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You searched for subject:(Cytology). Showing records 1 – 30 of 1364 total matches.

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Columbia University

1. Higuchi-Sanabria, Ryo. A Mother’s Sacrifice: The contribution of asymmetric cell division to lifespan regulation in Saccharomyces cerevisiae.

Degree: 2015, Columbia University

 Aging determinants are asymmetrically distributed during cell division in S. cerevisiae, which leads to production of an immaculate, age-free daughter cell. During this process, damaged… (more)

Subjects/Keywords: Cytology

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APA (6th Edition):

Higuchi-Sanabria, R. (2015). A Mother’s Sacrifice: The contribution of asymmetric cell division to lifespan regulation in Saccharomyces cerevisiae. (Doctoral Dissertation). Columbia University. Retrieved from https://doi.org/10.7916/D8J67GDW

Chicago Manual of Style (16th Edition):

Higuchi-Sanabria, Ryo. “A Mother’s Sacrifice: The contribution of asymmetric cell division to lifespan regulation in Saccharomyces cerevisiae.” 2015. Doctoral Dissertation, Columbia University. Accessed October 21, 2019. https://doi.org/10.7916/D8J67GDW.

MLA Handbook (7th Edition):

Higuchi-Sanabria, Ryo. “A Mother’s Sacrifice: The contribution of asymmetric cell division to lifespan regulation in Saccharomyces cerevisiae.” 2015. Web. 21 Oct 2019.

Vancouver:

Higuchi-Sanabria R. A Mother’s Sacrifice: The contribution of asymmetric cell division to lifespan regulation in Saccharomyces cerevisiae. [Internet] [Doctoral dissertation]. Columbia University; 2015. [cited 2019 Oct 21]. Available from: https://doi.org/10.7916/D8J67GDW.

Council of Science Editors:

Higuchi-Sanabria R. A Mother’s Sacrifice: The contribution of asymmetric cell division to lifespan regulation in Saccharomyces cerevisiae. [Doctoral Dissertation]. Columbia University; 2015. Available from: https://doi.org/10.7916/D8J67GDW


Columbia University

2. Nathwani, Bhavik Bharat. Structural characterization of primary cilia using accelerated piezoelectrically driven STED nanoscopy.

Degree: 2012, Columbia University

 Primary cilia are non-motile, hair-like projections occurring on most mammalian cell types. They play essential roles in transduction of chemical and mechanical signals across the… (more)

Subjects/Keywords: Cytology

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APA (6th Edition):

Nathwani, B. B. (2012). Structural characterization of primary cilia using accelerated piezoelectrically driven STED nanoscopy. (Doctoral Dissertation). Columbia University. Retrieved from https://doi.org/10.7916/D8NG4XR9

Chicago Manual of Style (16th Edition):

Nathwani, Bhavik Bharat. “Structural characterization of primary cilia using accelerated piezoelectrically driven STED nanoscopy.” 2012. Doctoral Dissertation, Columbia University. Accessed October 21, 2019. https://doi.org/10.7916/D8NG4XR9.

MLA Handbook (7th Edition):

Nathwani, Bhavik Bharat. “Structural characterization of primary cilia using accelerated piezoelectrically driven STED nanoscopy.” 2012. Web. 21 Oct 2019.

Vancouver:

Nathwani BB. Structural characterization of primary cilia using accelerated piezoelectrically driven STED nanoscopy. [Internet] [Doctoral dissertation]. Columbia University; 2012. [cited 2019 Oct 21]. Available from: https://doi.org/10.7916/D8NG4XR9.

Council of Science Editors:

Nathwani BB. Structural characterization of primary cilia using accelerated piezoelectrically driven STED nanoscopy. [Doctoral Dissertation]. Columbia University; 2012. Available from: https://doi.org/10.7916/D8NG4XR9


Columbia University

3. Crouch, Elizabeth. Adult Neural Stem Cells and Their Perivascular Niche.

Degree: 2013, Columbia University

 Stem cells reside in specialized niches that support their selfrenewal and differentiation. A balance between intrinsic and extrinsic signals mediates stem cell quiescence, activation and… (more)

Subjects/Keywords: Cytology

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APA (6th Edition):

Crouch, E. (2013). Adult Neural Stem Cells and Their Perivascular Niche. (Doctoral Dissertation). Columbia University. Retrieved from https://doi.org/10.7916/D8T1531D

Chicago Manual of Style (16th Edition):

Crouch, Elizabeth. “Adult Neural Stem Cells and Their Perivascular Niche.” 2013. Doctoral Dissertation, Columbia University. Accessed October 21, 2019. https://doi.org/10.7916/D8T1531D.

MLA Handbook (7th Edition):

Crouch, Elizabeth. “Adult Neural Stem Cells and Their Perivascular Niche.” 2013. Web. 21 Oct 2019.

Vancouver:

Crouch E. Adult Neural Stem Cells and Their Perivascular Niche. [Internet] [Doctoral dissertation]. Columbia University; 2013. [cited 2019 Oct 21]. Available from: https://doi.org/10.7916/D8T1531D.

Council of Science Editors:

Crouch E. Adult Neural Stem Cells and Their Perivascular Niche. [Doctoral Dissertation]. Columbia University; 2013. Available from: https://doi.org/10.7916/D8T1531D


Columbia University

4. Alaei, Sarah Rose. C-terminal lysines modulate Connexin32 turnover and its ability to suppress growth of Neuro-2a cell cultures.

Degree: 2013, Columbia University

 The extent of gap junction (GJ)-mediated coupling can be modulated through GJ channel gating. However, the amount of connexin protein available for incorporation into GJ,… (more)

Subjects/Keywords: Cytology

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APA (6th Edition):

Alaei, S. R. (2013). C-terminal lysines modulate Connexin32 turnover and its ability to suppress growth of Neuro-2a cell cultures. (Doctoral Dissertation). Columbia University. Retrieved from https://doi.org/10.7916/D8FN15M4

Chicago Manual of Style (16th Edition):

Alaei, Sarah Rose. “C-terminal lysines modulate Connexin32 turnover and its ability to suppress growth of Neuro-2a cell cultures.” 2013. Doctoral Dissertation, Columbia University. Accessed October 21, 2019. https://doi.org/10.7916/D8FN15M4.

MLA Handbook (7th Edition):

Alaei, Sarah Rose. “C-terminal lysines modulate Connexin32 turnover and its ability to suppress growth of Neuro-2a cell cultures.” 2013. Web. 21 Oct 2019.

Vancouver:

Alaei SR. C-terminal lysines modulate Connexin32 turnover and its ability to suppress growth of Neuro-2a cell cultures. [Internet] [Doctoral dissertation]. Columbia University; 2013. [cited 2019 Oct 21]. Available from: https://doi.org/10.7916/D8FN15M4.

