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You searched for +publisher:"University of Michigan" +contributor:("Gumucio, Deborah L"). Showing records 1 – 30 of 33 total matches.

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University of Michigan

1. Freddo, Andrew. New Perspectives on Intestinal Morphogenesis: The Role of Cell Division and Intraepithelial Forces in Villus Formation.

Degree: PhD, Cell & Developmental Biol PhD, 2018, University of Michigan

 Finger-like projections called villi convolute the intestinal surface, maximizing the area for nutrient absorption. Villi are rapidly formed and patterned during embryonic development; in the… (more)

Subjects/Keywords: small intestine; cell division; intestinal development; Molecular, Cellular and Developmental Biology; Health Sciences; Science

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APA (6th Edition):

Freddo, A. (2018). New Perspectives on Intestinal Morphogenesis: The Role of Cell Division and Intraepithelial Forces in Villus Formation. (Doctoral Dissertation). University of Michigan. Retrieved from http://hdl.handle.net/2027.42/144092

Chicago Manual of Style (16th Edition):

Freddo, Andrew. “New Perspectives on Intestinal Morphogenesis: The Role of Cell Division and Intraepithelial Forces in Villus Formation.” 2018. Doctoral Dissertation, University of Michigan. Accessed January 20, 2020. http://hdl.handle.net/2027.42/144092.

MLA Handbook (7th Edition):

Freddo, Andrew. “New Perspectives on Intestinal Morphogenesis: The Role of Cell Division and Intraepithelial Forces in Villus Formation.” 2018. Web. 20 Jan 2020.

Vancouver:

Freddo A. New Perspectives on Intestinal Morphogenesis: The Role of Cell Division and Intraepithelial Forces in Villus Formation. [Internet] [Doctoral dissertation]. University of Michigan; 2018. [cited 2020 Jan 20]. Available from: http://hdl.handle.net/2027.42/144092.

Council of Science Editors:

Freddo A. New Perspectives on Intestinal Morphogenesis: The Role of Cell Division and Intraepithelial Forces in Villus Formation. [Doctoral Dissertation]. University of Michigan; 2018. Available from: http://hdl.handle.net/2027.42/144092

2. Gurdziel, Katherine. Computational and Biological Approaches for Identification of Hedgehog Signaling Targets and Their Application to Intestinal Visceral Smooth Muscle Development in the Mouse.

Degree: PhD, Bioinformatics, 2016, University of Michigan

 The Hedgehog (Hh) pathway is an evolutionarily conserved cell-cell signaling pathway that controls organ development and homeostasis in embryos and adults. Hh signaling functions in… (more)

Subjects/Keywords: murine intestinal visceral smooth muscle development; Molecular, Cellular and Developmental Biology; Science

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APA (6th Edition):

Gurdziel, K. (2016). Computational and Biological Approaches for Identification of Hedgehog Signaling Targets and Their Application to Intestinal Visceral Smooth Muscle Development in the Mouse. (Doctoral Dissertation). University of Michigan. Retrieved from http://hdl.handle.net/2027.42/120838

Chicago Manual of Style (16th Edition):

Gurdziel, Katherine. “Computational and Biological Approaches for Identification of Hedgehog Signaling Targets and Their Application to Intestinal Visceral Smooth Muscle Development in the Mouse.” 2016. Doctoral Dissertation, University of Michigan. Accessed January 20, 2020. http://hdl.handle.net/2027.42/120838.

MLA Handbook (7th Edition):

Gurdziel, Katherine. “Computational and Biological Approaches for Identification of Hedgehog Signaling Targets and Their Application to Intestinal Visceral Smooth Muscle Development in the Mouse.” 2016. Web. 20 Jan 2020.

Vancouver:

Gurdziel K. Computational and Biological Approaches for Identification of Hedgehog Signaling Targets and Their Application to Intestinal Visceral Smooth Muscle Development in the Mouse. [Internet] [Doctoral dissertation]. University of Michigan; 2016. [cited 2020 Jan 20]. Available from: http://hdl.handle.net/2027.42/120838.

Council of Science Editors:

Gurdziel K. Computational and Biological Approaches for Identification of Hedgehog Signaling Targets and Their Application to Intestinal Visceral Smooth Muscle Development in the Mouse. [Doctoral Dissertation]. University of Michigan; 2016. Available from: http://hdl.handle.net/2027.42/120838


University of Michigan

3. Chiang, Chieh-Yin. A Novel Mechanism of Spermatogonia Death in Drosophila that Contributes to Tissue Homeostatis During Starvation.

Degree: PhD, Cell and Developmental Biology, 2016, University of Michigan

 Tissues are maintained in a homeostatic state by balancing the constant loss of old cells with the continued production of new cells. Importantly, dysfunction of… (more)

Subjects/Keywords: cell death; tissue homeostasis; phagocytosis; Molecular, Cellular and Developmental Biology; Science

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APA (6th Edition):

Chiang, C. (2016). A Novel Mechanism of Spermatogonia Death in Drosophila that Contributes to Tissue Homeostatis During Starvation. (Doctoral Dissertation). University of Michigan. Retrieved from http://hdl.handle.net/2027.42/135898

Chicago Manual of Style (16th Edition):

Chiang, Chieh-Yin. “A Novel Mechanism of Spermatogonia Death in Drosophila that Contributes to Tissue Homeostatis During Starvation.” 2016. Doctoral Dissertation, University of Michigan. Accessed January 20, 2020. http://hdl.handle.net/2027.42/135898.

MLA Handbook (7th Edition):

Chiang, Chieh-Yin. “A Novel Mechanism of Spermatogonia Death in Drosophila that Contributes to Tissue Homeostatis During Starvation.” 2016. Web. 20 Jan 2020.

Vancouver:

Chiang C. A Novel Mechanism of Spermatogonia Death in Drosophila that Contributes to Tissue Homeostatis During Starvation. [Internet] [Doctoral dissertation]. University of Michigan; 2016. [cited 2020 Jan 20]. Available from: http://hdl.handle.net/2027.42/135898.

Council of Science Editors:

Chiang C. A Novel Mechanism of Spermatogonia Death in Drosophila that Contributes to Tissue Homeostatis During Starvation. [Doctoral Dissertation]. University of Michigan; 2016. Available from: http://hdl.handle.net/2027.42/135898


University of Michigan

4. Burberry, Aaron Phillip. Understanding Pattern Recognition Receptor Signaling and its Effect on Hematopoietic Stem Cells.

Degree: PhD, Molecular & Cellular Pathology, 2013, University of Michigan

 Pattern recognition receptors (PRRs) sense unique and conserved structures common to many types of microorganisms and activate pro-inflammatory signaling cascades that are important for mounting… (more)

Subjects/Keywords: Genome-wide SiRNA Screen to Identify Regulators of NOD2; Model of Bacterial Infection to Assess HSC Function and Localization; Implications for Crohn's Disease and Extramedullary Hematopoiesis; Pathology; Health Sciences; Science

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APA (6th Edition):

Burberry, A. P. (2013). Understanding Pattern Recognition Receptor Signaling and its Effect on Hematopoietic Stem Cells. (Doctoral Dissertation). University of Michigan. Retrieved from http://hdl.handle.net/2027.42/102495

Chicago Manual of Style (16th Edition):

Burberry, Aaron Phillip. “Understanding Pattern Recognition Receptor Signaling and its Effect on Hematopoietic Stem Cells.” 2013. Doctoral Dissertation, University of Michigan. Accessed January 20, 2020. http://hdl.handle.net/2027.42/102495.

