Masato Obayashi

Spinocerebellar ataxia type 36 exists in diverse populations and can be caused by a short hexanucleotide GGCCTG repeat expansion

Masato Obayashi, Giovanni Stévanin, Matthis Synofzik et al. · Journal of Neurology Neurosurgery & Psychiatry · 2014 · 63 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

Abnormal <scp>RNA</scp> structures (<scp>RNA</scp> foci) containing a penta‐nucleotide repeat (<scp>UGGAA</scp>)_n in the <scp>P</scp>urkinje cell nucleus is associated with spinocerebellar ataxia type 31 pathogenesis

Yusuke Niimi, Makoto Takahashi, Emiko Sugawara et al. · Neuropathology · 2013 · 58 citations

Life Sciences, Genetics, Molecular Genetics +17

The carboxy-terminal fragment of α1A calcium channel preferentially aggregates in the cytoplasm of human spinocerebellar ataxia type 6 Purkinje cells

Taro Ishiguro, Kinya Ishikawa, Makoto Takahashi et al. · Acta Neuropathologica · 2009 · 56 citations · Full text

Life Sciences, Neurology, Neuroscience +17

Relocation of p25α/tubulin polymerization promoting protein from the nucleus to the perinuclear cytoplasm in the oligodendroglia of sporadic and COQ2 mutant multiple system atrophy

Kiyobumi Ota, Masato Obayashi, Kokoro Ozaki et al. · Acta Neuropathologica Communications · 2014 · 46 citations · Full text

Medicine, Neurology, Neuroscience +15

Reduced brain‐derived neurotrophic factor (BDNF) mRNA expression and presence of BDNF‐immunoreactive granules in the spinocerebellar ataxia type 6 (SCA6) cerebellum

Makoto Takahashi, Kinya Ishikawa, Nozomu Sato et al. · Neuropathology · 2012 · 34 citations · Full text

Life Sciences, Neurology, Neuroscience +17