Morel Y - Search Results

1

The molecular genetics of 21-hydroxylase deficiency.

Miller WL, Morel Y. Miller WL, et al. Among authors: morel y. Annu Rev Genet. 1989;23:371-93. doi: 10.1146/annurev.ge.23.120189.002103. Annu Rev Genet. 1989. PMID: 2694937 Review. No abstract available.

2

Transcript encoded on the opposite strand of the human steroid 21-hydroxylase/complement component C4 gene locus.

Morel Y, Bristow J, Gitelman SE, Miller WL. Morel Y, et al. Proc Natl Acad Sci U S A. 1989 Sep;86(17):6582-6. doi: 10.1073/pnas.86.17.6582. Proc Natl Acad Sci U S A. 1989. PMID: 2475872 Free PMC article.

3

Gene conversions and rearrangements cause discordance between inheritance of forms of 21-hydroxylase deficiency and HLA types.

Morel Y, David M, Forest MG, Betuel H, Hauptman G, Andre J, Bertrand J, Miller WL. Morel Y, et al. J Clin Endocrinol Metab. 1989 Mar;68(3):592-9. doi: 10.1210/jcem-68-3-592. J Clin Endocrinol Metab. 1989. PMID: 2783935

4

Analysis of the duplicated human C4/P450c21/X gene cluster.

Miller WL, Gitelman SE, Bristow J, Morel Y. Miller WL, et al. Among authors: morel y. J Steroid Biochem Mol Biol. 1992 Dec;43(8):961-71. doi: 10.1016/0960-0760(92)90324-C. J Steroid Biochem Mol Biol. 1992. PMID: 22217841

5

Clinical and molecular genetics of congenital adrenal hyperplasia due to 21-hydroxylase deficiency.

Morel Y, Miller WL. Morel Y, et al. Adv Hum Genet. 1991;20:1-68. doi: 10.1007/978-1-4684-5958-6_1. Adv Hum Genet. 1991. PMID: 1801590 Review. No abstract available.

6

Regulation of the gene for estrogenic 17-ketosteroid reductase lying on chromosome 17cen----q25.

Tremblay Y, Ringler GE, Morel Y, Mohandas TK, Labrie F, Strauss JF 3rd, Miller WL. Tremblay Y, et al. Among authors: morel y. J Biol Chem. 1989 Dec 5;264(34):20458-62. J Biol Chem. 1989. PMID: 2584224 Free article.

7

Assignment of the functional gene for human adrenodoxin to chromosome 11q13----qter and of adrenodoxin pseudogenes to chromosome 20cen----q13.1.

Morel Y, Picado-Leonard J, Wu DA, Chang CY, Mohandas TK, Chung BC, Miller WL. Morel Y, et al. Am J Hum Genet. 1988 Jul;43(1):52-9. Am J Hum Genet. 1988. PMID: 2837084 Free PMC article.

8

Human adrenodoxin reductase: two mRNAs encoded by a single gene on chromosome 17cen----q25 are expressed in steroidogenic tissues.

Solish SB, Picado-Leonard J, Morel Y, Kuhn RW, Mohandas TK, Hanukoglu I, Miller WL. Solish SB, et al. Among authors: morel y. Proc Natl Acad Sci U S A. 1988 Oct;85(19):7104-8. doi: 10.1073/pnas.85.19.7104. Proc Natl Acad Sci U S A. 1988. PMID: 2845396 Free PMC article.

9

Rearrangements and point mutations of P450c21 genes are distinguished by five restriction endonuclease haplotypes identified by a new probing strategy in 57 families with congenital adrenal hyperplasia.

Morel Y, André J, Uring-Lambert B, Hauptmann G, Bétuel H, Tossi M, Forest MG, David M, Bertrand J, Miller WL. Morel Y, et al. J Clin Invest. 1989 Feb;83(2):527-36. doi: 10.1172/JCI113914. J Clin Invest. 1989. PMID: 2913051 Free PMC article.

10

How a patient homozygous for a 30-kb deletion of the C4-CYP 21 genomic region can have a nonclassic form of 21-hydroxylase deficiency.

L'Allemand D, Tardy V, Grüters A, Schnabel D, Krude H, Morel Y. L'Allemand D, et al. Among authors: morel y. J Clin Endocrinol Metab. 2000 Dec;85(12):4562-7. doi: 10.1210/jcem.85.12.7018. J Clin Endocrinol Metab. 2000. PMID: 11134109

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