Council of Science Editors:

Alaei SR. C-terminal lysines modulate Connexin32 turnover and its ability to suppress growth of Neuro-2a cell cultures. [Doctoral Dissertation]. Columbia University; 2013. Available from: https://doi.org/10.7916/D8FN15M4


Columbia University

5. Guo, Yige. Molecular Mechanisms of Mitotic Spindle Assembly and Accurate Chromosome Segregation.

Degree: 2013, Columbia University

 During the cell cycle, duplicated DNA in S phase is segregated, in the form of chromatids, into two daughter cells in mitosis. The accuracy of… (more)

Subjects/Keywords: Cytology

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APA (6th Edition):

Guo, Y. (2013). Molecular Mechanisms of Mitotic Spindle Assembly and Accurate Chromosome Segregation. (Doctoral Dissertation). Columbia University. Retrieved from https://doi.org/10.7916/D8988FDC

Chicago Manual of Style (16th Edition):

Guo, Yige. “Molecular Mechanisms of Mitotic Spindle Assembly and Accurate Chromosome Segregation.” 2013. Doctoral Dissertation, Columbia University. Accessed October 21, 2019. https://doi.org/10.7916/D8988FDC.

MLA Handbook (7th Edition):

Guo, Yige. “Molecular Mechanisms of Mitotic Spindle Assembly and Accurate Chromosome Segregation.” 2013. Web. 21 Oct 2019.

Vancouver:

Guo Y. Molecular Mechanisms of Mitotic Spindle Assembly and Accurate Chromosome Segregation. [Internet] [Doctoral dissertation]. Columbia University; 2013. [cited 2019 Oct 21]. Available from: https://doi.org/10.7916/D8988FDC.

Council of Science Editors:

Guo Y. Molecular Mechanisms of Mitotic Spindle Assembly and Accurate Chromosome Segregation. [Doctoral Dissertation]. Columbia University; 2013. Available from: https://doi.org/10.7916/D8988FDC


Columbia University

6. Tung, Jennifer Jean. Evaluation of Chloride Intracellular Channels 4 and 1 Functions in Developmental and Pathological Angiogenesis.

Degree: 2012, Columbia University

 Members of the chloride intracellular channel (CLIC) protein family have been implicated as regulators of tubulogenesis, a critical step in the formation of new blood… (more)

Subjects/Keywords: Cytology

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APA (6th Edition):

Tung, J. J. (2012). Evaluation of Chloride Intracellular Channels 4 and 1 Functions in Developmental and Pathological Angiogenesis. (Doctoral Dissertation). Columbia University. Retrieved from https://doi.org/10.7916/D8T151QJ

Chicago Manual of Style (16th Edition):

Tung, Jennifer Jean. “Evaluation of Chloride Intracellular Channels 4 and 1 Functions in Developmental and Pathological Angiogenesis.” 2012. Doctoral Dissertation, Columbia University. Accessed October 21, 2019. https://doi.org/10.7916/D8T151QJ.

MLA Handbook (7th Edition):

Tung, Jennifer Jean. “Evaluation of Chloride Intracellular Channels 4 and 1 Functions in Developmental and Pathological Angiogenesis.” 2012. Web. 21 Oct 2019.

Vancouver:

Tung JJ. Evaluation of Chloride Intracellular Channels 4 and 1 Functions in Developmental and Pathological Angiogenesis. [Internet] [Doctoral dissertation]. Columbia University; 2012. [cited 2019 Oct 21]. Available from: https://doi.org/10.7916/D8T151QJ.

Council of Science Editors:

Tung JJ. Evaluation of Chloride Intracellular Channels 4 and 1 Functions in Developmental and Pathological Angiogenesis. [Doctoral Dissertation]. Columbia University; 2012. Available from: https://doi.org/10.7916/D8T151QJ


Florida State University

7. Wilson, Korey. The Dynamics of Replication Timing, Chromatin Compartments, and Gene Expression Changes during Lineage Specification of Stem Cells.

Degree: PhD, Biological Science, 2016, Florida State University

The temporal order in which segments of the genome are duplicated is referred to as the replication timing (RT) program. RT is established in each… (more)

Subjects/Keywords: Cytology

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APA (6th Edition):

Wilson, K. (2016). The Dynamics of Replication Timing, Chromatin Compartments, and Gene Expression Changes during Lineage Specification of Stem Cells. (Doctoral Dissertation). Florida State University. Retrieved from http://purl.flvc.org/fsu/fd/FSU_FA2016_Wilson_fsu_0071E_13444 ;

Chicago Manual of Style (16th Edition):

Wilson, Korey. “The Dynamics of Replication Timing, Chromatin Compartments, and Gene Expression Changes during Lineage Specification of Stem Cells.” 2016. Doctoral Dissertation, Florida State University. Accessed October 21, 2019. http://purl.flvc.org/fsu/fd/FSU_FA2016_Wilson_fsu_0071E_13444 ;.

MLA Handbook (7th Edition):

Wilson, Korey. “The Dynamics of Replication Timing, Chromatin Compartments, and Gene Expression Changes during Lineage Specification of Stem Cells.” 2016. Web. 21 Oct 2019.

Vancouver:

Wilson K. The Dynamics of Replication Timing, Chromatin Compartments, and Gene Expression Changes during Lineage Specification of Stem Cells. [Internet] [Doctoral dissertation]. Florida State University; 2016. [cited 2019 Oct 21]. Available from: http://purl.flvc.org/fsu/fd/FSU_FA2016_Wilson_fsu_0071E_13444 ;.

Council of Science Editors:

Wilson K. The Dynamics of Replication Timing, Chromatin Compartments, and Gene Expression Changes during Lineage Specification of Stem Cells. [Doctoral Dissertation]. Florida State University; 2016. Available from: http://purl.flvc.org/fsu/fd/FSU_FA2016_Wilson_fsu_0071E_13444 ;


Florida State University

8. Battaglia, Dana. Genome Wide DNA Replication Timing in Human Pluripotent and Leukemic Cell Types.

Degree: MS, Biological Science, 2011, Florida State University

Accurate replication of DNA once and only once per cell cycle is an essential process for all living organisms. Despite many studies aimed at understanding… (more)

Subjects/Keywords: Cytology

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APA (6th Edition):

Battaglia, D. (2011). Genome Wide DNA Replication Timing in Human Pluripotent and Leukemic Cell Types. (Masters Thesis). Florida State University. Retrieved from http://purl.flvc.org/fsu/fd/FSU_migr_etd-1132 ;

Chicago Manual of Style (16th Edition):

Battaglia, Dana. “Genome Wide DNA Replication Timing in Human Pluripotent and Leukemic Cell Types.” 2011. Masters Thesis, Florida State University. Accessed October 21, 2019. http://purl.flvc.org/fsu/fd/FSU_migr_etd-1132 ;.

