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Generation of the induced pluripotent stem cell line UHOMi001-A from a patient with mutations in CCDC40 gene causing Primary Ciliary Dyskinesia (PCD).
Ahmed, Engi; Sansac, Caroline; Fieldes, Mathieu; Bergougnoux, Anne; Bourguignon, Chloé; Mianné, Joffrey; Arnould, Cécile; Vachier, Isabelle; Assou, Said; Bourdin, Arnaud; De Vos, John.
Afiliação
  • Ahmed E; IRMB, Univ Montpellier, INSERM, CHU Montpellier, Montpellier, France.
  • Sansac C; IRMB, Univ Montpellier, INSERM, CHU Montpellier, Montpellier, France.
  • Fieldes M; IRMB, Univ Montpellier, INSERM, CHU Montpellier, Montpellier, France.
  • Bergougnoux A; Laboratory of Molecular Genetics, CHU Montpellier, Montpellier, France; Rare Genetic Diseases Laboratory, Institut Universitaire de Recherche Clinique, University of Montpellier, Montpellier, France.
  • Bourguignon C; IRMB, Univ Montpellier, INSERM, CHU Montpellier, Montpellier, France.
  • Mianné J; IRMB, Univ Montpellier, INSERM, CHU Montpellier, Montpellier, France.
  • Arnould C; Laboratory of Molecular Genetics, CHU Nîmes, Nîmes, France.
  • Vachier I; Department of Respiratory Diseases, CHU Montpellier, INSERM, Montpellier, France.
  • Assou S; IRMB, Univ Montpellier, INSERM, CHU Montpellier, Montpellier, France.
  • Bourdin A; Department of Respiratory Diseases, CHU Montpellier, INSERM, Montpellier, France. Electronic address: a-bourdin@chu-montpellier.fr.
  • De Vos J; IRMB, Univ Montpellier, INSERM, CHU Montpellier, Montpellier, France; Department of Cell and Tissue Engineering, CHU Montpellier, Montpellier, France. Electronic address: john.devos@inserm.fr.
Stem Cell Res ; 33: 15-19, 2018 12.
Article em En | MEDLINE | ID: mdl-30296669
Primary Ciliary Dyskinesia (PCD) is a rare heterogeneous genetic disorder affecting motile cilia structure and function leading to lung disease. We generated induced pluripotent stem cells (iPSCs) from dermal fibroblasts of a female PCD patient carrying disease-causing variants in the CCDC40 gene. Reprogramming was performed with the human OSKM transcription factors using the Sendai-virus delivery system. The resulting transgene free iPSCs had normal karyotype, expressed pluripotency markers, could differentiate into the three germ layers in vivo and retained the disease-causing CCDC40 mutations. This iPSC line could be useful to model PCD disease and test gene therapy strategies. Resource Table.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Prognostic_studies Limite: Adult / Female / Humans Idioma: En Ano de publicação: 2018 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Prognostic_studies Limite: Adult / Female / Humans Idioma: En Ano de publicação: 2018 Tipo de documento: Article