed immediately), CAM or in in vitro culture. Ovarian tissue fragments from both groups were removed on D1, D3 and D5 of culture, fixed, sectioned (5μm) and stained with H&E. The numbers of healthy and degenerated follicles, primordial and activated preantral (primary and secondary), and the number of infiltrated bovine and avian blood vessels were determined using standard stereological procedures. All grafts placed on the traumatized CAM demonstrated increased neovascularization over time. The healthy primordial follicle density decreased over time concomitant with an increase in degenerated (primordial and activated preantral) follicles in both treatment groups. Healthy activated preantral follicle density did not differ between the two culture systems at a given time. In CAM group, blood vessel density increased over time (p = 0.015). The second objective of this thesis was to develop a suitable vitrification protocol for bovine ovarian tissue. The viability of bovine ovarian tissue vitrified using two non-permeating cryoprotectants (sucrose and trehalose) and two cryodevices (cryotop and cryovial) was assessed. We hypothesized that during vitrification the higher cooling rate on the cryotop (open vitrification method) will yield better post-thaw viability of bovine ovarian tissue as compared to the cryovial (closed vitrification method). We also hypothesized that trehalose is a superior non-permeating cryoprotectant to sucrose for vitrification of bovine ovarian tissue. The ovarian tissue was fragmented (1-2mm3) and divided into 6 different treatment groups. Tissues were vitrified in TCM199 supplemented with 15% EG, 15% DMSO, 20% calf serum and 0.5M sucrose or trehalose then placed in a cryovial or on a cryotop. After warming, the vitrified tissues were either immediately placed in 10% formalin (control) or on the chorioallantoic membrane of a 10-day old chicken embryo for 5 days. Follicles from control and vitrified tissue were observed under a light microscope for normal morphology and the total, normal and degenerated follicle densities were determined by standard stereological procedures. Sucrose and trehalose did not differ, nor was a difference observed between the cryovial and the cryotop for total, healthy or… Advisors/Committee Members: Anzar, Muhammad, Singh, Jaswant, Honaramooz, Ali, Malhi, Pritpal.

Subjects/Keywords: CAM; cattle; chick embryo; cryodamage; cryotop; cryovial; follicle; in ovo culture; in vitro culture; ovary; sucrose; trehalose; vitrification;

14 more images…

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APA (6^th Edition):

Beck, K. (2015). VITRIFICATION AND CHORIOALLANTOIC MEMBRANE (CAM) CULTURE OF BOVINE OVARIAN TISSUE. (Thesis). University of Saskatchewan. Retrieved from http://hdl.handle.net/10388/ETD-2015-05-2051

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16^th Edition):

Beck, Kylie. “VITRIFICATION AND CHORIOALLANTOIC MEMBRANE (CAM) CULTURE OF BOVINE OVARIAN TISSUE.” 2015. Thesis, University of Saskatchewan. Accessed January 15, 2021. http://hdl.handle.net/10388/ETD-2015-05-2051.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7^th Edition):

Beck, Kylie. “VITRIFICATION AND CHORIOALLANTOIC MEMBRANE (CAM) CULTURE OF BOVINE OVARIAN TISSUE.” 2015. Web. 15 Jan 2021.

Vancouver:

Beck K. VITRIFICATION AND CHORIOALLANTOIC MEMBRANE (CAM) CULTURE OF BOVINE OVARIAN TISSUE. [Internet] [Thesis]. University of Saskatchewan; 2015. [cited 2021 Jan 15]. Available from: http://hdl.handle.net/10388/ETD-2015-05-2051.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Beck K. VITRIFICATION AND CHORIOALLANTOIC MEMBRANE (CAM) CULTURE OF BOVINE OVARIAN TISSUE. [Thesis]. University of Saskatchewan; 2015. Available from: http://hdl.handle.net/10388/ETD-2015-05-2051

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

16. 石川, 清乃. アスタキサンチンは抗酸化作用によって鶏胚におけるグルココルチコイド誘発白内障を抑制した : Effect of astaxanthin on cataract formation induced by glucocorticoids in the chick embryo.

Degree: 医学博士, 2015, Iwate Medical University / 岩手医科大学

URL: http://id.nii.ac.jp/1181/00005428/

2015

Subjects/Keywords: Cataract; glucocorticoid; astaxanthin; oxidative stress; chick embryo

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APA (6^th Edition):

石川, �. (2015). アスタキサンチンは抗酸化作用によって鶏胚におけるグルココルチコイド誘発白内障を抑制した : Effect of astaxanthin on cataract formation induced by glucocorticoids in the chick embryo. (Thesis). Iwate Medical University / 岩手医科大学. Retrieved from http://id.nii.ac.jp/1181/00005428/

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16^th Edition):

石川, 清乃. “アスタキサンチンは抗酸化作用によって鶏胚におけるグルココルチコイド誘発白内障を抑制した : Effect of astaxanthin on cataract formation induced by glucocorticoids in the chick embryo.” 2015. Thesis, Iwate Medical University / 岩手医科大学. Accessed January 15, 2021. http://id.nii.ac.jp/1181/00005428/.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7^th Edition):

石川, 清乃. “アスタキサンチンは抗酸化作用によって鶏胚におけるグルココルチコイド誘発白内障を抑制した : Effect of astaxanthin on cataract formation induced by glucocorticoids in the chick embryo.” 2015. Web. 15 Jan 2021.

Vancouver:

石川 �. アスタキサンチンは抗酸化作用によって鶏胚におけるグルココルチコイド誘発白内障を抑制した : Effect of astaxanthin on cataract formation induced by glucocorticoids in the chick embryo. [Internet] [Thesis]. Iwate Medical University / 岩手医科大学; 2015. [cited 2021 Jan 15]. Available from: http://id.nii.ac.jp/1181/00005428/.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

石川 �. アスタキサンチンは抗酸化作用によって鶏胚におけるグルココルチコイド誘発白内障を抑制した : Effect of astaxanthin on cataract formation induced by glucocorticoids in the chick embryo. [Thesis]. Iwate Medical University / 岩手医科大学; 2015. Available from: http://id.nii.ac.jp/1181/00005428/

