The overall objectives of the Mouse Phenotyping Core will be to provide DERC investigators with consultation, accurate and easily accessible mouse phenotyping, and the availability of both standard and certain unique mouse models of diabetes and its complications. Services provided by the Mouse Phenotyping Core to DERC investigators concentrate heavily on mouse metabolic, cardiovascular and pathologic phenotyping. These services particularly focus on interests of DERC members: 1) metabolic phenotyping relevant to the genesis of insulin resistance and the progression to type 2 diabetes; 2) cardiovascular physiological phenotyping relevant to models of atherosclerosis, diabetic cardiomyopathy and hypertension; 3) renal phenotyping relevant to hypertension and diabetic nephropathy. The existing strengths at UCSD in metabolic phenotyping and at UCLA in renal-cardiovascular phenotyping will be standardized and merged into one central, partially mobile Core. Seamless integration of phenotyping among DERC investigators at UCLA and UCSD will be facilitated by the Mobile Mouse Physiology Unit. This exciting and innovative concept permits delivery of many phenotyping services directly to the laboratory of DERC investigators, as well as provides needed transport of animals, cryopreserved embryos, equipment and other precious materials. Increased quality of data and substantial savings in costs to individual DERC investigators and the Core are anticipated through implementation of this unique concept. Dr. Gerald Levey, Provost UCLA, has committed to purchasing and equipping this Unit. Currently, the most heavily used services of the DERC include: oral glucose tolerance testing, plasma glucose determinations, renal function tests, non-invasive blood pressure measurements, osmotic minipump placement, cardiac fibrosis quantification, echocardiography, cardiac catheterization, and quantification of atherosclerosis. DERC funding will allow expansion of services and development of a new assay development component of this Core.

Agency
National Institute of Health (NIH)
Institute
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Type
Center Core Grants (P30)
Project #
1P30DK063491-01
Application #
6612269
Study Section
Special Emphasis Panel (ZDK1-GRB-7 (O1))
Project Start
2002-12-01
Project End
2007-11-30
Budget Start
Budget End
2004-04-30
Support Year
1
Fiscal Year
2003
Total Cost
$191,336
Indirect Cost
Name
University of California Los Angeles
Department
Type
DUNS #
092530369
City
Los Angeles
State
CA
Country
United States
Zip Code
90095
Eriguchi, Masahiro; Bernstein, Ellen A; Veiras, Luciana C et al. (2018) The Absence of the ACE N-Domain Decreases Renal Inflammation and Facilitates Sodium Excretion during Diabetic Kidney Disease. J Am Soc Nephrol 29:2546-2561
Turcot, Valérie (see original citation for additional authors) (2018) Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity. Nat Genet 50:26-41
Zhou, Zhenqi; Ribas, Vicent; Rajbhandari, Prashant et al. (2018) Estrogen receptor ? protects pancreatic ?-cells from apoptosis by preserving mitochondrial function and suppressing endoplasmic reticulum stress. J Biol Chem 293:4735-4751
Prins, Bram P; Mead, Timothy J; Brody, Jennifer A et al. (2018) Exome-chip meta-analysis identifies novel loci associated with cardiac conduction, including ADAMTS6. Genome Biol 19:87
Xu, Jiayi; Bartz, Traci M; Chittoor, Geetha et al. (2018) Meta-analysis across Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) consortium provides evidence for an association of serum vitamin D with pulmonary function. Br J Nutr 120:1159-1170
Keaton, Jacob M; Gao, Chuan; Guan, Meijian et al. (2018) Genome-wide interaction with the insulin secretion locus MTNR1B reveals CMIP as a novel type 2 diabetes susceptibility gene in African Americans. Genet Epidemiol 42:559-570
Skorobogatko, Yuliya; Dragan, Morgan; Cordon, Claudia et al. (2018) RalA controls glucose homeostasis by regulating glucose uptake in brown fat. Proc Natl Acad Sci U S A 115:7819-7824
Savji, Nazir; Meijers, Wouter C; Bartz, Traci M et al. (2018) The Association of Obesity and Cardiometabolic Traits With Incident HFpEF and HFrEF. JACC Heart Fail 6:701-709
Jiang, Xia; O'Reilly, Paul F; Aschard, Hugues et al. (2018) Genome-wide association study in 79,366 European-ancestry individuals informs the genetic architecture of 25-hydroxyvitamin D levels. Nat Commun 9:260
Balakrishnan, Poojitha; Jones, Miranda R; Vaidya, Dhananjay et al. (2018) Ethnic, Geographic, and Genetic Differences in Arsenic Metabolism at Low Arsenic Exposure: A Preliminary Analysis in the Multi-Ethnic Study of Atherosclerosis (MESA). Int J Environ Res Public Health 15:

Showing the most recent 10 out of 926 publications