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Journal of Neuropathology and Experimental Neurology|April 20, 2005
Dysferlin interacts with affixin (beta-parvin) at the sarcolemmaChie Matsuda, Kimihiko Kameyama, Kazuhiko Tagawa, et al.
Journal of the Neurological Sciences|May 28, 2003
Protein and gene analyses of dysferlinopathy in a large group of Japanese muscular dystrophy patientsKazuhiko Tagawa, Megumu Ogawa, Kiyokazu Kawabe, et al.
Acta Neuropathologica Communications|March 10, 2017
A novel form of necrosis, TRIAD, occurs in human Huntington's diseaseEmiko Yamanishi, Kazuko Hasegawa, Kyota Fujita, et al.
Journal of Neurochemistry|May 14, 2004
Distinct aggregation and cell death patterns among different types of primary neurons induced by mutant huntingtin proteinKazuhiko Tagawa, Masataka Hoshino, Tomohiro Okuda, et al.
Journal of Neurochemistry|September 13, 2003
Histone deacetylase activity is retained in primary neurons expressing mutant huntingtin proteinMasataka Hoshino, Kazuhiko Tagawa, Tomohiro Okuda, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|January 26, 2007
The induction levels of heat shock protein 70 differentiate the vulnerabilities to mutant huntingtin among neuronal subtypesKazuhiko Tagawa, Shigeki Marubuchi, Mei-Ling Qi, et al.
EMBO Molecular Medicine|December 17, 2014
HMGB1 facilitates repair of mitochondrial DNA damage and extends the lifespan of mutant ataxin-1 knock-in miceHikaru Ito, Kyota Fujita, Kazuhiko Tagawa, et al.
Nature Communications|February 1, 2018
Targeting Tyro3 ameliorates a model of PGRN-mutant FTLD-TDP via tau-mediated synaptic pathologyKyota Fujita, Xigui Chen, Hidenori Homma, et al.
Nature Communications|December 2, 2017
Developmental YAPdeltaC determines adult pathology in a model of spinocerebellar ataxia type 1Kyota Fujita, Ying Mao, Shigenori Uchida, et al.
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