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A hypomorphic PIGA gene mutation causes severe defects in neuron development and susceptibility to complement-mediated toxicity in a human iPSC model.
Yuan, Xuan; Li, Zhe; Baines, Andrea C; Gavriilaki, Eleni; Ye, Zhaohui; Wen, Zhexing; Braunstein, Evan M; Biesecker, Leslie G; Cheng, Linzhao; Dong, Xinzhong; Brodsky, Robert A.
Afiliação
  • Yuan X; Division of Hematology, Department of Medicine, Johns Hopkins University School of Medicine, Baltimore, MD, United States of America.
  • Li Z; Department of Neuroscience, Johns Hopkins University, School of Medicine, Baltimore, MD, United States of America.
  • Baines AC; Division of Hematology, Department of Medicine, Johns Hopkins University School of Medicine, Baltimore, MD, United States of America.
  • Gavriilaki E; Division of Hematology, Department of Medicine, Johns Hopkins University School of Medicine, Baltimore, MD, United States of America.
  • Ye Z; Division of Hematology, Department of Medicine, Johns Hopkins University School of Medicine, Baltimore, MD, United States of America.
  • Wen Z; Stem Cell Program in the Institute for Cell Engineering, Johns Hopkins University School of Medicine, Baltimore, MD, United States of America.
  • Braunstein EM; Stem Cell Program in the Institute for Cell Engineering, Johns Hopkins University School of Medicine, Baltimore, MD, United States of America.
  • Biesecker LG; Division of Hematology, Department of Medicine, Johns Hopkins University School of Medicine, Baltimore, MD, United States of America.
  • Cheng L; Genetic Disease Research Branch, National Human Genome Research Institute, National Institutes of Health, Bethesda, MD, United States of America.
  • Dong X; Division of Hematology, Department of Medicine, Johns Hopkins University School of Medicine, Baltimore, MD, United States of America.
  • Brodsky RA; Stem Cell Program in the Institute for Cell Engineering, Johns Hopkins University School of Medicine, Baltimore, MD, United States of America.
PLoS One ; 12(4): e0174074, 2017.
Article em En | MEDLINE | ID: mdl-28441409
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Proteínas do Sistema Complemento / Neurogênese / Células-Tronco Pluripotentes Induzidas / Células-Tronco Neurais / Proteínas de Membrana / Mutação Tipo de estudo: Etiology_studies Limite: Animals / Humans Idioma: En Revista: PLoS One Assunto da revista: CIENCIA / MEDICINA Ano de publicação: 2017 Tipo de documento: Article País de afiliação: Estados Unidos País de publicação: Estados Unidos
Texto completo
Adicionar na Minha BVS
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Proteínas do Sistema Complemento / Neurogênese / Células-Tronco Pluripotentes Induzidas / Células-Tronco Neurais / Proteínas de Membrana / Mutação Tipo de estudo: Etiology_studies Limite: Animals / Humans Idioma: En Revista: PLoS One Assunto da revista: CIENCIA / MEDICINA Ano de publicação: 2017 Tipo de documento: Article País de afiliação: Estados Unidos País de publicação: Estados Unidos