MLA Handbook (7th Edition):

Battaglia, Dana. “Genome Wide DNA Replication Timing in Human Pluripotent and Leukemic Cell Types.” 2011. Web. 21 Oct 2019.

Vancouver:

Battaglia D. Genome Wide DNA Replication Timing in Human Pluripotent and Leukemic Cell Types. [Internet] [Masters thesis]. Florida State University; 2011. [cited 2019 Oct 21]. Available from: http://purl.flvc.org/fsu/fd/FSU_migr_etd-1132 ;.

Council of Science Editors:

Battaglia D. Genome Wide DNA Replication Timing in Human Pluripotent and Leukemic Cell Types. [Masters Thesis]. Florida State University; 2011. Available from: http://purl.flvc.org/fsu/fd/FSU_migr_etd-1132 ;


University of Nottingham

9. Johnson, L. A. Integrative biological studies of anti-tumour agents.

Degree: PhD, 2009, University of Nottingham

 3, 11-difluoro-6, 8, 13-trimethyl-8H- quino [4, 3, 2-kl] acridinium methosulfate (RHPS4) is a member of a series of pentacyclic acridines developed at the University of… (more)

Subjects/Keywords: QH573 Cytology

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APA (6th Edition):

Johnson, L. A. (2009). Integrative biological studies of anti-tumour agents. (Doctoral Dissertation). University of Nottingham. Retrieved from http://eprints.nottingham.ac.uk/10800/ ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.514795

Chicago Manual of Style (16th Edition):

Johnson, L A. “Integrative biological studies of anti-tumour agents.” 2009. Doctoral Dissertation, University of Nottingham. Accessed October 21, 2019. http://eprints.nottingham.ac.uk/10800/ ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.514795.

MLA Handbook (7th Edition):

Johnson, L A. “Integrative biological studies of anti-tumour agents.” 2009. Web. 21 Oct 2019.

Vancouver:

Johnson LA. Integrative biological studies of anti-tumour agents. [Internet] [Doctoral dissertation]. University of Nottingham; 2009. [cited 2019 Oct 21]. Available from: http://eprints.nottingham.ac.uk/10800/ ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.514795.

Council of Science Editors:

Johnson LA. Integrative biological studies of anti-tumour agents. [Doctoral Dissertation]. University of Nottingham; 2009. Available from: http://eprints.nottingham.ac.uk/10800/ ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.514795


University of Nottingham

10. Fornari, Enzo. Bio-molecular gradient surfaces for biological recognition.

Degree: PhD, 2014, University of Nottingham

 The use of protein microfluidic systems is of growing interest for a variety of applications, including but not limited to tissue engineering, drug delivery and… (more)

Subjects/Keywords: QH573 Cytology

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APA (6th Edition):

Fornari, E. (2014). Bio-molecular gradient surfaces for biological recognition. (Doctoral Dissertation). University of Nottingham. Retrieved from http://eprints.nottingham.ac.uk/27734/ ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.639909

Chicago Manual of Style (16th Edition):

Fornari, Enzo. “Bio-molecular gradient surfaces for biological recognition.” 2014. Doctoral Dissertation, University of Nottingham. Accessed October 21, 2019. http://eprints.nottingham.ac.uk/27734/ ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.639909.

MLA Handbook (7th Edition):

Fornari, Enzo. “Bio-molecular gradient surfaces for biological recognition.” 2014. Web. 21 Oct 2019.

Vancouver:

Fornari E. Bio-molecular gradient surfaces for biological recognition. [Internet] [Doctoral dissertation]. University of Nottingham; 2014. [cited 2019 Oct 21]. Available from: http://eprints.nottingham.ac.uk/27734/ ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.639909.

Council of Science Editors:

Fornari E. Bio-molecular gradient surfaces for biological recognition. [Doctoral Dissertation]. University of Nottingham; 2014. Available from: http://eprints.nottingham.ac.uk/27734/ ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.639909


Central Connecticut State University

11. Reale, Virginia Danielle Hikel. Engineering a heterologous transforming growth factor-alpha promoter that is glucose-responsive in 293T cells / Virginia Danielle Hikel Reale.

Degree: Department of Biological Sciences, 2002, Central Connecticut State University

 Transforming growth factor-alpha (TGFa), a member of the endothelial growth factor (EGF) family of mitogens, was previously thought to exist solely in neoplastic cells and… (more)

Subjects/Keywords: Cytology

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APA (6th Edition):

Reale, V. D. H. (2002). Engineering a heterologous transforming growth factor-alpha promoter that is glucose-responsive in 293T cells / Virginia Danielle Hikel Reale. (Thesis). Central Connecticut State University. Retrieved from http://content.library.ccsu.edu/u?/ccsutheses,1495

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

Chicago Manual of Style (16th Edition):

Reale, Virginia Danielle Hikel. “Engineering a heterologous transforming growth factor-alpha promoter that is glucose-responsive in 293T cells / Virginia Danielle Hikel Reale.” 2002. Thesis, Central Connecticut State University. Accessed October 21, 2019. http://content.library.ccsu.edu/u?/ccsutheses,1495.

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

MLA Handbook (7th Edition):

Reale, Virginia Danielle Hikel. “Engineering a heterologous transforming growth factor-alpha promoter that is glucose-responsive in 293T cells / Virginia Danielle Hikel Reale.” 2002. Web. 21 Oct 2019.

Vancouver:

Reale VDH. Engineering a heterologous transforming growth factor-alpha promoter that is glucose-responsive in 293T cells / Virginia Danielle Hikel Reale. [Internet] [Thesis]. Central Connecticut State University; 2002. [cited 2019 Oct 21]. Available from: http://content.library.ccsu.edu/u?/ccsutheses,1495.

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

Council of Science Editors:

Reale VDH. Engineering a heterologous transforming growth factor-alpha promoter that is glucose-responsive in 293T cells / Virginia Danielle Hikel Reale. [Thesis]. Central Connecticut State University; 2002. Available from: http://content.library.ccsu.edu/u?/ccsutheses,1495

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


Columbia University

12. Lazarovici, Allan. Elucidating the sequence and structural specificities of DNA-binding factors.

Degree: 2014, Columbia University

 Characterizing the binding preferences of transcription factors is a major objective in molecular biology. Important processes such as development and responses to environmental stresses are… (more)

Subjects/Keywords: Biophysics; Cytology

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APA (6th Edition):

Lazarovici, A. (2014). Elucidating the sequence and structural specificities of DNA-binding factors. (Doctoral Dissertation). Columbia University. Retrieved from https://doi.org/10.7916/D8KP80R3

Chicago Manual of Style (16th Edition):

Lazarovici, Allan. “Elucidating the sequence and structural specificities of DNA-binding factors.” 2014. Doctoral Dissertation, Columbia University. Accessed October 21, 2019. https://doi.org/10.7916/D8KP80R3.

