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Glial pathology in a novel spontaneous mutant mouse of the Eif2b5 gene: a vanishing white matter disease model
Authors:Mika Terumitsu-Tsujita  Hiroki Kitaura  Ikuo Miura  Yuji Kiyama  Fumiko Goto  Yoshiko Muraki  Shiho Ominato  Norikazu Hara  Anna Simankova  Norihisa Bizen  Kazuhiro Kashiwagi  Takuhiro Ito  Yasuko Toyoshima  Akiyoshi Kakita  Toshiya Manabe  Shigeharu Wakana  Hirohide Takebayashi  Hironaka Igarashi
Affiliation:1. Center for Integrated Human Brain Science, Brain Research Institute, Niigata University, Niigata, Japan;2. Center for Integrated Human Brain Science, Brain Research Institute, Niigata University, Niigata, Japan

Department of Pathology, Brain Research Institute, Niigata University, Niigata, Japan;3. Technology and Development Team for Mouse Phenotype Analysis, The Japan Mouse Clinic, RIKEN BioResource Research Center, Ibaraki, Japan;4. Division of Neuronal Network, The Institute of Medical Science, The University of Tokyo, Tokyo, Japan;5. Department of Molecular Genetics, Brain Research Institute, Niigata University, Niigata, Japan;6. Division of Neurobiology and Anatomy, Graduate School of Medical and Dental Sciences, Niigata University, Niigata, Japan;7. Laboratory for Translation Structural Biology, RIKEN Center for Biosystems Dynamics Research, Tsurumi-ku, Yokohama, Japan;8. Department of Pathology, Brain Research Institute, Niigata University, Niigata, Japan

Abstract:
Keywords:Eif2b5  epilepsy  eukaryotic translation initiation factor 2B  guanine nucleotide exchange factor  missense mutation  vanishing white matter disease
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