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Characterization of the most frequent ATP7B mutation causing Wilson disease in hepatocytes from patient induced pluripotent stem cells.
Parisi, Silvia; Polishchuk, Elena V; Allocca, Simona; Ciano, Michela; Musto, Anna; Gallo, Maria; Perone, Lucia; Ranucci, Giusy; Iorio, Raffaele; Polishchuk, Roman S; Bonatti, Stefano.
Afiliação
  • Parisi S; Department of Molecular Medicine and Medical Biotechnology, University of Naples Federico II, Naples, Italy. silvia.parisi@unina.it.
  • Polishchuk EV; Telethon Institute of Genetics and Medicine, Pozzuoli, Italy.
  • Allocca S; Department of Molecular Medicine and Medical Biotechnology, University of Naples Federico II, Naples, Italy.
  • Ciano M; Department of Molecular Medicine and Medical Biotechnology, University of Naples Federico II, Naples, Italy.
  • Musto A; Department of Molecular Medicine and Medical Biotechnology, University of Naples Federico II, Naples, Italy.
  • Gallo M; Department of Molecular Medicine and Medical Biotechnology, University of Naples Federico II, Naples, Italy.
  • Perone L; Telethon Institute of Genetics and Medicine, Pozzuoli, Italy.
  • Ranucci G; Department of Translational Medical Science, Section of Pediatric, University of Naples Federico II, Naples, Italy.
  • Iorio R; Department of Translational Medical Science, Section of Pediatric, University of Naples Federico II, Naples, Italy.
  • Polishchuk RS; Telethon Institute of Genetics and Medicine, Pozzuoli, Italy. polish@tigem.it.
  • Bonatti S; Department of Molecular Medicine and Medical Biotechnology, University of Naples Federico II, Naples, Italy. bonatti@unina.it.
Sci Rep ; 8(1): 6247, 2018 04 19.
Article em En | MEDLINE | ID: mdl-29674751

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Polimorfismo de Nucleotídeo Único / Hepatócitos / Células-Tronco Pluripotentes Induzidas / ATPases Transportadoras de Cobre / Degeneração Hepatolenticular Limite: Humans Idioma: En Revista: Sci Rep Ano de publicação: 2018 Tipo de documento: Article País de afiliação: Itália

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Polimorfismo de Nucleotídeo Único / Hepatócitos / Células-Tronco Pluripotentes Induzidas / ATPases Transportadoras de Cobre / Degeneração Hepatolenticular Limite: Humans Idioma: En Revista: Sci Rep Ano de publicação: 2018 Tipo de documento: Article País de afiliação: Itália