Alumni
Placement of Graduates [pdf]
Dissertations List [pdf]
Recent Graduates
Brooks Scull, MS Spring 2009 | Brooks completed his thesis, "Intestinal regeneration after irradiation: Stem cells and Sox9," in the Lund lab. Brooks' student bio: Don’t let the picture fool you! I’ve been really happy here at UNC Chapel Hill for over 10 years and going. I graduated in Biology from UNC in 2002 and during that time I worked in Dr. Pagano’s lab as a Lab Assistant. After graduating, I became a Research Technician in Dr. Lund’s lab here in the Physiology department. In Dr. Lund’s lab, I’ve had the opportunity to be a part of many studies investigating gastrointestinal disease along with diet and obesity. I’ve recently become a graduate student studying intestinal regeneration after irradiation and identifying stem cell markers. Chapel Hill is a really fun place to live, and it’s great to be only hours from the beach and the mountains. |
Tiffany Thai, PhD Spring 2009 | Tiffany completed her thesis, "Functional characterization of ADP ribosyl cyclase signaling pathways in the renal microcirculation" under the direction of William Arendshorst, PhD. She and her family have recently relocated to the Atlanta, Georgia area. Tiffany's student bio: I am originally from Asheboro , NC and I received my BS in Biology here at UNC. As an undergraduate, I was initially interested in microbiology. My first laboratory work was done to investigate the importance of the Tat pathway in the secretory pathway of Mycobacterium tuberculosis under the direction of Dr. Miriam Braunstein. I quickly found, however, that the complexity of eukaryotic signaling mechanisms was more interesting to me. As a result, I began simultaneously studying the role of Igf-1 in migration and proliferation of aortic vascular smooth muscle cells. In order to continue studying vascular biology, I joined the Cell and Molecular Physiology department here at UNC and began my current work in Dr. Bill Arendshorst's lab where I am currently studying the role of the ADP ribosyl cyclase signaling pathway in renal hemodynamics. |
Xinshuo Wang, MS Spring 2009 | Xinshuo completed her thesis, "Glycogen Synthase Kinase-3 is required for axon growth and development," in the Snider lab in spring of 2009. Xinshuo's student bio: I come from Nanjing, one of the oldest and most beautiful cities in China. I got my Bachelor's degree in Biopharmaceuticals from China Pharmaceutical University, where I learned how drug therapies are created using biological technologies. But gradually I found that the molecular basis of a disease is more important than creating the drug itself. In 2003, with the hope of pursuing advanced degrees to enrich my knowledge and enhance my ability to do biomedical research, I came to the USA and joined Dr. Michal Zolkiewski's lab in the Department of Biochemistry at Kansas State University. My study there focused on a protein called TorsinA, which is the molecular origin of a neurological disease, early-onset torsion dystonia. In 2005, I joined the Department of Cell and Molecular Physiology at UNC to get closer to the studies that are related to human disease. After finishing two rotations in my first year, I have decided to join Dr. Snider's lab. Work in the Snider lab is directed at the role of neuronal growth factors in the development and regeneration of axons. I am currently studying the function and regulation of Glycogen Synthase Kinase 3 in axon development. |
Damon Jacobs, PhD | Damon's doctoral work in the Cheney lab culminated in his thesis, "Myosin Vc is a class V myosin that Functions in Secretory Granule Trafficking." He defended his thesis in December 2008 and accepted a postdoctoral position at the University of Kansas. The position is part of the IRACDA (Institutional Research and Academic Career Development Award) program that partners the University of Kansas with Haskell Indian Nations University, which is small, all American Indian university located across town in Lawrence, KS. Postdoctoral fellows are granted a three year appointment with two years working primarily at the bench performing research and 1 year focusing on teaching and mentoring at Haskell. Damon's student bio: Unconventional myosins (non-muscle, actin-based molecular motors) are the focus of Dr Cheney’s lab, and my research is mostly focused on a class V myosin, myosin 5c. Myosin 5c associates with secretory organelles and is involved in regulated secretion from epithelial cells. I am taking a high resolution imaging approach to study the role of Myosin 5c on stimulated secretion in human breast cancer cells. I also research myosin 10, which is a class of myosin involved in filopodia formation, cell adhesion, and possibly guidance during cellular migration, again taking an imaging approach in high spatial and temporal resolution. |
