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You searched for subject:(Cell AND Developmental Biology). Showing records 1 – 30 of 742 total matches.

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1. Sultana, Rifat. Lipid-Laden Macrophages Downregulate AKT Phosphorylation and Metabolize Lipid Droplets via Autophagy.

Degree: MS, Biology and Microbiology, 2017, South Dakota State University

  Macrophages contribute to plaque formation in atherosclerosis. Macrophages take up modified low-density lipoproteins and store excess cholesterol and triglycerides in lipid droplet organelles. Evidence… (more)

Subjects/Keywords: Biology; Cell and Developmental Biology

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

APA (6th Edition):

Sultana, R. (2017). Lipid-Laden Macrophages Downregulate AKT Phosphorylation and Metabolize Lipid Droplets via Autophagy. (Masters Thesis). South Dakota State University. Retrieved from http://openprairie.sdstate.edu/etd/1743

Chicago Manual of Style (16th Edition):

Sultana, Rifat. “Lipid-Laden Macrophages Downregulate AKT Phosphorylation and Metabolize Lipid Droplets via Autophagy.” 2017. Masters Thesis, South Dakota State University. Accessed June 23, 2018. http://openprairie.sdstate.edu/etd/1743.

MLA Handbook (7th Edition):

Sultana, Rifat. “Lipid-Laden Macrophages Downregulate AKT Phosphorylation and Metabolize Lipid Droplets via Autophagy.” 2017. Web. 23 Jun 2018.

Vancouver:

Sultana R. Lipid-Laden Macrophages Downregulate AKT Phosphorylation and Metabolize Lipid Droplets via Autophagy. [Internet] [Masters thesis]. South Dakota State University; 2017. [cited 2018 Jun 23]. Available from: http://openprairie.sdstate.edu/etd/1743.

Council of Science Editors:

Sultana R. Lipid-Laden Macrophages Downregulate AKT Phosphorylation and Metabolize Lipid Droplets via Autophagy. [Masters Thesis]. South Dakota State University; 2017. Available from: http://openprairie.sdstate.edu/etd/1743


Iowa State University

2. Farris, Caitlin. Starting small: Transcriptomics with single and small populations of cells.

Degree: 2014, Iowa State University

 Studying the transcriptome of organisms allows for the characterization of different aspects of development and disease progression. Studies of this kind are usually done with… (more)

Subjects/Keywords: Cell Biology; Developmental Biology; Genetics

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APA (6th Edition):

Farris, C. (2014). Starting small: Transcriptomics with single and small populations of cells. (Thesis). Iowa State University. Retrieved from https://lib.dr.iastate.edu/etd/14039

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):

Farris, Caitlin. “Starting small: Transcriptomics with single and small populations of cells.” 2014. Thesis, Iowa State University. Accessed June 23, 2018. https://lib.dr.iastate.edu/etd/14039.

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

MLA Handbook (7th Edition):

Farris, Caitlin. “Starting small: Transcriptomics with single and small populations of cells.” 2014. Web. 23 Jun 2018.

Vancouver:

Farris C. Starting small: Transcriptomics with single and small populations of cells. [Internet] [Thesis]. Iowa State University; 2014. [cited 2018 Jun 23]. Available from: https://lib.dr.iastate.edu/etd/14039.

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

Council of Science Editors:

Farris C. Starting small: Transcriptomics with single and small populations of cells. [Thesis]. Iowa State University; 2014. Available from: https://lib.dr.iastate.edu/etd/14039

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


University of Pennsylvania

3. Knight, Meghan Noelle. R-Spondin-2 Modulates Osteoblastogenesis And Bone Accrual.

Degree: 2017, University of Pennsylvania

 The R-spondin family of proteins are Wnt agonists, and the complete embryonic disruption of Rspo2 results in skeletal developmental defects that recapitulate the phenotype observed… (more)

Subjects/Keywords: Cell Biology; Developmental Biology

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APA (6th Edition):

Knight, M. N. (2017). R-Spondin-2 Modulates Osteoblastogenesis And Bone Accrual. (Thesis). University of Pennsylvania. Retrieved from https://repository.upenn.edu/edissertations/2398

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):

Knight, Meghan Noelle. “R-Spondin-2 Modulates Osteoblastogenesis And Bone Accrual.” 2017. Thesis, University of Pennsylvania. Accessed June 23, 2018. https://repository.upenn.edu/edissertations/2398.

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

MLA Handbook (7th Edition):

Knight, Meghan Noelle. “R-Spondin-2 Modulates Osteoblastogenesis And Bone Accrual.” 2017. Web. 23 Jun 2018.

Vancouver:

Knight MN. R-Spondin-2 Modulates Osteoblastogenesis And Bone Accrual. [Internet] [Thesis]. University of Pennsylvania; 2017. [cited 2018 Jun 23]. Available from: https://repository.upenn.edu/edissertations/2398.

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

Council of Science Editors:

Knight MN. R-Spondin-2 Modulates Osteoblastogenesis And Bone Accrual. [Thesis]. University of Pennsylvania; 2017. Available from: https://repository.upenn.edu/edissertations/2398

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


University of Pennsylvania

4. Aghajanian, Haig. Semaphorin 3d Signaling in Cardiovascular Development.

Degree: 2015, University of Pennsylvania

 Development of the heart is an intricate and complex process. Crucial to this process is vascular patterning and the signals that properly guide developing vessels.… (more)

Subjects/Keywords: Cell Biology; Developmental Biology

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APA (6th Edition):

Aghajanian, H. (2015). Semaphorin 3d Signaling in Cardiovascular Development. (Thesis). University of Pennsylvania. Retrieved from http://repository.upenn.edu/edissertations/1577

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):

Aghajanian, Haig. “Semaphorin 3d Signaling in Cardiovascular Development.” 2015. Thesis, University of Pennsylvania. Accessed June 23, 2018. http://repository.upenn.edu/edissertations/1577.

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

MLA Handbook (7th Edition):

Aghajanian, Haig. “Semaphorin 3d Signaling in Cardiovascular Development.” 2015. Web. 23 Jun 2018.

Vancouver:

Aghajanian H. Semaphorin 3d Signaling in Cardiovascular Development. [Internet] [Thesis]. University of Pennsylvania; 2015. [cited 2018 Jun 23]. Available from: http://repository.upenn.edu/edissertations/1577.

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

Council of Science Editors:

Aghajanian H. Semaphorin 3d Signaling in Cardiovascular Development. [Thesis]. University of Pennsylvania; 2015. Available from: http://repository.upenn.edu/edissertations/1577

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

5. Lou, Jieqiong. The Interplay of Signal Transduction and Membrane Traffic of the Macrophage Colony Stimulating Factor Receptor (MCSFR) Controls Macrophage Growth.

