Simpson ER - Search Results

1

Deletion within the CYP17 gene together with insertion of foreign DNA is the cause of combined complete 17 alpha-hydroxylase/17,20-lyase deficiency in an Italian patient.

Biason A, Mantero F, Scaroni C, Simpson ER, Waterman MR. Biason A, et al. Among authors: simpson er. Mol Endocrinol. 1991 Dec;5(12):2037-45. doi: 10.1210/mend-5-12-2037. Mol Endocrinol. 1991. PMID: 1665206

2

17 alpha-hydroxylase/17,20-lyase deficiency: from clinical investigation to molecular definition.

Yanase T, Simpson ER, Waterman MR. Yanase T, et al. Among authors: simpson er. Endocr Rev. 1991 Feb;12(1):91-108. doi: 10.1210/edrv-12-1-91. Endocr Rev. 1991. PMID: 2026124 Review. No abstract available.

3

Regulation of CYP11A (P450SCC) and CYP17 (P450(17) alpha) gene expression in bovine luteal cells in primary culture.

Lauber ME, Bengtson T, Waterman MR, Simpson ER. Lauber ME, et al. Among authors: simpson er. J Biol Chem. 1991 Jun 15;266(17):11170-5. J Biol Chem. 1991. PMID: 2040624 Free article.

4

Combined 17 alpha-hydroxylase/17,20-lyase deficiency due to a 7-basepair duplication in the N-terminal region of the cytochrome P45017 alpha (CYP17) gene.

Yanase T, Sanders D, Shibata A, Matsui N, Simpson ER, Waterman MR. Yanase T, et al. Among authors: simpson er. J Clin Endocrinol Metab. 1990 May;70(5):1325-9. doi: 10.1210/jcem-70-5-1325. J Clin Endocrinol Metab. 1990. PMID: 2335573

5

Vasoactive intestinal peptide regulates cholesterol side-chain cleavage cytochrome P-450 (P-450scc) gene expression in granulosa cells from immature rat ovaries.

Trzeciak WH, Waterman MR, Simpson ER, Ojeda SR. Trzeciak WH, et al. Among authors: simpson er. Mol Endocrinol. 1987 Jul;1(7):500-4. doi: 10.1210/mend-1-7-500. Mol Endocrinol. 1987. PMID: 2484721

6

Structural characterization of the bovine CYP17 (17 alpha-hydroxylase) gene.

Bhasker CR, Adler BS, Dee A, John ME, Kagimoto M, Zuber MX, Ahlgren R, Wang XD, Simpson ER, Waterman MR. Bhasker CR, et al. Among authors: simpson er. Arch Biochem Biophys. 1989 Jun;271(2):479-87. doi: 10.1016/0003-9861(89)90298-1. Arch Biochem Biophys. 1989. PMID: 2543297

7

Regulation of cholesterol side-chain cleavage and 17 alpha-hydroxylase/lyase activities in proliferating human theca interna cells in long term monolayer culture.

McAllister JM, Kerin JF, Trant JM, Estabrook RW, Mason JI, Waterman MR, Simpson ER. McAllister JM, et al. Among authors: simpson er. Endocrinology. 1989 Oct;125(4):1959-66. doi: 10.1210/endo-125-4-1959. Endocrinology. 1989. PMID: 2676474

8

Identification of a common molecular basis for combined 17 alpha-hydroxylase/17,20-lyase deficiency in two Mennonite families.

Kagimoto K, Waterman MR, Kagimoto M, Ferreira P, Simpson ER, Winter JS. Kagimoto K, et al. Among authors: simpson er. Hum Genet. 1989 Jun;82(3):285-6. doi: 10.1007/BF00291172. Hum Genet. 1989. PMID: 2786493

9

Deletion of a phenylalanine in the N-terminal region of human cytochrome P-450(17 alpha) results in partial combined 17 alpha-hydroxylase/17,20-lyase deficiency.

Yanase T, Kagimoto M, Suzuki S, Hashiba K, Simpson ER, Waterman MR. Yanase T, et al. Among authors: simpson er. J Biol Chem. 1989 Oct 25;264(30):18076-82. J Biol Chem. 1989. PMID: 2808364 Free article.

10

Regulation of the synthesis of 3-hydroxy-3-methylglutaryl coenzyme A reductase in the bovine ovary in vivo and in vitro.

Rodgers RJ, Mason JI, Waterman MR, Simpson ER. Rodgers RJ, et al. Among authors: simpson er. Mol Endocrinol. 1987 Feb;1(2):172-80. doi: 10.1210/mend-1-2-172. Mol Endocrinol. 1987. PMID: 2842664

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