This subproject is one of many research subprojects utilizing the resources provided by a Center grant funded by NIH/NCRR. The subproject and investigator (PI) may have received primary funding from another NIH source, and thus could be represented in other CRISP entries. The institution listed is for the Center, which is not necessarily the institution for the investigator.
The Specific Aims of our Center of Biomedical Research Excellence are: (1) Expand the critical mass of of investigators in the cell biology of obesity/diabetes research;(2) mentor junior faculty displaying great promise in setting priorities and multi-tasking, critical thinking, hypothesis formulation, experimental planning, oral and written communication, laboratory management, and career planning;(3) implement evaluation criteria for junior investigators that increases their odds for acquiring continuous independent RO1 funding;(4) foster a collaborative and interactive research environment in which junior investigators may conduct nationally recognized research, and (5) strengthen the research infrastructure for obesity/diabetes research by establishing a Cell Biology Core and by increasing support for the Genomics Core at PBRC. The overall goal of our COBRE program is to graduate our junior scientists to independent funding and increase retention of these promising young scientists at PBRC and within Louisiana.

Agency
National Institute of Health (NIH)
Institute
National Center for Research Resources (NCRR)
Type
Exploratory Grants (P20)
Project #
5P20RR021945-04
Application #
7959982
Study Section
Special Emphasis Panel (ZRR1-RI-8 (01))
Project Start
2009-07-01
Project End
2010-06-30
Budget Start
2009-07-01
Budget End
2010-06-30
Support Year
4
Fiscal Year
2009
Total Cost
$323,525
Indirect Cost
Name
Lsu Pennington Biomedical Research Center
Department
Type
Organized Research Units
DUNS #
611012324
City
Baton Rouge
State
LA
Country
United States
Zip Code
70808
Stephens, Jacqueline M; Bailey, Jennifer L; Hang, Hardy et al. (2018) Adipose Tissue Dysfunction Occurs Independently of Obesity in Adipocyte-Specific Oncostatin Receptor Knockout Mice. Obesity (Silver Spring) 26:1439-1447
Chang, Ji Suk; Ghosh, Sujoy; Newman, Susan et al. (2018) A map of the PGC-1?- and NT-PGC-1?-regulated transcriptional network in brown adipose tissue. Sci Rep 8:7876
Forney, Laura A; Stone, Kirsten P; Wanders, Desiree et al. (2018) The role of suppression of hepatic SCD1 expression in the metabolic effects of dietary methionine restriction. Appl Physiol Nutr Metab 43:123-130
Sarzynski, Mark A; Ruiz-Ramie, Jonathan J; Barber, Jacob L et al. (2018) Effects of Increasing Exercise Intensity and Dose on Multiple Measures of HDL (High-Density Lipoprotein) Function. Arterioscler Thromb Vasc Biol 38:943-952
Yu, Sangho; François, Marie; Huesing, Clara et al. (2018) The Hypothalamic Preoptic Area and Body Weight Control. Neuroendocrinology 106:187-194
Wanders, Desiree; Forney, Laura A; Stone, Kirsten P et al. (2018) The Components of Age-Dependent Effects of Dietary Methionine Restriction on Energy Balance in Rats. Obesity (Silver Spring) 26:740-746
François, Marie; Qualls-Creekmore, Emily; Berthoud, Hans-Rudolf et al. (2018) Genetics-based manipulation of adipose tissue sympathetic innervation. Physiol Behav 190:21-27
Kruger, Claudia; Burke, Susan J; Collier, J Jason et al. (2018) Lipid peroxidation regulates podocyte migration and cytoskeletal structure through redox sensitive RhoA signaling. Redox Biol 16:248-254
Yu, Sangho; Münzberg, Heike (2018) Testing Effects of Chronic Chemogenetic Neuronal Stimulation on Energy Balance by Indirect Calorimetry. Bio Protoc 8:
Forney, Laura A; Stone, Kirsten P; Wanders, Desiree et al. (2018) Sensing and signaling mechanisms linking dietary methionine restriction to the behavioral and physiological components of the response. Front Neuroendocrinol 51:36-45

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