Degree: PhD, Chemistry and Biochemistry, 2013, South Dakota State University

  Macrophage colony stimulating factor receptor (MCSFR a.k.a CSF-1R), is a receptor tyrosine kinase (RTK) that is essential for the growth of myeloid stem cells,… (more)

Subjects/Keywords: Cell and Developmental Biology

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APA (6th Edition):

Lou, J. (2013). The Interplay of Signal Transduction and Membrane Traffic of the Macrophage Colony Stimulating Factor Receptor (MCSFR) Controls Macrophage Growth. (Doctoral Dissertation). South Dakota State University. Retrieved from http://openprairie.sdstate.edu/etd/1462

Chicago Manual of Style (16th Edition):

Lou, Jieqiong. “The Interplay of Signal Transduction and Membrane Traffic of the Macrophage Colony Stimulating Factor Receptor (MCSFR) Controls Macrophage Growth.” 2013. Doctoral Dissertation, South Dakota State University. Accessed June 23, 2018. http://openprairie.sdstate.edu/etd/1462.

MLA Handbook (7th Edition):

Lou, Jieqiong. “The Interplay of Signal Transduction and Membrane Traffic of the Macrophage Colony Stimulating Factor Receptor (MCSFR) Controls Macrophage Growth.” 2013. Web. 23 Jun 2018.

Vancouver:

Lou J. The Interplay of Signal Transduction and Membrane Traffic of the Macrophage Colony Stimulating Factor Receptor (MCSFR) Controls Macrophage Growth. [Internet] [Doctoral dissertation]. South Dakota State University; 2013. [cited 2018 Jun 23]. Available from: http://openprairie.sdstate.edu/etd/1462.

Council of Science Editors:

Lou J. The Interplay of Signal Transduction and Membrane Traffic of the Macrophage Colony Stimulating Factor Receptor (MCSFR) Controls Macrophage Growth. [Doctoral Dissertation]. South Dakota State University; 2013. Available from: http://openprairie.sdstate.edu/etd/1462

6. Tortelote, Giovane G. An Extra-Embryonic Wnt Signaling Event Controls Gastrulation in Mice: A Dissertation.

Degree: Graduate School of Biomedical Sciences, Program in Cell Biology, 2012, U of Massachusetts : Med

  The formation of the anterior-posterior axis requires a symmetry-breaking event that starts gastrulation. Ultimately, the morphogenetic movements of gastrulation reshape the embryo to its… (more)

Subjects/Keywords: Cell and Developmental Biology

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APA (6th Edition):

Tortelote, G. G. (2012). An Extra-Embryonic Wnt Signaling Event Controls Gastrulation in Mice: A Dissertation. (Doctoral Dissertation). U of Massachusetts : Med. Retrieved from http://escholarship.umassmed.edu/gsbs_diss/643

Chicago Manual of Style (16th Edition):

Tortelote, Giovane G. “An Extra-Embryonic Wnt Signaling Event Controls Gastrulation in Mice: A Dissertation.” 2012. Doctoral Dissertation, U of Massachusetts : Med. Accessed June 23, 2018. http://escholarship.umassmed.edu/gsbs_diss/643.

MLA Handbook (7th Edition):

Tortelote, Giovane G. “An Extra-Embryonic Wnt Signaling Event Controls Gastrulation in Mice: A Dissertation.” 2012. Web. 23 Jun 2018.

Vancouver:

Tortelote GG. An Extra-Embryonic Wnt Signaling Event Controls Gastrulation in Mice: A Dissertation. [Internet] [Doctoral dissertation]. U of Massachusetts : Med; 2012. [cited 2018 Jun 23]. Available from: http://escholarship.umassmed.edu/gsbs_diss/643.

Council of Science Editors:

Tortelote GG. An Extra-Embryonic Wnt Signaling Event Controls Gastrulation in Mice: A Dissertation. [Doctoral Dissertation]. U of Massachusetts : Med; 2012. Available from: http://escholarship.umassmed.edu/gsbs_diss/643

7. Porpiglia, Ermelinda. Digital and Analog STAT5 Signaling in Erythropoiesis: A Dissertation.

Degree: Graduate School of Biomedical Sciences, Program in Immunology and Virology, 2011, U of Massachusetts : Med

  Erythropoietin (Epo) modulates red blood cell production (erythropoiesis) by binding to its receptor and activating STAT5, a Signal Transducer and Activator of Transcription (STAT)… (more)

Subjects/Keywords: Cell and Developmental Biology

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APA (6th Edition):

Porpiglia, E. (2011). Digital and Analog STAT5 Signaling in Erythropoiesis: A Dissertation. (Doctoral Dissertation). U of Massachusetts : Med. Retrieved from http://escholarship.umassmed.edu/gsbs_diss/553

Chicago Manual of Style (16th Edition):

Porpiglia, Ermelinda. “Digital and Analog STAT5 Signaling in Erythropoiesis: A Dissertation.” 2011. Doctoral Dissertation, U of Massachusetts : Med. Accessed June 23, 2018. http://escholarship.umassmed.edu/gsbs_diss/553.

MLA Handbook (7th Edition):

Porpiglia, Ermelinda. “Digital and Analog STAT5 Signaling in Erythropoiesis: A Dissertation.” 2011. Web. 23 Jun 2018.

Vancouver:

Porpiglia E. Digital and Analog STAT5 Signaling in Erythropoiesis: A Dissertation. [Internet] [Doctoral dissertation]. U of Massachusetts : Med; 2011. [cited 2018 Jun 23]. Available from: http://escholarship.umassmed.edu/gsbs_diss/553.

Council of Science Editors:

Porpiglia E. Digital and Analog STAT5 Signaling in Erythropoiesis: A Dissertation. [Doctoral Dissertation]. U of Massachusetts : Med; 2011. Available from: http://escholarship.umassmed.edu/gsbs_diss/553

8. Johnston, Brian T. Serotonin-Expressing Cells in the Corpus of the Stomach Originate from Bone Marrow: A Master’s Thesis.

Degree: Graduate School of Biomedical Sciences, Interdisciplinary Graduate Program, 2012, U of Massachusetts : Med

  Neurogenin 3 and its downstream target NeuroD are basic helix-loop-helix transcription factors which promote endocrine differentiation in the gastrointestinal tract. However, mice lacking Ngn3… (more)

Subjects/Keywords: Cell and Developmental Biology

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APA (6th Edition):

Johnston, B. T. (2012). Serotonin-Expressing Cells in the Corpus of the Stomach Originate from Bone Marrow: A Master’s Thesis. (Masters Thesis). U of Massachusetts : Med. Retrieved from http://escholarship.umassmed.edu/gsbs_diss/639

Chicago Manual of Style (16th Edition):

Johnston, Brian T. “Serotonin-Expressing Cells in the Corpus of the Stomach Originate from Bone Marrow: A Master’s Thesis.” 2012. Masters Thesis, U of Massachusetts : Med. Accessed June 23, 2018. http://escholarship.umassmed.edu/gsbs_diss/639.