MLA Handbook (7th Edition):

Burberry, Aaron Phillip. “Understanding Pattern Recognition Receptor Signaling and its Effect on Hematopoietic Stem Cells.” 2013. Web. 20 Jan 2020.

Vancouver:

Burberry AP. Understanding Pattern Recognition Receptor Signaling and its Effect on Hematopoietic Stem Cells. [Internet] [Doctoral dissertation]. University of Michigan; 2013. [cited 2020 Jan 20]. Available from: http://hdl.handle.net/2027.42/102495.

Council of Science Editors:

Burberry AP. Understanding Pattern Recognition Receptor Signaling and its Effect on Hematopoietic Stem Cells. [Doctoral Dissertation]. University of Michigan; 2013. Available from: http://hdl.handle.net/2027.42/102495


University of Michigan

5. Slawny, Nicole A. Tri-lineage Differentiation of Embryonic Stem Cells: Role of Wnt Signaling.

Degree: PhD, Cell and Developmental Biology, 2010, University of Michigan

 Since embryonic stem cells (ESC) and the epiblast share a gene expression profile and an attenuated cell cycle, ESC are an attractive model system to… (more)

Subjects/Keywords: Tri-lineage Differentiation of Embryonic Stem Cells: Role of Wnt Signaling; Molecular, Cellular and Developmental Biology; Science

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APA (6th Edition):

Slawny, N. A. (2010). Tri-lineage Differentiation of Embryonic Stem Cells: Role of Wnt Signaling. (Doctoral Dissertation). University of Michigan. Retrieved from http://hdl.handle.net/2027.42/77753

Chicago Manual of Style (16th Edition):

Slawny, Nicole A. “Tri-lineage Differentiation of Embryonic Stem Cells: Role of Wnt Signaling.” 2010. Doctoral Dissertation, University of Michigan. Accessed January 20, 2020. http://hdl.handle.net/2027.42/77753.

MLA Handbook (7th Edition):

Slawny, Nicole A. “Tri-lineage Differentiation of Embryonic Stem Cells: Role of Wnt Signaling.” 2010. Web. 20 Jan 2020.

Vancouver:

Slawny NA. Tri-lineage Differentiation of Embryonic Stem Cells: Role of Wnt Signaling. [Internet] [Doctoral dissertation]. University of Michigan; 2010. [cited 2020 Jan 20]. Available from: http://hdl.handle.net/2027.42/77753.

Council of Science Editors:

Slawny NA. Tri-lineage Differentiation of Embryonic Stem Cells: Role of Wnt Signaling. [Doctoral Dissertation]. University of Michigan; 2010. Available from: http://hdl.handle.net/2027.42/77753


University of Michigan

6. Shao, Yue. Bioengineered in vitro Model for Peri-implantation Human Embryogenesis.

Degree: PhD, Mechanical Engineering, 2017, University of Michigan

 Implantation is a critical developmental milestone for early human embryogenesis and successful pregnancy. During implantation, the pluripotent epiblast gives rise to the squamous amnion and… (more)

Subjects/Keywords: Human pluripotent stem cells; In vitro developmental models; Mechanobiology; Biomaterials; Micro-engineering; Human embryology; Biomedical Engineering; Mechanical Engineering; Engineering

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APA (6th Edition):

Shao, Y. (2017). Bioengineered in vitro Model for Peri-implantation Human Embryogenesis. (Doctoral Dissertation). University of Michigan. Retrieved from http://hdl.handle.net/2027.42/136956

Chicago Manual of Style (16th Edition):

Shao, Yue. “Bioengineered in vitro Model for Peri-implantation Human Embryogenesis.” 2017. Doctoral Dissertation, University of Michigan. Accessed January 20, 2020. http://hdl.handle.net/2027.42/136956.

MLA Handbook (7th Edition):

Shao, Yue. “Bioengineered in vitro Model for Peri-implantation Human Embryogenesis.” 2017. Web. 20 Jan 2020.

Vancouver:

Shao Y. Bioengineered in vitro Model for Peri-implantation Human Embryogenesis. [Internet] [Doctoral dissertation]. University of Michigan; 2017. [cited 2020 Jan 20]. Available from: http://hdl.handle.net/2027.42/136956.

Council of Science Editors:

Shao Y. Bioengineered in vitro Model for Peri-implantation Human Embryogenesis. [Doctoral Dissertation]. University of Michigan; 2017. Available from: http://hdl.handle.net/2027.42/136956

7. Chin, Alana. Elucidating a novel WNT/?-CATENIN Signaling-Independent Environment that Precedes Villus Morphogenesis in the Embryonic Intestine.

Degree: PhD, Cell and Developmental Biology, 2017, University of Michigan

 The intestine is a vital organ responsible for several functions, including excretion of waste, acting as a major site of host immunity, and most importantly,… (more)

Subjects/Keywords: intestinal development; villus morphogenesis; cell signaling; Wnt/beta-catenin signaling pathway; Molecular, Cellular and Developmental Biology; Health Sciences

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APA (6th Edition):

Chin, A. (2017). Elucidating a novel WNT/?-CATENIN Signaling-Independent Environment that Precedes Villus Morphogenesis in the Embryonic Intestine. (Doctoral Dissertation). University of Michigan. Retrieved from http://hdl.handle.net/2027.42/136965

Chicago Manual of Style (16th Edition):

Chin, Alana. “Elucidating a novel WNT/?-CATENIN Signaling-Independent Environment that Precedes Villus Morphogenesis in the Embryonic Intestine.” 2017. Doctoral Dissertation, University of Michigan. Accessed January 20, 2020. http://hdl.handle.net/2027.42/136965.

MLA Handbook (7th Edition):

Chin, Alana. “Elucidating a novel WNT/?-CATENIN Signaling-Independent Environment that Precedes Villus Morphogenesis in the Embryonic Intestine.” 2017. Web. 20 Jan 2020.

Vancouver:

Chin A. Elucidating a novel WNT/?-CATENIN Signaling-Independent Environment that Precedes Villus Morphogenesis in the Embryonic Intestine. [Internet] [Doctoral dissertation]. University of Michigan; 2017. [cited 2020 Jan 20]. Available from: http://hdl.handle.net/2027.42/136965.

Council of Science Editors:

Chin A. Elucidating a novel WNT/?-CATENIN Signaling-Independent Environment that Precedes Villus Morphogenesis in the Embryonic Intestine. [Doctoral Dissertation]. University of Michigan; 2017. Available from: http://hdl.handle.net/2027.42/136965

8. Carulli, Alexis J. The Dynamic Regulation of Intestinal Stem Cells by Notch Signaling.

Degree: PhD, Molecular and Integrative Physiology, 2016, University of Michigan

 The intestinal epithelium has one of the fastest cellular turnover rates in the body, a process fueled by a highly active intestinal stem cell (ISC)… (more)

Subjects/Keywords: intestinal stem cell; Notch signaling; Physiology; Science

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APA (6th Edition):

Carulli, A. J. (2016). The Dynamic Regulation of Intestinal Stem Cells by Notch Signaling. (Doctoral Dissertation). University of Michigan. Retrieved from http://hdl.handle.net/2027.42/120757

Chicago Manual of Style (16th Edition):

Carulli, Alexis J. “The Dynamic Regulation of Intestinal Stem Cells by Notch Signaling.” 2016. Doctoral Dissertation, University of Michigan. Accessed January 20, 2020. http://hdl.handle.net/2027.42/120757.

