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Abnormal morphology and function in retinal ganglion cells derived from patients-specific iPSCs generated from individuals with Leber's hereditary optic neuropathy.
Nie, Zhipeng; Wang, Chenghui; Chen, Jiarong; Ji, Yanchun; Zhang, Hongxing; Zhao, Fuxin; Zhou, Xiangtian; Guan, Min-Xin.
Afiliação
  • Nie Z; Division of Medical Genetics and Genomics, The Children's Hospital, Zhejiang University School of Medicine and National Clinical Research Center for Child Health, Hangzhou, Zhejiang, China.
  • Wang C; Institute of Genetics and Department of Human Genetics, Zhejiang University School of Medicine, Hangzhou, Zhejiang, China.
  • Chen J; Institute of Genetics and Department of Human Genetics, Zhejiang University School of Medicine, Hangzhou, Zhejiang, China.
  • Ji Y; Division of Medical Genetics and Genomics, The Children's Hospital, Zhejiang University School of Medicine and National Clinical Research Center for Child Health, Hangzhou, Zhejiang, China.
  • Zhang H; Institute of Genetics and Department of Human Genetics, Zhejiang University School of Medicine, Hangzhou, Zhejiang, China.
  • Zhao F; Division of Medical Genetics and Genomics, The Children's Hospital, Zhejiang University School of Medicine and National Clinical Research Center for Child Health, Hangzhou, Zhejiang, China.
  • Zhou X; Institute of Genetics and Department of Human Genetics, Zhejiang University School of Medicine, Hangzhou, Zhejiang, China.
  • Guan MX; Department of Ophthalmology, The First Affiliated Hospital, Shandong First Medical University, Jinan, Shandong, China.
Hum Mol Genet ; 32(2): 231-243, 2023 01 06.
Article em En | MEDLINE | ID: mdl-35947995
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Atrofia Óptica Hereditária de Leber / Células-Tronco Pluripotentes Induzidas Tipo de estudo: Prognostic_studies Limite: Animals Idioma: En Revista: Hum Mol Genet Assunto da revista: BIOLOGIA MOLECULAR / GENETICA MEDICA Ano de publicação: 2023 Tipo de documento: Article País de afiliação: China
Texto completo
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PubMed Links
Buscar no Google

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Atrofia Óptica Hereditária de Leber / Células-Tronco Pluripotentes Induzidas Tipo de estudo: Prognostic_studies Limite: Animals Idioma: En Revista: Hum Mol Genet Assunto da revista: BIOLOGIA MOLECULAR / GENETICA MEDICA Ano de publicação: 2023 Tipo de documento: Article País de afiliação: China