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Loss of mitochondrial ClpP,Lonp1, and Tfam triggers transcriptional induction of Rnf213, a susceptibility factor for moyamoya disease |
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| Authors: | Key Jana Maletzko Antonia Kohli Aneesha Gispert Suzana Torres-Odio Sylvia Wittig Ilka Heidler Juliana Bárcena Clea López-Otín Carlos Lei Yuanjiu West A. Phillip Münch Christian Auburger Georg |
| Affiliation: | 1.Experimental Neurology, Goethe University Medical School, 60590, Frankfurt am Main, Germany ;2.Faculty of Biosciences, Goethe-University, Frankfurt am Main, Germany ;3.Functional Proteomics Group, Goethe-University Hospital, 60590, Frankfurt am Main, Germany ;4.Departamento de Bioquímica y Biología Molecular, Facultad de Medicina, Instituto Universitario de Oncología, Universidad de Oviedo, 33006, Oviedo, Spain ;5.Department of Microbial Pathogenesis and Immunology, Texas A&M University, College Station, TX, USA ;6.Institute of Biochemistry II, Goethe University Medical School, 60590, Frankfurt am Main, Germany ; |
| Abstract: | neurogenetics - Human RNF213, which encodes the protein mysterin, is a known susceptibility gene for moyamoya disease (MMD), a cerebrovascular condition with occlusive lesions and compensatory... |
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