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MSTO1 is a cytoplasmic pro-mitochondrial fusion protein, whose mutation induces myopathy and ataxia in humans.
Gal, Aniko; Balicza, Peter; Weaver, David; Naghdi, Shamim; Joseph, Suresh K; Várnai, Péter; Gyuris, Tibor; Horváth, Attila; Nagy, Laszlo; Seifert, Erin L; Molnar, Maria Judit; Hajnóczky, György.
Afiliação
  • Gal A; MitoCare Center for Mitochondrial Imaging Research and Diagnostics, Department of Pathology, Anatomy and Cell Biology, Thomas Jefferson University, Philadelphia, PA, USA.
  • Balicza P; Institute of Genomic Medicine and Rare Disorders, Semmelweis University, Budapest, Hungary.
  • Weaver D; Institute of Genomic Medicine and Rare Disorders, Semmelweis University, Budapest, Hungary.
  • Naghdi S; MitoCare Center for Mitochondrial Imaging Research and Diagnostics, Department of Pathology, Anatomy and Cell Biology, Thomas Jefferson University, Philadelphia, PA, USA.
  • Joseph SK; MitoCare Center for Mitochondrial Imaging Research and Diagnostics, Department of Pathology, Anatomy and Cell Biology, Thomas Jefferson University, Philadelphia, PA, USA.
  • Várnai P; MitoCare Center for Mitochondrial Imaging Research and Diagnostics, Department of Pathology, Anatomy and Cell Biology, Thomas Jefferson University, Philadelphia, PA, USA.
  • Gyuris T; Department of Physiology, Semmelweis University, Budapest, Hungary.
  • Horváth A; Department of Biochemistry and Molecular Biology, University of Debrecen, Debrecen, Hungary.
  • Nagy L; Department of Biochemistry and Molecular Biology, University of Debrecen, Debrecen, Hungary.
  • Seifert EL; Department of Biochemistry and Molecular Biology, University of Debrecen, Debrecen, Hungary.
  • Molnar MJ; MitoCare Center for Mitochondrial Imaging Research and Diagnostics, Department of Pathology, Anatomy and Cell Biology, Thomas Jefferson University, Philadelphia, PA, USA.
  • Hajnóczky G; Institute of Genomic Medicine and Rare Disorders, Semmelweis University, Budapest, Hungary.
EMBO Mol Med ; 9(7): 967-984, 2017 07.
Article em En | MEDLINE | ID: mdl-28554942
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Ataxia / Proteínas de Ciclo Celular / Proteínas do Citoesqueleto / Dinâmica Mitocondrial / Doenças Musculares / Mutação Tipo de estudo: Prognostic_studies Limite: Adult / Female / Humans / Male / Middle aged Idioma: En Revista: EMBO Mol Med Ano de publicação: 2017 Tipo de documento: Article
Texto completo
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Ataxia / Proteínas de Ciclo Celular / Proteínas do Citoesqueleto / Dinâmica Mitocondrial / Doenças Musculares / Mutação Tipo de estudo: Prognostic_studies Limite: Adult / Female / Humans / Male / Middle aged Idioma: En Revista: EMBO Mol Med Ano de publicação: 2017 Tipo de documento: Article