MLA Handbook (7th Edition):

Carulli, Alexis J. “The Dynamic Regulation of Intestinal Stem Cells by Notch Signaling.” 2016. Web. 20 Jan 2020.

Vancouver:

Carulli AJ. The Dynamic Regulation of Intestinal Stem Cells by Notch Signaling. [Internet] [Doctoral dissertation]. University of Michigan; 2016. [cited 2020 Jan 20]. Available from: http://hdl.handle.net/2027.42/120757.

Council of Science Editors:

Carulli AJ. The Dynamic Regulation of Intestinal Stem Cells by Notch Signaling. [Doctoral Dissertation]. University of Michigan; 2016. Available from: http://hdl.handle.net/2027.42/120757


University of Michigan

9. Dosch, Joseph Scott. Examining the Role of Hedgehog Signaling in the Pancreatic Tumor Microenvironment.

Degree: PhD, Cellular & Molecular Biology, 2011, University of Michigan

 The Hedgehog (Hh) pathway is a conserved signaling network that plays a critical role during embryonic development as well as in the maintenance of adult… (more)

Subjects/Keywords: Pancreatic Cancer; Hedgehog Pathway; Health Sciences

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APA (6th Edition):

Dosch, J. S. (2011). Examining the Role of Hedgehog Signaling in the Pancreatic Tumor Microenvironment. (Doctoral Dissertation). University of Michigan. Retrieved from http://hdl.handle.net/2027.42/86276

Chicago Manual of Style (16th Edition):

Dosch, Joseph Scott. “Examining the Role of Hedgehog Signaling in the Pancreatic Tumor Microenvironment.” 2011. Doctoral Dissertation, University of Michigan. Accessed January 20, 2020. http://hdl.handle.net/2027.42/86276.

MLA Handbook (7th Edition):

Dosch, Joseph Scott. “Examining the Role of Hedgehog Signaling in the Pancreatic Tumor Microenvironment.” 2011. Web. 20 Jan 2020.

Vancouver:

Dosch JS. Examining the Role of Hedgehog Signaling in the Pancreatic Tumor Microenvironment. [Internet] [Doctoral dissertation]. University of Michigan; 2011. [cited 2020 Jan 20]. Available from: http://hdl.handle.net/2027.42/86276.

Council of Science Editors:

Dosch JS. Examining the Role of Hedgehog Signaling in the Pancreatic Tumor Microenvironment. [Doctoral Dissertation]. University of Michigan; 2011. Available from: http://hdl.handle.net/2027.42/86276


University of Michigan

10. Kiel, Mark Julin. Identification, Localization, and Characterization of Hematopoietic Stem Cells and Their Niche.

Degree: PhD, Cell and Developmental Biology, 2010, University of Michigan

 To improve our ability to identify HSCs and their localization in vivo we compared the gene expression profiles of highly purified hematopoietic stem cells (HSCs)… (more)

Subjects/Keywords: Hematopoietic Stem Cells; CD150; N-cadherin; Immortal Strand; Molecular, Cellular and Developmental Biology; Health Sciences

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APA (6th Edition):

Kiel, M. J. (2010). Identification, Localization, and Characterization of Hematopoietic Stem Cells and Their Niche. (Doctoral Dissertation). University of Michigan. Retrieved from http://hdl.handle.net/2027.42/75797

Chicago Manual of Style (16th Edition):

Kiel, Mark Julin. “Identification, Localization, and Characterization of Hematopoietic Stem Cells and Their Niche.” 2010. Doctoral Dissertation, University of Michigan. Accessed January 20, 2020. http://hdl.handle.net/2027.42/75797.

MLA Handbook (7th Edition):

Kiel, Mark Julin. “Identification, Localization, and Characterization of Hematopoietic Stem Cells and Their Niche.” 2010. Web. 20 Jan 2020.

Vancouver:

Kiel MJ. Identification, Localization, and Characterization of Hematopoietic Stem Cells and Their Niche. [Internet] [Doctoral dissertation]. University of Michigan; 2010. [cited 2020 Jan 20]. Available from: http://hdl.handle.net/2027.42/75797.

Council of Science Editors:

Kiel MJ. Identification, Localization, and Characterization of Hematopoietic Stem Cells and Their Niche. [Doctoral Dissertation]. University of Michigan; 2010. Available from: http://hdl.handle.net/2027.42/75797


University of Michigan

11. Mathew, Esha. Stromal Contribution to Pancreatic Cancer Pathogenesis.

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

 The overarching goal of this work is to understand the contribution of the stroma to pancreatic tumorigenesis. Pancreatic cancer is among the deadliest of human… (more)

Subjects/Keywords: pancreatic cancer; microenvironment; Hedgehog signaling; Molecular, Cellular and Developmental Biology; Science (General); Health Sciences; Science

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APA (6th Edition):

Mathew, E. (2015). Stromal Contribution to Pancreatic Cancer Pathogenesis. (Doctoral Dissertation). University of Michigan. Retrieved from http://hdl.handle.net/2027.42/116776

Chicago Manual of Style (16th Edition):

Mathew, Esha. “Stromal Contribution to Pancreatic Cancer Pathogenesis.” 2015. Doctoral Dissertation, University of Michigan. Accessed January 20, 2020. http://hdl.handle.net/2027.42/116776.

MLA Handbook (7th Edition):

Mathew, Esha. “Stromal Contribution to Pancreatic Cancer Pathogenesis.” 2015. Web. 20 Jan 2020.

Vancouver:

Mathew E. Stromal Contribution to Pancreatic Cancer Pathogenesis. [Internet] [Doctoral dissertation]. University of Michigan; 2015. [cited 2020 Jan 20]. Available from: http://hdl.handle.net/2027.42/116776.

Council of Science Editors:

Mathew E. Stromal Contribution to Pancreatic Cancer Pathogenesis. [Doctoral Dissertation]. University of Michigan; 2015. Available from: http://hdl.handle.net/2027.42/116776

12. Anderson, Erik Ryan. The Role of Hypoxia-Inducible Factors in the Regulation of Systemic Iron Homeostasis.

Degree: PhD, Cellular & Molecular Biology, 2013, University of Michigan

 Disorders of Iron Homeostasis affect over a billion people worldwide. These disorders can be grouped according to iron deficiency, the major cause of anemia, and… (more)

Subjects/Keywords: Iron Homeostasis; Hypoxia; Molecular, Cellular and Developmental Biology; Physiology; Science (General); Health Sciences; Science

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APA (6th Edition):

Anderson, E. R. (2013). The Role of Hypoxia-Inducible Factors in the Regulation of Systemic Iron Homeostasis. (Doctoral Dissertation). University of Michigan. Retrieved from http://hdl.handle.net/2027.42/98036

Chicago Manual of Style (16th Edition):

Anderson, Erik Ryan. “The Role of Hypoxia-Inducible Factors in the Regulation of Systemic Iron Homeostasis.” 2013. Doctoral Dissertation, University of Michigan. Accessed January 20, 2020. http://hdl.handle.net/2027.42/98036.

