Elzaïat M - Search Results

1

A specific role for PRND in goat foetal Leydig cells is suggested by prion family gene expression during gonad development in goats and mice.

Allais-Bonnet A, Castille J, Pannetier M, Passet B, Elzaïat M, André M, Montazer-Torbati F, Moazami-Goudarzi K, Vilotte JL, Pailhoux E. Allais-Bonnet A, et al. Among authors: elzaiat m. FEBS Open Bio. 2016 Jan 14;6(1):4-15. doi: 10.1002/2211-5463.12002. eCollection 2016 Jan. FEBS Open Bio. 2016. PMID: 27047737 Free PMC article.

2

FOXL2 is a female sex-determining gene in the goat.

Boulanger L, Pannetier M, Gall L, Allais-Bonnet A, Elzaiat M, Le Bourhis D, Daniel N, Richard C, Cotinot C, Ghyselinck NB, Pailhoux E. Boulanger L, et al. Among authors: elzaiat m. Curr Biol. 2014 Feb 17;24(4):404-8. doi: 10.1016/j.cub.2013.12.039. Epub 2014 Jan 30. Curr Biol. 2014. PMID: 24485832 Free article.

3

High-throughput sequencing analyses of XX genital ridges lacking FOXL2 reveal DMRT1 up-regulation before SOX9 expression during the sex-reversal process in goats.

Elzaiat M, Jouneau L, Thépot D, Klopp C, Allais-Bonnet A, Cabau C, André M, Chaffaux S, Cribiu EP, Pailhoux E, Pannetier M. Elzaiat M, et al. Biol Reprod. 2014 Dec;91(6):153. doi: 10.1095/biolreprod.114.122796. Epub 2014 Nov 13. Biol Reprod. 2014. PMID: 25395674

4

Dual role of DMXL2 in olfactory information transmission and the first wave of spermatogenesis.

Gobé C, Elzaiat M, Meunier N, André M, Sellem E, Congar P, Jouneau L, Allais-Bonnet A, Naciri I, Passet B, Pailhoux E, Pannetier M. Gobé C, et al. Among authors: elzaiat m. PLoS Genet. 2019 Feb 8;15(2):e1007909. doi: 10.1371/journal.pgen.1007909. eCollection 2019 Feb. PLoS Genet. 2019. PMID: 30735494 Free PMC article.

5

Telling the story of XX sex reversal in the goat: highlighting the sex-crossroad in domestic mammals.

Pannetier M, Elzaiat M, Thépot D, Pailhoux E. Pannetier M, et al. Among authors: elzaiat m. Sex Dev. 2012;6(1-3):33-45. doi: 10.1159/000334056. Epub 2011 Nov 16. Sex Dev. 2012. PMID: 22094227 Review.

6

The genetic make-up of ovarian development and function: the focus on the transcription factor FOXL2.

Elzaiat M, Todeschini AL, Caburet S, Veitia RA. Elzaiat M, et al. Clin Genet. 2017 Feb;91(2):173-182. doi: 10.1111/cge.12862. Epub 2016 Sep 29. Clin Genet. 2017. PMID: 27604691 Review.

7

DHH pathogenic variants involved in 46,XY disorders of sex development differentially impact protein self-cleavage and structural conformation.

Elzaiat M, Flatters D, Sierra-Díaz DC, Legois B, Laissue P, Veitia RA. Elzaiat M, et al. Hum Genet. 2020 Nov;139(11):1455-1470. doi: 10.1007/s00439-020-02189-5. Epub 2020 Jun 5. Hum Genet. 2020. PMID: 32504121

8

A homozygous donor splice-site mutation in the meiotic gene MSH4 causes primary ovarian insufficiency.

Carlosama C, Elzaiat M, Patiño LC, Mateus HE, Veitia RA, Laissue P. Carlosama C, et al. Among authors: elzaiat m. Hum Mol Genet. 2017 Aug 15;26(16):3161-3166. doi: 10.1093/hmg/ddx199. Hum Mol Genet. 2017. PMID: 28541421

9

High-throughput Exploration of the Network Dependent on AKT1 in Mouse Ovarian Granulosa Cells.

Elzaiat M, Herman L, Legois B, Léger T, Todeschini AL, Veitia RA. Elzaiat M, et al. Mol Cell Proteomics. 2019 Jul;18(7):1307-1319. doi: 10.1074/mcp.RA119.0014613. Epub 2019 Apr 16. Mol Cell Proteomics. 2019. PMID: 30992313 Free PMC article.

10

[No title available]

[No authors listed] [No authors listed] PMID: 33451517

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