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Hidehiro Mizusawa

Showing results (201-210 of 302) with videos related to

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Biochemical and Biophysical Research Communications|February 1, 2018
Biochemical features of genetic Creutzfeldt-Jakob disease with valine-to-isoleucine substitution at codon 180 on the prion protein geneYoko Ito, Nobuo Sanjo, Masaki Hizume, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|June 28, 2025
Spinocerebellar ataxia type 2 followed by amyotrophic lateral sclerosis due to a pure CAG repeat expansion in ATXN2: a case report and literature reviewShohei Ono, Masataka Nakamura, Takeshi Ikegami, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 26, 2003
Tumor necrosis factor-related apoptosis-inducing ligand induces neuronal death in a murine model of HIV central nervous system infectionYoshiharu Miura, Naoko Misawa, Yuji Kawano, et al.
Acta Neuropathologica|March 1, 2005
Constant and severe involvement of Betz cells in corticobasal degeneration is not consistent with pyramidal signs: a clinicopathological study of ten autopsy casesKuniaki Tsuchiya, Shigeo Murayama, Kazuko Mitani, et al.
Journal of Human Genetics|July 6, 2007
Redefining the disease locus of 16q22.1-linked autosomal dominant cerebellar ataxiaTakeshi Amino, Kinya Ishikawa, Shuta Toru, et al.
Human Gene Therapy|July 24, 2010
In vivo application of an RNAi strategy for the selective suppression of a mutant alleleTakayuki Kubodera, Hiromi Yamada, Masayuki Anzai, et al.
Neuroscience Letters|August 3, 2010
Localization and trafficking of endogenous anterior pharynx-defective 1, a component of Alzheimer's disease related gamma-secretaseNobuo Sanjo, Taiichi Katayama, Hiroshi Hasegawa, et al.
Neuromuscular Disorders : NMD|December 7, 2002
Down-regulation of an ankyrin repeat-containing protein, V-1, during skeletal muscle differentiation and its re-expression in the regenerative process of muscular dystrophyYuko Furukawa, Naohiro Hashimoto, Tohru Yamakuni, et al.
BMJ Open|August 27, 2013
Graft-related disease progression in dura mater graft-associated Creutzfeldt-Jakob disease: a cross-sectional studyKenji Sakai, Tsuyoshi Hamaguchi, Moeko Noguchi-Shinohara, et al.
Plos Medicine|May 31, 2007
Lithium therapy improves neurological function and hippocampal dendritic arborization in a spinocerebellar ataxia type 1 mouse modelKei Watase, Jennifer R Gatchel, Yaling Sun, et al.
Pageof 31

Showing results (201-210 of 302) with videos related to

Sort By:
Pageof 31
Biochemical and Biophysical Research Communications|February 1, 2018
Biochemical features of genetic Creutzfeldt-Jakob disease with valine-to-isoleucine substitution at codon 180 on the prion protein geneYoko Ito, Nobuo Sanjo, Masaki Hizume, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|June 28, 2025
Spinocerebellar ataxia type 2 followed by amyotrophic lateral sclerosis due to a pure CAG repeat expansion in ATXN2: a case report and literature reviewShohei Ono, Masataka Nakamura, Takeshi Ikegami, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 26, 2003
Tumor necrosis factor-related apoptosis-inducing ligand induces neuronal death in a murine model of HIV central nervous system infectionYoshiharu Miura, Naoko Misawa, Yuji Kawano, et al.
Acta Neuropathologica|March 1, 2005
Constant and severe involvement of Betz cells in corticobasal degeneration is not consistent with pyramidal signs: a clinicopathological study of ten autopsy casesKuniaki Tsuchiya, Shigeo Murayama, Kazuko Mitani, et al.
Journal of Human Genetics|July 6, 2007
Redefining the disease locus of 16q22.1-linked autosomal dominant cerebellar ataxiaTakeshi Amino, Kinya Ishikawa, Shuta Toru, et al.
Human Gene Therapy|July 24, 2010
In vivo application of an RNAi strategy for the selective suppression of a mutant alleleTakayuki Kubodera, Hiromi Yamada, Masayuki Anzai, et al.
Neuroscience Letters|August 3, 2010
Localization and trafficking of endogenous anterior pharynx-defective 1, a component of Alzheimer's disease related gamma-secretaseNobuo Sanjo, Taiichi Katayama, Hiroshi Hasegawa, et al.
Neuromuscular Disorders : NMD|December 7, 2002
Down-regulation of an ankyrin repeat-containing protein, V-1, during skeletal muscle differentiation and its re-expression in the regenerative process of muscular dystrophyYuko Furukawa, Naohiro Hashimoto, Tohru Yamakuni, et al.
BMJ Open|August 27, 2013
Graft-related disease progression in dura mater graft-associated Creutzfeldt-Jakob disease: a cross-sectional studyKenji Sakai, Tsuyoshi Hamaguchi, Moeko Noguchi-Shinohara, et al.
Plos Medicine|May 31, 2007
Lithium therapy improves neurological function and hippocampal dendritic arborization in a spinocerebellar ataxia type 1 mouse modelKei Watase, Jennifer R Gatchel, Yaling Sun, et al.
Pageof 31