MLA Handbook (7th Edition):

Anderson, Erik Ryan. “The Role of Hypoxia-Inducible Factors in the Regulation of Systemic Iron Homeostasis.” 2013. Web. 20 Jan 2020.

Vancouver:

Anderson ER. The Role of Hypoxia-Inducible Factors in the Regulation of Systemic Iron Homeostasis. [Internet] [Doctoral dissertation]. University of Michigan; 2013. [cited 2020 Jan 20]. Available from: http://hdl.handle.net/2027.42/98036.

Council of Science Editors:

Anderson ER. The Role of Hypoxia-Inducible Factors in the Regulation of Systemic Iron Homeostasis. [Doctoral Dissertation]. University of Michigan; 2013. Available from: http://hdl.handle.net/2027.42/98036

13. Swinehart, Ilea T. HOX11 Function in Musculoskeletal Development and Repair.

Degree: PhD, Cellular & Molecular Biology, 2013, University of Michigan

 Previous genetic analyses of Hox loss-of-function phenotypes have demonstrated that these genes are essential regulators of skeletal patterning. However, as studies of Hox function in… (more)

Subjects/Keywords: Hox Genes; Musculoskeletal Development; Fracture Repair; Connective Tissue; Molecular, Cellular and Developmental Biology; Science

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APA (6th Edition):

Swinehart, I. T. (2013). HOX11 Function in Musculoskeletal Development and Repair. (Doctoral Dissertation). University of Michigan. Retrieved from http://hdl.handle.net/2027.42/99922

Chicago Manual of Style (16th Edition):

Swinehart, Ilea T. “HOX11 Function in Musculoskeletal Development and Repair.” 2013. Doctoral Dissertation, University of Michigan. Accessed January 20, 2020. http://hdl.handle.net/2027.42/99922.

MLA Handbook (7th Edition):

Swinehart, Ilea T. “HOX11 Function in Musculoskeletal Development and Repair.” 2013. Web. 20 Jan 2020.

Vancouver:

Swinehart IT. HOX11 Function in Musculoskeletal Development and Repair. [Internet] [Doctoral dissertation]. University of Michigan; 2013. [cited 2020 Jan 20]. Available from: http://hdl.handle.net/2027.42/99922.

Council of Science Editors:

Swinehart IT. HOX11 Function in Musculoskeletal Development and Repair. [Doctoral Dissertation]. University of Michigan; 2013. Available from: http://hdl.handle.net/2027.42/99922

14. Wang, Shih-Kai. Tooth Development: Learn from "The Normal" and "The Abnormal".

Degree: PhD, Oral Health Sciences, 2014, University of Michigan

 For the past decades, tooth development has been extensively studied as a model for understanding organogenesis of ectoderm-derived structures. Much has been learned from the… (more)

Subjects/Keywords: Tooth Development; Tooth Agenesis; Amelogenesis Imperfecta; FAM83H; Dental Enamel; Protein-protein Interaction; Dentistry; Health Sciences

…different institutes. Sequencing data generated at the University of Michigan DNA Sequencing Core… …was analyzed by Drs. James Cavalcoli, Manjusha Pande, and Yongsheng Bai at the University of… …Michigan Bioinformatics Core. Commercial services from Edge BioSystems (Gaithersburg, MD… 

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APA (6th Edition):

Wang, S. (2014). Tooth Development: Learn from "The Normal" and "The Abnormal". (Doctoral Dissertation). University of Michigan. Retrieved from http://hdl.handle.net/2027.42/107122

Chicago Manual of Style (16th Edition):

Wang, Shih-Kai. “Tooth Development: Learn from "The Normal" and "The Abnormal".” 2014. Doctoral Dissertation, University of Michigan. Accessed January 20, 2020. http://hdl.handle.net/2027.42/107122.

MLA Handbook (7th Edition):

Wang, Shih-Kai. “Tooth Development: Learn from "The Normal" and "The Abnormal".” 2014. Web. 20 Jan 2020.

Vancouver:

Wang S. Tooth Development: Learn from "The Normal" and "The Abnormal". [Internet] [Doctoral dissertation]. University of Michigan; 2014. [cited 2020 Jan 20]. Available from: http://hdl.handle.net/2027.42/107122.

Council of Science Editors:

Wang S. Tooth Development: Learn from "The Normal" and "The Abnormal". [Doctoral Dissertation]. University of Michigan; 2014. Available from: http://hdl.handle.net/2027.42/107122

15. He, Shenghui. Transcriptional Regulation of Stem Cell Self-Renewal.

Degree: PhD, Cellular & Molecular Biology, 2010, University of Michigan

 Self-renewal is a defining feature that distinguishes stem cells from transiently amplifying progenitors. Regulation of stem cell self-renewal involves precise control of cell cycle progression,… (more)

Subjects/Keywords: Stem Cells; Self-renewal; Bmi-1; Sox17; Molecular, Cellular and Developmental Biology; Science

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APA (6th Edition):

He, S. (2010). Transcriptional Regulation of Stem Cell Self-Renewal. (Doctoral Dissertation). University of Michigan. Retrieved from http://hdl.handle.net/2027.42/78905

Chicago Manual of Style (16th Edition):

He, Shenghui. “Transcriptional Regulation of Stem Cell Self-Renewal.” 2010. Doctoral Dissertation, University of Michigan. Accessed January 20, 2020. http://hdl.handle.net/2027.42/78905.

MLA Handbook (7th Edition):

He, Shenghui. “Transcriptional Regulation of Stem Cell Self-Renewal.” 2010. Web. 20 Jan 2020.

Vancouver:

He S. Transcriptional Regulation of Stem Cell Self-Renewal. [Internet] [Doctoral dissertation]. University of Michigan; 2010. [cited 2020 Jan 20]. Available from: http://hdl.handle.net/2027.42/78905.

Council of Science Editors:

He S. Transcriptional Regulation of Stem Cell Self-Renewal. [Doctoral Dissertation]. University of Michigan; 2010. Available from: http://hdl.handle.net/2027.42/78905

16. Prakash, Ajay. Development and Pathology of the Mammalian Pylorus.

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

 The pylorus is the junction between the stomach and the small intestine. It regulates food movement between the two organs and prevents the regurgitation of… (more)

Subjects/Keywords: Gata3; Nkx2-5; pyloric development; Sox9; Molecular, Cellular and Developmental Biology; Health Sciences

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APA (6th Edition):

Prakash, A. (2015). Development and Pathology of the Mammalian Pylorus. (Doctoral Dissertation). University of Michigan. Retrieved from http://hdl.handle.net/2027.42/111521

Chicago Manual of Style (16th Edition):

Prakash, Ajay. “Development and Pathology of the Mammalian Pylorus.” 2015. Doctoral Dissertation, University of Michigan. Accessed January 20, 2020. http://hdl.handle.net/2027.42/111521.

