During the past four years the DERC with its core laboratories and support for pilot and feasibility studies has greatly contributed to expansion in scope and intensity of the research at the Joslin. Over this period there has been more than doubling of research at the Joslin. Over this period there has been more than doubling of research fellows and a 50% increase of faculty in the Research Division. Recognizing the importance of this expansion and the resulting space shortage it has created, the Trustees have committed to expansion of the Joslin Diabetes Center by adding three floors to the current building (adding over 40,000 square feet of additional research space). In its financial import and support of interdisciplinary studies utilizing multiple tools of biomedical research and its support of junior faculty, the DERG is an essential component of this planned expansion as well as for the maintenance of current efforts. In this renewal, we have proposed a reduction in some current activities to accommodate two new cores (Transgenic Mouse Facility, Electron Microscopy), and a new subcore (Genetics). We have expanded the mission of the radio- iodination facility to that of a Peptide Biochemistry Core with the availability of a peptide synthesizer. We have also planned the addition of one pilot and feasibility grant to our Center for use by scientists outside the joslin in the Longwood area and affiliated Harvard hospitals.

Agency
National Institute of Health (NIH)
Institute
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Type
Center Core Grants (P30)
Project #
2P30DK036836-06
Application #
3102116
Study Section
Diabetes, Endocrinology and Metabolic Diseases B Subcommittee (DDK)
Project Start
1986-09-30
Project End
1996-11-30
Budget Start
1992-02-01
Budget End
1992-11-30
Support Year
6
Fiscal Year
1992
Total Cost
Indirect Cost
Name
Joslin Diabetes Center
Department
Type
DUNS #
071723084
City
Boston
State
MA
Country
United States
Zip Code
02215
Viana-Huete, Vanesa; Guillén, Carlos; García, Gema et al. (2018) Male Brown Fat-Specific Double Knockout of IGFIR/IR: Atrophy, Mitochondrial Fission Failure, Impaired Thermogenesis, and Obesity. Endocrinology 159:323-340
Peterson, Claire M; Young-Hyman, Deborah; Fischer, Sarah et al. (2018) Examination of Psychosocial and Physiological Risk for Bulimic Symptoms in Youth With Type 1 Diabetes Transitioning to an Insulin Pump: A Pilot Study. J Pediatr Psychol 43:83-93
Rotroff, Daniel M; Pijut, Sonja S; Marvel, Skylar W et al. (2018) Genetic Variants in HSD17B3, SMAD3, and IPO11 Impact Circulating Lipids in Response to Fenofibrate in Individuals With Type 2 Diabetes. Clin Pharmacol Ther 103:712-721
Leitner, Brooks P; Weiner, Lauren S; Desir, Matthew et al. (2018) Kinetics of human brown adipose tissue activation and deactivation. Int J Obes (Lond) :
Commissariat, Persis V; Volkening, Lisa K; Guo, Zijing et al. (2018) Associations between major life events and adherence, glycemic control, and psychosocial characteristics in teens with type 1 diabetes. Pediatr Diabetes 19:85-91
Barbour, Linda A; Scifres, Christina; Valent, Amy M et al. (2018) A cautionary response to SMFM statement: pharmacological treatment of gestational diabetes. Am J Obstet Gynecol 219:367.e1-367.e7
Lammer, Jan; Karst, Sonja G; Lin, Michael M et al. (2018) Association of Microaneurysms on Adaptive Optics Scanning Laser Ophthalmoscopy With Surrounding Neuroretinal Pathology and Visual Function in Diabetes. Invest Ophthalmol Vis Sci 59:5633-5640
Gordin, Daniel; King, George L (2018) Response to Comment on Gordin et al. Differential Association of Microvascular Attributions With Cardiovascular Disease in Patients With Long Duration of Type 1 Diabetes. Diabetes Care 2018;41:815-822. Diabetes Care 41:e128
Karatepe, Kutay; Zhu, Haiyan; Zhang, Xiaoyu et al. (2018) Proteinase 3 Limits the Number of Hematopoietic Stem and Progenitor Cells in Murine Bone Marrow. Stem Cell Reports 11:1092-1105
Sustarsic, Elahu G; Ma, Tao; Lynes, Matthew D et al. (2018) Cardiolipin Synthesis in Brown and Beige Fat Mitochondria Is Essential for Systemic Energy Homeostasis. Cell Metab 28:159-174.e11

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