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4 results for Dipietromaria,+Aurélie

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ArticlesPeer ReviewedFull Text
Functional Exploration of the Adult Ovarian Granulosa Cell Tumor-Associated Somatic FOXL2 Mutation p.Cys134Trp (c.402C>G)
Author / Creator:Benayoun, Bérénice A. ; Caburet, Sandrine ; Dipietromaria, Aurélie ; Georges, Adrien ; D'Haene, Barbara ; Pandaranayaka, P. J. Eswari ; L'Hôte, David ; Todeschini, Anne-Laure ; Krishnaswamy, Sankaran ; Fellous, Marc ; De Baere, Elfride ; Veitia, Reiner A.
Publisher:United States: Public Library of Science
Journal title:PloS one, 2010-01, Vol.5 (1), p.e8789-e8789
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Genome-Wide Linkage in a Highly Consanguineous Pedigree Reveals Two Novel Loci on Chromosome 7 for Non-Syndromic Familial Premature Ovarian Failure
Author / Creator:Caburet, Sandrine ; Zavadakova, Petra ; Ben-Neriah, Ziva ; Bouhali, Kamal ; Dipietromaria, Aurélie ; Charon, Céline ; Besse, Céline ; Laissue, Paul ; Chalifa-Caspi, Vered ; Christin-Maitre, Sophie ; Vaiman, Daniel ; Levi, Giovanni ; Veitia, Reiner A. ; Fellous, Marc
Publisher:United States: Public Library of Science
Journal title:PloS one, 2012-03, Vol.7 (3), p.e33412-e33412
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SUMOylation of the Forkhead Transcription Factor FOXL2 Promotes Its Stabilization/Activation through Transient Recruitment to PML Bodies
Author / Creator:Georges, Adrien ; Benayoun, Bérénice A. ; Marongiu, Mara ; Dipietromaria, Aurélie ; L'Hôte, David ; Todeschini, Anne-Laure ; Auer, Jana ; Crisponi, Laura ; Veitia, Reiner A.
Publisher:United States: Public Library of Science
Journal title:PloS one, 2011-10, Vol.6 (10), p.e25463-e25463
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Functional evidence implicating FOXL2 in non-syndromic premature ovarian failure and in the regulation of the transcription factor OSR2
Author / Creator:Laissue, P ; Lakhal, B ; Benayoun, B A ; Dipietromaria, A ; Braham, R ; Elghezal, H ; Philibert, P ; Saâd, A ; Sultan, C ; Fellous, M ; Veitia, R A
Publisher:England: BMJ Publishing Group Ltd
Journal title:Journal of medical genetics, 2009-07, Vol.46 (7), p.455-457
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Functional Exploration of the Adult Ovarian Granulosa Cell Tumor-Associated Somatic FOXL2 Mutation p.Cys134Trp (c.402C>G)

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Genome-Wide Linkage in a Highly Consanguineous Pedigree Reveals Two Novel Loci on Chromosome 7 for Non-Syndromic Familial Premature Ovarian Failure

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SUMOylation of the Forkhead Transcription Factor FOXL2 Promotes Its Stabilization/Activation through Transient Recruitment to PML Bodies

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Functional evidence implicating FOXL2 in non-syndromic premature ovarian failure and in the regulation of the transcription factor OSR2

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