Agency
National Institute of Health (NIH)
Institute
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Type
Clinical Investigator Award (CIA) (K08)
Project #
1K08DK002387-01
Application #
2134330
Study Section
Special Emphasis Panel (SRC)
Project Start
1996-09-01
Project End
2001-08-31
Budget Start
1996-09-01
Budget End
1997-08-31
Support Year
1
Fiscal Year
1996
Total Cost
Indirect Cost
Name
University of California San Francisco
Department
Pediatrics
Type
Schools of Medicine
DUNS #
073133571
City
San Francisco
State
CA
Country
United States
Zip Code
94143
Costa-Santos, Marivania; Kater, Claudio E; Dias, Eduardo P et al. (2004) Two intronic mutations cause 17-hydroxylase deficiency by disrupting splice acceptor sites: direct demonstration of aberrant splicing and absent enzyme activity by expression of the entire CYP17 gene in HEK-293 cells. J Clin Endocrinol Metab 89:43-8
Costa-Santos, Marivania; Kater, Claudio E; Auchus, Richard J et al. (2004) Two prevalent CYP17 mutations and genotype-phenotype correlations in 24 Brazilian patients with 17-hydroxylase deficiency. J Clin Endocrinol Metab 89:49-60
Khan, Naveed; Sharma, Kamalesh K; Andersson, Stefan et al. (2004) Human 17beta-hydroxysteroid dehydrogenases types 1, 2, and 3 catalyze bi-directional equilibrium reactions, rather than unidirectional metabolism, in HEK-293 cells. Arch Biochem Biophys 429:50-9
Fluck, Christa E; Miller, Walter L; Auchus, Richard J (2003) The 17, 20-lyase activity of cytochrome p450c17 from human fetal testis favors the delta5 steroidogenic pathway. J Clin Endocrinol Metab 88:3762-6
Gupta, Manisha K; Guryev, Oleg L; Auchus, Richard J (2003) 5alpha-reduced C21 steroids are substrates for human cytochrome P450c17. Arch Biochem Biophys 418:151-60
Sherbet, Daniel P; Tiosano, Dov; Kwist, Kerri M et al. (2003) CYP17 mutation E305G causes isolated 17,20-lyase deficiency by selectively altering substrate binding. J Biol Chem 278:48563-9
Wilson, Jean D; Auchus, Richard J; Leihy, Michael W et al. (2003) 5alpha-androstane-3alpha,17beta-diol is formed in tammar wallaby pouch young testes by a pathway involving 5alpha-pregnane-3alpha,17alpha-diol-20-one as a key intermediate. Endocrinology 144:575-80
Mathieu, Axel P; LeHoux, Jean Guy; Auchus, Richard J (2003) Molecular dynamics of substrate complexes with hamster cytochrome P450c17 (CYP17): mechanistic approach to understanding substrate binding and activities. Biochim Biophys Acta 1619:291-300
Auchus, Richard J; Sampath Kumar, A; Andrew Boswell, C et al. (2003) The enantiomer of progesterone (ent-progesterone) is a competitive inhibitor of human cytochromes P450c17 and P450c21. Arch Biochem Biophys 409:134-44
Arlt, Wiebke; Martens, John W M; Song, Maengseok et al. (2002) Molecular evolution of adrenarche: structural and functional analysis of p450c17 from four primate species. Endocrinology 143:4665-72

Showing the most recent 10 out of 20 publications