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6 results for Drévillon,+Loïc

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ArticlesPeer ReviewedFull Text
Two new cases of interstitial 7q35q36.1 deletion including CNTNAP2 and KMT2C
Author / Creator:Tosca, Lucie ; Drévillon, Loïc ; Mouka, Aurélie ; Lecerf, Laure ; Briand, Audrey ; Ortonne, Valérie ; Benoit, Virginie ; Brisset, Sophie ; Van Maldergem, Lionel ; Laudouar, Quitterie ; Heide, Solveig ; Goossens, Michel ; Giurgea, Irina ; Tachdjian, Gérard ; Métay, Corinne
Publisher:United States: John Wiley & Sons, Inc
Journal title:Molecular genetics & genomic medicine, 2021-11, Vol.9 (11), p.e1645-n/a
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iPSCs derived from infertile men carrying complex genetic abnormalities can generate primordial germ-like cells
Author / Creator:Mouka, Aurélie ; Arkoun, Brahim ; Moison, Pauline ; Drévillon, Loïc ; Jarray, Rafika ; Brisset, Sophie ; Mayeur, Anne ; Bouligand, Jérôme ; Boland-Auge, Anne ; Deleuze, Jean-François ; Yates, Frank ; Lemonnier, Thomas ; Callier, Patrick ; Duffourd, Yannis ; Nitschke, Patrick ; Ollivier, Emmanuelle ; Bourdin, Arnaud ; De Vos, John ; Livera, Gabriel ; Tachdjian, Gérard ; Maouche-Chrétien, Leïla ; Tosca, Lucie
Publisher:London: Nature Publishing Group UK
Journal title:Scientific reports, 2022-08, Vol.12 (1), p.14302-14, Article 14302
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COMMD1-Mediated Ubiquitination Regulates CFTR Trafficking
Author / Creator:Drévillon, Loïc ; Tanguy, Gaëlle ; Hinzpeter, Alexandre ; Arous, Nicole ; de Becdelièvre, Alix ; Aissat, Abdel ; Tarze, Agathe ; Goossens, Michel ; Fanen, Pascale
Publisher:United States: Public Library of Science
Journal title:PloS one, 2011-03, Vol.6 (3), p.e18334-e18334
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Induced pluripotent stem cell generation from a man carrying a complex chromosomal rearrangement as a genetic model for infertility studies
Author / Creator:Mouka, Aurélie ; Izard, Vincent ; Tachdjian, Gérard ; Brisset, Sophie ; Yates, Frank ; Mayeur, Anne ; Drévillon, Loïc ; Jarray, Rafika ; Leboulch, Philippe ; Maouche-Chrétien, Leila ; Tosca, Lucie
Publisher:London: Nature Publishing Group UK
Journal title:Scientific reports, 2017-01, Vol.7 (1), p.39760, Article 39760
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Prenatal Diagnosis of a 2.5 Mb De Novo 17q24.1q24.2 Deletion Encompassing KPNA2 and PSMD12 Genes in a Fetus with Craniofacial Dysmorphism, Equinovarus Feet, and Syndactyly
Author / Creator:Tachdjian, Gérard ; Brisset, Sophie ; Drévillon, Loïc ; Métay, Corinne ; Saada, Julien ; Martinovic, Jelena ; Tosca, Lucie ; Naud, Marie-Emmanuelle ; Benoit, Virginie
Publisher:Cairo, Egypt: Hindawi Publishing Corporation
Journal title:Case reports in genetics, 2017-01, Vol.2017 (2017), p.1-5
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Prenatal Diagnosis of a 2.5 Mb De Novo 17q24.1q24.2 Deletion Encompassing KPNA2 and PSMD12 Genes in a Fetus with Craniofacial Dysmorphism, Equinovarus Feet, and Syndactyly
Author / Creator:Naud, Marie-Emmanuelle ; Tosca, Lucie ; Martinovic, Jelena ; Saada, Julien ; Métay, Corinne ; Drévillon, Loïc ; Benoit, Virginie ; Brisset, Sophie ; Tachdjian, Gérard
Journal title:Case reports in genetics, 2017, Vol.2017, p.7803136-7803136
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Two new cases of interstitial 7q35q36.1 deletion including CNTNAP2 and KMT2C

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iPSCs derived from infertile men carrying complex genetic abnormalities can generate primordial germ-like cells

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COMMD1-Mediated Ubiquitination Regulates CFTR Trafficking

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Induced pluripotent stem cell generation from a man carrying a complex chromosomal rearrangement as a genetic model for infertility studies

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Prenatal Diagnosis of a 2.5 Mb De Novo 17q24.1q24.2 Deletion Encompassing KPNA2 and PSMD12 Genes in a Fetus with Craniofacial Dysmorphism, Equinovarus Feet, and Syndactyly

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Prenatal Diagnosis of a 2.5 Mb De Novo 17q24.1q24.2 Deletion Encompassing KPNA2 and PSMD12 Genes in a Fetus with Craniofacial Dysmorphism, Equinovarus Feet, and Syndactyly

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