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Masato Hasegawa

Showing results (211-220 of 286) with videos related to

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Frontiers in Neuroscience|November 30, 2020
Comparison of Common and Disease-Specific Post-translational Modifications of Pathological Tau Associated With a Wide Range of TauopathiesFuyuki Kametani, Mari Yoshida, Tomoyasu Matsubara, et al.
Internal Medicine (Tokyo, Japan)|February 16, 2010
TDP-43 M337V mutation in familial amyotrophic lateral sclerosis in JapanAkira Tamaoka, Makoto Arai, Masanari Itokawa, et al.
Neuropathology : Official Journal of the Japanese Society of Neuropathology|May 8, 2024
An autopsy case of type A FTLD-TDP with a GRN mutation presenting with the logopenic variant of primary progressive aphasia at onset and with corticobasal syndrome subsequentlyTakafumi Tomenaga, Shinobu Minatani, Hiroto Namba, et al.
Neuropathology : Official Journal of the Japanese Society of Neuropathology|January 28, 2010
Phosphorylated and cleaved TDP-43 in ALS, FTLD and other neurodegenerative disorders and in cellular models of TDP-43 proteinopathyTetsuaki Arai, Masato Hasegawa, Takashi Nonoka, et al.
Neuropathology : Official Journal of the Japanese Society of Neuropathology|January 27, 2023
Neuropathology of spinocerebellar ataxia type 8: Common features and unique tauopathyYuki Yonenobu, Goichi Beck, Kansuke Kido, et al.
Annals of Neurology|June 12, 2008
Phosphorylated TDP-43 in frontotemporal lobar degeneration and amyotrophic lateral sclerosisMasato Hasegawa, Tetsuaki Arai, Takashi Nonaka, et al.
FEBS Open Bio|June 20, 2023
Cryo-EM structures of tau filaments from SH-SY5Y cells seeded with brain extracts from cases of Alzheimer's disease and corticobasal degenerationAiri Tarutani, Sofia Lövestam, Xianjun Zhang, et al.
Neuropathology : Official Journal of the Japanese Society of Neuropathology|July 5, 2021
Amyotrophic lateral sclerosis with speech apraxia, predominant upper motor neuron signs, and prominent iron accumulation in the frontal operculum and precentral gyrusTomoki T Mitani, Goichi Beck, Kansuke Kido, et al.
Acta Neuropathologica Communications|November 21, 2013
Extensive deamidation at asparagine residue 279 accounts for weak immunoreactivity of tau with RD4 antibody in Alzheimer's disease brainAyaho Dan, Muneaki Takahashi, Masami Masuda-Suzukake, et al.
Acta Neuropathologica Communications|July 31, 2024
Pure argyrophilic grain disease revisited: independent effects on limbic, neocortical, and striato-pallido-nigral degeneration and the development of dementia in a series with a low to moderate Braak stageOsamu Yokota, Tomoko Miki, Hanae Nakashima-Yasuda, et al.
Pageof 29

Showing results (211-220 of 286) with videos related to

Sort By:
Pageof 29
Frontiers in Neuroscience|November 30, 2020
Comparison of Common and Disease-Specific Post-translational Modifications of Pathological Tau Associated With a Wide Range of TauopathiesFuyuki Kametani, Mari Yoshida, Tomoyasu Matsubara, et al.
Internal Medicine (Tokyo, Japan)|February 16, 2010
TDP-43 M337V mutation in familial amyotrophic lateral sclerosis in JapanAkira Tamaoka, Makoto Arai, Masanari Itokawa, et al.
Neuropathology : Official Journal of the Japanese Society of Neuropathology|May 8, 2024
An autopsy case of type A FTLD-TDP with a GRN mutation presenting with the logopenic variant of primary progressive aphasia at onset and with corticobasal syndrome subsequentlyTakafumi Tomenaga, Shinobu Minatani, Hiroto Namba, et al.
Neuropathology : Official Journal of the Japanese Society of Neuropathology|January 28, 2010
Phosphorylated and cleaved TDP-43 in ALS, FTLD and other neurodegenerative disorders and in cellular models of TDP-43 proteinopathyTetsuaki Arai, Masato Hasegawa, Takashi Nonoka, et al.
Neuropathology : Official Journal of the Japanese Society of Neuropathology|January 27, 2023
Neuropathology of spinocerebellar ataxia type 8: Common features and unique tauopathyYuki Yonenobu, Goichi Beck, Kansuke Kido, et al.
Annals of Neurology|June 12, 2008
Phosphorylated TDP-43 in frontotemporal lobar degeneration and amyotrophic lateral sclerosisMasato Hasegawa, Tetsuaki Arai, Takashi Nonaka, et al.
FEBS Open Bio|June 20, 2023
Cryo-EM structures of tau filaments from SH-SY5Y cells seeded with brain extracts from cases of Alzheimer's disease and corticobasal degenerationAiri Tarutani, Sofia Lövestam, Xianjun Zhang, et al.
Neuropathology : Official Journal of the Japanese Society of Neuropathology|July 5, 2021
Amyotrophic lateral sclerosis with speech apraxia, predominant upper motor neuron signs, and prominent iron accumulation in the frontal operculum and precentral gyrusTomoki T Mitani, Goichi Beck, Kansuke Kido, et al.
Acta Neuropathologica Communications|November 21, 2013
Extensive deamidation at asparagine residue 279 accounts for weak immunoreactivity of tau with RD4 antibody in Alzheimer's disease brainAyaho Dan, Muneaki Takahashi, Masami Masuda-Suzukake, et al.
Acta Neuropathologica Communications|July 31, 2024
Pure argyrophilic grain disease revisited: independent effects on limbic, neocortical, and striato-pallido-nigral degeneration and the development of dementia in a series with a low to moderate Braak stageOsamu Yokota, Tomoko Miki, Hanae Nakashima-Yasuda, et al.
Pageof 29