MLA Handbook (7th Edition):

Lazarovici, Allan. “Elucidating the sequence and structural specificities of DNA-binding factors.” 2014. Web. 21 Oct 2019.

Vancouver:

Lazarovici A. Elucidating the sequence and structural specificities of DNA-binding factors. [Internet] [Doctoral dissertation]. Columbia University; 2014. [cited 2019 Oct 21]. Available from: https://doi.org/10.7916/D8KP80R3.

Council of Science Editors:

Lazarovici A. Elucidating the sequence and structural specificities of DNA-binding factors. [Doctoral Dissertation]. Columbia University; 2014. Available from: https://doi.org/10.7916/D8KP80R3


Columbia University

13. Hu, Daniel Jun-Kit. Roles for Cytoplasmic Dynein and the Unconventional Kinesin, KIF1a, during Cortical Development.

Degree: 2015, Columbia University

 Radial glial progenitor (RGP) cells are neural stem cells that give rise to the majority of neurons, glia, and adult stem cells during cortical development.… (more)

Subjects/Keywords: Cytology; Neurosciences

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APA (6th Edition):

Hu, D. J. (2015). Roles for Cytoplasmic Dynein and the Unconventional Kinesin, KIF1a, during Cortical Development. (Doctoral Dissertation). Columbia University. Retrieved from https://doi.org/10.7916/D8Z89BG9

Chicago Manual of Style (16th Edition):

Hu, Daniel Jun-Kit. “Roles for Cytoplasmic Dynein and the Unconventional Kinesin, KIF1a, during Cortical Development.” 2015. Doctoral Dissertation, Columbia University. Accessed October 21, 2019. https://doi.org/10.7916/D8Z89BG9.

MLA Handbook (7th Edition):

Hu, Daniel Jun-Kit. “Roles for Cytoplasmic Dynein and the Unconventional Kinesin, KIF1a, during Cortical Development.” 2015. Web. 21 Oct 2019.

Vancouver:

Hu DJ. Roles for Cytoplasmic Dynein and the Unconventional Kinesin, KIF1a, during Cortical Development. [Internet] [Doctoral dissertation]. Columbia University; 2015. [cited 2019 Oct 21]. Available from: https://doi.org/10.7916/D8Z89BG9.

Council of Science Editors:

Hu DJ. Roles for Cytoplasmic Dynein and the Unconventional Kinesin, KIF1a, during Cortical Development. [Doctoral Dissertation]. Columbia University; 2015. Available from: https://doi.org/10.7916/D8Z89BG9


Columbia University

14. Stachowiak, Matthew R. Mechanisms of Actomyosin Contractility in Cells.

Degree: 2011, Columbia University

 Many fundamental cellular processes hinge on the ability of cells to exert contractile force. Contractility is used by cells to divide, to migrate, to heal… (more)

Subjects/Keywords: Biophysics; Cytology

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APA (6th Edition):

Stachowiak, M. R. (2011). Mechanisms of Actomyosin Contractility in Cells. (Doctoral Dissertation). Columbia University. Retrieved from https://doi.org/10.7916/D8F76KHH

Chicago Manual of Style (16th Edition):

Stachowiak, Matthew R. “Mechanisms of Actomyosin Contractility in Cells.” 2011. Doctoral Dissertation, Columbia University. Accessed October 21, 2019. https://doi.org/10.7916/D8F76KHH.

MLA Handbook (7th Edition):

Stachowiak, Matthew R. “Mechanisms of Actomyosin Contractility in Cells.” 2011. Web. 21 Oct 2019.

Vancouver:

Stachowiak MR. Mechanisms of Actomyosin Contractility in Cells. [Internet] [Doctoral dissertation]. Columbia University; 2011. [cited 2019 Oct 21]. Available from: https://doi.org/10.7916/D8F76KHH.

Council of Science Editors:

Stachowiak MR. Mechanisms of Actomyosin Contractility in Cells. [Doctoral Dissertation]. Columbia University; 2011. Available from: https://doi.org/10.7916/D8F76KHH


Columbia University

15. Sommer, Julia. Control of Neuronal Circuit Assembly by Gtpase Regulators.

Degree: 2011, Columbia University

 One of the most remarkable features of the central nervous system is the exquisite specificity of its synaptic connections, which is crucial for the functioning… (more)

Subjects/Keywords: Neurosciences; Cytology

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APA (6th Edition):

Sommer, J. (2011). Control of Neuronal Circuit Assembly by Gtpase Regulators. (Doctoral Dissertation). Columbia University. Retrieved from https://doi.org/10.7916/D81J9HZ1

Chicago Manual of Style (16th Edition):

Sommer, Julia. “Control of Neuronal Circuit Assembly by Gtpase Regulators.” 2011. Doctoral Dissertation, Columbia University. Accessed October 21, 2019. https://doi.org/10.7916/D81J9HZ1.

MLA Handbook (7th Edition):

Sommer, Julia. “Control of Neuronal Circuit Assembly by Gtpase Regulators.” 2011. Web. 21 Oct 2019.

Vancouver:

Sommer J. Control of Neuronal Circuit Assembly by Gtpase Regulators. [Internet] [Doctoral dissertation]. Columbia University; 2011. [cited 2019 Oct 21]. Available from: https://doi.org/10.7916/D81J9HZ1.

Council of Science Editors:

Sommer J. Control of Neuronal Circuit Assembly by Gtpase Regulators. [Doctoral Dissertation]. Columbia University; 2011. Available from: https://doi.org/10.7916/D81J9HZ1


Columbia University

16. Pan, Kally Zhang. Cell Size Control in Fission Yeast.

Degree: 2013, Columbia University

 Among all living organisms, there is almost much variety in cell size as there is for cell function and cell type. However, within each cell… (more)

Subjects/Keywords: Cytology; Genetics

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APA (6th Edition):

Pan, K. Z. (2013). Cell Size Control in Fission Yeast. (Doctoral Dissertation). Columbia University. Retrieved from https://doi.org/10.7916/D8028ZXF

Chicago Manual of Style (16th Edition):

Pan, Kally Zhang. “Cell Size Control in Fission Yeast.” 2013. Doctoral Dissertation, Columbia University. Accessed October 21, 2019. https://doi.org/10.7916/D8028ZXF.

MLA Handbook (7th Edition):

Pan, Kally Zhang. “Cell Size Control in Fission Yeast.” 2013. Web. 21 Oct 2019.

