This application is for a competing renewal in the Cardiovascular Pathophysiology training program at UAB for pre-doctoral students which is currently in its 9th year. We have successfully recruited a significant proportion of minorities, MD/Ph.D students and women trainees. Since the appointment of the first trainees in late 1999 24 students have entered the training program with 16 having completed their graduate studies and developed science related careers in respected national research centers and universities. The training will be undertaken by faculty from six separate departments at the institution (four basic science and two clinical) with a expertise in a broad range of research areas relevant to cardiovascular research. This training program recognizes the integrated and multi-disciplinary nature of modern cardiovascular research and includes faculty from six research centers at UAB encompassing institutional areas of strength in Free Radical Biology, Nephrology Research, Clinical Nutrition, BioMatrix Engineering and Regenerative Medicine Comprehensive Diabetes and Hypertension. The students will earn degrees in the graduate programs in pathology, physiology or integrated biomedical sciences (IBS). Students supported by the proposal will have completed the first year, selected a project and mentor with cardiovascular relevance and demonstrated excellence in their studies and research potential. The program plan consists of a didactic component that emphasizes cardiovascular disease in the context of other pathologies with particular emphasis on molecular mechanisms of disease. An area of increasing significance in cardiovascular research and a strength at UAB. We also include courses that encompass career enhancement components including preparation for research applications, review of papers, and preparation of review articles. In addition we have included an emerging and important area in graduate education in the development of the management and personnel skills necessary to direct a research group. No overlap with current training programs at this institution exist.

Agency
National Institute of Health (NIH)
Institute
National Heart, Lung, and Blood Institute (NHLBI)
Type
Institutional National Research Service Award (T32)
Project #
5T32HL007918-12
Application #
7828073
Study Section
NHLBI Institutional Training Mechanism Review Committee (NITM)
Program Officer
Commarato, Michael
Project Start
1999-07-01
Project End
2014-06-30
Budget Start
2010-07-01
Budget End
2011-06-30
Support Year
12
Fiscal Year
2010
Total Cost
$201,614
Indirect Cost
Name
University of Alabama Birmingham
Department
Pathology
Type
Schools of Medicine
DUNS #
063690705
City
Birmingham
State
AL
Country
United States
Zip Code
35294
Holdbrooks, Andrew T; Britain, Colleen M; Bellis, Susan L (2018) ST6Gal-I sialyltransferase promotes tumor necrosis factor (TNF)-mediated cancer cell survival via sialylation of the TNF receptor 1 (TNFR1) death receptor. J Biol Chem 293:1610-1622
Owusu, Benjamin Y; Zimmerman, Kurt A; Murphy-Ullrich, Joanne E (2018) The role of the endoplasmic reticulum protein calreticulin in mediating TGF-?-stimulated extracellular matrix production in fibrotic disease. J Cell Commun Signal 12:289-299
Lambert, James A; Carlisle, Matthew A; Lam, Adam et al. (2017) Mechanisms and Treatment of Halogen Inhalation-Induced Pulmonary and Systemic Injuries in Pregnant Mice. Hypertension 70:390-400
Willig, Amanda L; Kramer, Philip A; Chacko, Balu K et al. (2017) Monocyte bioenergetic function is associated with body composition in virologically suppressed HIV-infected women. Redox Biol 12:648-656
Kandasamy, Jegen; Olave, Nelida; Ballinger, Scott W et al. (2017) Vascular Endothelial Mitochondrial Function Predicts Death or Pulmonary Outcomes in Preterm Infants. Am J Respir Crit Care Med 196:1040-1049
Fetterman, Jessica L; Sammy, Melissa J; Ballinger, Scott W (2017) Mitochondrial toxicity of tobacco smoke and air pollution. Toxicology 391:18-33
Grabner, Alexander; Schramm, Karla; Silswal, Neerupma et al. (2017) FGF23/FGFR4-mediated left ventricular hypertrophy is reversible. Sci Rep 7:1993
Quiles, Justin M; Narasimhan, Madhusudhanan; Mosbruger, Timothy et al. (2017) Identification of transcriptome signature for myocardial reductive stress. Redox Biol 13:568-580
Kesterson, Robert A; Johnson, Larry W; Lambert, Laura J et al. (2016) Generation of Mitochondrial-nuclear eXchange Mice via Pronuclear Transfer. Bio Protoc 6:
Fetterman, Jessica L; Holbrook, Monica; Westbrook, David G et al. (2016) Mitochondrial DNA damage and vascular function in patients with diabetes mellitus and atherosclerotic cardiovascular disease. Cardiovasc Diabetol 15:53

Showing the most recent 10 out of 89 publications