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

East Carolina University

17. Jiang, Qixiao. Perfluorooctanoic acid-induced developmental cardiotoxicity in an avian model.

Degree: PhD, Pharmacology and Toxicology, 2013, East Carolina University

URL: http://hdl.handle.net/10342/1818

► Perfluorooctanoic acid (PFOA) is a synthetic chemical used in polyfluormer production. It is a widespread environmental contaminant and is known to induce developmental toxicity in… (more)

▼ Perfluorooctanoic acid (PFOA) is a synthetic chemical used in polyfluormer production. It is a widespread environmental contaminant and is known to induce developmental toxicity in rodent models. As several related compounds also induce developmental cardiotoxicity in avian models, a series of experiments were carried out in chicken embryos and hatchling chickens to assess the effects of PFOA on developing hearts and to explore underlying mechanisms. Histology was used to assess late stage embryo hearts and echocardiography was used to assess morphological and functional parameters of hearts in living one-day-old hatchlings. Hearts of exposed embryos had a thinned right ventricular wall and multiple morphological and functional changes were detected in the left ventricles of exposed hatchlings. As PFOA is known to activate the peroxisome proliferator activated receptor Ã¡ (PPARÃ¡) in rodent models, the PPARÃ¡ agonist WY 14,643 was used to assess the role of PPARÃ¡ in PFOA-induced developmental cardiotoxicity. Real-time polymerase chain reaction (PCR) and western blot were used to assess hearts of early stage embryos for expression of genes related to heart development. WY 14,643 partially mimicked the morphological and functional effects of PFOA only in the left ventricle of hearts of hatchling chickens and bone morphogenic protein 2 (BMP2) signaling pathways were involved in mediating the process. Additionally, primary cardiomyocyte cultures were used to explore mechanisms of toxicity at the cellular level. Viability, contractility, and reactive oxygen species (ROS) generation were evaluated in primary cardiomyocytes isolated from hearts of embryos exposed to PFOA in ovo or were exposed in vitro. Primary cardiomyocytes isolated from embryos exposed to PFOA in ovo functioned similarly to hearts of exposed hatchling chickens. Primary cardiomyocytes exposed in vitro responded differently, suggesting that the cardiotoxicity is likely from interference of PFOA in an early stage of heart development rather than from overt cytotoxicity to cardiomyocytes. In conclusion, this dissertation work indicates that PFOA induces morphological and functional alterations in hearts of chicken embryos and hatchling chickens, that mechanisms of the cardiotoxicity may involve PPARÃ¡ and BMP2 signaling pathways, and that PFOA is likely interfering in an early stage of heart development.Â Â Advisors/Committee Members: DeWitt, Jamie C. (advisor).

Subjects/Keywords: Toxicology; Avian; Cardiotoxicity; Developmental toxicity; Perfluorooctanoic acid; Fluorocarbons – toxicity; Chick Embryo – embryology; Heart – embryology; Models, Animal

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APA (6^th Edition):

Jiang, Q. (2013). Perfluorooctanoic acid-induced developmental cardiotoxicity in an avian model. (Doctoral Dissertation). East Carolina University. Retrieved from http://hdl.handle.net/10342/1818

Chicago Manual of Style (16^th Edition):

Jiang, Qixiao. “Perfluorooctanoic acid-induced developmental cardiotoxicity in an avian model.” 2013. Doctoral Dissertation, East Carolina University. Accessed January 15, 2021. http://hdl.handle.net/10342/1818.

MLA Handbook (7^th Edition):

Jiang, Qixiao. “Perfluorooctanoic acid-induced developmental cardiotoxicity in an avian model.” 2013. Web. 15 Jan 2021.

Vancouver:

Jiang Q. Perfluorooctanoic acid-induced developmental cardiotoxicity in an avian model. [Internet] [Doctoral dissertation]. East Carolina University; 2013. [cited 2021 Jan 15]. Available from: http://hdl.handle.net/10342/1818.

Council of Science Editors:

Jiang Q. Perfluorooctanoic acid-induced developmental cardiotoxicity in an avian model. [Doctoral Dissertation]. East Carolina University; 2013. Available from: http://hdl.handle.net/10342/1818

University of Saskatchewan

18. Karunarathna, Ruwani. Incidence and pathogenesis of enterococcus associated chicken embryo and neonatal mortality.

Degree: 2019, University of Saskatchewan

URL: http://hdl.handle.net/10388/12511

► Chicken embryo mortality and yolk sac infections (YSI) of neonatal chickens cause a significant economic loss to the poultry industry. In recent years, an emergence… (more)

▼ Chicken embryo mortality and yolk sac infections (YSI) of neonatal chickens cause a significant economic loss to the poultry industry. In recent years, an emergence of Enterococcus associated YSI in neonatal broiler chickens was reported in many countries around the world including Canada, but reasons associated with the emergence of enterococcal infections in poultry were not understood. Although Escherichia coli was predominantly isolated from dead embryos and YSI in neonatal chickens in the past, enterococci emerged as the main bacterial species from these incidents in the western Canadian poultry industry. Hence, our main objectives were to identify the incidence of enterococci in commercial hatcheries in western Canada associated with embryonic death and to study the pathogenesis of embryonic and neonatal death related with enterococci. Chicken embryo death could result from many reasons, but as described in Chapter 2, 65.82% of yolk materials from non-viable chicken embryos were positive for at least one bacterial species. Enterococci was predominantly isolated from non-viable chicken embryos followed by E. coli. E. faecalis was the predominant enterococcal isolate followed by E. faecium. While polymicrobial growths were common, 56% of the embryos were co-infected with E. faecalis and E. coli. We have demonstrated that matrix-assisted laser desorption/ionization time-of-flight mass spectrometry can distinguish enterococci into the species level with 97.18% accuracy, and can be applied for use in routine poultry pathogen identification. In the third chapter, we have demonstrated that the majority of isolated enterococci and E. coli are multidrug resistant and highlighted the urgency of antimicrobial resistance surveillance in this reservoir of non-viable chicken embryos to understand antimicrobial resistance dissemination and its control. In the fourth chapter, we have utilized an egg infection model to understand the pathogenesis of enterococci and E. coli. We were able to demonstrate that E. faecalis was able to penetrate the eggshell, and colonize internal organs of chicken embryos without causing inflammation or death. However, once E. faecalis co-infected with E. coli, it led to high chick mortality due to septicemia and associated increased proinflammatory cytokines prior to hatch. Overall, our research findings highlight the importance of maintaining proper hygienic and biosecurity measures in commercial hatcheries and poultry production facilities in order to minimize bacterial contamination of hatching eggs to control neonatal chicken mortality. Advisors/Committee Members: Gomis, Susantha, Ngeleka, Musangu, Wobeser, Bruce, Willson, Philip, Simko, Elemir.

