application): The goal of the GC is to provide CNRU investigators: 1) assistance in the development, analysis and use of genetically defined mouse models relevant to nutrition research, and 2) state-of-the-art molecular methodologies. The GC has been designed to accomplish the following major aims: 1.Relative to use of genetically defined mouse models, the GC will a. Provide the expertise and technology necessary for development and use of genetically defined mouse models to CNRU investigators. This will include facilitating the analysis and development of congenic strains by CNRU investigators, e.g., through such development procedures known as """"""""speed congenics"""""""" (1). Many of the models are used primarily in studies of dyslipidemia diseases, diabetes and obesity and include mutant mouse strains entirely unique to this resource. b.Provide expertise in the development of transgene constructs or gene knockout vectors for producing transgenic of gene knockout mouse models. The actual mice can be produced in the UAB Transgenic Animal/ES Cell Resource (see section IV.E. below). c.Provide expertise for the design and analysis of mice for biochemical, metabolic and gene expression studies in conjunction with Component II of the GC and with the CNRU Energy Metabolism/Body Composition Core (Core A). 2.Relative to the development of genetic methods, the GC will provide access to a range of techniques related to gene expression, polymorphism detection, verification of genetic constructs and molecular scanning of candidate genes for nutrition-related diseases. 3.The GC will enhance research in progress, consolidate manpower effort, improve research quality, and contribute to cost-effectiveness in terms of providing laboratory services at less cost and higher quality. 4.The GC will support a Core facility that will act as a platform for promoting multi-disciplinary research and training in clinical nutrition and obesity across the UAB Campus. 5.The GC will offer advice and training to graduate students, fellows, and investigators on the specific measurements, and to attract new investigators to the area of nutrition/obesity-related research.

Agency
National Institute of Health (NIH)
Institute
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Type
Center Core Grants (P30)
Project #
5P30DK056336-03
Application #
6616909
Study Section
Special Emphasis Panel (ZDK1)
Project Start
2002-06-01
Project End
2003-05-31
Budget Start
Budget End
Support Year
3
Fiscal Year
2002
Total Cost
$162,000
Indirect Cost
Name
University of Alabama Birmingham
Department
Type
DUNS #
004514360
City
Birmingham
State
AL
Country
United States
Zip Code
35294
Ejima, K; Pavela, G; Li, P et al. (2018) Generalized lambda distribution for flexibly testing differences beyond the mean in the distribution of a dependent variable such as body mass index. Int J Obes (Lond) 42:930-933
Watanabe, Louis P; Riddle, Nicole C (2018) Measuring Exercise Levels in Drosophila melanogaster Using the Rotating Exercise Quantification System (REQS). J Vis Exp :
Buford, Thomas W; Carter, Christy S; VanDerPol, William J et al. (2018) Composition and richness of the serum microbiome differ by age and link to systemic inflammation. Geroscience 40:257-268
Smith Jr, D L; Thomas, D M; Siu, C O et al. (2018) Regression to the mean, apparent data errors and biologically extraordinary results: letter regarding 'changes in telomere length 3-5 years after gastric bypass surgery'. Int J Obes (Lond) 42:949-950
George, Brandon J; Li, Peng; Lieberman, Harris R et al. (2018) Randomization to randomization probability: Estimating treatment effects under actual conditions of use. Psychol Methods 23:337-350
Ejima, Keisuke; Thomas, Diana M; Allison, David B (2018) A Mathematical Model for Predicting Obesity Transmission with Both Genetic and Nongenetic Heredity. Obesity (Silver Spring) 26:927-933
Dhurandhar, Emily J; Pavela, Gregory; Kaiser, Kathryn A et al. (2018) Body Mass Index and Subjective Social Status: The Coronary Artery Risk Development in Young Adults Study. Obesity (Silver Spring) 26:426-431
Schneider, C R; Biggio, J R; Chandler-Laney, P C (2018) Association of early pregnancy body mass index with post-partum weight change among African-American women. Clin Obes 8:170-175
Kim, Teayoun; Nason, Shelly; Holleman, Cassie et al. (2018) Glucagon Receptor Signaling Regulates Energy Metabolism via Hepatic Farnesoid X Receptor and Fibroblast Growth Factor 21. Diabetes 67:1773-1782
Borges, Juliano H; Carter, Stephen J; Singh, Harshvardhan et al. (2018) Inverse relationship between changes of maximal aerobic capacity and changes in walking economy after weight loss. Eur J Appl Physiol :

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