MLA Handbook (7th Edition):

Johnston, Brian T. “Serotonin-Expressing Cells in the Corpus of the Stomach Originate from Bone Marrow: A Master’s Thesis.” 2012. Web. 23 Jun 2018.

Vancouver:

Johnston BT. Serotonin-Expressing Cells in the Corpus of the Stomach Originate from Bone Marrow: A Master’s Thesis. [Internet] [Masters thesis]. U of Massachusetts : Med; 2012. [cited 2018 Jun 23]. Available from: http://escholarship.umassmed.edu/gsbs_diss/639.

Council of Science Editors:

Johnston BT. Serotonin-Expressing Cells in the Corpus of the Stomach Originate from Bone Marrow: A Master’s Thesis. [Masters Thesis]. U of Massachusetts : Med; 2012. Available from: http://escholarship.umassmed.edu/gsbs_diss/639


Brigham Young University

9. Folsom, Ryan J. Rapid Adaptation of Dopamine D2 Receptor Responses in the Brain and Blood Following Acute Ethanol.

Degree: MS, 2014, Brigham Young University

 Dopamine (DA) D2 receptor expression parallels DA levels in the brain and these autoreceptors have been shown to be modulated by long-term ethanol exposure. We… (more)

Subjects/Keywords: Cell and Developmental Biology; Physiology

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APA (6th Edition):

Folsom, R. J. (2014). Rapid Adaptation of Dopamine D2 Receptor Responses in the Brain and Blood Following Acute Ethanol. (Thesis). Brigham Young University. Retrieved from https://scholarsarchive.byu.edu/etd/5248

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):

Folsom, Ryan J. “Rapid Adaptation of Dopamine D2 Receptor Responses in the Brain and Blood Following Acute Ethanol.” 2014. Thesis, Brigham Young University. Accessed June 23, 2018. https://scholarsarchive.byu.edu/etd/5248.

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

MLA Handbook (7th Edition):

Folsom, Ryan J. “Rapid Adaptation of Dopamine D2 Receptor Responses in the Brain and Blood Following Acute Ethanol.” 2014. Web. 23 Jun 2018.

Vancouver:

Folsom RJ. Rapid Adaptation of Dopamine D2 Receptor Responses in the Brain and Blood Following Acute Ethanol. [Internet] [Thesis]. Brigham Young University; 2014. [cited 2018 Jun 23]. Available from: https://scholarsarchive.byu.edu/etd/5248.

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

Council of Science Editors:

Folsom RJ. Rapid Adaptation of Dopamine D2 Receptor Responses in the Brain and Blood Following Acute Ethanol. [Thesis]. Brigham Young University; 2014. Available from: https://scholarsarchive.byu.edu/etd/5248

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


Brigham Young University

10. Mabey, Jennifer Kei. Synaptic Plasticity in GABAergic Inhibition of VTA Neurons.

Degree: MS, 2014, Brigham Young University

 Past research has demonstrated that the motivational effects of opiates causes a change in ventral tegmental area (VTA) γ-amino butyric acid (GABA) subtype A receptor… (more)

Subjects/Keywords: Cell and Developmental Biology; Physiology

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APA (6th Edition):

Mabey, J. K. (2014). Synaptic Plasticity in GABAergic Inhibition of VTA Neurons. (Thesis). Brigham Young University. Retrieved from https://scholarsarchive.byu.edu/etd/5256

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):

Mabey, Jennifer Kei. “Synaptic Plasticity in GABAergic Inhibition of VTA Neurons.” 2014. Thesis, Brigham Young University. Accessed June 23, 2018. https://scholarsarchive.byu.edu/etd/5256.

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

MLA Handbook (7th Edition):

Mabey, Jennifer Kei. “Synaptic Plasticity in GABAergic Inhibition of VTA Neurons.” 2014. Web. 23 Jun 2018.

Vancouver:

Mabey JK. Synaptic Plasticity in GABAergic Inhibition of VTA Neurons. [Internet] [Thesis]. Brigham Young University; 2014. [cited 2018 Jun 23]. Available from: https://scholarsarchive.byu.edu/etd/5256.

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

Council of Science Editors:

Mabey JK. Synaptic Plasticity in GABAergic Inhibition of VTA Neurons. [Thesis]. Brigham Young University; 2014. Available from: https://scholarsarchive.byu.edu/etd/5256

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


Eastern Illinois University

11. Shah, Anit. The Role of CREG1 and PITX1 as Master Regulators of Liver Function.

Degree: MS, Biological Sciences, 2015, Eastern Illinois University

  Development in mammals requires a complex array of positive and negative regulatory signals and responses. The liver is a major organ that has been… (more)

Subjects/Keywords: Cell and Developmental Biology

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APA (6th Edition):

Shah, A. (2015). The Role of CREG1 and PITX1 as Master Regulators of Liver Function. (Masters Thesis). Eastern Illinois University. Retrieved from http://thekeep.eiu.edu/theses/2373

Chicago Manual of Style (16th Edition):

Shah, Anit. “The Role of CREG1 and PITX1 as Master Regulators of Liver Function.” 2015. Masters Thesis, Eastern Illinois University. Accessed June 23, 2018. http://thekeep.eiu.edu/theses/2373.

MLA Handbook (7th Edition):

Shah, Anit. “The Role of CREG1 and PITX1 as Master Regulators of Liver Function.” 2015. Web. 23 Jun 2018.

Vancouver:

Shah A. The Role of CREG1 and PITX1 as Master Regulators of Liver Function. [Internet] [Masters thesis]. Eastern Illinois University; 2015. [cited 2018 Jun 23]. Available from: http://thekeep.eiu.edu/theses/2373.

Council of Science Editors:

Shah A. The Role of CREG1 and PITX1 as Master Regulators of Liver Function. [Masters Thesis]. Eastern Illinois University; 2015. Available from: http://thekeep.eiu.edu/theses/2373


Brigham Young University

12. Chavez Matias, Elizabeth Murayama. Expression of Osteoarthritis Biomarkers in Temporomandibular Joints of Mice with and Without Receptor for Advanced Glycation End Products (RAGE).

Degree: MS, 2014, Brigham Young University

 This thesis will be organized into three chapters discussing the mechanism underlying the onset and progression of osteoarthritis (OA) in the temporomandibular joint (TMJ). Understanding… (more)

Subjects/Keywords: Cell and Developmental Biology; Physiology

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APA (6th Edition):

Chavez Matias, E. M. (2014). Expression of Osteoarthritis Biomarkers in Temporomandibular Joints of Mice with and Without Receptor for Advanced Glycation End Products (RAGE). (Thesis). Brigham Young University. Retrieved from https://scholarsarchive.byu.edu/etd/5242

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):

Chavez Matias, Elizabeth Murayama. “Expression of Osteoarthritis Biomarkers in Temporomandibular Joints of Mice with and Without Receptor for Advanced Glycation End Products (RAGE).” 2014. Thesis, Brigham Young University. Accessed June 23, 2018. https://scholarsarchive.byu.edu/etd/5242.