Subjects/Keywords: Enterococci; E. coli; Chicken embryo death; Neonatal Chick Mortality; Yolk sac infections; Multidrug resistant enterococci; Pathogenesis

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APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6^th Edition):

Karunarathna, R. (2019). Incidence and pathogenesis of enterococcus associated chicken embryo and neonatal mortality. (Thesis). University of Saskatchewan. Retrieved from http://hdl.handle.net/10388/12511

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16^th Edition):

Karunarathna, Ruwani. “Incidence and pathogenesis of enterococcus associated chicken embryo and neonatal mortality.” 2019. Thesis, University of Saskatchewan. Accessed January 15, 2021. http://hdl.handle.net/10388/12511.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7^th Edition):

Karunarathna, Ruwani. “Incidence and pathogenesis of enterococcus associated chicken embryo and neonatal mortality.” 2019. Web. 15 Jan 2021.

Vancouver:

Karunarathna R. Incidence and pathogenesis of enterococcus associated chicken embryo and neonatal mortality. [Internet] [Thesis]. University of Saskatchewan; 2019. [cited 2021 Jan 15]. Available from: http://hdl.handle.net/10388/12511.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Karunarathna R. Incidence and pathogenesis of enterococcus associated chicken embryo and neonatal mortality. [Thesis]. University of Saskatchewan; 2019. Available from: http://hdl.handle.net/10388/12511

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

19. Bertacini, Paula Valença. Material particulado fino presente no ar da cidade de São Paulo promove alterações nas células de Purkinje: um estudo experimental em embrião de galinha.

Degree: PhD, Fisiopatologia Experimental, 2011, University of São Paulo

URL: http://www.teses.usp.br/teses/disponiveis/5/5160/tde-24052011-145330/ ;

►

A poluição do ar é associada a diferentes patologias inclusive as que afetam o sistema nervoso central. O objetivo deste estudo foi avaliar o efeito… (more)

▼

A poluição do ar é associada a diferentes patologias inclusive as que afetam o sistema nervoso central. O objetivo deste estudo foi avaliar o efeito do material particulado fino (PM2,5) da cidade de São Paulo nas células de Purkinje de embriões de galinha. Dose única de PM2,5 em suspensão (1,5 ou 20,0 Pg.100Pl-1) foi injetada em ovos fertilizados de galinha em E0 foram artificialmente incubados por 18 dias (E18). Análises morfométricas no cerebelo foram realizadas em material submetido à reação imuno-histoquímica com anticorpos dirigidos à calbindina (CB), ao fator neurotrófico derivado do encéfalo (BDNF) e à caspase 3 (CAS) para avaliação da densidade de células de Purkinje, de seus dendritos e da taxa de apoptose nestas células. A expressão do BDNF no cerebelo foi determinada pelo método de immunoblotting. A ocorrência de elementos traço e de peroxidação lipídica no cerebelo foi avaliada, assim como a atividade da superóxido dismutase (SOD) e da catalase. Não foram observadas diferenças no desenvolvimento geral e na taxa de mortalidade dos embriões submetidos ao PM2,5 em comparação aos controles. Embora o PM2.5 em suspensão tenha apresentado elevada quantidade de elementos traço, depleção na concentrações de elementos como Cu, Mg, Mn, Se e Zn foi observada no cerebelo dos animais. Comparados ao controle salina, animais submetidos às concentrações de PM2,5 apresentaram diminuição da densidade de células de Purkinje CB+ nos grupos PM2,5 (18% no PM2,51,5 Pg e 23% no grupo PM2,5 20,0 Pg). Aumento de 45% na densidade de dendritos das células de Purkinje no grupo exposto a PM2,5 20,0 Pg foi observado. Redução significativa na expressão de BDNF no cerebelo e também na densidade de células de Purkinje BDNF+ no grupo PM2,5 20,0 Pg foi observada em relação aos controles e ao grupo PM2,51,5 Pg. A ocorrência de células de Purkinje apoptóticas não variou entre os grupos deste estudo da mesma forma em que a peroxidação lipídica e a atividade de SOD também não variaram. Contudo, foi observada maior atividade da catalase no cerebelo dos animais expostos ao material particulado. Conclusão: O material particulado fino da cidade de São Paulo afetou o desenvolvimento embrionário das células de Purkinje no modelo empregado e promoveu a ativação de mecanismos antioxidantes. A composição elementar do material particulado da cidade de São Paulo pode estar associada à perturbação da poda dendrítica nas células de Purkinje

Air pollutants are associated to several diseases including those related to central nervous system. The aim of this work was to evaluate the effect of urban fine particles (PM2.5) in chicken embryo Purkinje cells. A single dose of PM2.5 suspension in two different concentrations (1.5 or 20.0 Pg.100Pl-1) was injected in fresh laid fertilized eggs on E0. Control groups were performed (intact and saline groups). After 18 days of embryo incubation (E18), no differences in general abnormal development and mortality ratio were found between groups. Cerebellar morphometrical analysis for neuronal density, dendritic outgrowth…

Advisors/Committee Members: Negri, Elnara Márcia.

Subjects/Keywords: Air pollution; Células de Purkinje; Cerebellum; Cerebelo; Chick embryo; Desenvolvimento embrionário; Embrião de galinha; Embryo development; Material particulado; Particulate matter; Poluição do ar; Purkinje cells

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APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6^th Edition):

Bertacini, P. V. (2011). Material particulado fino presente no ar da cidade de São Paulo promove alterações nas células de Purkinje: um estudo experimental em embrião de galinha. (Doctoral Dissertation). University of São Paulo. Retrieved from http://www.teses.usp.br/teses/disponiveis/5/5160/tde-24052011-145330/ ;

Chicago Manual of Style (16^th Edition):

Bertacini, Paula Valença. “Material particulado fino presente no ar da cidade de São Paulo promove alterações nas células de Purkinje: um estudo experimental em embrião de galinha.” 2011. Doctoral Dissertation, University of São Paulo. Accessed January 15, 2021. http://www.teses.usp.br/teses/disponiveis/5/5160/tde-24052011-145330/ ;.

