application) The Molecular Biology Core is dedicated to providing cost-effective access to services common to most applications of modern molecular biology and to provide training and technology to exploit a variety of more advanced gene discovery tools. The application of molecular genetic approaches to the study of diabetes is widely recognized as a crucial element in the progress toward an understanding of the detailed mechanism of glucose homeostasis and of the still poorly understood pathophysiology of adult onset diabetes. In addition, molecular tools have already played an essential role in elucidating some of the factors contributing to the immunological derangements responsible for the inception of the beta cell destruction underlying juvenile diabetes mellitus. However, the application of the powerful tools of molecular biology increasingly requires the mastery of a broad spectrum of technologies. Common to many of these technologies is a requirement for facile gene isolation and manipulation, which in turn calls for the libraries, cell lines, and protein and nucleic acid probes needed to isolate genes and analyze them. The speed and convenience with which nucleic acids can be manipulated are in turn dependent on key reagents and services which can be expensive and time-consuming to develop on an individual laboratory basis. In addition to making available the approaches in use for expression-based discovery of gene products and their interactions, the Molecular Biology Core will, by consolidating the intellectually broader user base of the diabetes research community with the very high volume of activity ongoing in the Department of Molecular Biology, afford substantial incremental savings for Center-affiliated investigators for reagents and services, such as the provision of synthetic oligonucleotides, automated DNA sequencing, colony picking, and DNA arraying.

Agency
National Institute of Health (NIH)
Institute
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Type
Center Core Grants (P30)
Project #
5P30DK057521-03
Application #
6597597
Study Section
Special Emphasis Panel (ZDK1)
Project Start
2002-06-03
Project End
2003-03-31
Budget Start
Budget End
Support Year
3
Fiscal Year
2002
Total Cost
Indirect Cost
Name
Massachusetts General Hospital
Department
Type
DUNS #
City
Boston
State
MA
Country
United States
Zip Code
02199
Vujic, Ana; Lerchenmüller, Carolin; Wu, Ting-Di et al. (2018) Exercise induces new cardiomyocyte generation in the adult mammalian heart. Nat Commun 9:1659
Fulzele, Keertik; Dedic, Christopher; Lai, Forest et al. (2018) Loss of Gs? in osteocytes leads to osteopenia due to sclerostin induced suppression of osteoblast activity. Bone 117:138-148
Battistone, Maria A; Nair, Anil V; Barton, Claire R et al. (2018) Extracellular Adenosine Stimulates Vacuolar ATPase-Dependent Proton Secretion in Medullary Intercalated Cells. J Am Soc Nephrol 29:545-556
Cheung, Pui W; Terlouw, Abby; Janssen, Sam Antoon et al. (2018) Inhibition of non-receptor tyrosine kinase Src induces phosphoserine 256-independent aquaporin-2 membrane accumulation. J Physiol :
Karim, Lamya; Moulton, Julia; Van Vliet, Miranda et al. (2018) Bone microarchitecture, biomechanical properties, and advanced glycation end-products in the proximal femur of adults with type 2 diabetes. Bone 114:32-39
Kolar, Matthew J; Nelson, Andrew T; Chang, Tina et al. (2018) Faster Protocol for Endogenous Fatty Acid Esters of Hydroxy Fatty Acid (FAHFA) Measurements. Anal Chem 90:5358-5365
Todd, William D; Fenselau, Henning; Wang, Joshua L et al. (2018) A hypothalamic circuit for the circadian control of aggression. Nat Neurosci 21:717-724
Cox, Kimberly H; Oliveira, Luciana M B; Plummer, Lacey et al. (2018) Modeling mutant/wild-type interactions to ascertain pathogenicity of PROKR2 missense variants in patients with isolated GnRH deficiency. Hum Mol Genet 27:338-350
Aguayo-Mazzucato, Cristina; Bonner-Weir, Susan (2018) Pancreatic ? Cell Regeneration as a Possible Therapy for Diabetes. Cell Metab 27:57-67
McKeown, Nicola M; Dashti, Hassan S; Ma, Jiantao et al. (2018) Sugar-sweetened beverage intake associations with fasting glucose and insulin concentrations are not modified by selected genetic variants in a ChREBP-FGF21 pathway: a meta-analysis. Diabetologia 61:317-330

Showing the most recent 10 out of 389 publications