Agency
National Institute of Health (NIH)
Institute
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Type
Method to Extend Research in Time (MERIT) Award (R37)
Project #
5R37DK015070-25
Application #
2136891
Study Section
Special Emphasis Panel (NSS)
Project Start
1979-07-15
Project End
1997-06-30
Budget Start
1996-07-08
Budget End
1997-06-30
Support Year
25
Fiscal Year
1996
Total Cost
Indirect Cost
Name
University of Chicago
Department
Internal Medicine/Medicine
Type
Schools of Medicine
DUNS #
225410919
City
Chicago
State
IL
Country
United States
Zip Code
60637
Bellelli, Roberto; Vitagliano, Donata; Federico, Giorgia et al. (2018) Oncogene-induced senescence and its evasion in a mouse model of thyroid neoplasia. Mol Cell Endocrinol 460:24-35
Cangul, Hakan; Liao, Xiao-Hui; Schoenmakers, Erik et al. (2018) Homozygous loss-of-function mutations in SLC26A7 cause goitrous congenital hypothyroidism. JCI Insight 3:
Watanabe, Y; Sharwood, E; Goodwin, B et al. (2018) A novel mutation in the TG gene (G2322S) causing congenital hypothyroidism in a Sudanese family: a case report. BMC Med Genet 19:69
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Ohba, Kenji; Sinha, Rohit Anthony; Singh, Brijesh Kumar et al. (2017) Changes in Hepatic TR? Protein Expression, Lipogenic Gene Expression, and Long-Chain Acylcarnitine Levels During Chronic Hyperthyroidism and Triiodothyronine Withdrawal in a Mouse Model. Thyroid 27:852-860
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