This program will train 6 postdoctoral fellows annually in mechanisms and Innovation in vascular disease. The program goals include rigorous training in the scientific method, critical analysis, logical reasoning and independent thinking, all within a highly collaborative working group. Trainees will develop a focused area of translational vascular research expertise and will be exposed to a wide range of complementary research techniques. Mentors will provide collegial and productive collaboration, and help to hone skills in oral and written communication, and to instill respect for the responsible conduct of research. Fellows will undergo a minimum two-year education and research program, although we only intend to fund the first year through the institutional T32. Fellows will be encouraged and mentored in their development of funding proposals for the second year. The overarching goal for this program is to produce researchers who are well-schooled in the fundamental problems of vascular disease, and are driven to find innovative strategies to tackle those problems, thereby translating basic research into clinical success. Fellows will receive their training in a multidisciplinary milieu of fundamental, translational and clinical research in vascular biology and disease. The Stanford Cardiovascular Institute (CVI) offers a unique platform by which to train the next generation of basic and translational scientists. Mentors for the proposed program, all members of the CVI, come not only from vascular medicine, but also from materials science, bioengineering, imaging, and health research and policy. Brought together in a collaborative Institute, these scientists share a common interest in the mechanisms behind vascular development and disease.

Agency
National Institute of Health (NIH)
Institute
National Heart, Lung, and Blood Institute (NHLBI)
Type
Institutional National Research Service Award (T32)
Project #
5T32HL098049-05
Application #
8699255
Study Section
NHLBI Institutional Training Mechanism Review Committee (NITM)
Program Officer
Scott, Jane
Project Start
2010-07-01
Project End
2015-06-30
Budget Start
2014-07-01
Budget End
2015-06-30
Support Year
5
Fiscal Year
2014
Total Cost
Indirect Cost
Name
Stanford University
Department
Internal Medicine/Medicine
Type
Schools of Medicine
DUNS #
City
Stanford
State
CA
Country
United States
Zip Code
94304
Tamosiuniene, Rasa; Manouvakhova, Olga; Mesange, Paul et al. (2018) Dominant Role for Regulatory T Cells in Protecting Females Against Pulmonary Hypertension. Circ Res 122:1689-1702
Lu, Ake T; Xue, Luting; Salfati, Elias L et al. (2018) GWAS of epigenetic aging rates in blood reveals a critical role for TERT. Nat Commun 9:387
Tran, Kenneth; Ullery, Brant W; Itoga, Nathan et al. (2018) Polar orientation of renal grafts within the proximal seal zone affects risk of early type IA endoleaks after chimney endovascular aneurysm repair. J Vasc Surg 67:1034-1041
Piening, Brian D; Zhou, Wenyu; Contrepois, Kévin et al. (2018) Integrative Personal Omics Profiles during Periods of Weight Gain and Loss. Cell Syst 6:157-170.e8
Foster, Abbygail A; Dewi, Ruby E; Cai, Lei et al. (2018) Protein-engineered hydrogels enhance the survival of induced pluripotent stem cell-derived endothelial cells for treatment of peripheral arterial disease. Biomater Sci 6:614-622
Keating, Brendan J; Pereira, Alexandre C; Snyder, Michael et al. (2018) Applying genomics in heart transplantation. Transpl Int 31:278-290
Itoga, Nathan K; Wu, Tiffany; Dake, Michael D et al. (2018) Acute Type B Dissection Causing Collapse of EVAR Endograft and Iliac Limb Occlusion. Ann Vasc Surg 46:206.e1-206.e4
Rajaei, Sheeva; Rigdon, Joseph; Crowe, Susan et al. (2018) Breastfeeding Duration and the Risk of Coronary Artery Disease. J Womens Health (Larchmt) :
Mardinoglu, Adil; Wu, Hao; Bjornson, Elias et al. (2018) An Integrated Understanding of the Rapid Metabolic Benefits of a Carbohydrate-Restricted Diet on Hepatic Steatosis in Humans. Cell Metab 27:559-571.e5
Itoga, Nathan K; Tawfik, Daniel S; Lee, Charles K et al. (2018) Association of Blood Pressure Measurements With Peripheral Artery Disease Events. Circulation 138:1805-1814

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