Fellous M - Search Results

1

The human doublesex-related gene, DMRT2, is homologous to a gene involved in somitogenesis and encodes a potential bicistronic transcript.

Ottolenghi C, Veitia R, Barbieri M, Fellous M, McElreavey K. Ottolenghi C, et al. Among authors: fellous m. Genomics. 2000 Mar 1;64(2):179-86. doi: 10.1006/geno.2000.6120. Genomics. 2000. PMID: 10729224

2

Novel paralogy relations among human chromosomes support a link between the phylogeny of doublesex-related genes and the evolution of sex determination.

Ottolenghi C, Fellous M, Barbieri M, McElreavey K. Ottolenghi C, et al. Among authors: fellous m. Genomics. 2002 Mar;79(3):333-43. doi: 10.1006/geno.2002.6711. Genomics. 2002. PMID: 11863363

3

Deletions of distal 9p associated with 46,XY male to female sex reversal: definition of the breakpoints at 9p23.3-p24.1.

Veitia R, Nunes M, Brauner R, Doco-Fenzy M, Joanny-Flinois O, Jaubert F, Lortat-Jacob S, Fellous M, McElreavey K. Veitia R, et al. Among authors: fellous m. Genomics. 1997 Apr 15;41(2):271-4. doi: 10.1006/geno.1997.4648. Genomics. 1997. PMID: 9143505

4

Conservation of Y chromosome-specific sequences immediately 5' to the testis determining gene in primates.

Veitia RA, Fellous M, McElreavey K. Veitia RA, et al. Among authors: fellous m. Gene. 1997 Oct 15;199(1-2):63-70. doi: 10.1016/s0378-1119(97)00347-8. Gene. 1997. PMID: 9358040

5

The region on 9p associated with 46,XY sex reversal contains several transcripts expressed in the urogenital system and a novel doublesex-related domain.

Ottolenghi C, Veitia R, Quintana-Murci L, Torchard D, Scapoli L, Souleyreau-Therville N, Beckmann J, Fellous M, McElreavey K. Ottolenghi C, et al. Among authors: fellous m. Genomics. 2000 Mar 1;64(2):170-8. doi: 10.1006/geno.2000.6121. Genomics. 2000. PMID: 10729223

6

Absence of mutations involving the LIM homeobox domain gene LHX9 in 46,XY gonadal agenesis and dysgenesis.

Ottolenghi C, Moreira-Filho C, Mendonça BB, Barbieri M, Fellous M, Berkovitz GD, McElreavey K. Ottolenghi C, et al. Among authors: fellous m. J Clin Endocrinol Metab. 2001 Jun;86(6):2465-9. doi: 10.1210/jcem.86.6.7539. J Clin Endocrinol Metab. 2001. PMID: 11397841

7

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: fellous m. Genomics. 1992 Jul;13(3):838-40. doi: 10.1016/0888-7543(92)90164-n. Genomics. 1992. PMID: 1639410

8

Sense and antisense Foxl2 transcripts in mouse.

Cocquet J, Pannetier M, Fellous M, Veitia RA. Cocquet J, et al. Among authors: fellous m. Genomics. 2005 May;85(5):531-41. doi: 10.1016/j.ygeno.2005.01.007. Genomics. 2005. PMID: 15820304

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: fellous m. C R Acad Sci III. 1993;316(4):375-83. C R Acad Sci III. 1993. PMID: 8402263

10

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: fellous m. 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.

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