Generation of the human induced pluripotent stem cell line UKWNLi002-A from dermal fibroblasts of a woman with a heterozygous c.608 C>T (p.Thr203Met) mutation in exon 3 of the nerve growth factor gene potentially associated with hereditary sensory and autonomic neuropathy type 5.

Klein, Thomas; Henkel, Lisa; Klug, Katharina; Kwok, Chee Keong; Klopocki, Eva; Üçeyler, Nurcan

Klein, Thomas; Henkel, Lisa; Klug, Katharina; Kwok, Chee Keong; Klopocki, Eva; Üçeyler, Nurcan.

Afiliação

Klein T; Department of Neurology, University of Würzburg, Würzburg, Germany.
Henkel L; Department of Neurology, University of Würzburg, Würzburg, Germany.
Klug K; Department of Neurology, University of Würzburg, Würzburg, Germany.
Kwok CK; Institute of Anatomy and Cell Biology II, University of Würzburg, Würzburg, Germany.
Klopocki E; Institute of Human Genetics, Biocentre, University of Würzburg, Würzburg, Germany.
Üçeyler N; Department of Neurology, University of Würzburg, Würzburg, Germany. Electronic address: ueceyler_n@ukw.de.

Stem Cell Res ; 33: 171-174, 2018 12.

Article em En | MEDLINE | ID: mdl-30384131

Assuntos

Reprogramação Celular/genética; Éxons/genética; Fibroblastos/metabolismo; Neuropatias Hereditárias Sensoriais e Autônomas/genética; Células-Tronco Pluripotentes Induzidas/metabolismo; Idoso; Diferenciação Celular; Feminino; Humanos; Mutação

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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neuropatias Hereditárias Sensoriais e Autônomas / Éxons / Reprogramação Celular / Células-Tronco Pluripotentes Induzidas / Fibroblastos Tipo de estudo: Risk_factors_studies Limite: Aged / Female / Humans Idioma: En Ano de publicação: 2018 Tipo de documento: Article

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