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

MLA Handbook (7th Edition):

Chavez Matias, Elizabeth Murayama. “Expression of Osteoarthritis Biomarkers in Temporomandibular Joints of Mice with and Without Receptor for Advanced Glycation End Products (RAGE).” 2014. Web. 23 Jun 2018.

Vancouver:

Chavez Matias EM. Expression of Osteoarthritis Biomarkers in Temporomandibular Joints of Mice with and Without Receptor for Advanced Glycation End Products (RAGE). [Internet] [Thesis]. Brigham Young University; 2014. [cited 2018 Jun 23]. Available from: https://scholarsarchive.byu.edu/etd/5242.

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

Council of Science Editors:

Chavez Matias EM. Expression of Osteoarthritis Biomarkers in Temporomandibular Joints of Mice with and Without Receptor for Advanced Glycation End Products (RAGE). [Thesis]. Brigham Young University; 2014. Available from: https://scholarsarchive.byu.edu/etd/5242

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


Brigham Young University

13. Moore, Timothy Michael. Examination of Anabolic Signaling and Muscle Growth with Caffeine Treatment in Overloaded Hindlimb Muscle and Electrically Stimulated Muscle Lacking Liver Kinase B1.

Degree: MS, 2014, Brigham Young University

 Skeletal muscle has the ability to increase in size (hypertrophy) after resistance is placed upon it. This hypertrophy is marked by significant upregulation of the… (more)

Subjects/Keywords: Cell and Developmental Biology; Physiology

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APA (6th Edition):

Moore, T. M. (2014). Examination of Anabolic Signaling and Muscle Growth with Caffeine Treatment in Overloaded Hindlimb Muscle and Electrically Stimulated Muscle Lacking Liver Kinase B1. (Thesis). Brigham Young University. Retrieved from https://scholarsarchive.byu.edu/etd/5260

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):

Moore, Timothy Michael. “Examination of Anabolic Signaling and Muscle Growth with Caffeine Treatment in Overloaded Hindlimb Muscle and Electrically Stimulated Muscle Lacking Liver Kinase B1.” 2014. Thesis, Brigham Young University. Accessed June 23, 2018. https://scholarsarchive.byu.edu/etd/5260.

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

MLA Handbook (7th Edition):

Moore, Timothy Michael. “Examination of Anabolic Signaling and Muscle Growth with Caffeine Treatment in Overloaded Hindlimb Muscle and Electrically Stimulated Muscle Lacking Liver Kinase B1.” 2014. Web. 23 Jun 2018.

Vancouver:

Moore TM. Examination of Anabolic Signaling and Muscle Growth with Caffeine Treatment in Overloaded Hindlimb Muscle and Electrically Stimulated Muscle Lacking Liver Kinase B1. [Internet] [Thesis]. Brigham Young University; 2014. [cited 2018 Jun 23]. Available from: https://scholarsarchive.byu.edu/etd/5260.

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

Council of Science Editors:

Moore TM. Examination of Anabolic Signaling and Muscle Growth with Caffeine Treatment in Overloaded Hindlimb Muscle and Electrically Stimulated Muscle Lacking Liver Kinase B1. [Thesis]. Brigham Young University; 2014. Available from: https://scholarsarchive.byu.edu/etd/5260

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


Loyola University Chicago

14. Silva, Diane. Regulation of Gonad Morphogenesis in Drosophila Melanogaster by Broad Complex, Tramtrack and Bric à Brac Transcription Factors.

Degree: MS, Biology, 2016, Loyola University Chicago

  During embryogenesis, primordial germ cells (PGCs) and somatic gonadal precursor cells (SGPs) migrate and coalesce to form the early gonad. A failure of SGPs… (more)

Subjects/Keywords: Cell and Developmental Biology

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APA (6th Edition):

Silva, D. (2016). Regulation of Gonad Morphogenesis in Drosophila Melanogaster by Broad Complex, Tramtrack and Bric à Brac Transcription Factors. (Thesis). Loyola University Chicago. Retrieved from http://ecommons.luc.edu/luc_theses/3271

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):

Silva, Diane. “Regulation of Gonad Morphogenesis in Drosophila Melanogaster by Broad Complex, Tramtrack and Bric à Brac Transcription Factors.” 2016. Thesis, Loyola University Chicago. Accessed June 23, 2018. http://ecommons.luc.edu/luc_theses/3271.

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

MLA Handbook (7th Edition):

Silva, Diane. “Regulation of Gonad Morphogenesis in Drosophila Melanogaster by Broad Complex, Tramtrack and Bric à Brac Transcription Factors.” 2016. Web. 23 Jun 2018.

Vancouver:

Silva D. Regulation of Gonad Morphogenesis in Drosophila Melanogaster by Broad Complex, Tramtrack and Bric à Brac Transcription Factors. [Internet] [Thesis]. Loyola University Chicago; 2016. [cited 2018 Jun 23]. Available from: http://ecommons.luc.edu/luc_theses/3271.

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

Council of Science Editors:

Silva D. Regulation of Gonad Morphogenesis in Drosophila Melanogaster by Broad Complex, Tramtrack and Bric à Brac Transcription Factors. [Thesis]. Loyola University Chicago; 2016. Available from: http://ecommons.luc.edu/luc_theses/3271

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


University of Kansas

15. Wang, Xiaochen. Forward and reverse genetic approaches to identify genes involved in leg morphogenesis in Drosophila.

Degree: PhD, Molecular Biosciences, 2010, University of Kansas

 Development of Drosophila leg imaginal discs provides an ideal model to study hormone-regulated morphogenesis. During the onset of metamorphosis, a pulse of ecdysone triggers the… (more)

Subjects/Keywords: Biology; Genetics; Developmental biology; Cell biology

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APA (6th Edition):

Wang, X. (2010). Forward and reverse genetic approaches to identify genes involved in leg morphogenesis in Drosophila. (Doctoral Dissertation). University of Kansas. Retrieved from http://hdl.handle.net/1808/6402

Chicago Manual of Style (16th Edition):

Wang, Xiaochen. “Forward and reverse genetic approaches to identify genes involved in leg morphogenesis in Drosophila.” 2010. Doctoral Dissertation, University of Kansas. Accessed June 23, 2018. http://hdl.handle.net/1808/6402.

MLA Handbook (7th Edition):

Wang, Xiaochen. “Forward and reverse genetic approaches to identify genes involved in leg morphogenesis in Drosophila.” 2010. Web. 23 Jun 2018.

