Quigley CA - Search Results

1

Characterization of mutant androgen receptors causing partial androgen insensitivity syndrome.

De Bellis A, Quigley CA, Marschke KB, el-Awady MK, Lane MV, Smith EP, Sar M, Wilson EM, French FS. De Bellis A, et al. Among authors: quigley ca. J Clin Endocrinol Metab. 1994 Mar;78(3):513-22. doi: 10.1210/jcem.78.3.8126121. J Clin Endocrinol Metab. 1994. PMID: 8126121

2

Partial androgen insensitivity with phenotypic variation caused by androgen receptor mutations that disrupt activation function 2 and the NH(2)- and carboxyl-terminal interaction.

Quigley CA, Tan JA, He B, Zhou ZX, Mebarki F, Morel Y, Forest MG, Chatelain P, Ritzén EM, French FS, Wilson EM. Quigley CA, et al. Mech Ageing Dev. 2004 Oct-Nov;125(10-11):683-95. doi: 10.1016/j.mad.2004.08.007. Mech Ageing Dev. 2004. PMID: 15541764

3

Complete deletion of the androgen receptor gene: definition of the null phenotype of the androgen insensitivity syndrome and determination of carrier status.

Quigley CA, Friedman KJ, Johnson A, Lafreniere RG, Silverman LM, Lubahn DB, Brown TR, Wilson EM, Willard HF, French FS. Quigley CA, et al. J Clin Endocrinol Metab. 1992 Apr;74(4):927-33. doi: 10.1210/jcem.74.4.1347772. J Clin Endocrinol Metab. 1992. PMID: 1347772

4

Single base mutations in the human androgen receptor gene causing complete androgen insensitivity: rapid detection by a modified denaturing gradient gel electrophoresis technique.

De Bellis A, Quigley CA, Cariello NF, el-Awady MK, Sar M, Lane MV, Wilson EM, French FS. De Bellis A, et al. Among authors: quigley ca. Mol Endocrinol. 1992 Nov;6(11):1909-20. doi: 10.1210/mend.6.11.1480178. Mol Endocrinol. 1992. PMID: 1480178

5

Complete androgen insensitivity due to deletion of exon C of the androgen receptor gene highlights the functional importance of the second zinc finger of the androgen receptor in vivo.

Quigley CA, Evans BA, Simental JA, Marschke KB, Sar M, Lubahn DB, Davies P, Hughes IA, Wilson EM, French FS. Quigley CA, et al. Mol Endocrinol. 1992 Jul;6(7):1103-12. doi: 10.1210/mend.6.7.1508223. Mol Endocrinol. 1992. PMID: 1508223

6

Molecular basis of androgen insensitivity.

French FS, Lubahn DB, Brown TR, Simental JA, Quigley CA, Yarbrough WG, Tan JA, Sar M, Joseph DR, Evans BA, et al. French FS, et al. Among authors: quigley ca. Recent Prog Horm Res. 1990;46:1-38; discussion 38-42. doi: 10.1016/b978-0-12-571146-3.50005-5. Recent Prog Horm Res. 1990. PMID: 2281183 Review. No abstract available.

7

Androgen receptor defects: historical, clinical, and molecular perspectives.

Quigley CA, De Bellis A, Marschke KB, el-Awady MK, Wilson EM, French FS. Quigley CA, et al. Endocr Rev. 1995 Jun;16(3):271-321. doi: 10.1210/edrv-16-3-271. Endocr Rev. 1995. PMID: 7671849 Review. No abstract available.

8

Androgen insensitivity syndromes.

Quigley CA, French FS. Quigley CA, et al. Curr Ther Endocrinol Metab. 1994;5:342-51. Curr Ther Endocrinol Metab. 1994. PMID: 7704751 No abstract available.

9

A novel missense mutation in the amino-terminal domain of the human androgen receptor gene in a family with partial androgen insensitivity syndrome causes reduced efficiency of protein translation.

Choong CS, Quigley CA, French FS, Wilson EM. Choong CS, et al. Among authors: quigley ca. J Clin Invest. 1996 Sep 15;98(6):1423-31. doi: 10.1172/JCI118930. J Clin Invest. 1996. PMID: 8823308 Free PMC article.

10

Male pseudohermaphroditism.

Kupfer SR, Quigley CA, French FS. Kupfer SR, et al. Among authors: quigley ca. Semin Perinatol. 1992 Oct;16(5):319-31. Semin Perinatol. 1992. PMID: 1485188 Review. No abstract available.

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