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Generation of two induced pluripotent stem cell lines (UQACi002-A and UQACi005-A) from two patients with KRT14 epidermolysis bullosa simplex mutations.
Bchetnia, Mbarka; Martineau, Laurie; Racine, Véronique; Powell, Julie; McCuaig, Catherine; Morin, Charles; Dupérée, Audrey; Gros-Louis, François; Laprise, Catherine.
Afiliación
  • Bchetnia M; Université du Québec à Chicoutimi, Département des sciences fondamentales, Saguenay, QC, Canada.
  • Martineau L; Centre hospitalier universitaire (CHU) de Québec-Université Laval, Québec, QC, Canada.
  • Racine V; Centre hospitalier universitaire (CHU) de Québec-Université Laval, Québec, QC, Canada.
  • Powell J; CHU Sainte-Justine, Montréal, QC, Canada.
  • McCuaig C; CHU Sainte-Justine, Montréal, QC, Canada.
  • Morin C; Centre intégré universitaire de santé et de services sociaux (CIUSSS) du Saguenay-Lac-Saint-Jean, Saguenay, QC, Canada.
  • Dupérée A; Centre intégré universitaire de santé et de services sociaux (CIUSSS) du Saguenay-Lac-Saint-Jean, Saguenay, QC, Canada.
  • Gros-Louis F; Centre hospitalier universitaire (CHU) de Québec-Université Laval, Québec, QC, Canada.
  • Laprise C; Université du Québec à Chicoutimi, Département des sciences fondamentales, Saguenay, QC, Canada; Centre intégré universitaire de santé et de services sociaux (CIUSSS) du Saguenay-Lac-Saint-Jean, Saguenay, QC, Canada. Electronic address: catherine.laprise@uqac.ca.
Stem Cell Res ; 61: 102750, 2022 05.
Article en En | MEDLINE | ID: mdl-35334406
More than 107 pathogenic variations were identified in Keratin 14 gene (KRT14) in patients affected by epidermolysis bullosa simplex (EBS), a rare skin disease with still no curative treatment. Disease models as human induced pluripotent stem cells (hiPSCs) are promising tool for further advance the knowledge about this disorder and accelerate therapies development. Here, two hiPSC lines were reprogrammed from skin fibroblasts of two EBS patients carrying mutations within KRT14 by using CytoTune®Sendai virus. These iPSCs display pluripotent cell morphology, pluripotent markers expression, and the capability to differentiate into the three germ layers.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Epidermólisis Ampollosa Simple / Células Madre Pluripotentes Inducidas Tipo de estudio: Prognostic_studies Límite: Humans Idioma: En Revista: Stem Cell Res Año: 2022 Tipo del documento: Article País de afiliación: Canadá Pais de publicación: Reino Unido

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Epidermólisis Ampollosa Simple / Células Madre Pluripotentes Inducidas Tipo de estudio: Prognostic_studies Límite: Humans Idioma: En Revista: Stem Cell Res Año: 2022 Tipo del documento: Article País de afiliación: Canadá Pais de publicación: Reino Unido