Vancouver:

Wang X. Forward and reverse genetic approaches to identify genes involved in leg morphogenesis in Drosophila. [Internet] [Doctoral dissertation]. University of Kansas; 2010. [cited 2018 Jun 23]. Available from: http://hdl.handle.net/1808/6402.

Council of Science Editors:

Wang X. Forward and reverse genetic approaches to identify genes involved in leg morphogenesis in Drosophila. [Doctoral Dissertation]. University of Kansas; 2010. Available from: http://hdl.handle.net/1808/6402


University of Western Ontario

16. Evered, Caitlin L. Inhibition Of MT1-MMP Proteolytic Function And ERK1/2 Signalling Influences Breast Cancer Cell Migration And Invasion Through Changes In MMP-2 And MMP-9 Expression.

Degree: 2016, University of Western Ontario

 Membrane-type 1 matrix metalloproteinase (MT1-MMP) is a multifunctional protease that invokes changes extracellularly via cleavages of ECM substrates, and intracellularly through induction of cell signalling… (more)

Subjects/Keywords: Cancer Biology; Cell Biology; Developmental Biology

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APA (6th Edition):

Evered, C. L. (2016). Inhibition Of MT1-MMP Proteolytic Function And ERK1/2 Signalling Influences Breast Cancer Cell Migration And Invasion Through Changes In MMP-2 And MMP-9 Expression. (Thesis). University of Western Ontario. Retrieved from https://ir.lib.uwo.ca/etd/3900

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):

Evered, Caitlin L. “Inhibition Of MT1-MMP Proteolytic Function And ERK1/2 Signalling Influences Breast Cancer Cell Migration And Invasion Through Changes In MMP-2 And MMP-9 Expression.” 2016. Thesis, University of Western Ontario. Accessed June 23, 2018. https://ir.lib.uwo.ca/etd/3900.

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

MLA Handbook (7th Edition):

Evered, Caitlin L. “Inhibition Of MT1-MMP Proteolytic Function And ERK1/2 Signalling Influences Breast Cancer Cell Migration And Invasion Through Changes In MMP-2 And MMP-9 Expression.” 2016. Web. 23 Jun 2018.

Vancouver:

Evered CL. Inhibition Of MT1-MMP Proteolytic Function And ERK1/2 Signalling Influences Breast Cancer Cell Migration And Invasion Through Changes In MMP-2 And MMP-9 Expression. [Internet] [Thesis]. University of Western Ontario; 2016. [cited 2018 Jun 23]. Available from: https://ir.lib.uwo.ca/etd/3900.

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

Council of Science Editors:

Evered CL. Inhibition Of MT1-MMP Proteolytic Function And ERK1/2 Signalling Influences Breast Cancer Cell Migration And Invasion Through Changes In MMP-2 And MMP-9 Expression. [Thesis]. University of Western Ontario; 2016. Available from: https://ir.lib.uwo.ca/etd/3900

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


University of Cambridge

17. Finegan, Tara May. The localisation and role of Sidekick at apical vertices in Drosophila epithelial morphogenesis .

Degree: 2018, University of Cambridge

 During animal development, epithelial tissues undergo morphogenesis in order to build tissues, organs and body structure. A key driving force in epithelial morphogenesis is cell(more)

Subjects/Keywords: Morphogenesis; Developmental Biology; Drosophila; Cell biology

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APA (6th Edition):

Finegan, T. M. (2018). The localisation and role of Sidekick at apical vertices in Drosophila epithelial morphogenesis . (Thesis). University of Cambridge. Retrieved from https://www.repository.cam.ac.uk/handle/1810/274873

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):

Finegan, Tara May. “The localisation and role of Sidekick at apical vertices in Drosophila epithelial morphogenesis .” 2018. Thesis, University of Cambridge. Accessed June 23, 2018. https://www.repository.cam.ac.uk/handle/1810/274873.

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

MLA Handbook (7th Edition):

Finegan, Tara May. “The localisation and role of Sidekick at apical vertices in Drosophila epithelial morphogenesis .” 2018. Web. 23 Jun 2018.

Vancouver:

Finegan TM. The localisation and role of Sidekick at apical vertices in Drosophila epithelial morphogenesis . [Internet] [Thesis]. University of Cambridge; 2018. [cited 2018 Jun 23]. Available from: https://www.repository.cam.ac.uk/handle/1810/274873.

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

Council of Science Editors:

Finegan TM. The localisation and role of Sidekick at apical vertices in Drosophila epithelial morphogenesis . [Thesis]. University of Cambridge; 2018. Available from: https://www.repository.cam.ac.uk/handle/1810/274873

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

18. Gannon, Hugh S. Mdm2-p53 Signaling in Tissue Homeostasis and the DNA Damage Response: A Dissertation.

Degree: Graduate School of Biomedical Sciences, Program in Cell Biology, 2012, U of Massachusetts : Med

  The p53 transcription factor responds to various cellular stressors by regulating the expression of numerous target genes involved in cellular processes such as cell(more)

Subjects/Keywords: Cancer Biology; Cell and Developmental Biology

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APA (6th Edition):

Gannon, H. S. (2012). Mdm2-p53 Signaling in Tissue Homeostasis and the DNA Damage Response: A Dissertation. (Doctoral Dissertation). U of Massachusetts : Med. Retrieved from http://escholarship.umassmed.edu/gsbs_diss/631

Chicago Manual of Style (16th Edition):

Gannon, Hugh S. “Mdm2-p53 Signaling in Tissue Homeostasis and the DNA Damage Response: A Dissertation.” 2012. Doctoral Dissertation, U of Massachusetts : Med. Accessed June 23, 2018. http://escholarship.umassmed.edu/gsbs_diss/631.

MLA Handbook (7th Edition):

Gannon, Hugh S. “Mdm2-p53 Signaling in Tissue Homeostasis and the DNA Damage Response: A Dissertation.” 2012. Web. 23 Jun 2018.

Vancouver:

Gannon HS. Mdm2-p53 Signaling in Tissue Homeostasis and the DNA Damage Response: A Dissertation. [Internet] [Doctoral dissertation]. U of Massachusetts : Med; 2012. [cited 2018 Jun 23]. Available from: http://escholarship.umassmed.edu/gsbs_diss/631.