MLA Handbook (7^th Edition):

Bertacini, Paula Valença. “Material particulado fino presente no ar da cidade de São Paulo promove alterações nas células de Purkinje: um estudo experimental em embrião de galinha.” 2011. Web. 15 Jan 2021.

Vancouver:

Bertacini PV. Material particulado fino presente no ar da cidade de São Paulo promove alterações nas células de Purkinje: um estudo experimental em embrião de galinha. [Internet] [Doctoral dissertation]. University of São Paulo; 2011. [cited 2021 Jan 15]. Available from: http://www.teses.usp.br/teses/disponiveis/5/5160/tde-24052011-145330/ ;.

Council of Science Editors:

Bertacini PV. Material particulado fino presente no ar da cidade de São Paulo promove alterações nas células de Purkinje: um estudo experimental em embrião de galinha. [Doctoral Dissertation]. University of São Paulo; 2011. Available from: http://www.teses.usp.br/teses/disponiveis/5/5160/tde-24052011-145330/ ;

20. Picard, Cyril. Caractérisation de nouvelles subpopulations de progéniteurs musculaires au cours du développement embryonnaire des amniotes : Nanocomposites poreux à base de nanoparticules métalliques : de la synthèse vers des applications dans le domaine de l'adsorption.

Degree: Docteur es, Biologie du developpement, 2013, Aix Marseille Université

URL: http://www.theses.fr/2013AIXM4000

►

Chez les vertébrés, les muscles squelettiques du corps sont dérivés de la partie dorsale dessomites, le dermomyotome, structure transitoire mésodermique. Une première étape demyogenèse aboutit… (more)

▼

Chez les vertébrés, les muscles squelettiques du corps sont dérivés de la partie dorsale dessomites, le dermomyotome, structure transitoire mésodermique. Une première étape demyogenèse aboutit à la formation d’un muscle primitif, le myotome primaire, à partir desbordures du dermomyotome : ces cellules constituent les premières fibres musculaires, et formentl’architecture de base du futur muscle. Dans un second temps, une population de progéniteursmusculaires émerge de la région centrale du dermomyotome. Cette population est primordialedans la constitution du muscle. Elle prolifère, et une partie d’entre elle fusionne aux fibresexistantes pour donner les fibres multinucléées adultes. Finalement, une partie des progéniteursmusculaires reste indifférenciée jusqu’à l’âge adulte et compose la population de cellules souchesmusculaires, les cellules satellites. Ainsi, les progéniteurs musculaires contribuent audéveloppement musculaire tout au long du développement embryonnaire et foetal, mais égalementà la myogenèse post-natale avec les cellules satellites.Lors de ma thèse, je me suis intéressé à cette population de progéniteurs musculaires. Deux souspopulationsde progéniteurs musculaires ont précédemment été identifiées dans notre laboratoireau cours de l’embryogénèse précoce de poulet, l’une exprimant le facteur de transcription Pax7,l’autre co-exprimant Pax7 et le facteur de différenciation myogénique précoce Myf5. Face àl’absence de données concernant les progéniteurs musculaires, et à l’importance de cettepopulation pour la myogenèse, j’ai réalisé une étude systématique des progéniteurs musculairestout au long du développement embryonnaire et foetal de deux organismes modèles : le poulet etla souris. J’ai pu montrer que ces deux sous-populations coexistent tout au long dudéveloppement, depuis l’émergence des progéniteurs de la partie centrale du dermomyotome,jusqu’au moment où ces cellules deviennent des cellules satellites à la fin du développementfoetal. De manière très intéressante, j’ai pu montrer qu’au sein des progéniteurs musculaires, lapopulation principale co-exprime Pax7 et Myf5, et prolifère activement, alors que la populationPax7 est mineure et prolifère à un taux moins élevé. Cette dernière entre de manière importanteen quiescence à la fin du développement embryonnaire. Ces caractéristiques sont semblablesentre le poulet et la souris, et montrent que des stratégies cellulaires et moléculaires similairessont conservées au sein des amniotes.

Duringembryonicandfetallife,skeletalmusclegrowthisdependentupontheproliferationandthedifferentiationofapopulationofresidentmuscleprogenitors,fromwhichderivethemusclestemcellsof theadult,thesatellitecells.Underpoorlydefinedextrinsicandintrinsicinfluences,muscleprogenitorsproliferate,differentiateorenteraquiescentstatetobecomereservesatellitecells.Despitetheir…

Advisors/Committee Members: Marcelle, Christophe (thesis director).

Subjects/Keywords: Progéniteurs musculaires; Pax7; Myf5; Embryon de poulet; Embryon de souris; Myogénèse; Resident muscle progenitor; Pax7; Myf5; Chick embryo; Mouse embryo; Myogenesis; 571.8

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APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6^th Edition):

Picard, C. (2013). Caractérisation de nouvelles subpopulations de progéniteurs musculaires au cours du développement embryonnaire des amniotes : Nanocomposites poreux à base de nanoparticules métalliques : de la synthèse vers des applications dans le domaine de l'adsorption. (Doctoral Dissertation). Aix Marseille Université. Retrieved from http://www.theses.fr/2013AIXM4000

Chicago Manual of Style (16^th Edition):

Picard, Cyril. “Caractérisation de nouvelles subpopulations de progéniteurs musculaires au cours du développement embryonnaire des amniotes : Nanocomposites poreux à base de nanoparticules métalliques : de la synthèse vers des applications dans le domaine de l'adsorption.” 2013. Doctoral Dissertation, Aix Marseille Université. Accessed January 15, 2021. http://www.theses.fr/2013AIXM4000.

MLA Handbook (7^th Edition):

Picard, Cyril. “Caractérisation de nouvelles subpopulations de progéniteurs musculaires au cours du développement embryonnaire des amniotes : Nanocomposites poreux à base de nanoparticules métalliques : de la synthèse vers des applications dans le domaine de l'adsorption.” 2013. Web. 15 Jan 2021.

Vancouver:

Picard C. Caractérisation de nouvelles subpopulations de progéniteurs musculaires au cours du développement embryonnaire des amniotes : Nanocomposites poreux à base de nanoparticules métalliques : de la synthèse vers des applications dans le domaine de l'adsorption. [Internet] [Doctoral dissertation]. Aix Marseille Université 2013. [cited 2021 Jan 15]. Available from: http://www.theses.fr/2013AIXM4000.

