Elzaiat M - Search Results

1

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.

2

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.

3

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

4

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

5

A truncating variant of RAD51B associated with primary ovarian insufficiency provides insights into its meiotic and somatic functions.

Franca MM, Condezo YB, Elzaiat M, Felipe-Medina N, Sánchez-Sáez F, Muñoz S, Sainz-Urruela R, Martín-Hervás MR, García-Valiente R, Sánchez-Martín MA, Astudillo A, Mendez J, Llano E, Veitia RA, Mendonca BB, Pendás AM. Franca MM, et al. Among authors: elzaiat m. Cell Death Differ. 2022 Dec;29(12):2347-2361. doi: 10.1038/s41418-022-01021-z. Epub 2022 May 27. Cell Death Differ. 2022. PMID: 35624308 Free PMC article.

6

Genetics of 46,XY gonadal dysgenesis.

Elzaiat M, McElreavey K, Bashamboo A. Elzaiat M, et al. Best Pract Res Clin Endocrinol Metab. 2022 Jan;36(1):101633. doi: 10.1016/j.beem.2022.101633. Epub 2022 Feb 25. Best Pract Res Clin Endocrinol Metab. 2022. PMID: 35249806 Review.

7

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.

8

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.

9

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

10

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.

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