Council of Science Editors:

Gannon HS. Mdm2-p53 Signaling in Tissue Homeostasis and the DNA Damage Response: A Dissertation. [Doctoral Dissertation]. U of Massachusetts : Med; 2012. Available from: http://escholarship.umassmed.edu/gsbs_diss/631

19. Ramkumar, Charusheila. Antagonistic Pleiotropy: The Role of Smurf2 in Cancer and Aging: A Dissertation.

Degree: Graduate School of Biomedical Sciences, Cell Biology, 2012, U of Massachusetts : Med

  In response to telomere shortening, oxidative stress, DNA damage or aberrant activation of oncogenes, normal somatic cells exit the cell cycle and enter an… (more)

Subjects/Keywords: Cancer Biology; Cell and Developmental Biology

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APA (6th Edition):

Ramkumar, C. (2012). Antagonistic Pleiotropy: The Role of Smurf2 in Cancer and Aging: A Dissertation. (Doctoral Dissertation). U of Massachusetts : Med. Retrieved from http://escholarship.umassmed.edu/gsbs_diss/634

Chicago Manual of Style (16th Edition):

Ramkumar, Charusheila. “Antagonistic Pleiotropy: The Role of Smurf2 in Cancer and Aging: A Dissertation.” 2012. Doctoral Dissertation, U of Massachusetts : Med. Accessed June 23, 2018. http://escholarship.umassmed.edu/gsbs_diss/634.

MLA Handbook (7th Edition):

Ramkumar, Charusheila. “Antagonistic Pleiotropy: The Role of Smurf2 in Cancer and Aging: A Dissertation.” 2012. Web. 23 Jun 2018.

Vancouver:

Ramkumar C. Antagonistic Pleiotropy: The Role of Smurf2 in Cancer and Aging: A Dissertation. [Internet] [Doctoral dissertation]. U of Massachusetts : Med; 2012. [cited 2018 Jun 23]. Available from: http://escholarship.umassmed.edu/gsbs_diss/634.

Council of Science Editors:

Ramkumar C. Antagonistic Pleiotropy: The Role of Smurf2 in Cancer and Aging: A Dissertation. [Doctoral Dissertation]. U of Massachusetts : Med; 2012. Available from: http://escholarship.umassmed.edu/gsbs_diss/634


Iowa State University

20. Haage, Amanda Michelle. Microenvironment regulation of matrix metalloproteinase activity in pancreatic cancer cells.

Degree: 2014, Iowa State University

 Currently there are no reliable treatment options for cancer metastasis. The complex cascade of events leading to metastasis reveals a multitude of therapeutic targets, but… (more)

Subjects/Keywords: Molecular, Cellular, and Developmental Biology; Cell Biology

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APA (6th Edition):

Haage, A. M. (2014). Microenvironment regulation of matrix metalloproteinase activity in pancreatic cancer cells. (Thesis). Iowa State University. Retrieved from https://lib.dr.iastate.edu/etd/14152

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):

Haage, Amanda Michelle. “Microenvironment regulation of matrix metalloproteinase activity in pancreatic cancer cells.” 2014. Thesis, Iowa State University. Accessed June 23, 2018. https://lib.dr.iastate.edu/etd/14152.

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

MLA Handbook (7th Edition):

Haage, Amanda Michelle. “Microenvironment regulation of matrix metalloproteinase activity in pancreatic cancer cells.” 2014. Web. 23 Jun 2018.

Vancouver:

Haage AM. Microenvironment regulation of matrix metalloproteinase activity in pancreatic cancer cells. [Internet] [Thesis]. Iowa State University; 2014. [cited 2018 Jun 23]. Available from: https://lib.dr.iastate.edu/etd/14152.

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

Council of Science Editors:

Haage AM. Microenvironment regulation of matrix metalloproteinase activity in pancreatic cancer cells. [Thesis]. Iowa State University; 2014. Available from: https://lib.dr.iastate.edu/etd/14152

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


Purdue University

21. Henderson, Jonathan T. Intranuclear strain measured by iterative warping in cells under mechanical and osmotic stress.

Degree: PhD, Biomedical Engineering, 2014, Purdue University

  The nucleus is a membrane bound organelle and regulation center for gene expression in the cell. Mechanical forces transfer to the nucleus directly and… (more)

Subjects/Keywords: Biology; Biomechanics and Biotransport; Biophysics; Cell and Developmental Biology; Cell Biology

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APA (6th Edition):

Henderson, J. T. (2014). Intranuclear strain measured by iterative warping in cells under mechanical and osmotic stress. (Doctoral Dissertation). Purdue University. Retrieved from http://docs.lib.purdue.edu/open_access_dissertations/283

Chicago Manual of Style (16th Edition):

Henderson, Jonathan T. “Intranuclear strain measured by iterative warping in cells under mechanical and osmotic stress.” 2014. Doctoral Dissertation, Purdue University. Accessed June 23, 2018. http://docs.lib.purdue.edu/open_access_dissertations/283.

MLA Handbook (7th Edition):

Henderson, Jonathan T. “Intranuclear strain measured by iterative warping in cells under mechanical and osmotic stress.” 2014. Web. 23 Jun 2018.

Vancouver:

Henderson JT. Intranuclear strain measured by iterative warping in cells under mechanical and osmotic stress. [Internet] [Doctoral dissertation]. Purdue University; 2014. [cited 2018 Jun 23]. Available from: http://docs.lib.purdue.edu/open_access_dissertations/283.

Council of Science Editors:

Henderson JT. Intranuclear strain measured by iterative warping in cells under mechanical and osmotic stress. [Doctoral Dissertation]. Purdue University; 2014. Available from: http://docs.lib.purdue.edu/open_access_dissertations/283

22. Yildirim, Ozlem. Chromatin Dynamics in Pluripotency and Differentiation: A Dissertation.

Degree: Graduate School of Biomedical Sciences, Interdisciplinary Graduate Program, 2012, U of Massachusetts : Med

  Different cell types in multi-cellular organisms heritably maintain different gene expression patterns despite carrying the same genome; a phenomenon termed epigenetics. It is widely… (more)

Subjects/Keywords: Cell and Developmental Biology; Genetics and Genomics

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APA (6th Edition):

Yildirim, O. (2012). Chromatin Dynamics in Pluripotency and Differentiation: A Dissertation. (Doctoral Dissertation). U of Massachusetts : Med. Retrieved from http://escholarship.umassmed.edu/gsbs_diss/623

Chicago Manual of Style (16th Edition):

Yildirim, Ozlem. “Chromatin Dynamics in Pluripotency and Differentiation: A Dissertation.” 2012. Doctoral Dissertation, U of Massachusetts : Med. Accessed June 23, 2018. http://escholarship.umassmed.edu/gsbs_diss/623.

MLA Handbook (7th Edition):

Yildirim, Ozlem. “Chromatin Dynamics in Pluripotency and Differentiation: A Dissertation.” 2012. Web. 23 Jun 2018.

Vancouver:

Yildirim O. Chromatin Dynamics in Pluripotency and Differentiation: A Dissertation. [Internet] [Doctoral dissertation]. U of Massachusetts : Med; 2012. [cited 2018 Jun 23]. Available from: http://escholarship.umassmed.edu/gsbs_diss/623.