Council of Science Editors:

Picard C. Caractérisation de nouvelles subpopulations de progéniteurs musculaires au cours du développement embryonnaire des amniotes : Nanocomposites poreux à base de nanoparticules métalliques : de la synthèse vers des applications dans le domaine de l'adsorption. [Doctoral Dissertation]. Aix Marseille Université 2013. Available from: http://www.theses.fr/2013AIXM4000

21. 前田, 可奈子. Effect of green tea polyphenols on glucocorticoid-induced cataract formation in chick embryo : ステロイド誘発鶏胚白内障モデルにおける緑茶ポリフェノールの効果.

Degree: 医学博士, 2017, Iwate Medical University / 岩手医科大学

URL: http://id.nii.ac.jp/1181/00008804/

2016

Subjects/Keywords: cataract; glucocorticoid; green tea polyphenols; oxidative stress; chick embryo; cataract; glucocorticoid; green tea polyphenols; oxidative stress; chick embryo

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APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6^th Edition):

前田, �. (2017). Effect of green tea polyphenols on glucocorticoid-induced cataract formation in chick embryo : ステロイド誘発鶏胚白内障モデルにおける緑茶ポリフェノールの効果. (Thesis). Iwate Medical University / 岩手医科大学. Retrieved from http://id.nii.ac.jp/1181/00008804/

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16^th Edition):

前田, 可奈子. “Effect of green tea polyphenols on glucocorticoid-induced cataract formation in chick embryo : ステロイド誘発鶏胚白内障モデルにおける緑茶ポリフェノールの効果.” 2017. Thesis, Iwate Medical University / 岩手医科大学. Accessed January 15, 2021. http://id.nii.ac.jp/1181/00008804/.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7^th Edition):

前田, 可奈子. “Effect of green tea polyphenols on glucocorticoid-induced cataract formation in chick embryo : ステロイド誘発鶏胚白内障モデルにおける緑茶ポリフェノールの効果.” 2017. Web. 15 Jan 2021.

Vancouver:

前田 �. Effect of green tea polyphenols on glucocorticoid-induced cataract formation in chick embryo : ステロイド誘発鶏胚白内障モデルにおける緑茶ポリフェノールの効果. [Internet] [Thesis]. Iwate Medical University / 岩手医科大学; 2017. [cited 2021 Jan 15]. Available from: http://id.nii.ac.jp/1181/00008804/.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

前田 �. Effect of green tea polyphenols on glucocorticoid-induced cataract formation in chick embryo : ステロイド誘発鶏胚白内障モデルにおける緑茶ポリフェノールの効果. [Thesis]. Iwate Medical University / 岩手医科大学; 2017. Available from: http://id.nii.ac.jp/1181/00008804/

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Oregon State University

22. Stauber, Leah. Involvement of the Ets-1 transcription factor in early bovine and porcine embryo development.

Degree: PhD, Animal Science, 2010, Oregon State University

URL: http://hdl.handle.net/1957/19626

► Early embryo development is dependent on maternally derived RNA and protein synthesized during oogenesis. In the bovine embryo this dependence lasts until the 8-16 cell… (more)

Subjects/Keywords: embryo

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APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6^th Edition):

Stauber, L. (2010). Involvement of the Ets-1 transcription factor in early bovine and porcine embryo development. (Doctoral Dissertation). Oregon State University. Retrieved from http://hdl.handle.net/1957/19626

Chicago Manual of Style (16^th Edition):

Stauber, Leah. “Involvement of the Ets-1 transcription factor in early bovine and porcine embryo development.” 2010. Doctoral Dissertation, Oregon State University. Accessed January 15, 2021. http://hdl.handle.net/1957/19626.

MLA Handbook (7^th Edition):

Stauber, Leah. “Involvement of the Ets-1 transcription factor in early bovine and porcine embryo development.” 2010. Web. 15 Jan 2021.

Vancouver:

Stauber L. Involvement of the Ets-1 transcription factor in early bovine and porcine embryo development. [Internet] [Doctoral dissertation]. Oregon State University; 2010. [cited 2021 Jan 15]. Available from: http://hdl.handle.net/1957/19626.

Council of Science Editors:

Stauber L. Involvement of the Ets-1 transcription factor in early bovine and porcine embryo development. [Doctoral Dissertation]. Oregon State University; 2010. Available from: http://hdl.handle.net/1957/19626

23. Finn, Thomas P. The role of chick ciliary neurotrophic factor in regulating cell death in ciliary ganglion neurons.

Degree: PhD, 1997, Oregon Health Sciences University

URL: doi:10.6083/M4736P4C ; http://digitalcommons.ohsu.edu/etd/2653

Subjects/Keywords: Nerve Growth Factors; Chick Embryo; Nerve Tissue Proteins; Neurons; Ganglia; Cell Death

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APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6^th Edition):

Finn, T. P. (1997). The role of chick ciliary neurotrophic factor in regulating cell death in ciliary ganglion neurons. (Doctoral Dissertation). Oregon Health Sciences University. Retrieved from doi:10.6083/M4736P4C ; http://digitalcommons.ohsu.edu/etd/2653

Chicago Manual of Style (16^th Edition):

Finn, Thomas P. “The role of chick ciliary neurotrophic factor in regulating cell death in ciliary ganglion neurons.” 1997. Doctoral Dissertation, Oregon Health Sciences University. Accessed January 15, 2021. doi:10.6083/M4736P4C ; http://digitalcommons.ohsu.edu/etd/2653.

MLA Handbook (7^th Edition):

Finn, Thomas P. “The role of chick ciliary neurotrophic factor in regulating cell death in ciliary ganglion neurons.” 1997. Web. 15 Jan 2021.

Vancouver:

Finn TP. The role of chick ciliary neurotrophic factor in regulating cell death in ciliary ganglion neurons. [Internet] [Doctoral dissertation]. Oregon Health Sciences University; 1997. [cited 2021 Jan 15]. Available from: doi:10.6083/M4736P4C ; http://digitalcommons.ohsu.edu/etd/2653.