Vancouver:

Pan KZ. Cell Size Control in Fission Yeast. [Internet] [Doctoral dissertation]. Columbia University; 2013. [cited 2019 Oct 21]. Available from: https://doi.org/10.7916/D8028ZXF.

Council of Science Editors:

Pan KZ. Cell Size Control in Fission Yeast. [Doctoral Dissertation]. Columbia University; 2013. Available from: https://doi.org/10.7916/D8028ZXF


Columbia University

17. Palmer, Colin James. The transcription factor Zfx is required for tumorigenesis caused by Hedgehog pathway activation.

Degree: 2013, Columbia University

 The Hedgehog (Hh) signaling pathway regulates normal development and cell proliferation across the metazoa. Upon its aberrant activation, mammalian Hh signaling can also cause tumor… (more)

Subjects/Keywords: Cytology; Genetics

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APA (6th Edition):

Palmer, C. J. (2013). The transcription factor Zfx is required for tumorigenesis caused by Hedgehog pathway activation. (Doctoral Dissertation). Columbia University. Retrieved from https://doi.org/10.7916/D8VQ391B

Chicago Manual of Style (16th Edition):

Palmer, Colin James. “The transcription factor Zfx is required for tumorigenesis caused by Hedgehog pathway activation.” 2013. Doctoral Dissertation, Columbia University. Accessed October 21, 2019. https://doi.org/10.7916/D8VQ391B.

MLA Handbook (7th Edition):

Palmer, Colin James. “The transcription factor Zfx is required for tumorigenesis caused by Hedgehog pathway activation.” 2013. Web. 21 Oct 2019.

Vancouver:

Palmer CJ. The transcription factor Zfx is required for tumorigenesis caused by Hedgehog pathway activation. [Internet] [Doctoral dissertation]. Columbia University; 2013. [cited 2019 Oct 21]. Available from: https://doi.org/10.7916/D8VQ391B.

Council of Science Editors:

Palmer CJ. The transcription factor Zfx is required for tumorigenesis caused by Hedgehog pathway activation. [Doctoral Dissertation]. Columbia University; 2013. Available from: https://doi.org/10.7916/D8VQ391B


Columbia University

18. Kupferman, Justine. Targeting Ion Channels to Distal Dendrites.

Degree: 2013, Columbia University

 Neurons are divided into functional compartments: the soma houses the DNA and transcriptional machinery, the axons conduct action potentials, presynaptic boutons transmit synaptic signals, and… (more)

Subjects/Keywords: Neurosciences; Cytology

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APA (6th Edition):

Kupferman, J. (2013). Targeting Ion Channels to Distal Dendrites. (Doctoral Dissertation). Columbia University. Retrieved from https://doi.org/10.7916/D86H4QT1

Chicago Manual of Style (16th Edition):

Kupferman, Justine. “Targeting Ion Channels to Distal Dendrites.” 2013. Doctoral Dissertation, Columbia University. Accessed October 21, 2019. https://doi.org/10.7916/D86H4QT1.

MLA Handbook (7th Edition):

Kupferman, Justine. “Targeting Ion Channels to Distal Dendrites.” 2013. Web. 21 Oct 2019.

Vancouver:

Kupferman J. Targeting Ion Channels to Distal Dendrites. [Internet] [Doctoral dissertation]. Columbia University; 2013. [cited 2019 Oct 21]. Available from: https://doi.org/10.7916/D86H4QT1.

Council of Science Editors:

Kupferman J. Targeting Ion Channels to Distal Dendrites. [Doctoral Dissertation]. Columbia University; 2013. Available from: https://doi.org/10.7916/D86H4QT1


Columbia University

19. Uh, Minji. Notch Signaling Determines Lymphatic Cell Fate and Regulates Sprouting Lymphangiogenesis.

Degree: 2013, Columbia University

 The lymphatic vascular system is necessary for physiological regulation of tissue fluid homeostasis and absorption of dietary fat. Lymphatics also function in the inflammatory response… (more)

Subjects/Keywords: Cytology; Pharmacology

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APA (6th Edition):

Uh, M. (2013). Notch Signaling Determines Lymphatic Cell Fate and Regulates Sprouting Lymphangiogenesis. (Doctoral Dissertation). Columbia University. Retrieved from https://doi.org/10.7916/D85H7PN6

Chicago Manual of Style (16th Edition):

Uh, Minji. “Notch Signaling Determines Lymphatic Cell Fate and Regulates Sprouting Lymphangiogenesis.” 2013. Doctoral Dissertation, Columbia University. Accessed October 21, 2019. https://doi.org/10.7916/D85H7PN6.

MLA Handbook (7th Edition):

Uh, Minji. “Notch Signaling Determines Lymphatic Cell Fate and Regulates Sprouting Lymphangiogenesis.” 2013. Web. 21 Oct 2019.

Vancouver:

Uh M. Notch Signaling Determines Lymphatic Cell Fate and Regulates Sprouting Lymphangiogenesis. [Internet] [Doctoral dissertation]. Columbia University; 2013. [cited 2019 Oct 21]. Available from: https://doi.org/10.7916/D85H7PN6.

Council of Science Editors:

Uh M. Notch Signaling Determines Lymphatic Cell Fate and Regulates Sprouting Lymphangiogenesis. [Doctoral Dissertation]. Columbia University; 2013. Available from: https://doi.org/10.7916/D85H7PN6


Columbia University

20. Ruggles, Kelly Valentine. Cellular Fatty Acid Toxicity: Extrapolating Yeast Screens into Mammalian Models.

Degree: 2012, Columbia University

 Fatty acid deposition in non-adipose tissue leads to a cellular dysfunction known as lipotoxicity. Neutral lipid synthesis is known to protect against lipotoxicity but many… (more)

Subjects/Keywords: Nutrition; Cytology

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APA (6th Edition):

Ruggles, K. V. (2012). Cellular Fatty Acid Toxicity: Extrapolating Yeast Screens into Mammalian Models. (Doctoral Dissertation). Columbia University. Retrieved from https://doi.org/10.7916/D84B2ZC0

Chicago Manual of Style (16th Edition):

Ruggles, Kelly Valentine. “Cellular Fatty Acid Toxicity: Extrapolating Yeast Screens into Mammalian Models.” 2012. Doctoral Dissertation, Columbia University. Accessed October 21, 2019. https://doi.org/10.7916/D84B2ZC0.

MLA Handbook (7th Edition):

Ruggles, Kelly Valentine. “Cellular Fatty Acid Toxicity: Extrapolating Yeast Screens into Mammalian Models.” 2012. Web. 21 Oct 2019.

Vancouver:

Ruggles KV. Cellular Fatty Acid Toxicity: Extrapolating Yeast Screens into Mammalian Models. [Internet] [Doctoral dissertation]. Columbia University; 2012. [cited 2019 Oct 21]. Available from: https://doi.org/10.7916/D84B2ZC0.