Council of Science Editors:

Yildirim O. Chromatin Dynamics in Pluripotency and Differentiation: A Dissertation. [Doctoral Dissertation]. U of Massachusetts : Med; 2012. Available from: http://escholarship.umassmed.edu/gsbs_diss/623


Iowa State University

23. Lin, Haining. Insights into the rice and Arabidopsis genomes: intron fates, paralogs, and lineage-specific genes.

Degree: 2009, Iowa State University

 With the availability of near-complete rice genome sequence, high-quality annotation data, and large expression profile datasets, we examined segmental duplication, intron turnover, and paralogous protein… (more)

Subjects/Keywords: Cell and Developmental Biology; Genetics and Genomics

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APA (6th Edition):

Lin, H. (2009). Insights into the rice and Arabidopsis genomes: intron fates, paralogs, and lineage-specific genes. (Thesis). Iowa State University. Retrieved from https://lib.dr.iastate.edu/etd/12194

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):

Lin, Haining. “Insights into the rice and Arabidopsis genomes: intron fates, paralogs, and lineage-specific genes.” 2009. Thesis, Iowa State University. Accessed June 23, 2018. https://lib.dr.iastate.edu/etd/12194.

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

MLA Handbook (7th Edition):

Lin, Haining. “Insights into the rice and Arabidopsis genomes: intron fates, paralogs, and lineage-specific genes.” 2009. Web. 23 Jun 2018.

Vancouver:

Lin H. Insights into the rice and Arabidopsis genomes: intron fates, paralogs, and lineage-specific genes. [Internet] [Thesis]. Iowa State University; 2009. [cited 2018 Jun 23]. Available from: https://lib.dr.iastate.edu/etd/12194.

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

Council of Science Editors:

Lin H. Insights into the rice and Arabidopsis genomes: intron fates, paralogs, and lineage-specific genes. [Thesis]. Iowa State University; 2009. Available from: https://lib.dr.iastate.edu/etd/12194

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


Iowa State University

24. Liu, Xiayan. var2 genetic suppressors.

Degree: 2010, Iowa State University

 The Arabidopsis variegation2 (var2) mutant, displaying a conspicuous green and white sectoring phenotype, is one of the most well-characterized variegation mutants and is the caused… (more)

Subjects/Keywords: Cell and Developmental Biology; Genetics and Genomics

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APA (6th Edition):

Liu, X. (2010). var2 genetic suppressors. (Thesis). Iowa State University. Retrieved from https://lib.dr.iastate.edu/etd/11956

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):

Liu, Xiayan. “var2 genetic suppressors.” 2010. Thesis, Iowa State University. Accessed June 23, 2018. https://lib.dr.iastate.edu/etd/11956.

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

MLA Handbook (7th Edition):

Liu, Xiayan. “var2 genetic suppressors.” 2010. Web. 23 Jun 2018.

Vancouver:

Liu X. var2 genetic suppressors. [Internet] [Thesis]. Iowa State University; 2010. [cited 2018 Jun 23]. Available from: https://lib.dr.iastate.edu/etd/11956.

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

Council of Science Editors:

Liu X. var2 genetic suppressors. [Thesis]. Iowa State University; 2010. Available from: https://lib.dr.iastate.edu/etd/11956

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

25. Dillard, Paulette Rawley. Intracrine regulation of androgen receptor in prostate cancer.

Degree: PhD, Biology, 2010, Clark University Atlanta

  The proliferation and differentiation of normal prostate epithelial cells depend upon the action of the androgens, testosterone and dihydrotestosterone. Prostate cancer cells retain the… (more)

Subjects/Keywords: Prostate Cancer; Cell and Developmental Biology

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APA (6th Edition):

Dillard, P. R. (2010). Intracrine regulation of androgen receptor in prostate cancer. (Doctoral Dissertation). Clark University Atlanta. Retrieved from http://digitalcommons.auctr.edu/dissertations/161

Chicago Manual of Style (16th Edition):

Dillard, Paulette Rawley. “Intracrine regulation of androgen receptor in prostate cancer.” 2010. Doctoral Dissertation, Clark University Atlanta. Accessed June 23, 2018. http://digitalcommons.auctr.edu/dissertations/161.

MLA Handbook (7th Edition):

Dillard, Paulette Rawley. “Intracrine regulation of androgen receptor in prostate cancer.” 2010. Web. 23 Jun 2018.

Vancouver:

Dillard PR. Intracrine regulation of androgen receptor in prostate cancer. [Internet] [Doctoral dissertation]. Clark University Atlanta; 2010. [cited 2018 Jun 23]. Available from: http://digitalcommons.auctr.edu/dissertations/161.

Council of Science Editors:

Dillard PR. Intracrine regulation of androgen receptor in prostate cancer. [Doctoral Dissertation]. Clark University Atlanta; 2010. Available from: http://digitalcommons.auctr.edu/dissertations/161


University of Pennsylvania

26. Zhu, Wenting. Mechanisms of HDAC2 Function in the Regulation of Adult Cardiac Hypertrophy and Embryonic Myocyte Proliferation.

Degree: 2010, University of Pennsylvania

 HDACs can modify the structure and function of chromatin to regulate gene expression and can also modify many non-histone proteins that regulate cell function and… (more)

Subjects/Keywords: Cell and Developmental Biology; Life Sciences

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APA (6th Edition):

Zhu, W. (2010). Mechanisms of HDAC2 Function in the Regulation of Adult Cardiac Hypertrophy and Embryonic Myocyte Proliferation. (Thesis). University of Pennsylvania. Retrieved from http://repository.upenn.edu/edissertations/294

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):

Zhu, Wenting. “Mechanisms of HDAC2 Function in the Regulation of Adult Cardiac Hypertrophy and Embryonic Myocyte Proliferation.” 2010. Thesis, University of Pennsylvania. Accessed June 23, 2018. http://repository.upenn.edu/edissertations/294.

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

MLA Handbook (7th Edition):

Zhu, Wenting. “Mechanisms of HDAC2 Function in the Regulation of Adult Cardiac Hypertrophy and Embryonic Myocyte Proliferation.” 2010. Web. 23 Jun 2018.

Vancouver:

Zhu W. Mechanisms of HDAC2 Function in the Regulation of Adult Cardiac Hypertrophy and Embryonic Myocyte Proliferation. [Internet] [Thesis]. University of Pennsylvania; 2010. [cited 2018 Jun 23]. Available from: http://repository.upenn.edu/edissertations/294.