Council of Science Editors:

Finn TP. The role of chick ciliary neurotrophic factor in regulating cell death in ciliary ganglion neurons. [Doctoral Dissertation]. Oregon Health Sciences University; 1997. Available from: doi:10.6083/M4736P4C ; http://digitalcommons.ohsu.edu/etd/2653

24. Le, Anh-Chi N. Regulation of gap junctional intercellular communication in the vertebrate lens.

Degree: PhD, 2000, Oregon Health Sciences University

URL: doi:10.6083/M45X277G ; http://digitalcommons.ohsu.edu/etd/3289

Subjects/Keywords: Lens, Crystalline; Gap Junctions; Cell Communication; Chick Embryo; Fibroblast Growth Factors

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APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6^th Edition):

Le, A. N. (2000). Regulation of gap junctional intercellular communication in the vertebrate lens. (Doctoral Dissertation). Oregon Health Sciences University. Retrieved from doi:10.6083/M45X277G ; http://digitalcommons.ohsu.edu/etd/3289

Chicago Manual of Style (16^th Edition):

Le, Anh-Chi N. “Regulation of gap junctional intercellular communication in the vertebrate lens.” 2000. Doctoral Dissertation, Oregon Health Sciences University. Accessed January 15, 2021. doi:10.6083/M45X277G ; http://digitalcommons.ohsu.edu/etd/3289.

MLA Handbook (7^th Edition):

Le, Anh-Chi N. “Regulation of gap junctional intercellular communication in the vertebrate lens.” 2000. Web. 15 Jan 2021.

Vancouver:

Le AN. Regulation of gap junctional intercellular communication in the vertebrate lens. [Internet] [Doctoral dissertation]. Oregon Health Sciences University; 2000. [cited 2021 Jan 15]. Available from: doi:10.6083/M45X277G ; http://digitalcommons.ohsu.edu/etd/3289.

Council of Science Editors:

Le AN. Regulation of gap junctional intercellular communication in the vertebrate lens. [Doctoral Dissertation]. Oregon Health Sciences University; 2000. Available from: doi:10.6083/M45X277G ; http://digitalcommons.ohsu.edu/etd/3289

25. Ho, Alex Tsung-Lin. Myelination in the developing chicken ciliary ganglion.

Degree: PhD, 2003, Oregon Health Sciences University

URL: doi:10.6083/M4TD9VNP ; http://digitalcommons.ohsu.edu/etd/3136

Subjects/Keywords: Myelin Sheath; Ciliary Body – innervation; Neuregulins; Schwann Cells; Chick Embryo; Chickens

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APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6^th Edition):

Ho, A. T. (2003). Myelination in the developing chicken ciliary ganglion. (Doctoral Dissertation). Oregon Health Sciences University. Retrieved from doi:10.6083/M4TD9VNP ; http://digitalcommons.ohsu.edu/etd/3136

Chicago Manual of Style (16^th Edition):

Ho, Alex Tsung-Lin. “Myelination in the developing chicken ciliary ganglion.” 2003. Doctoral Dissertation, Oregon Health Sciences University. Accessed January 15, 2021. doi:10.6083/M4TD9VNP ; http://digitalcommons.ohsu.edu/etd/3136.

MLA Handbook (7^th Edition):

Ho, Alex Tsung-Lin. “Myelination in the developing chicken ciliary ganglion.” 2003. Web. 15 Jan 2021.

Vancouver:

Ho AT. Myelination in the developing chicken ciliary ganglion. [Internet] [Doctoral dissertation]. Oregon Health Sciences University; 2003. [cited 2021 Jan 15]. Available from: doi:10.6083/M4TD9VNP ; http://digitalcommons.ohsu.edu/etd/3136.

Council of Science Editors:

Ho AT. Myelination in the developing chicken ciliary ganglion. [Doctoral Dissertation]. Oregon Health Sciences University; 2003. Available from: doi:10.6083/M4TD9VNP ; http://digitalcommons.ohsu.edu/etd/3136

26. Linakis, James G. Prenatal exposure to alcohol : effects on discrimination learning and conditioned inhibition in the chick :.

Degree: PhD, 1980, Oregon Health Sciences University

URL: doi:10.6083/M47P8WK9 ; http://digitalcommons.ohsu.edu/etd/2320

Subjects/Keywords: Ethanol; Chick Embryo; Discrimination Learning; Fetal Alcohol Syndrome; Inhibition (Psychology)

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APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6^th Edition):

Linakis, J. G. (1980). Prenatal exposure to alcohol : effects on discrimination learning and conditioned inhibition in the chick :. (Doctoral Dissertation). Oregon Health Sciences University. Retrieved from doi:10.6083/M47P8WK9 ; http://digitalcommons.ohsu.edu/etd/2320

Chicago Manual of Style (16^th Edition):

Linakis, James G. “Prenatal exposure to alcohol : effects on discrimination learning and conditioned inhibition in the chick :.” 1980. Doctoral Dissertation, Oregon Health Sciences University. Accessed January 15, 2021. doi:10.6083/M47P8WK9 ; http://digitalcommons.ohsu.edu/etd/2320.

MLA Handbook (7^th Edition):

Linakis, James G. “Prenatal exposure to alcohol : effects on discrimination learning and conditioned inhibition in the chick :.” 1980. Web. 15 Jan 2021.

Vancouver:

Linakis JG. Prenatal exposure to alcohol : effects on discrimination learning and conditioned inhibition in the chick :. [Internet] [Doctoral dissertation]. Oregon Health Sciences University; 1980. [cited 2021 Jan 15]. Available from: doi:10.6083/M47P8WK9 ; http://digitalcommons.ohsu.edu/etd/2320.

Council of Science Editors:

Linakis JG. Prenatal exposure to alcohol : effects on discrimination learning and conditioned inhibition in the chick :. [Doctoral Dissertation]. Oregon Health Sciences University; 1980. Available from: doi:10.6083/M47P8WK9 ; http://digitalcommons.ohsu.edu/etd/2320

University of Cambridge

27. Baillie-Johnson, Peter. The Generation of a Candidate Axial Precursor in Three Dimensional Aggregates of Mouse Embryonic Stem Cells.