Christy Stack, MS | Christy completed her thesis, "The role of palladin in pancreatic cancer," in the Otey lab. Christy's student bio: I received my BS from New Mexico State University in Las Cruces, NM. While in my freshman year there, I decided that I wanted to go to graduate school and quickly pursued a job in a lab so I could get as much experience as possible. One of the people willing to take such a plucky undergrad was Dr. Brad Shuster, whom I worked with for all four years of college. Initially I had wanted to study Microbiology, but his projects involving cytokinesis in sea urchin embryos lured me away from bacteria, and I have been in love with cell biology ever since. |
Jason Clayton, PhD
| Jason completed his thesis work on the “Role of Vascular Endothelial Growth Factor-A in Collateral Growth and Development” in August 2008 and has returned to medical school to complete the MD requirements of his MD/PhD. Jason's student bio: I am an MD/PhD student and after finishing two years of Medical School, I decided to join the Faber lab where we study mechanisms of vascular growth and remodeling. My primary area of interest is in the process of arteriogenesis. Embryologically, specialized arteriole-to-arteriole anastomoses are formed which connect two parallel arteries. In the adult, if one of these parallel arteries becomes stenosed, or blocked, arteriogenesis occurs resulting in the positive (outward) remodeling of these pre-existing arteriole-to-arteriole anastomoses. Arteriogenesis also involves new growth (de novo) of blood vessels and their subsequent maturation into conduit arteries. Unlike angiogenesis, little is known about the mechanism or regulation of arteriogenesis. Because arteriogenesis provides a crucial endogenous bypass system, it is imperative to identify growth pathways that may be potential targets for therapeutic intervention. I am studying the role of VEGF signaling in the growth of these specialized vessels. In the lab, we use genetic and pharmacological approaches, combined with physiological measurements of blood flow, tissue perfusion, and blood pressure, to better understand the mechanism of arteriogenesis. |
Rebecca Sayers, PhD Graduated
| Rebecca's thesis, entitled “Focal Adhesion Kinase and its Endogenous Inhibitor, FRNK, in Vascular Development and Injury,” was done under the direction of Joan Taylor in the Department of Pathology and Laboratory Medicine. Rebecca accepted a position as a Medical Writer/Editor at Education and Training Systems International in Chapel Hill, NC. Rebecca's student bio: I am in the laboratory of Dr. Joan Taylor, a professor in the Department of Pathology, where my research is focused on investigating the role of FRNK (Focal Adhesion Kinase-Related Non-Kinase) in vascular smooth muscle cells (VSMC). FRNK is an endogenously expressed, dominant negative form of FAK (focal adhesion kinase) that is selectively expressed in smooth muscle. This expression is predominantly in conduit arteries and veins and also in the bronchioles of the lung. In particular, I am trying to determine how FRNK expression is regulated in VSMC and the role it plays in controlling cell proliferation and migration in vascular disease. |
Alicia Blaker, PhD Graduated | Alicia conducted her doctoral research on "Regulation of Smooth Muscle Specific Transcriptions by Serum Response Factor and Formin Homology Domain Containing Protein-1” in the laboratory of Chris Mack in the Department of Pathology and Laboratory Medicine. She will pursue her postdoctoral training in the Boston area. Alicia's student bio: My current lab focuses on cardiovascular physiology and pathology. I study Serum Response Factor, a transcription factor that is required for expression of nearly all of the vascular smooth muscle genes. We have identified post-translational modifications in SRF that stimulate aberrant changes in the smooth muscle phenotype and have used SRF -/- murine embryonic stem cells to study these changes. |
Department of Cell and Molecular Physiology - UNC School of Medicine