The primary mission of the Translational Research Core (TRC) is to promote high-quality diabetes translational research for members of the Einstein-Mount Sinai Diabetes Research Center (ES-DRC), through delivery of services including consultation, training and mentoring in clinical research methods that are specifically applicable to diabetes, its complications and related metabolic defects. Core services derive from the broad expertise of Core investigators, encompassing studies in clinical physiology, clinical trials involving diabetes and obesity as well as patient-centered outcomes research, thus spanning the spectrum of translational research. The unique strengths of our TRC position us to promote the continued growth of diabetes-related translational research at the Albert Einstein College of Medicine (Einstein) and to expand our reach to include the expertise of diabetes investigators at the Icahn School of Medicine at Mount Sinai (Mount Sinai) and other regional partners. We provide resources for diabetes research via faculty consultation and collaborative efforts for other programs and projects. Importantly, the TRC also leverages resources of the recently renewed Einstein Clinical and Translational Science Award (CTSA, known as the Institute for Clinical and Translational Research, ICTR) and the Mount Sinai Institutes for Translational Sciences (Conduits). Further, the TRC also receives substantial Institutional support, which further extends our reach and capabilities. The Einstein and Mount Sinai CTSAs provide critical research infrastructure and facilitate access to other institutionally sponsored services, while the TRC in partnership with the CTSAs will focus specifically on support of the unique diabetes, obesity and metabolism research needs. We view the CTSA programs as an important partner in our efforts and have developed this Core to fill critical gaps in the resources needed to promote the broad range of diabetes clinical and translational research. The TRC therefore has the following specific aims: 1) To facilitate the development of novel diabetes-related ?T1? translational research programs based upon novel collaborations between basic scientists and `translational' researchers; 2) To provide specialized expertise in the design and implementation of diabetes ?T2-T3? research programs; and 3) To provide consultation, infrastructure and training to build capacity for diabetes community-based (?T4?) research at the local, regional and national levels.

Public Health Relevance

The Translational Research Core provides cost effective, thoughtful design and implementation of human- based clinical and population based studies with Einstein-Mount Sinai Diabetes Research Center members to improve our understanding and treatment of patients with diabetes.

Agency
National Institute of Health (NIH)
Institute
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Type
Center Core Grants (P30)
Project #
5P30DK020541-41
Application #
9272883
Study Section
Special Emphasis Panel (ZDK1-GRB-S)
Project Start
Project End
Budget Start
2017-04-01
Budget End
2018-03-31
Support Year
41
Fiscal Year
2017
Total Cost
$189,511
Indirect Cost
$68,922
Name
Albert Einstein College of Medicine, Inc
Department
Type
Domestic Higher Education
DUNS #
079783367
City
Bronx
State
NY
Country
United States
Zip Code
10461
Ackeifi, Courtney A; Swartz, Ethan A; Wang, Peng (2018) Cell-Based Methods to Identify Inducers of Human Pancreatic Beta-Cell Proliferation. Methods Mol Biol 1787:87-100
Walters, Ryan O; Arias, Esperanza; Diaz, Antonio et al. (2018) Sarcosine Is Uniquely Modulated by Aging and Dietary Restriction in Rodents and Humans. Cell Rep 25:663-676.e6
Schwartz, Gary J (2018) Roles for gut vagal sensory signals in determining energy availability and energy expenditure. Brain Res 1693:151-153
Guan, Fangxia; Tabrizian, Tahmineh; Novaj, Ardijana et al. (2018) Dietary Walnuts Protect Against Obesity-Driven Intestinal Stem Cell Decline and Tumorigenesis. Front Nutr 5:37
Tang, Yan; Kwon, Hyokjoon; Neel, Brian A et al. (2018) The fructose-2,6-bisphosphatase TIGAR suppresses NF-?B signaling by directly inhibiting the linear ubiquitin assembly complex LUBAC. J Biol Chem 293:7578-7591
Lontchi-Yimagou, Eric; You, Jee Young; Carey, Michelle et al. (2018) Potential approaches to prevent hypoglycemia-associated autonomic failure. J Investig Med 66:641-647
Chemaly, Elie R; Troncone, Luca; Lebeche, Djamel (2018) SERCA control of cell death and survival. Cell Calcium 69:46-61
Wang, Peng; Karakose, Esra; Liu, Hongtao et al. (2018) Combined Inhibition of DYRK1A, SMAD, and Trithorax Pathways Synergizes to Induce Robust Replication in Adult Human Beta Cells. Cell Metab :
Jeong, Jae Hoon; Chang, Ji Suk; Jo, Young-Hwan (2018) Intracellular glycolysis in brown adipose tissue is essential for optogenetically induced nonshivering thermogenesis in mice. Sci Rep 8:6672
Willis, Ian M; Moir, Robyn D; Hernandez, Nouria (2018) Metabolic programming a lean phenotype by deregulation of RNA polymerase III. Proc Natl Acad Sci U S A 115:12182-12187

Showing the most recent 10 out of 533 publications