Degree: PhD, 2017, University of Cambridge

URL: https://www.repository.cam.ac.uk/handle/1810/267818

► Textbook accounts of vertebrate embryonic development have been based largely upon experiments on amphibian embryos, which have shown that the tissues of the trunk and… (more)

▼ Textbook accounts of vertebrate embryonic development have been based largely upon experiments on amphibian embryos, which have shown that the tissues of the trunk and tail are organised from distinct precursors that existed during gastrulation. In the mouse and chick, however, retrospective clonal analyses and transplantation experiments have demonstrated that the amniote body instead arises progressively from a population of axial precursors that are common to both the neural and mesodermal tissues of the trunk and tail. For this reason, they are known as neuro-mesodermal progenitors (NMps). Detailed studies of NMps have been precluded by their lack of a unique gene expression profile and the technical difficulties associated with isolating them from the embryo. Mouse embryonic stem cells (ESCs) provide the possibility of instead deriving them in vitro. ESCs have been used to model developmental processes, partly through large cellular aggregates known as embryoid bodies. These structures do not, however, resemble the axial organisation of the embryo and they develop in a disordered manner. This thesis presents a novel culture system of small, three-dimensional aggregates of ESCs (gastruloids) that can recreate the events of early post-implantation development, including axial elongation. Gastruloids are the first ESC-based model for axial elongation morphogenesis; this body of work characterises their development and identifies a candidate population of NMps within their elongating tissues. Additionally, this work establishes a xenotransplantation assay for testing the functional properties of in vitro-derived NMp populations in the chicken embryo and applies it to NMps from gastruloid cultures. The results of this assay show that gastruloids are a credible source of NMps in vitro and therefore offer a new experimental means to interrogate their properties. The use of gastruloids to recreate embryonic development has implications for basic research as a synthetic system and for the therapeutic derivation of other embryonic progenitors through bioengineering.

Subjects/Keywords: Gastruloid; Neuro-mesodermal Progenitor; Bioengineering; Embryonic stem cell; Spinal Cord; Embryo; Axial Elongation; Gastrulation; Mouse; Chick; Xenotransplantation; 3D; EPSRC; Anteroposterior; Organoids; Embryonic Organoids

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APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6^th Edition):

Baillie-Johnson, P. (2017). The Generation of a Candidate Axial Precursor in Three Dimensional Aggregates of Mouse Embryonic Stem Cells. (Doctoral Dissertation). University of Cambridge. Retrieved from https://www.repository.cam.ac.uk/handle/1810/267818

Chicago Manual of Style (16^th Edition):

Baillie-Johnson, Peter. “The Generation of a Candidate Axial Precursor in Three Dimensional Aggregates of Mouse Embryonic Stem Cells.” 2017. Doctoral Dissertation, University of Cambridge. Accessed January 15, 2021. https://www.repository.cam.ac.uk/handle/1810/267818.

MLA Handbook (7^th Edition):

Baillie-Johnson, Peter. “The Generation of a Candidate Axial Precursor in Three Dimensional Aggregates of Mouse Embryonic Stem Cells.” 2017. Web. 15 Jan 2021.

Vancouver:

Baillie-Johnson P. The Generation of a Candidate Axial Precursor in Three Dimensional Aggregates of Mouse Embryonic Stem Cells. [Internet] [Doctoral dissertation]. University of Cambridge; 2017. [cited 2021 Jan 15]. Available from: https://www.repository.cam.ac.uk/handle/1810/267818.

Council of Science Editors:

Baillie-Johnson P. The Generation of a Candidate Axial Precursor in Three Dimensional Aggregates of Mouse Embryonic Stem Cells. [Doctoral Dissertation]. University of Cambridge; 2017. Available from: https://www.repository.cam.ac.uk/handle/1810/267818

28. ZANG ZHIJIANG. Regulation of the TRIP-BR1 proto-oncoprotein - a potential therapeutic target for human cutaneous and intracavitory proliferative lesions.

Degree: 2008, National University of Singapore

URL: http://scholarbank.nus.edu.sg/handle/10635/27843

Subjects/Keywords: TRIP-Br1; PP2A; protein phosphatase; E2F; Neoplasm; chick embryo chorioallantoic membrane

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APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6^th Edition):

ZHIJIANG, Z. (2008). Regulation of the TRIP-BR1 proto-oncoprotein - a potential therapeutic target for human cutaneous and intracavitory proliferative lesions. (Thesis). National University of Singapore. Retrieved from http://scholarbank.nus.edu.sg/handle/10635/27843

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16^th Edition):

ZHIJIANG, ZANG. “Regulation of the TRIP-BR1 proto-oncoprotein - a potential therapeutic target for human cutaneous and intracavitory proliferative lesions.” 2008. Thesis, National University of Singapore. Accessed January 15, 2021. http://scholarbank.nus.edu.sg/handle/10635/27843.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7^th Edition):

ZHIJIANG, ZANG. “Regulation of the TRIP-BR1 proto-oncoprotein - a potential therapeutic target for human cutaneous and intracavitory proliferative lesions.” 2008. Web. 15 Jan 2021.

Vancouver:

ZHIJIANG Z. Regulation of the TRIP-BR1 proto-oncoprotein - a potential therapeutic target for human cutaneous and intracavitory proliferative lesions. [Internet] [Thesis]. National University of Singapore; 2008. [cited 2021 Jan 15]. Available from: http://scholarbank.nus.edu.sg/handle/10635/27843.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

ZHIJIANG Z. Regulation of the TRIP-BR1 proto-oncoprotein - a potential therapeutic target for human cutaneous and intracavitory proliferative lesions. [Thesis]. National University of Singapore; 2008. Available from: http://scholarbank.nus.edu.sg/handle/10635/27843

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

University of Cape Town

29. Stander, Cornelia Steynberg. An ultrastructural and light microscopic study of melanocyte differentiation in chick embryos.

