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Items: 9

1.

A truncating MEIOB mutation responsible for familial primary ovarian insufficiency abolishes its interaction with its partner SPATA22 and their recruitment to DNA double-strand breaks.

Caburet S, Todeschini AL, Petrillo C, Martini E, Farran ND, Legois B, Livera G, Younis JS, Shalev S, Veitia RA.

EBioMedicine. 2019 Apr;42:524-531. doi: 10.1016/j.ebiom.2019.03.075. Epub 2019 Apr 15.

2.

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.

Mol Cell Proteomics. 2019 Jul;18(7):1307-1319. doi: 10.1074/mcp.RA119.001461. Epub 2019 Apr 16.

PMID:
30992313
3.

A homozygous FANCM mutation underlies a familial case of non-syndromic primary ovarian insufficiency.

Fouquet B, Pawlikowska P, Caburet S, Guigon C, Mäkinen M, Tanner L, Hietala M, Urbanska K, Bellutti L, Legois B, Bessieres B, Gougeon A, Benachi A, Livera G, Rosselli F, Veitia RA, Misrahi M.

Elife. 2017 Dec 12;6. pii: e30490. doi: 10.7554/eLife.30490.

4.

A novel variant of DHH in a familial case of 46,XY disorder of sex development: Insights from molecular dynamics simulations.

Paris F, Flatters D, Caburet S, Legois B, Servant N, Lefebvre H, Sultan C, Veitia RA.

Clin Endocrinol (Oxf). 2017 Nov;87(5):539-544. doi: 10.1111/cen.13420. Epub 2017 Aug 13.

PMID:
28708305
5.

A homozygous mutation of GNRHR in a familial case diagnosed with polycystic ovary syndrome.

Caburet S, Fruchter RB, Legois B, Fellous M, Shalev S, Veitia RA.

Eur J Endocrinol. 2017 May;176(5):K9-K14. doi: 10.1530/EJE-16-0968.

PMID:
28348023
6.

A non-sense MCM9 mutation in a familial case of primary ovarian insufficiency.

Fauchereau F, Shalev S, Chervinsky E, Beck-Fruchter R, Legois B, Fellous M, Caburet S, Veitia RA.

Clin Genet. 2016 May;89(5):603-7. doi: 10.1111/cge.12736. Epub 2016 Feb 10.

PMID:
26771056
7.

Molecular analyses of juvenile granulosa cell tumors bearing AKT1 mutations provide insights into tumor biology and therapeutic leads.

Auguste A, Bessière L, Todeschini AL, Caburet S, Sarnacki S, Prat J, D'angelo E, De La Grange P, Ariste O, Lemoine F, Legois B, Sultan C, Zider A, Galmiche L, Kalfa N, Veitia RA.

Hum Mol Genet. 2015 Dec 1;24(23):6687-98. doi: 10.1093/hmg/ddv373. Epub 2015 Sep 11.

PMID:
26362254
8.

A Hot-spot of In-frame Duplications Activates the Oncoprotein AKT1 in Juvenile Granulosa Cell Tumors.

Bessière L, Todeschini AL, Auguste A, Sarnacki S, Flatters D, Legois B, Sultan C, Kalfa N, Galmiche L, Veitia RA.

EBioMedicine. 2015 Mar 6;2(5):421-31. doi: 10.1016/j.ebiom.2015.03.002. eCollection 2015 May.

9.

The transcription factor FOXL2 mobilizes estrogen signaling to maintain the identity of ovarian granulosa cells.

Georges A, L'Hôte D, Todeschini AL, Auguste A, Legois B, Zider A, Veitia RA.

Elife. 2014 Nov 4;3. doi: 10.7554/eLife.04207.

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