Vilain E - Search Results

1

[The analysis of SRY doesn't explain all the pathology of sex determination].

Vilain E, McElreavey K, Vidaud M, Richaud F, Fellous M. Vilain E, et al. Ann Endocrinol (Paris). 1991;52(6):435-6. Ann Endocrinol (Paris). 1991. PMID: 1824496 French. No abstract available.

2

[Sex genetics].

Vilain E, Elreavey KM, Richaud F, Fellous M. Vilain E, et al. Presse Med. 1992 May 16;21(18):852-6. Presse Med. 1992. PMID: 1535151 Review. French.

3

Familial case with sequence variant in the testis-determining region associated with two sex phenotypes.

Vilain E, McElreavey K, Jaubert F, Raymond JP, Richaud F, Fellous M. Vilain E, et al. Am J Hum Genet. 1992 May;50(5):1008-11. Am J Hum Genet. 1992. PMID: 1570829 Free PMC article.

4

XY sex reversal associated with a nonsense mutation in SRY.

McElreavey KD, Vilain E, Boucekkine C, Vidaud M, Jaubert F, Richaud F, Fellous M. McElreavey KD, et al. Among authors: vilain e. Genomics. 1992 Jul;13(3):838-40. doi: 10.1016/0888-7543(92)90164-n. Genomics. 1992. PMID: 1639410

5

[Study of sex determination gene (SRY) in 46,XY gonadal dysgenesis].

Boucekkine C, Vilain E, McElreavey K, Jaubert F, Brauner R, Thibaud E, Battin J, Toublanc JE, Kucheria K, Chaabouni S, et al. Boucekkine C, et al. Among authors: vilain e. Ann Endocrinol (Paris). 1994;54(5):315-21. Ann Endocrinol (Paris). 1994. PMID: 8085778 French.

6

Control of sex determination in animals.

McElreavey K, Vilain E, Cotinot C, Payen E, Fellous M. McElreavey K, et al. Among authors: vilain e. Eur J Biochem. 1993 Dec 15;218(3):769-83. doi: 10.1111/j.1432-1033.1993.tb18432.x. Eur J Biochem. 1993. PMID: 8281929 Free article. Review. No abstract available.

7

A regulatory cascade hypothesis for mammalian sex determination: SRY represses a negative regulator of male development.

McElreavey K, Vilain E, Abbas N, Herskowitz I, Fellous M. McElreavey K, et al. Among authors: vilain e. Proc Natl Acad Sci U S A. 1993 Apr 15;90(8):3368-72. doi: 10.1073/pnas.90.8.3368. Proc Natl Acad Sci U S A. 1993. PMID: 8475082 Free PMC article.

8

A minority of 46,XX true hermaphrodites are positive for the Y-DNA sequence including SRY.

McElreavey K, Rappaport R, Vilain E, Abbas N, Richaud F, Lortat-Jacob S, Berger R, Le Coniat M, Boucekkine C, Kucheria K, et al. McElreavey K, et al. Among authors: vilain e. Hum Genet. 1992 Sep-Oct;90(1-2):121-5. doi: 10.1007/BF00210754. Hum Genet. 1992. PMID: 1427767

9

Familial case of 46,XX male and 46,XX true hermaphrodite associated with a paternal-derived SRY-bearing X chromosome.

Abbas N, McElreavey K, Leconiat M, Vilain E, Jaubert F, Berger R, Nihoul-Fekete C, Rappaport R, Fellous M. Abbas N, et al. Among authors: vilain e. C R Acad Sci III. 1993;316(4):375-83. C R Acad Sci III. 1993. PMID: 8402263

10

Pathology of 46,XY pure gonadal dysgenesis: absence of testis differentiation associated with mutations in the testis-determining factor.

Vilain E, Jaubert F, Fellous M, McElreavey K. Vilain E, et al. Differentiation. 1993 Jan;52(2):151-9. doi: 10.1111/j.1432-0436.1993.tb00625.x. Differentiation. 1993. PMID: 8472885

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