MLA Handbook (7th Edition):

Prakash, Ajay. “Development and Pathology of the Mammalian Pylorus.” 2015. Web. 20 Jan 2020.

Vancouver:

Prakash A. Development and Pathology of the Mammalian Pylorus. [Internet] [Doctoral dissertation]. University of Michigan; 2015. [cited 2020 Jan 20]. Available from: http://hdl.handle.net/2027.42/111521.

Council of Science Editors:

Prakash A. Development and Pathology of the Mammalian Pylorus. [Doctoral Dissertation]. University of Michigan; 2015. Available from: http://hdl.handle.net/2027.42/111521

17. Cao, Siyan. Endoplasmic Reticulum Stress in Intestinal Epithelial Cells and Inflammatory Bowel Disease.

Degree: PhD, Biological Chemistry, 2013, University of Michigan

 Recent studies linked endoplasmic reticulum stress and the unfolded protein response (UPR) to inflammatory bowel disease (IBD), which includes Crohn’s disease and ulcerative colitis. My… (more)

Subjects/Keywords: Endoplasmic Reticulum Stress; Inflammatory Bowel Disease; Intestinal Epithelial Cells; Biological Chemistry; Health Sciences

…x28;ULAM) at the University of Michigan Medical Center with free access to water and… …guidelines approved by the University of Michigan Committee on the Use and Care of Animals (… 

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APA (6th Edition):

Cao, S. (2013). Endoplasmic Reticulum Stress in Intestinal Epithelial Cells and Inflammatory Bowel Disease. (Doctoral Dissertation). University of Michigan. Retrieved from http://hdl.handle.net/2027.42/99965

Chicago Manual of Style (16th Edition):

Cao, Siyan. “Endoplasmic Reticulum Stress in Intestinal Epithelial Cells and Inflammatory Bowel Disease.” 2013. Doctoral Dissertation, University of Michigan. Accessed January 20, 2020. http://hdl.handle.net/2027.42/99965.

MLA Handbook (7th Edition):

Cao, Siyan. “Endoplasmic Reticulum Stress in Intestinal Epithelial Cells and Inflammatory Bowel Disease.” 2013. Web. 20 Jan 2020.

Vancouver:

Cao S. Endoplasmic Reticulum Stress in Intestinal Epithelial Cells and Inflammatory Bowel Disease. [Internet] [Doctoral dissertation]. University of Michigan; 2013. [cited 2020 Jan 20]. Available from: http://hdl.handle.net/2027.42/99965.

Council of Science Editors:

Cao S. Endoplasmic Reticulum Stress in Intestinal Epithelial Cells and Inflammatory Bowel Disease. [Doctoral Dissertation]. University of Michigan; 2013. Available from: http://hdl.handle.net/2027.42/99965

18. Holtz, Alexander. Novel Mechanisms that Antagonize Hedgehog Signaling at the Cell Surface During Vertebrate Embryogenesis.

Degree: PhD, Cellular & Molec Biology PhD, 2017, University of Michigan

 Hedgehog (HH) signaling is a conserved mode of cell-cell communication that is indispensible for embryogenesis. HH proteins are secreted ligands that travel over long distances… (more)

Subjects/Keywords: Hedgehog; negative feedback; neural tube; lung; heparan sulfate; basement membrane; Genetics; Molecular, Cellular and Developmental Biology; Neurosciences; Health Sciences; Science

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APA (6th Edition):

Holtz, A. (2017). Novel Mechanisms that Antagonize Hedgehog Signaling at the Cell Surface During Vertebrate Embryogenesis. (Doctoral Dissertation). University of Michigan. Retrieved from http://hdl.handle.net/2027.42/137137

Chicago Manual of Style (16th Edition):

Holtz, Alexander. “Novel Mechanisms that Antagonize Hedgehog Signaling at the Cell Surface During Vertebrate Embryogenesis.” 2017. Doctoral Dissertation, University of Michigan. Accessed January 20, 2020. http://hdl.handle.net/2027.42/137137.

MLA Handbook (7th Edition):

Holtz, Alexander. “Novel Mechanisms that Antagonize Hedgehog Signaling at the Cell Surface During Vertebrate Embryogenesis.” 2017. Web. 20 Jan 2020.

Vancouver:

Holtz A. Novel Mechanisms that Antagonize Hedgehog Signaling at the Cell Surface During Vertebrate Embryogenesis. [Internet] [Doctoral dissertation]. University of Michigan; 2017. [cited 2020 Jan 20]. Available from: http://hdl.handle.net/2027.42/137137.

Council of Science Editors:

Holtz A. Novel Mechanisms that Antagonize Hedgehog Signaling at the Cell Surface During Vertebrate Embryogenesis. [Doctoral Dissertation]. University of Michigan; 2017. Available from: http://hdl.handle.net/2027.42/137137

19. Gifford, Gail B. Notch1 and Notch2 Receptors Regulate Human and Mouse Gastric Epithelial Cell Homeostasis.

Degree: PhD, Molecular and Integrative Physiology, 2016, University of Michigan

 The gastric epithelium undergoes constant turnover that is maintained by a population of gastric stem cells. Gastric stem cells are under the regulation of multiple… (more)

Subjects/Keywords: gastric physiology; stem cells; Notch signaling pathway; Physiology; Health Sciences

…approved by the University of Michigan Committee on the Use and Care of Animals. Mouse Organoid… 

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APA (6th Edition):

Gifford, G. B. (2016). Notch1 and Notch2 Receptors Regulate Human and Mouse Gastric Epithelial Cell Homeostasis. (Doctoral Dissertation). University of Michigan. Retrieved from http://hdl.handle.net/2027.42/120753

Chicago Manual of Style (16th Edition):

Gifford, Gail B. “Notch1 and Notch2 Receptors Regulate Human and Mouse Gastric Epithelial Cell Homeostasis.” 2016. Doctoral Dissertation, University of Michigan. Accessed January 20, 2020. http://hdl.handle.net/2027.42/120753.

MLA Handbook (7th Edition):

Gifford, Gail B. “Notch1 and Notch2 Receptors Regulate Human and Mouse Gastric Epithelial Cell Homeostasis.” 2016. Web. 20 Jan 2020.

Vancouver:

Gifford GB. Notch1 and Notch2 Receptors Regulate Human and Mouse Gastric Epithelial Cell Homeostasis. [Internet] [Doctoral dissertation]. University of Michigan; 2016. [cited 2020 Jan 20]. Available from: http://hdl.handle.net/2027.42/120753.

Council of Science Editors:

Gifford GB. Notch1 and Notch2 Receptors Regulate Human and Mouse Gastric Epithelial Cell Homeostasis. [Doctoral Dissertation]. University of Michigan; 2016. Available from: http://hdl.handle.net/2027.42/120753

20. Krill, Kenneth Thomas. Effects of Dicer Inactivation in the Developing Mouse Adrenal Cortex and Micro-RNAs in Adrenocortical Carcinoma.

