Agency
National Institute of Health (NIH)
Institute
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Type
Research Project (R01)
Project #
5R01DK038146-06
Application #
2140298
Study Section
Endocrinology Study Section (END)
Project Start
1988-09-20
Project End
1997-02-28
Budget Start
1995-03-01
Budget End
1997-02-28
Support Year
6
Fiscal Year
1995
Total Cost
Indirect Cost
Name
University of Texas MD Anderson Cancer Center
Department
Internal Medicine/Medicine
Type
Other Domestic Higher Education
DUNS #
001910777
City
Houston
State
TX
Country
United States
Zip Code
77030
Lou, H; Gagel, R F (2001) Alternative ribonucleic acid processing in endocrine systems. Endocr Rev 22:205-25
Hoff, A O; Cote, G J; Fritsche Jr, H A et al. (1999) Calcium-induced activation of a mutant G-protein-coupled receptor causes in vitro transformation of NIH/3T3 cells. Neoplasia 1:485-91
Lou, H; Helfman, D M; Gagel, R F et al. (1999) Polypyrimidine tract-binding protein positively regulates inclusion of an alternative 3'-terminal exon. Mol Cell Biol 19:78-85
Lou, H; Gagel, R F (1998) Alternative RNA processing--its role in regulating expression of calcitonin/calcitonin gene-related peptide. J Endocrinol 156:401-5
Lou, H; Neugebauer, K M; Gagel, R F et al. (1998) Regulation of alternative polyadenylation by U1 snRNPs and SRp20. Mol Cell Biol 18:4977-85
Thomas, P M; Wohllk, N; Huang, E et al. (1996) Inactivation of the first nucleotide-binding fold of the sulfonylurea receptor, and familial persistent hyperinsulinemic hypoglycemia of infancy. Am J Hum Genet 59:510-8
Wohllk, N; Cote, G J; Bugalho, M M et al. (1996) Relevance of RET proto-oncogene mutations in sporadic medullary thyroid carcinoma. J Clin Endocrinol Metab 81:3740-5
Lou, H; Gagel, R F; Berget, S M (1996) An intron enhancer recognized by splicing factors activates polyadenylation. Genes Dev 10:208-19
Lou, H; Yang, Y; Cote, G J et al. (1995) An intron enhancer containing a 5' splice site sequence in the human calcitonin/calcitonin gene-related peptide gene. Mol Cell Biol 15:7135-42
Thomas, P M; Cote, G J; Wohllk, N et al. (1995) Mutations in the sulfonylurea receptor gene in familial persistent hyperinsulinemic hypoglycemia of infancy. Science 268:426-9

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