In this renewal application for Phase II of the NURSA project, we will detail, as space permits, the tremendous progress that this project has enjoyed over the past 4 years. This work could be considered a 'labor of love' for a talented and committed group of investigators in the field of Nuclear Receptors (NRs). Certainly, the money available for each project/core has been minimal and well below that available in an normal R01 application. However, it was felt that for the field of NRs and coregulators (CoRs) to advance more rapidly and toward translational goals, a large amount of experimental non-RO1-type data, data bases for information on all NR and CoR molecules and their physiologic/pathologic ramifications, and an efficient electronic distribution mechanism had to be created. Initiated from an inactive base as a 'completely new' project, it has had great success and has far exceeded many of its original goals over the past 4 years. In Phase II of the NURSA project in the next 5 years, we will complete this mission with advanced genomic and proteomic data that extends and now ties our fundamental NURSA information base into context with cellular signaling and human disease.

Agency
National Institute of Health (NIH)
Institute
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Type
Research Program--Cooperative Agreements (U19)
Project #
3U19DK062434-07S1
Application #
7669862
Study Section
Special Emphasis Panel (ZDK1-GRB-9 (M1))
Program Officer
Margolis, Ronald N
Project Start
2002-08-15
Project End
2012-06-30
Budget Start
2008-08-01
Budget End
2009-06-30
Support Year
7
Fiscal Year
2008
Total Cost
$37,500
Indirect Cost
Name
Baylor College of Medicine
Department
Anatomy/Cell Biology
Type
Schools of Medicine
DUNS #
051113330
City
Houston
State
TX
Country
United States
Zip Code
77030
Kim, Kang Ho; Choi, Sungwoo; Zhou, Ying et al. (2017) Hepatic FXR/SHP axis modulates systemic glucose and fatty acid homeostasis in aged mice. Hepatology 66:498-509
Fleet, Tiffany; Stashi, Erin; Zhu, Bokai et al. (2016) Genetic and Environmental Models of Circadian Disruption Link SRC-2 Function to Hepatic Pathology. J Biol Rhythms 31:443-60
Wagner, Martin; Choi, Sungwoo; Panzitt, Katrin et al. (2016) Liver receptor homolog-1 is a critical determinant of methyl-pool metabolism. Hepatology 63:95-106
Han, Sang Jun; Begum, Khurshida; Foulds, Charles E et al. (2016) The Dual Estrogen Receptor ? Inhibitory Effects of the Tissue-Selective Estrogen Complex for Endometrial and Breast Safety. Mol Pharmacol 89:14-26
Han, Sang Jun; Jung, Sung Yun; Wu, San-Pin et al. (2015) Estrogen Receptor ? Modulates Apoptosis Complexes and the Inflammasome to Drive the Pathogenesis of Endometriosis. Cell 163:960-74
Wu, San-Pin; Kao, Chung-Yang; Wang, Leiming et al. (2015) Increased COUP-TFII expression in adult hearts induces mitochondrial dysfunction resulting in heart failure. Nat Commun 6:8245
Tang, Ke; Tsai, Sophia Y; Tsai, Ming-Jer (2015) COUP-TFs and eye development. Biochim Biophys Acta 1849:201-9
Xu, Pingwen; Cao, Xuehong; He, Yanlin et al. (2015) Estrogen receptor-? in medial amygdala neurons regulates body weight. J Clin Invest 125:2861-76
Kang, Yun Kyoung; Putluri, Nagireddy; Maity, Suman et al. (2015) CAPER is vital for energy and redox homeostasis by integrating glucose-induced mitochondrial functions via ERR-?-Gabpa and stress-induced adaptive responses via NF-?B-cMYC. PLoS Genet 11:e1005116
Kida, Yasuyuki S; Kawamura, Teruhisa; Wei, Zong et al. (2015) ERRs Mediate a Metabolic Switch Required for Somatic Cell Reprogramming to Pluripotency. Cell Stem Cell 16:547-55

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