Degree: PhD, Cellular and Molecular Biology, 2014, University of Michigan

 Adrenocortical carcinoma (ACC) is a rare yet highly aggressive form of cancer with limited treatment options and poor prognosis. Insulin-like growth factor 2 (IGF2) is… (more)

Subjects/Keywords: MiRNA; MicroRNA; Adrenal Gland; Adrenal Cancer; Adrenal Development; Nr6a1; Molecular, Cellular and Developmental Biology; Science

…and characterized. Jerome W. Conn, a University of Michigan Medical School alumnus and… 

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APA (6th Edition):

Krill, K. T. (2014). Effects of Dicer Inactivation in the Developing Mouse Adrenal Cortex and Micro-RNAs in Adrenocortical Carcinoma. (Doctoral Dissertation). University of Michigan. Retrieved from http://hdl.handle.net/2027.42/107297

Chicago Manual of Style (16th Edition):

Krill, Kenneth Thomas. “Effects of Dicer Inactivation in the Developing Mouse Adrenal Cortex and Micro-RNAs in Adrenocortical Carcinoma.” 2014. Doctoral Dissertation, University of Michigan. Accessed January 20, 2020. http://hdl.handle.net/2027.42/107297.

MLA Handbook (7th Edition):

Krill, Kenneth Thomas. “Effects of Dicer Inactivation in the Developing Mouse Adrenal Cortex and Micro-RNAs in Adrenocortical Carcinoma.” 2014. Web. 20 Jan 2020.

Vancouver:

Krill KT. Effects of Dicer Inactivation in the Developing Mouse Adrenal Cortex and Micro-RNAs in Adrenocortical Carcinoma. [Internet] [Doctoral dissertation]. University of Michigan; 2014. [cited 2020 Jan 20]. Available from: http://hdl.handle.net/2027.42/107297.

Council of Science Editors:

Krill KT. Effects of Dicer Inactivation in the Developing Mouse Adrenal Cortex and Micro-RNAs in Adrenocortical Carcinoma. [Doctoral Dissertation]. University of Michigan; 2014. Available from: http://hdl.handle.net/2027.42/107297

21. Yadlapalli, Swathi. Non-Random Sister Chromatid Segregation During Stem Cell Division in Drosophila Melanogaster Testis.

Degree: PhD, Cell and Developmental Biology, 2013, University of Michigan

 Adult stem cells undergo asymmetric cell division to self-renew and to produce differentiated cells throughout the life of an organism. This increases the risk of… (more)

Subjects/Keywords: Non-random Sister Chromatid Segregation; Drosophila Male Germline Stem Cell; Molecular, Cellular and Developmental Biology; Health Sciences

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APA (6th Edition):

Yadlapalli, S. (2013). Non-Random Sister Chromatid Segregation During Stem Cell Division in Drosophila Melanogaster Testis. (Doctoral Dissertation). University of Michigan. Retrieved from http://hdl.handle.net/2027.42/102306

Chicago Manual of Style (16th Edition):

Yadlapalli, Swathi. “Non-Random Sister Chromatid Segregation During Stem Cell Division in Drosophila Melanogaster Testis.” 2013. Doctoral Dissertation, University of Michigan. Accessed January 20, 2020. http://hdl.handle.net/2027.42/102306.

MLA Handbook (7th Edition):

Yadlapalli, Swathi. “Non-Random Sister Chromatid Segregation During Stem Cell Division in Drosophila Melanogaster Testis.” 2013. Web. 20 Jan 2020.

Vancouver:

Yadlapalli S. Non-Random Sister Chromatid Segregation During Stem Cell Division in Drosophila Melanogaster Testis. [Internet] [Doctoral dissertation]. University of Michigan; 2013. [cited 2020 Jan 20]. Available from: http://hdl.handle.net/2027.42/102306.

Council of Science Editors:

Yadlapalli S. Non-Random Sister Chromatid Segregation During Stem Cell Division in Drosophila Melanogaster Testis. [Doctoral Dissertation]. University of Michigan; 2013. Available from: http://hdl.handle.net/2027.42/102306

22. Li, Xing. Bioinformatic Analysis of Epithelial:Mesenchymal Crosstalk during Mouse Gut Development and Patterning.

Degree: PhD, Bioinformatics, 2009, University of Michigan

 ABSTRACT BIOINFORMATIC ANALYSIS OF EPITHELIAL:MESENCHYMAL CROSSTALK DURING MOUSE GUT DEVELOPMENT AND PATTERNING By Xing Li Chair: Deborah L. Gumucio The small intestine develops from a… (more)

Subjects/Keywords: Bioinformatic Analysis; Gut Development; Epithelial-mesenchymal Crosstalk; Health Sciences; Science

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APA (6th Edition):

Li, X. (2009). Bioinformatic Analysis of Epithelial:Mesenchymal Crosstalk during Mouse Gut Development and Patterning. (Doctoral Dissertation). University of Michigan. Retrieved from http://hdl.handle.net/2027.42/62198

Chicago Manual of Style (16th Edition):

Li, Xing. “Bioinformatic Analysis of Epithelial:Mesenchymal Crosstalk during Mouse Gut Development and Patterning.” 2009. Doctoral Dissertation, University of Michigan. Accessed January 20, 2020. http://hdl.handle.net/2027.42/62198.

MLA Handbook (7th Edition):

Li, Xing. “Bioinformatic Analysis of Epithelial:Mesenchymal Crosstalk during Mouse Gut Development and Patterning.” 2009. Web. 20 Jan 2020.

Vancouver:

Li X. Bioinformatic Analysis of Epithelial:Mesenchymal Crosstalk during Mouse Gut Development and Patterning. [Internet] [Doctoral dissertation]. University of Michigan; 2009. [cited 2020 Jan 20]. Available from: http://hdl.handle.net/2027.42/62198.

Council of Science Editors:

Li X. Bioinformatic Analysis of Epithelial:Mesenchymal Crosstalk during Mouse Gut Development and Patterning. [Doctoral Dissertation]. University of Michigan; 2009. Available from: http://hdl.handle.net/2027.42/62198

23. Waghray, Meghna. Cell Specific Regulation of Sonic Hedgehog in Adult Stomach: Understanding Mechanisms Leading to Gastric Atrophy/Metaplasia. Mechanisms Leading to Gastric Atrophy/Metaplasia.

Degree: PhD, Cell and Developmental Biology, 2009, University of Michigan

 Helicobacter induced gastritis of the corpus results in loss of parietal cell function, loss of the oxyntic gland (atrophy), changes that predispose to gastric cancer.… (more)

Subjects/Keywords: Helicobacter Induced IL-1b Regulation of Sonic Hedgehog; Health Sciences; Science

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APA (6th Edition):

Waghray, M. (2009). Cell Specific Regulation of Sonic Hedgehog in Adult Stomach: Understanding Mechanisms Leading to Gastric Atrophy/Metaplasia. Mechanisms Leading to Gastric Atrophy/Metaplasia. (Doctoral Dissertation). University of Michigan. Retrieved from http://hdl.handle.net/2027.42/62276

Chicago Manual of Style (16th Edition):

Waghray, Meghna. “Cell Specific Regulation of Sonic Hedgehog in Adult Stomach: Understanding Mechanisms Leading to Gastric Atrophy/Metaplasia. Mechanisms Leading to Gastric Atrophy/Metaplasia.” 2009. Doctoral Dissertation, University of Michigan. Accessed January 20, 2020. http://hdl.handle.net/2027.42/62276.

