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PD-linked CHCHD2 mutations impair CHCHD10 and MICOS complex leading to mitochondria dysfunction.
Zhou, Wei; Ma, Dongrui; Sun, Alfred Xuyang; Tran, Hoang-Dai; Ma, Dong-Liang; Singh, Brijesh K; Zhou, Jin; Zhang, Jinyan; Wang, Danlei; Zhao, Yi; Yen, Paul M; Goh, Eyleen; Tan, Eng-King.
Afiliação
  • Zhou W; Neuroscience Research Laboratory, National Neuroscience Institute, Singapore.
  • Ma D; Department of Neurology, Singapore General Hospital, Singapore.
  • Sun AX; Neuroscience Research Laboratory, National Neuroscience Institute, Singapore.
  • Tran HD; Stem Cell and Regenerative Biology Laboratory, Genome Institute of Singapore, Singapore.
  • Ma DL; Neuroscience Research Laboratory, National Neuroscience Institute, Singapore.
  • Singh BK; Stem Cell and Regenerative Biology Laboratory, Genome Institute of Singapore, Singapore.
  • Zhou J; Neuroregeneration Laboratory, Singhealth Duke-NUS Neuroscience Academic Clinical Program, Singapore.
  • Zhang J; Programs in Metabolic and Cardiovascular Disorders, Duke-NUS Graduate Medical School, Singapore.
  • Wang D; Programs in Metabolic and Cardiovascular Disorders, Duke-NUS Graduate Medical School, Singapore.
  • Zhao Y; Department of Neurology, Singapore General Hospital, Singapore.
  • Yen PM; Stem Cell and Regenerative Biology Laboratory, Genome Institute of Singapore, Singapore.
  • Goh E; Department of Clinical Research, Singapore General Hospital, Singapore.
  • Tan EK; Programs in Metabolic and Cardiovascular Disorders, Duke-NUS Graduate Medical School, Singapore.
Hum Mol Genet ; 28(7): 1100-1116, 2019 04 01.
Article em En | MEDLINE | ID: mdl-30496485

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Fatores de Transcrição / Doenças Mitocondriais / Proteínas Mitocondriais Tipo de estudo: Prognostic_studies Limite: Animals / Humans / Male Idioma: En Revista: Hum Mol Genet Assunto da revista: BIOLOGIA MOLECULAR / GENETICA MEDICA Ano de publicação: 2019 Tipo de documento: Article País de afiliação: Singapura

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Fatores de Transcrição / Doenças Mitocondriais / Proteínas Mitocondriais Tipo de estudo: Prognostic_studies Limite: Animals / Humans / Male Idioma: En Revista: Hum Mol Genet Assunto da revista: BIOLOGIA MOLECULAR / GENETICA MEDICA Ano de publicação: 2019 Tipo de documento: Article País de afiliação: Singapura