Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Christel Vache"'
Autor:
Carla Sanjurjo-Soriano, Nejla Erkilic, Christel Vache, Gregor Dubois, Anne-Françoise Roux, Isabelle Meunier, Vasiliki Kalatzis
Publikováno v:
Stem Cell Research, Vol 60, Iss , Pp 102738- (2022)
We report here the generation of the human iPSC line INMi005-A from a patient with non-syndromic autosomal recessive retinitis pigmentosa caused by compound heterozygous mutations in the USH2A gene. The reprogramming of primary human dermal fibroblas
Externí odkaz:
https://doaj.org/article/80ebaca8f2e7443683df77b81e1672fa
Autor:
Serge Pellier, Chantal Vaury, Olivier Camares, Annie Meiniel, Eva Leoz-Garziandia, Christel Vache, Bernard Dastugue, Fabienne De Graeve, Mahchid Bamdad
Publikováno v:
Environmental Toxicology and Chemistry. 25:572
Polycyclic aromatic hydrocarbons (PAHs) are well-known ubiquitous environmental contaminants. Permeability glycoprotein (P-gp) is a transmembrane detoxification efflux pump transporting various lipophilic xenobiotics, such as PAHs, out of the cells.
Autor:
Christel Vaché, Jacques Puechberty, Valérie Faugère, Floriane Darmaisin, Alessandro Liquori, David Baux, Catherine Blanchet, Gema Garcia-Garcia, Isabelle Meunier, Franck Pellestor, Michel Koenig, Anne-Françoise Roux
Publikováno v:
Frontiers in Genetics, Vol 11 (2020)
Usher type 1 syndrome is a rare autosomal recessive disorder involving congenital severe-to-profound hearing loss, development of vision impairment in the first decade, and severe balance difficulties. The PCDH15 gene, one of the five genes implicate
Externí odkaz:
https://doaj.org/article/7b788bb3d7c2403c815d579012188e3e
Autor:
Luke Mansard, Christel Vaché, Julie Bianchi, Corinne Baudoin, Isabelle Perthus, Bertrand Isidor, Catherine Blanchet, David Baux, Michel Koenig, Vasiliki Kalatzis, Anne-Françoise Roux
Publikováno v:
Diagnostics, Vol 12, Iss 1, p 207 (2022)
GSDME, also known as DFNA5, is a gene implicated in autosomal dominant nonsyndromic hearing loss (ADNSHL), affecting, at first, the high frequencies with a subsequent progression over all frequencies. To date, all the GSDME pathogenic variants associ
Externí odkaz:
https://doaj.org/article/1a0d5f9b33f8483ba90ee067fe0abd44
Autor:
Luke Mansard, David Baux, Christel Vaché, Catherine Blanchet, Isabelle Meunier, Marjolaine Willems, Valérie Faugère, Corinne Baudoin, Melody Moclyn, Julie Bianchi, Helene Dollfus, Brigitte Gilbert-Dussardier, Delphine Dupin-Deguine, Dominique Bonneau, Isabelle Drumare, Sylvie Odent, Xavier Zanlonghi, Mireille Claustres, Michel Koenig, Vasiliki Kalatzis, Anne-Françoise Roux
Publikováno v:
International Journal of Molecular Sciences, Vol 22, Iss 24, p 13294 (2021)
Usher syndrome is an autosomal recessive disorder characterized by congenital hearing loss combined with retinitis pigmentosa, and in some cases, vestibular areflexia. Three clinical subtypes are distinguished, and MYO7A and USH2A represent the two m
Externí odkaz:
https://doaj.org/article/60bf793686c64932a496b57b4a231434
Autor:
Camille Cenni, Luke Mansard, Catherine Blanchet, David Baux, Christel Vaché, Corinne Baudoin, Mélodie Moclyn, Valérie Faugère, Michel Mondain, Eric Jeziorski, Anne-Françoise Roux, Marjolaine Willems
Publikováno v:
Diagnostics, Vol 11, Iss 9, p 1636 (2021)
We describe a family with both hearing loss (HL) and thrombocytopenia, caused by pathogenic variants in three genes. The proband was a child with neonatal thrombocytopenia, childhood-onset HL, hyper-laxity and severe myopia. The child’s mother (and
Externí odkaz:
https://doaj.org/article/e6a6cf451298483093b82e2edbc31bdc
Autor:
Thomas Besnard, Gema García‐García, David Baux, Christel Vaché, Valérie Faugère, Lise Larrieu, Susana Léonard, Jose M. Millan, Sue Malcolm, Mireille Claustres, Anne‐Françoise Roux
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 2, Iss 1, Pp 30-43 (2014)
Abstract We show that massively parallel targeted sequencing of 19 genes provides a new and reliable strategy for molecular diagnosis of Usher syndrome (USH) and nonsyndromic deafness, particularly appropriate for these disorders characterized by a h
Externí odkaz:
https://doaj.org/article/b950ebe4483b4138a4518e0fbe7b6143
Autor:
Radulfus WN Slijkerman, Christel Vaché, Margo Dona, Gema García-García, Mireille Claustres, Lisette Hetterschijt, Theo A Peters, Bas P Hartel, Ronald JE Pennings, José M Millan, Elena Aller, Alejandro Garanto, Rob WJ Collin, Hannie Kremer, Anne-Françoise Roux, Erwin Van Wijk
Publikováno v:
Molecular Therapy: Nucleic Acids, Vol 5, Iss C (2016)
Usher syndrome (USH) is the most common cause of combined deaf-blindness in man. The hearing loss can be partly compensated by providing patients with hearing aids or cochlear implants, but the loss of vision is currently untreatable. In general, mut
Externí odkaz:
https://doaj.org/article/630403874b684cdf82cd8b7633db40fd