MLA Handbook (7th Edition):

Waghray, Meghna. “Cell Specific Regulation of Sonic Hedgehog in Adult Stomach: Understanding Mechanisms Leading to Gastric Atrophy/Metaplasia. Mechanisms Leading to Gastric Atrophy/Metaplasia.” 2009. Web. 20 Jan 2020.

Vancouver:

Waghray M. Cell Specific Regulation of Sonic Hedgehog in Adult Stomach: Understanding Mechanisms Leading to Gastric Atrophy/Metaplasia. Mechanisms Leading to Gastric Atrophy/Metaplasia. [Internet] [Doctoral dissertation]. University of Michigan; 2009. [cited 2020 Jan 20]. Available from: http://hdl.handle.net/2027.42/62276.

Council of Science Editors:

Waghray M. Cell Specific Regulation of Sonic Hedgehog in Adult Stomach: Understanding Mechanisms Leading to Gastric Atrophy/Metaplasia. Mechanisms Leading to Gastric Atrophy/Metaplasia. [Doctoral Dissertation]. University of Michigan; 2009. Available from: http://hdl.handle.net/2027.42/62276

24. Staubach Grosse, Ann Marie. Evidence for a New Model of Intestinal Morphogenesis.

Degree: PhD, Cellular & Molecular Biology, 2011, University of Michigan

 During vertebrate intestinal development, coordinated morphogenetic movements between E12.5 and E16.5 transform the epithelial layer from a flat surface into evaginating villi and simultaneously generate… (more)

Subjects/Keywords: Intestinal Development; Lumen Formation; Epithelial Remodeling; Mouse Morphogenesis; Pseudostratified Epithelium; Intestinal Lengthening; Molecular, Cellular and Developmental Biology; Science

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APA (6th Edition):

Staubach Grosse, A. M. (2011). Evidence for a New Model of Intestinal Morphogenesis. (Doctoral Dissertation). University of Michigan. Retrieved from http://hdl.handle.net/2027.42/86275

Chicago Manual of Style (16th Edition):

Staubach Grosse, Ann Marie. “Evidence for a New Model of Intestinal Morphogenesis.” 2011. Doctoral Dissertation, University of Michigan. Accessed January 20, 2020. http://hdl.handle.net/2027.42/86275.

MLA Handbook (7th Edition):

Staubach Grosse, Ann Marie. “Evidence for a New Model of Intestinal Morphogenesis.” 2011. Web. 20 Jan 2020.

Vancouver:

Staubach Grosse AM. Evidence for a New Model of Intestinal Morphogenesis. [Internet] [Doctoral dissertation]. University of Michigan; 2011. [cited 2020 Jan 20]. Available from: http://hdl.handle.net/2027.42/86275.

Council of Science Editors:

Staubach Grosse AM. Evidence for a New Model of Intestinal Morphogenesis. [Doctoral Dissertation]. University of Michigan; 2011. Available from: http://hdl.handle.net/2027.42/86275

25. Yang, Hoseong. Hedgehog-Wnt Interactions during Pathologic Epithelial Bud Development and Skin Tumorigenesis.

Degree: PhD, Cellular & Molecular Biology, 2010, University of Michigan

 The Hedgehog (Hh) and canonical Wnt/beta-catenin signaling pathways are involved in various embryonic processes, and when aberrantly activated after birth in certain cell types or… (more)

Subjects/Keywords: Hedgehog, Wnt, BCC, Skin, Epithelial Bud; Dermatology; Molecular, Cellular and Developmental Biology; Health Sciences

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APA (6th Edition):

Yang, H. (2010). Hedgehog-Wnt Interactions during Pathologic Epithelial Bud Development and Skin Tumorigenesis. (Doctoral Dissertation). University of Michigan. Retrieved from http://hdl.handle.net/2027.42/75879

Chicago Manual of Style (16th Edition):

Yang, Hoseong. “Hedgehog-Wnt Interactions during Pathologic Epithelial Bud Development and Skin Tumorigenesis.” 2010. Doctoral Dissertation, University of Michigan. Accessed January 20, 2020. http://hdl.handle.net/2027.42/75879.

MLA Handbook (7th Edition):

Yang, Hoseong. “Hedgehog-Wnt Interactions during Pathologic Epithelial Bud Development and Skin Tumorigenesis.” 2010. Web. 20 Jan 2020.

Vancouver:

Yang H. Hedgehog-Wnt Interactions during Pathologic Epithelial Bud Development and Skin Tumorigenesis. [Internet] [Doctoral dissertation]. University of Michigan; 2010. [cited 2020 Jan 20]. Available from: http://hdl.handle.net/2027.42/75879.

Council of Science Editors:

Yang H. Hedgehog-Wnt Interactions during Pathologic Epithelial Bud Development and Skin Tumorigenesis. [Doctoral Dissertation]. University of Michigan; 2010. Available from: http://hdl.handle.net/2027.42/75879

26. Zacharias, William John. Homeostatic Roles for Adult Intestinal Hedgehog Signaling: Insight into Smooth Muscle Maintenance and Inflammatory Control.

Degree: PhD, Cell and Developmental Biology, 2011, University of Michigan

 The Hedgehog (Hh) signaling pathway is a critical regulator of cell migration, proliferation, and fate specification during mammalian development. In the gastrointestinal tract, Hh signals… (more)

Subjects/Keywords: Hedgehog Signaling; Intestine; Inflammation; Smooth Muscle; Molecular, Cellular and Developmental Biology; Science

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APA (6th Edition):

Zacharias, W. J. (2011). Homeostatic Roles for Adult Intestinal Hedgehog Signaling: Insight into Smooth Muscle Maintenance and Inflammatory Control. (Doctoral Dissertation). University of Michigan. Retrieved from http://hdl.handle.net/2027.42/84506

Chicago Manual of Style (16th Edition):

Zacharias, William John. “Homeostatic Roles for Adult Intestinal Hedgehog Signaling: Insight into Smooth Muscle Maintenance and Inflammatory Control.” 2011. Doctoral Dissertation, University of Michigan. Accessed January 20, 2020. http://hdl.handle.net/2027.42/84506.

MLA Handbook (7th Edition):

Zacharias, William John. “Homeostatic Roles for Adult Intestinal Hedgehog Signaling: Insight into Smooth Muscle Maintenance and Inflammatory Control.” 2011. Web. 20 Jan 2020.

Vancouver:

Zacharias WJ. Homeostatic Roles for Adult Intestinal Hedgehog Signaling: Insight into Smooth Muscle Maintenance and Inflammatory Control. [Internet] [Doctoral dissertation]. University of Michigan; 2011. [cited 2020 Jan 20]. Available from: http://hdl.handle.net/2027.42/84506.