Council of Science Editors:

Ruggles KV. Cellular Fatty Acid Toxicity: Extrapolating Yeast Screens into Mammalian Models. [Doctoral Dissertation]. Columbia University; 2012. Available from: https://doi.org/10.7916/D84B2ZC0


Florida State University

21. Wang, Mian. Scc3 Is Required for Sister Chromatid Cohesion and Rec8 Production during Meiosis in Sacchromyces Cerevisiae.

Degree: MS, Biological Science, 2010, Florida State University

Accurate chromosome segregation during meiosis is critical for generating genetic diversity and for producing gametes with the correct number of chromosomes. After meiotic S-phase, homologs… (more)

Subjects/Keywords: Biology; Cytology

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APA (6th Edition):

Wang, M. (2010). Scc3 Is Required for Sister Chromatid Cohesion and Rec8 Production during Meiosis in Sacchromyces Cerevisiae. (Masters Thesis). Florida State University. Retrieved from http://purl.flvc.org/fsu/fd/FSU_migr_etd-4619 ;

Chicago Manual of Style (16th Edition):

Wang, Mian. “Scc3 Is Required for Sister Chromatid Cohesion and Rec8 Production during Meiosis in Sacchromyces Cerevisiae.” 2010. Masters Thesis, Florida State University. Accessed October 21, 2019. http://purl.flvc.org/fsu/fd/FSU_migr_etd-4619 ;.

MLA Handbook (7th Edition):

Wang, Mian. “Scc3 Is Required for Sister Chromatid Cohesion and Rec8 Production during Meiosis in Sacchromyces Cerevisiae.” 2010. Web. 21 Oct 2019.

Vancouver:

Wang M. Scc3 Is Required for Sister Chromatid Cohesion and Rec8 Production during Meiosis in Sacchromyces Cerevisiae. [Internet] [Masters thesis]. Florida State University; 2010. [cited 2019 Oct 21]. Available from: http://purl.flvc.org/fsu/fd/FSU_migr_etd-4619 ;.

Council of Science Editors:

Wang M. Scc3 Is Required for Sister Chromatid Cohesion and Rec8 Production during Meiosis in Sacchromyces Cerevisiae. [Masters Thesis]. Florida State University; 2010. Available from: http://purl.flvc.org/fsu/fd/FSU_migr_etd-4619 ;


Florida State University

22. Beyrouthy, Maroun J., 1976-. The Subcellular Localization of the Transcription Factor YY1 during Cellular Life and Death.

Degree: PhD, Biological Science, 2007, Florida State University

One of the events leading to a cell's commitment to a new cell cycle resulting in cell division is upregulation of the replication-dependent histone gene… (more)

Subjects/Keywords: Cytology

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APA (6th Edition):

Beyrouthy, Maroun J., 1. (2007). The Subcellular Localization of the Transcription Factor YY1 during Cellular Life and Death. (Doctoral Dissertation). Florida State University. Retrieved from http://purl.flvc.org/fsu/fd/FSU_migr_etd-1402 ;

Chicago Manual of Style (16th Edition):

Beyrouthy, Maroun J., 1976-. “The Subcellular Localization of the Transcription Factor YY1 during Cellular Life and Death.” 2007. Doctoral Dissertation, Florida State University. Accessed October 21, 2019. http://purl.flvc.org/fsu/fd/FSU_migr_etd-1402 ;.

MLA Handbook (7th Edition):

Beyrouthy, Maroun J., 1976-. “The Subcellular Localization of the Transcription Factor YY1 during Cellular Life and Death.” 2007. Web. 21 Oct 2019.

Vancouver:

Beyrouthy, Maroun J. 1. The Subcellular Localization of the Transcription Factor YY1 during Cellular Life and Death. [Internet] [Doctoral dissertation]. Florida State University; 2007. [cited 2019 Oct 21]. Available from: http://purl.flvc.org/fsu/fd/FSU_migr_etd-1402 ;.

Council of Science Editors:

Beyrouthy, Maroun J. 1. The Subcellular Localization of the Transcription Factor YY1 during Cellular Life and Death. [Doctoral Dissertation]. Florida State University; 2007. Available from: http://purl.flvc.org/fsu/fd/FSU_migr_etd-1402 ;


Florida State University

23. Lee, Emily M. (Emily Michelle). Elucidating a Mechanism for Hepatitis C Virus Induced Steatosis and Identification of Anti-Viral Compounds for Treating Zika Virus Infection.

Degree: PhD, Biological Science, 2018, Florida State University

 During the past 30 years, there have been several Flaviviridae threats. Among them, Hepatatis C virus (HCV) emerged in the Western hemisphere as the previously… (more)

Subjects/Keywords: Virology; Cytology

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APA (6th Edition):

Lee, E. M. (. M. (2018). Elucidating a Mechanism for Hepatitis C Virus Induced Steatosis and Identification of Anti-Viral Compounds for Treating Zika Virus Infection. (Doctoral Dissertation). Florida State University. Retrieved from http://purl.flvc.org/fsu/fd/2018_Sp_Lee_fsu_0071E_14503 ;

Chicago Manual of Style (16th Edition):

Lee, Emily M (Emily Michelle). “Elucidating a Mechanism for Hepatitis C Virus Induced Steatosis and Identification of Anti-Viral Compounds for Treating Zika Virus Infection.” 2018. Doctoral Dissertation, Florida State University. Accessed October 21, 2019. http://purl.flvc.org/fsu/fd/2018_Sp_Lee_fsu_0071E_14503 ;.

MLA Handbook (7th Edition):

Lee, Emily M (Emily Michelle). “Elucidating a Mechanism for Hepatitis C Virus Induced Steatosis and Identification of Anti-Viral Compounds for Treating Zika Virus Infection.” 2018. Web. 21 Oct 2019.

Vancouver:

Lee EM(M. Elucidating a Mechanism for Hepatitis C Virus Induced Steatosis and Identification of Anti-Viral Compounds for Treating Zika Virus Infection. [Internet] [Doctoral dissertation]. Florida State University; 2018. [cited 2019 Oct 21]. Available from: http://purl.flvc.org/fsu/fd/2018_Sp_Lee_fsu_0071E_14503 ;.