Degree: Image, Division of Cell Biology, 1991, University of Cape Town

URL: http://hdl.handle.net/11427/27149

► The embryonic source and chemical nature of those factor/s directing the in vivo differentiation of melanocytes from crest cells are as yet unknown. To begin… (more)

▼ The embryonic source and chemical nature of those factor/s directing the in vivo differentiation of melanocytes from crest cells are as yet unknown. To begin to address this issue, it is important to establish exactly when and where these signa/s first exert their effects. Therefore, in the present study, overtly differentiated melanocytes containing melanin were quantitated in developing Black Australorp X New Hampshire Red chick embryos. In contrast to previous studies, it was found that embryos synthesize melanin from as early as Day 5 of development, and that at this stage, the melanocytes are predominantly dermally located. Between 5 and 8 days, the numbers of both dermal and epidermal melanocytes increase, after which the dermal melanocyte population declines rapidly while the number of epidermal melanocytes continues to increase. These findings suggest that premelanocytes do not have to be epidermally located to initiate terminal differentiation and implicate the dermis as a possible source of melanocyte inducing factor/s. The next step was to examine stages of development prior to the onset of pigment production. For this reason, tyrosinase was purified for use as antigen in the production of a polyclonal antibody. The antibody was tested for specificity by western blotting, - immunocytochemistry and immunoinhibition procedures. Lack of specificity was demonstrated, rendering it unsuitable as an antibody marker for early melanocytes. Fowl melanocytes are thought to differentiate into either eumelanosome- or pheomelanosome synthesizing cells. To test the validity of this concept, embryonic skin of the red/black cross breed were screened for possible mixed type melanocytes by electron microscopy. The melanocytes contained melanosomes with a matrix of irregularly arranged filaments amongst typical eumelanogenic melanosomes. This suggests that these chick melanocytes may synthesize both eumelanosomes and pheomelanosomes in single cells. In a further study on pure breeding New Hampshire Reds, it was found that the melanocytes contained a mixture of typical and less typical pheomelanosomes. Outer membrane indentations in the latter melanosome type suggest that tyrosinase may enter these pheomelanosomes by a mechanism related to that proposed for the melanosomes of goldfish. Advisors/Committee Members: Kidson, Susan H (advisor).

Subjects/Keywords: Cell Biology; Cell differentiation.; Chick embryo - Embryology.; Melanins.; Melanocytes - Ultrastructure

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APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6^th Edition):

Stander, C. S. (1991). An ultrastructural and light microscopic study of melanocyte differentiation in chick embryos. (Thesis). University of Cape Town. Retrieved from http://hdl.handle.net/11427/27149

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16^th Edition):

Stander, Cornelia Steynberg. “An ultrastructural and light microscopic study of melanocyte differentiation in chick embryos.” 1991. Thesis, University of Cape Town. Accessed January 15, 2021. http://hdl.handle.net/11427/27149.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7^th Edition):

Stander, Cornelia Steynberg. “An ultrastructural and light microscopic study of melanocyte differentiation in chick embryos.” 1991. Web. 15 Jan 2021.

Vancouver:

Stander CS. An ultrastructural and light microscopic study of melanocyte differentiation in chick embryos. [Internet] [Thesis]. University of Cape Town; 1991. [cited 2021 Jan 15]. Available from: http://hdl.handle.net/11427/27149.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Stander CS. An ultrastructural and light microscopic study of melanocyte differentiation in chick embryos. [Thesis]. University of Cape Town; 1991. Available from: http://hdl.handle.net/11427/27149

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

30. Baillie-Johnson, Peter. The generation of a candidate axial precursor in three dimensional aggregates of mouse embryonic stem cells.

Degree: PhD, 2017, University of Cambridge

URL: https://doi.org/10.17863/CAM.13742 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.725553

► Textbook accounts of vertebrate embryonic development have been based largely upon experiments on amphibian embryos, which have shown that the tissues of the trunk and… (more)

▼ Textbook accounts of vertebrate embryonic development have been based largely upon experiments on amphibian embryos, which have shown that the tissues of the trunk and tail are organised from distinct precursors that existed during gastrulation. In the mouse and chick, however, retrospective clonal analyses and transplantation experiments have demonstrated that the amniote body instead arises progressively from a population of axial precursors that are common to both the neural and mesodermal tissues of the trunk and tail. For this reason, they are known as neuro-mesodermal progenitors (NMps). Detailed studies of NMps have been precluded by their lack of a unique gene expression profile and the technical difficulties associated with isolating them from the embryo. Mouse embryonic stem cells (ESCs) provide the possibility of instead deriving them in vitro. ESCs have been used to model developmental processes, partly through large cellular aggregates known as embryoid bodies. These structures do not, however, resemble the axial organisation of the embryo and they develop in a disordered manner. This thesis presents a novel culture system of small, three-dimensional aggregates of ESCs (gastruloids) that can recreate the events of early post-implantation development, including axial elongation. Gastruloids are the first ESC-based model for axial elongation morphogenesis; this body of work characterises their development and identifies a candidate population of NMps within their elongating tissues. Additionally, this work establishes a xenotransplantation assay for testing the functional properties of in vitro-derived NMp populations in the chicken embryo and applies it to NMps from gastruloid cultures. The results of this assay show that gastruloids are a credible source of NMps in vitro and therefore offer a new experimental means to interrogate their properties. The use of gastruloids to recreate embryonic development has implications for basic research as a synthetic system and for the therapeutic derivation of other embryonic progenitors through bioengineering.

Subjects/Keywords: 612.6; Gastruloid; Neuro-mesodermal Progenitor; Bioengineering; Embryonic stem cell; Spinal Cord; Embryo; Axial Elongation; Gastrulation; Mouse; Chick; Xenotransplantation; 3D; EPSRC; Anteroposterior; Organoids; Embryonic Organoids

10 more images…

Record Details Similar Records Cite « Share

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APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6^th Edition):

Baillie-Johnson, P. (2017). The generation of a candidate axial precursor in three dimensional aggregates of mouse embryonic stem cells. (Doctoral Dissertation). University of Cambridge. Retrieved from https://doi.org/10.17863/CAM.13742 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.725553

Chicago Manual of Style (16^th Edition):

Baillie-Johnson, Peter. “The generation of a candidate axial precursor in three dimensional aggregates of mouse embryonic stem cells.” 2017. Doctoral Dissertation, University of Cambridge. Accessed January 15, 2021. https://doi.org/10.17863/CAM.13742 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.725553.

MLA Handbook (7^th Edition):

Baillie-Johnson, Peter. “The generation of a candidate axial precursor in three dimensional aggregates of mouse embryonic stem cells.” 2017. Web. 15 Jan 2021.

Vancouver:

Baillie-Johnson P. The generation of a candidate axial precursor in three dimensional aggregates of mouse embryonic stem cells. [Internet] [Doctoral dissertation]. University of Cambridge; 2017. [cited 2021 Jan 15]. Available from: https://doi.org/10.17863/CAM.13742 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.725553.

Council of Science Editors:

Baillie-Johnson P. The generation of a candidate axial precursor in three dimensional aggregates of mouse embryonic stem cells. [Doctoral Dissertation]. University of Cambridge; 2017. Available from: https://doi.org/10.17863/CAM.13742 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.725553

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