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

Council of Science Editors:

Zhu W. Mechanisms of HDAC2 Function in the Regulation of Adult Cardiac Hypertrophy and Embryonic Myocyte Proliferation. [Thesis]. University of Pennsylvania; 2010. Available from: http://repository.upenn.edu/edissertations/294

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


McMaster University

27. Mahmood, Tanya F. Biological Activity of Natural Cleavage Products of Slit in the Developing Drosophila Heart.

Degree: MSc, 2011, McMaster University

The Slit morphogen is a secreted glycoprotein that is naturally cleaved into two fragments. The amino fragment (N-Slit) contains Leucine Rich Repeats (LRR) that… (more)

Subjects/Keywords: Drosophila; heart; Slit; Robo; lumen; axons; Cell and Developmental Biology; Cell and Developmental Biology

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APA (6th Edition):

Mahmood, T. F. (2011). Biological Activity of Natural Cleavage Products of Slit in the Developing Drosophila Heart. (Masters Thesis). McMaster University. Retrieved from http://hdl.handle.net/11375/11180

Chicago Manual of Style (16th Edition):

Mahmood, Tanya F. “Biological Activity of Natural Cleavage Products of Slit in the Developing Drosophila Heart.” 2011. Masters Thesis, McMaster University. Accessed June 23, 2018. http://hdl.handle.net/11375/11180.

MLA Handbook (7th Edition):

Mahmood, Tanya F. “Biological Activity of Natural Cleavage Products of Slit in the Developing Drosophila Heart.” 2011. Web. 23 Jun 2018.

Vancouver:

Mahmood TF. Biological Activity of Natural Cleavage Products of Slit in the Developing Drosophila Heart. [Internet] [Masters thesis]. McMaster University; 2011. [cited 2018 Jun 23]. Available from: http://hdl.handle.net/11375/11180.

Council of Science Editors:

Mahmood TF. Biological Activity of Natural Cleavage Products of Slit in the Developing Drosophila Heart. [Masters Thesis]. McMaster University; 2011. Available from: http://hdl.handle.net/11375/11180


University of Michigan

28. Gu, Fangwei. Characterization of the Role of CSLD proteins in Arabidopsis Cell Wall Deposition.

Degree: PhD, Molecular, Cellular and Developmental Biology, 2015, University of Michigan

 Plant cells are surrounded by the plant cell wall, which defines the plant cell shape as well as provides structural integrity to plant tissues and… (more)

Subjects/Keywords: Plant Biology; Cell Biology; Cell Wall; Cell Cycle; Molecular, Cellular and Developmental Biology; Science

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APA (6th Edition):

Gu, F. (2015). Characterization of the Role of CSLD proteins in Arabidopsis Cell Wall Deposition. (Doctoral Dissertation). University of Michigan. Retrieved from http://hdl.handle.net/2027.42/116730

Chicago Manual of Style (16th Edition):

Gu, Fangwei. “Characterization of the Role of CSLD proteins in Arabidopsis Cell Wall Deposition.” 2015. Doctoral Dissertation, University of Michigan. Accessed June 23, 2018. http://hdl.handle.net/2027.42/116730.

MLA Handbook (7th Edition):

Gu, Fangwei. “Characterization of the Role of CSLD proteins in Arabidopsis Cell Wall Deposition.” 2015. Web. 23 Jun 2018.

Vancouver:

Gu F. Characterization of the Role of CSLD proteins in Arabidopsis Cell Wall Deposition. [Internet] [Doctoral dissertation]. University of Michigan; 2015. [cited 2018 Jun 23]. Available from: http://hdl.handle.net/2027.42/116730.

Council of Science Editors:

Gu F. Characterization of the Role of CSLD proteins in Arabidopsis Cell Wall Deposition. [Doctoral Dissertation]. University of Michigan; 2015. Available from: http://hdl.handle.net/2027.42/116730


UCLA

29. Seet, Christopher. In Vitro Generation of Adaptive Immunity from Hematopoietic Stem Cells.

Degree: Cellular & Molecular Pathology, 2018, UCLA

 The engagement of a dendritic cell with a T cell expressing a cognate T cell receptor is the defining even in the initiation of adaptive… (more)

Subjects/Keywords: Immunology; Developmental biology; Cellular biology; Dendritic cell; Hematopoiesis; Immunotherapy; T cell

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APA (6th Edition):

Seet, C. (2018). In Vitro Generation of Adaptive Immunity from Hematopoietic Stem Cells. (Thesis). UCLA. Retrieved from http://www.escholarship.org/uc/item/7qx121wd

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):

Seet, Christopher. “In Vitro Generation of Adaptive Immunity from Hematopoietic Stem Cells.” 2018. Thesis, UCLA. Accessed June 23, 2018. http://www.escholarship.org/uc/item/7qx121wd.

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

MLA Handbook (7th Edition):

Seet, Christopher. “In Vitro Generation of Adaptive Immunity from Hematopoietic Stem Cells.” 2018. Web. 23 Jun 2018.

Vancouver:

Seet C. In Vitro Generation of Adaptive Immunity from Hematopoietic Stem Cells. [Internet] [Thesis]. UCLA; 2018. [cited 2018 Jun 23]. Available from: http://www.escholarship.org/uc/item/7qx121wd.

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

Council of Science Editors:

Seet C. In Vitro Generation of Adaptive Immunity from Hematopoietic Stem Cells. [Thesis]. UCLA; 2018. Available from: http://www.escholarship.org/uc/item/7qx121wd

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


University of Pennsylvania

30. Yzaguirre, Amanda Danielle. The Specification Of Hemogenic Endothelium During Embryogenesis And Beyond.

Degree: 2017, University of Pennsylvania

 The primary goal of regenerative medicine is the in vitro derivation of cells that are functional and safe for transplantation into patients. Although progress has… (more)

Subjects/Keywords: Confocal microscopy; Development; Embryo; Hematopoiesis; Runx1; Biology; Cell Biology; Developmental Biology

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

APA (6th Edition):

Yzaguirre, A. D. (2017). The Specification Of Hemogenic Endothelium During Embryogenesis And Beyond. (Thesis). University of Pennsylvania. Retrieved from https://repository.upenn.edu/edissertations/2659

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):

Yzaguirre, Amanda Danielle. “The Specification Of Hemogenic Endothelium During Embryogenesis And Beyond.” 2017. Thesis, University of Pennsylvania. Accessed June 23, 2018. https://repository.upenn.edu/edissertations/2659.

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

MLA Handbook (7th Edition):

Yzaguirre, Amanda Danielle. “The Specification Of Hemogenic Endothelium During Embryogenesis And Beyond.” 2017. Web. 23 Jun 2018.

Vancouver:

Yzaguirre AD. The Specification Of Hemogenic Endothelium During Embryogenesis And Beyond. [Internet] [Thesis]. University of Pennsylvania; 2017. [cited 2018 Jun 23]. Available from: https://repository.upenn.edu/edissertations/2659.

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

Council of Science Editors:

Yzaguirre AD. The Specification Of Hemogenic Endothelium During Embryogenesis And Beyond. [Thesis]. University of Pennsylvania; 2017. Available from: https://repository.upenn.edu/edissertations/2659

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

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