Council of Science Editors:

Zacharias WJ. Homeostatic Roles for Adult Intestinal Hedgehog Signaling: Insight into Smooth Muscle Maintenance and Inflammatory Control. [Doctoral Dissertation]. University of Michigan; 2011. Available from: http://hdl.handle.net/2027.42/84506

27. Michael, Lowell Evan. Bmi1 and Hedgehog Signaling in Medulloblastoma Pathogenesis.

Degree: PhD, Cellular & Molecular Biology, 2010, University of Michigan

 Medulloblastoma is the most common malignant brain tumor in children, and occurs in up to 5% of patients with Gorlin syndrome, a familial cancer susceptibility… (more)

Subjects/Keywords: Bmi1; Hedgehog Signaling; Medulloblastoma Pathogenesis; Mouse Models of Cancer; Molecular, Cellular and Developmental Biology; Science

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APA (6th Edition):

Michael, L. E. (2010). Bmi1 and Hedgehog Signaling in Medulloblastoma Pathogenesis. (Doctoral Dissertation). University of Michigan. Retrieved from http://hdl.handle.net/2027.42/75987

Chicago Manual of Style (16th Edition):

Michael, Lowell Evan. “Bmi1 and Hedgehog Signaling in Medulloblastoma Pathogenesis.” 2010. Doctoral Dissertation, University of Michigan. Accessed January 20, 2020. http://hdl.handle.net/2027.42/75987.

MLA Handbook (7th Edition):

Michael, Lowell Evan. “Bmi1 and Hedgehog Signaling in Medulloblastoma Pathogenesis.” 2010. Web. 20 Jan 2020.

Vancouver:

Michael LE. Bmi1 and Hedgehog Signaling in Medulloblastoma Pathogenesis. [Internet] [Doctoral dissertation]. University of Michigan; 2010. [cited 2020 Jan 20]. Available from: http://hdl.handle.net/2027.42/75987.

Council of Science Editors:

Michael LE. Bmi1 and Hedgehog Signaling in Medulloblastoma Pathogenesis. [Doctoral Dissertation]. University of Michigan; 2010. Available from: http://hdl.handle.net/2027.42/75987

28. VanDussen, Kelli L. Notch-Regulated Mechanisms of Epithelial Cell Fate Selection in the Intestine.

Degree: PhD, Molecular and Integrative Physiology, 2010, University of Michigan

 Throughout the lifetime of an organism, progenitor cells in the intestine proliferate and differentiate to form cells of the secretory and absorptive lineages. Many intercellular… (more)

Subjects/Keywords: Intestine; Cellular Differentiation; Notch Signaling; Stem Cell; Molecular, Cellular and Developmental Biology; Physiology; Science

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APA (6th Edition):

VanDussen, K. L. (2010). Notch-Regulated Mechanisms of Epithelial Cell Fate Selection in the Intestine. (Doctoral Dissertation). University of Michigan. Retrieved from http://hdl.handle.net/2027.42/77890

Chicago Manual of Style (16th Edition):

VanDussen, Kelli L. “Notch-Regulated Mechanisms of Epithelial Cell Fate Selection in the Intestine.” 2010. Doctoral Dissertation, University of Michigan. Accessed January 20, 2020. http://hdl.handle.net/2027.42/77890.

MLA Handbook (7th Edition):

VanDussen, Kelli L. “Notch-Regulated Mechanisms of Epithelial Cell Fate Selection in the Intestine.” 2010. Web. 20 Jan 2020.

Vancouver:

VanDussen KL. Notch-Regulated Mechanisms of Epithelial Cell Fate Selection in the Intestine. [Internet] [Doctoral dissertation]. University of Michigan; 2010. [cited 2020 Jan 20]. Available from: http://hdl.handle.net/2027.42/77890.

Council of Science Editors:

VanDussen KL. Notch-Regulated Mechanisms of Epithelial Cell Fate Selection in the Intestine. [Doctoral Dissertation]. University of Michigan; 2010. Available from: http://hdl.handle.net/2027.42/77890

29. Udager, Aaron Mark. Cell-specific Gene Expression: Pylorus Morphogenesis and Hedgehog-regulated Enhancers.

Degree: PhD, Cell and Developmental Biology, 2012, University of Michigan

 The precise spatiotemporal control of gene expression is integral to the survival of all organisms. Inappropriate gene expression can lead to developmental defects in newborns,… (more)

Subjects/Keywords: Computational Biology; Intestine Development; Hedgehog Signaling; Pyloric Sphincter; Gata3; Enhancers; Molecular, Cellular and Developmental Biology; Health Sciences

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APA (6th Edition):

Udager, A. M. (2012). Cell-specific Gene Expression: Pylorus Morphogenesis and Hedgehog-regulated Enhancers. (Doctoral Dissertation). University of Michigan. Retrieved from http://hdl.handle.net/2027.42/91524

Chicago Manual of Style (16th Edition):

Udager, Aaron Mark. “Cell-specific Gene Expression: Pylorus Morphogenesis and Hedgehog-regulated Enhancers.” 2012. Doctoral Dissertation, University of Michigan. Accessed January 20, 2020. http://hdl.handle.net/2027.42/91524.

MLA Handbook (7th Edition):

Udager, Aaron Mark. “Cell-specific Gene Expression: Pylorus Morphogenesis and Hedgehog-regulated Enhancers.” 2012. Web. 20 Jan 2020.

Vancouver:

Udager AM. Cell-specific Gene Expression: Pylorus Morphogenesis and Hedgehog-regulated Enhancers. [Internet] [Doctoral dissertation]. University of Michigan; 2012. [cited 2020 Jan 20]. Available from: http://hdl.handle.net/2027.42/91524.

Council of Science Editors:

Udager AM. Cell-specific Gene Expression: Pylorus Morphogenesis and Hedgehog-regulated Enhancers. [Doctoral Dissertation]. University of Michigan; 2012. Available from: http://hdl.handle.net/2027.42/91524


University of Michigan

30. Brandt, William D. The Role of Gata2 in Hematopoietic and Vascular Development.

Degree: PhD, Cellular & Molecular Biology, 2009, University of Michigan

 Transcription factors play demonstrably critical roles in development. The transcription factor Gata2 is required for the proliferation of hematopoietic progenitors and proper urogenital development. Gata2… (more)

Subjects/Keywords: Development; Transcription; GATA; Hematopoiesis; Vasculature; Molecular, Cellular and Developmental Biology; Science

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APA (6th Edition):

Brandt, W. D. (2009). The Role of Gata2 in Hematopoietic and Vascular Development. (Doctoral Dissertation). University of Michigan. Retrieved from http://hdl.handle.net/2027.42/64600

Chicago Manual of Style (16th Edition):

Brandt, William D. “The Role of Gata2 in Hematopoietic and Vascular Development.” 2009. Doctoral Dissertation, University of Michigan. Accessed January 20, 2020. http://hdl.handle.net/2027.42/64600.

MLA Handbook (7th Edition):

Brandt, William D. “The Role of Gata2 in Hematopoietic and Vascular Development.” 2009. Web. 20 Jan 2020.

Vancouver:

Brandt WD. The Role of Gata2 in Hematopoietic and Vascular Development. [Internet] [Doctoral dissertation]. University of Michigan; 2009. [cited 2020 Jan 20]. Available from: http://hdl.handle.net/2027.42/64600.

Council of Science Editors:

Brandt WD. The Role of Gata2 in Hematopoietic and Vascular Development. [Doctoral Dissertation]. University of Michigan; 2009. Available from: http://hdl.handle.net/2027.42/64600

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