Council of Science Editors:

Lee EM(M. Elucidating a Mechanism for Hepatitis C Virus Induced Steatosis and Identification of Anti-Viral Compounds for Treating Zika Virus Infection. [Doctoral Dissertation]. Florida State University; 2018. Available from: http://purl.flvc.org/fsu/fd/2018_Sp_Lee_fsu_0071E_14503 ;


Florida State University

24. Summerill, Corinne Alethea Oriana. The Cryo-EM 3D Reconstruction of Isolated Lethocerus Z-Discs.

Degree: MS, Biological Science, 2016, Florida State University

 Electron microscopy is an important technique for observing macromolecular structures, such as DNA and viruses, which would be too small to see under light microscopy.… (more)

Subjects/Keywords: Biology; Cytology

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APA (6th Edition):

Summerill, C. A. O. (2016). The Cryo-EM 3D Reconstruction of Isolated Lethocerus Z-Discs. (Masters Thesis). Florida State University. Retrieved from http://purl.flvc.org/fsu/fd/FSU_FA2016_Summerill_fsu_0071N_13636 ;

Chicago Manual of Style (16th Edition):

Summerill, Corinne Alethea Oriana. “The Cryo-EM 3D Reconstruction of Isolated Lethocerus Z-Discs.” 2016. Masters Thesis, Florida State University. Accessed October 21, 2019. http://purl.flvc.org/fsu/fd/FSU_FA2016_Summerill_fsu_0071N_13636 ;.

MLA Handbook (7th Edition):

Summerill, Corinne Alethea Oriana. “The Cryo-EM 3D Reconstruction of Isolated Lethocerus Z-Discs.” 2016. Web. 21 Oct 2019.

Vancouver:

Summerill CAO. The Cryo-EM 3D Reconstruction of Isolated Lethocerus Z-Discs. [Internet] [Masters thesis]. Florida State University; 2016. [cited 2019 Oct 21]. Available from: http://purl.flvc.org/fsu/fd/FSU_FA2016_Summerill_fsu_0071N_13636 ;.

Council of Science Editors:

Summerill CAO. The Cryo-EM 3D Reconstruction of Isolated Lethocerus Z-Discs. [Masters Thesis]. Florida State University; 2016. Available from: http://purl.flvc.org/fsu/fd/FSU_FA2016_Summerill_fsu_0071N_13636 ;


Drexel University

25. Austin, Timothy Ottum. New understanding of the effects of microtubule-associated proteins on dynamic instability, including the role of tau in neuronal function and disease.

Degree: 2018, Drexel University

As morphologically complex and polarized structures, neurons are critically dependent on cytoskeletal function. Neuronal processes are formed and maintained on a backbone of microtubules, which… (more)

Subjects/Keywords: Neurosciences; Cytology

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APA (6th Edition):

Austin, T. O. (2018). New understanding of the effects of microtubule-associated proteins on dynamic instability, including the role of tau in neuronal function and disease. (Thesis). Drexel University. Retrieved from https://idea.library.drexel.edu/islandora/object/idea%3A7967

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

Chicago Manual of Style (16th Edition):

Austin, Timothy Ottum. “New understanding of the effects of microtubule-associated proteins on dynamic instability, including the role of tau in neuronal function and disease.” 2018. Thesis, Drexel University. Accessed October 21, 2019. https://idea.library.drexel.edu/islandora/object/idea%3A7967.

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

MLA Handbook (7th Edition):

Austin, Timothy Ottum. “New understanding of the effects of microtubule-associated proteins on dynamic instability, including the role of tau in neuronal function and disease.” 2018. Web. 21 Oct 2019.

Vancouver:

Austin TO. New understanding of the effects of microtubule-associated proteins on dynamic instability, including the role of tau in neuronal function and disease. [Internet] [Thesis]. Drexel University; 2018. [cited 2019 Oct 21]. Available from: https://idea.library.drexel.edu/islandora/object/idea%3A7967.

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

Council of Science Editors:

Austin TO. New understanding of the effects of microtubule-associated proteins on dynamic instability, including the role of tau in neuronal function and disease. [Thesis]. Drexel University; 2018. Available from: https://idea.library.drexel.edu/islandora/object/idea%3A7967

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


University of Nottingham

26. Shaikh Qureshi, Wasay Mohiuddin. The chick cardiomyocyte micromass system and stem cell differentiation along specific pathways : prediction of embryotoxic effects and their mechanism.

Degree: PhD, 2012, University of Nottingham

 Malformations in humans at birth have been recorded since ancient times. These malformations are anatomical or physiological anomalies present at the time of birth that… (more)

Subjects/Keywords: 612; QH573 Cytology

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APA (6th Edition):

Shaikh Qureshi, W. M. (2012). The chick cardiomyocyte micromass system and stem cell differentiation along specific pathways : prediction of embryotoxic effects and their mechanism. (Doctoral Dissertation). University of Nottingham. Retrieved from http://eprints.nottingham.ac.uk/12773/ ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.568698

Chicago Manual of Style (16th Edition):

Shaikh Qureshi, Wasay Mohiuddin. “The chick cardiomyocyte micromass system and stem cell differentiation along specific pathways : prediction of embryotoxic effects and their mechanism.” 2012. Doctoral Dissertation, University of Nottingham. Accessed October 21, 2019. http://eprints.nottingham.ac.uk/12773/ ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.568698.

MLA Handbook (7th Edition):

Shaikh Qureshi, Wasay Mohiuddin. “The chick cardiomyocyte micromass system and stem cell differentiation along specific pathways : prediction of embryotoxic effects and their mechanism.” 2012. Web. 21 Oct 2019.

Vancouver:

Shaikh Qureshi WM. The chick cardiomyocyte micromass system and stem cell differentiation along specific pathways : prediction of embryotoxic effects and their mechanism. [Internet] [Doctoral dissertation]. University of Nottingham; 2012. [cited 2019 Oct 21]. Available from: http://eprints.nottingham.ac.uk/12773/ ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.568698.

Council of Science Editors:

Shaikh Qureshi WM. The chick cardiomyocyte micromass system and stem cell differentiation along specific pathways : prediction of embryotoxic effects and their mechanism. [Doctoral Dissertation]. University of Nottingham; 2012. Available from: http://eprints.nottingham.ac.uk/12773/ ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.568698


University of Nottingham

27. Carter, David Andrew. Sourcing cells for gut tissue engineering : understanding and inducing embryonic stem cell differentiation to the intestinal cell lineage.

Degree: 2012, University of Nottingham

 Tissue engineering of any tissue type requires the combination of a supporting scaffold, a range of biological factors and a suitable source of cells. This… (more)

Subjects/Keywords: 616.027; QH573 Cytology

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APA (6th Edition):

Carter, D. A. (2012). Sourcing cells for gut tissue engineering : understanding and inducing embryonic stem cell differentiation to the intestinal cell lineage. (Doctoral Dissertation). University of Nottingham. Retrieved from http://eprints.nottingham.ac.uk/12713/ ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.559695

Chicago Manual of Style (16th Edition):

Carter, David Andrew. “Sourcing cells for gut tissue engineering : understanding and inducing embryonic stem cell differentiation to the intestinal cell lineage.” 2012. Doctoral Dissertation, University of Nottingham. Accessed October 21, 2019. http://eprints.nottingham.ac.uk/12713/ ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.559695.

