Generation of an ipsc line (imagini022-a) ...
Type de document :
Article dans une revue scientifique: Article original
PMID :
URL permanente :
Titre :
Generation of an ipsc line (imagini022-a) from a patient carrying a sox10 missense mutation and presenting with deafness, depigmentation and progressive neurological impairment
Auteur(s) :
Banal, Celine [Auteur]
Quelennec, Eddy [Auteur]
Bertani-Torres, William [Auteur]
Gacem, Nadjet [Auteur]
Amiel, Jeanne [Auteur]
Marlin, Sandrine [Auteur]
Petit, Florence [Auteur]
Pingault, Veronique [Auteur]
Lefort, Nathalie [Auteur]
Bondurand, Nadege [Auteur]
Quelennec, Eddy [Auteur]
Bertani-Torres, William [Auteur]
Gacem, Nadjet [Auteur]
Amiel, Jeanne [Auteur]
Marlin, Sandrine [Auteur]
Petit, Florence [Auteur]
Pingault, Veronique [Auteur]
Lefort, Nathalie [Auteur]
Bondurand, Nadege [Auteur]
Titre de la revue :
Stem cell research
Nom court de la revue :
Stem Cell Res
Numéro :
48
Pagination :
101936
Date de publication :
2020-08-02
ISSN :
1876-7753
Discipline(s) HAL :
Sciences du Vivant [q-bio]
Résumé en anglais : [en]
Mutations of SOX10 result in a broad range of phenotypes including Waardenburg syndrome (WS types 2 and 4) that can be found in association with peripheral demyelinating neuropathy and/or central dysmyelinating leukodystrophy. ...
Lire la suite >Mutations of SOX10 result in a broad range of phenotypes including Waardenburg syndrome (WS types 2 and 4) that can be found in association with peripheral demyelinating neuropathy and/or central dysmyelinating leukodystrophy. Here, we generated induced pluripotent stem cells (iPSCs) from a patient carrying a de novo heterozygous missense mutation in the SOX10 gene (MIM* 602229, NM006941.3c.523C > G; p.Pro175Ala) presenting with deafness, depigmentation and progressive neurological impairment. Cells were reprogrammed by non-integrative viral transduction from blood sample, have normal karyotype, express pluripotency markers and are able to differentiate into the three germ cell layers.Lire moins >
Lire la suite >Mutations of SOX10 result in a broad range of phenotypes including Waardenburg syndrome (WS types 2 and 4) that can be found in association with peripheral demyelinating neuropathy and/or central dysmyelinating leukodystrophy. Here, we generated induced pluripotent stem cells (iPSCs) from a patient carrying a de novo heterozygous missense mutation in the SOX10 gene (MIM* 602229, NM006941.3c.523C > G; p.Pro175Ala) presenting with deafness, depigmentation and progressive neurological impairment. Cells were reprogrammed by non-integrative viral transduction from blood sample, have normal karyotype, express pluripotency markers and are able to differentiate into the three germ cell layers.Lire moins >
Langue :
Anglais
Audience :
Internationale
Vulgarisation :
Non
Établissement(s) :
Université de Lille
Collections :
Date de dépôt :
2021-09-02T07:01:40Z