MLA Handbook (7th Edition):

Carter, David Andrew. “Sourcing cells for gut tissue engineering : understanding and inducing embryonic stem cell differentiation to the intestinal cell lineage.” 2012. Web. 21 Oct 2019.

Vancouver:

Carter DA. Sourcing cells for gut tissue engineering : understanding and inducing embryonic stem cell differentiation to the intestinal cell lineage. [Internet] [Doctoral dissertation]. University of Nottingham; 2012. [cited 2019 Oct 21]. Available from: http://eprints.nottingham.ac.uk/12713/ ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.559695.

Council of Science Editors:

Carter DA. Sourcing cells for gut tissue engineering : understanding and inducing embryonic stem cell differentiation to the intestinal cell lineage. [Doctoral Dissertation]. University of Nottingham; 2012. Available from: http://eprints.nottingham.ac.uk/12713/ ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.559695


University of Nottingham

28. Thansa, Kwanta. Novel approaches to the isolation of farm animal embryonic stem cells.

Degree: 2009, University of Nottingham

 The establishment of stable immortal ES cell lines using embryos as a source of isolation in domesticated farm animals, in particular for pigs, which are… (more)

Subjects/Keywords: 636.089; QH573 Cytology

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APA (6th Edition):

Thansa, K. (2009). Novel approaches to the isolation of farm animal embryonic stem cells. (Doctoral Dissertation). University of Nottingham. Retrieved from http://eprints.nottingham.ac.uk/10918/ ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.508214

Chicago Manual of Style (16th Edition):

Thansa, Kwanta. “Novel approaches to the isolation of farm animal embryonic stem cells.” 2009. Doctoral Dissertation, University of Nottingham. Accessed October 21, 2019. http://eprints.nottingham.ac.uk/10918/ ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.508214.

MLA Handbook (7th Edition):

Thansa, Kwanta. “Novel approaches to the isolation of farm animal embryonic stem cells.” 2009. Web. 21 Oct 2019.

Vancouver:

Thansa K. Novel approaches to the isolation of farm animal embryonic stem cells. [Internet] [Doctoral dissertation]. University of Nottingham; 2009. [cited 2019 Oct 21]. Available from: http://eprints.nottingham.ac.uk/10918/ ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.508214.

Council of Science Editors:

Thansa K. Novel approaches to the isolation of farm animal embryonic stem cells. [Doctoral Dissertation]. University of Nottingham; 2009. Available from: http://eprints.nottingham.ac.uk/10918/ ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.508214


University of Nottingham

29. Uhiara, Chukwuemeka Obinna. The role of extracellular signal-regulated kinase in beta-adrenoceptor-mediated vasodilatation.

Degree: 2012, University of Nottingham

 Beta-Adrenoceptors (B-ARs) mediate vasodilatation by activating various mechanisms that collectively contribute to vascular smooth muscle (VSM) relaxation. It has been shown that B2-AR stimulation in… (more)

Subjects/Keywords: 615.1; QH573 Cytology

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APA (6th Edition):

Uhiara, C. O. (2012). The role of extracellular signal-regulated kinase in beta-adrenoceptor-mediated vasodilatation. (Doctoral Dissertation). University of Nottingham. Retrieved from http://eprints.nottingham.ac.uk/12695/ ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.559690

Chicago Manual of Style (16th Edition):

Uhiara, Chukwuemeka Obinna. “The role of extracellular signal-regulated kinase in beta-adrenoceptor-mediated vasodilatation.” 2012. Doctoral Dissertation, University of Nottingham. Accessed October 21, 2019. http://eprints.nottingham.ac.uk/12695/ ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.559690.

MLA Handbook (7th Edition):

Uhiara, Chukwuemeka Obinna. “The role of extracellular signal-regulated kinase in beta-adrenoceptor-mediated vasodilatation.” 2012. Web. 21 Oct 2019.

Vancouver:

Uhiara CO. The role of extracellular signal-regulated kinase in beta-adrenoceptor-mediated vasodilatation. [Internet] [Doctoral dissertation]. University of Nottingham; 2012. [cited 2019 Oct 21]. Available from: http://eprints.nottingham.ac.uk/12695/ ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.559690.

Council of Science Editors:

Uhiara CO. The role of extracellular signal-regulated kinase in beta-adrenoceptor-mediated vasodilatation. [Doctoral Dissertation]. University of Nottingham; 2012. Available from: http://eprints.nottingham.ac.uk/12695/ ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.559690


University of Nottingham

30. Kachel, Hamid Saeid. Inhibition of mammalian nicotinic acetylcholine receptors by philanthotoxin analogues is strongly influenced by subunit composition.

Degree: PhD, 2015, University of Nottingham

 Philanthotoxin-433 (PhTX-433) is an active component of the Egyptian solitary digger wasp, Philanthus triangulum, venom which non-selectively inhibits several excitatory ion channels. With the aim… (more)

Subjects/Keywords: 571.6; QH573 Cytology

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APA (6th Edition):

Kachel, H. S. (2015). Inhibition of mammalian nicotinic acetylcholine receptors by philanthotoxin analogues is strongly influenced by subunit composition. (Doctoral Dissertation). University of Nottingham. Retrieved from http://eprints.nottingham.ac.uk/27912/ ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.666900

Chicago Manual of Style (16th Edition):

Kachel, Hamid Saeid. “Inhibition of mammalian nicotinic acetylcholine receptors by philanthotoxin analogues is strongly influenced by subunit composition.” 2015. Doctoral Dissertation, University of Nottingham. Accessed October 21, 2019. http://eprints.nottingham.ac.uk/27912/ ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.666900.

MLA Handbook (7th Edition):

Kachel, Hamid Saeid. “Inhibition of mammalian nicotinic acetylcholine receptors by philanthotoxin analogues is strongly influenced by subunit composition.” 2015. Web. 21 Oct 2019.

Vancouver:

Kachel HS. Inhibition of mammalian nicotinic acetylcholine receptors by philanthotoxin analogues is strongly influenced by subunit composition. [Internet] [Doctoral dissertation]. University of Nottingham; 2015. [cited 2019 Oct 21]. Available from: http://eprints.nottingham.ac.uk/27912/ ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.666900.

Council of Science Editors:

Kachel HS. Inhibition of mammalian nicotinic acetylcholine receptors by philanthotoxin analogues is strongly influenced by subunit composition. [Doctoral Dissertation]. University of Nottingham; 2015. Available from: http://eprints.nottingham.ac.uk/27912/ ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.666900

[1] [2] [3] [4] [5] … [46]

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