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Masato Hasegawa

Showing results (241-250 of 286) with videos related to

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Acta Neuropathologica|November 6, 2015
Biochemical classification of tauopathies by immunoblot, protein sequence and mass spectrometric analyses of sarkosyl-insoluble and trypsin-resistant tauSayuri Taniguchi-Watanabe, Tetsuaki Arai, Fuyuki Kametani, et al.
Communications Biology|July 16, 2021
Essential roles of plexin-B3<sup>+</sup> oligodendrocyte precursor cells in the pathogenesis of Alzheimer's diseaseNaomi Nihonmatsu-Kikuchi, Xiu-Jun Yu, Yoshiki Matsuda, et al.
Acta Neuropathologica Communications|August 10, 2023
A heterozygous splicing variant IVS9-7A > T in intron 9 of the MAPT gene in a patient with right-temporal variant frontotemporal dementia with atypical 4 repeat tauopathyKohji Mori, Kazue Shigenobu, Goichi Beck, et al.
Nature|February 13, 2020
Novel tau filament fold in corticobasal degenerationWenjuan Zhang, Airi Tarutani, Kathy L Newell, et al.
Acta Neuropathologica Communications|January 4, 2026
Co-aggregation of annexin A11 and TDP-43 in FTLD/MND with primary lateral sclerosis phenotypeAiri Tarutani, Takashi Nonaka, Reiko Ohtani, et al.
Scientific Reports|August 11, 2017
TDP-43 stabilises the processing intermediates of mitochondrial transcriptsKeiichi Izumikawa, Yuko Nobe, Harunori Yoshikawa, et al.
Neuropathology and Applied Neurobiology|September 5, 2014
Accumulation of dipeptide repeat proteins predates that of TDP-43 in frontotemporal lobar degeneration associated with hexanucleotide repeat expansions in C9ORF72 geneAtik Baborie, Timothy D Griffiths, Evelyn Jaros, et al.
Journal of the Neurological Sciences|June 12, 2016
TDP-43 in the hypoglossal nucleus identifies amyotrophic lateral sclerosis in behavioral variant frontotemporal dementiaGlenda M Halliday, Matthew C Kiernan, Jillian J Kril, et al.
Acta Neuropathologica Communications|August 29, 2020
Unclassified four-repeat tauopathy associated with familial parkinsonism and progressive respiratory failureMasayoshi Nakano, Yuichi Riku, Kenya Nishioka, et al.
Acta Neuropathologica|August 13, 2025
Biallelic variants in DNAJC7 cause familial amyotrophic lateral sclerosis with the TDP-43 pathologyToru Yamashita, Osamu Yokota, Daiki Ousaka, et al.
Pageof 29

Showing results (241-250 of 286) with videos related to

Sort By:
Pageof 29
Acta Neuropathologica|November 6, 2015
Biochemical classification of tauopathies by immunoblot, protein sequence and mass spectrometric analyses of sarkosyl-insoluble and trypsin-resistant tauSayuri Taniguchi-Watanabe, Tetsuaki Arai, Fuyuki Kametani, et al.
Communications Biology|July 16, 2021
Essential roles of plexin-B3<sup>+</sup> oligodendrocyte precursor cells in the pathogenesis of Alzheimer's diseaseNaomi Nihonmatsu-Kikuchi, Xiu-Jun Yu, Yoshiki Matsuda, et al.
Acta Neuropathologica Communications|August 10, 2023
A heterozygous splicing variant IVS9-7A > T in intron 9 of the MAPT gene in a patient with right-temporal variant frontotemporal dementia with atypical 4 repeat tauopathyKohji Mori, Kazue Shigenobu, Goichi Beck, et al.
Nature|February 13, 2020
Novel tau filament fold in corticobasal degenerationWenjuan Zhang, Airi Tarutani, Kathy L Newell, et al.
Acta Neuropathologica Communications|January 4, 2026
Co-aggregation of annexin A11 and TDP-43 in FTLD/MND with primary lateral sclerosis phenotypeAiri Tarutani, Takashi Nonaka, Reiko Ohtani, et al.
Scientific Reports|August 11, 2017
TDP-43 stabilises the processing intermediates of mitochondrial transcriptsKeiichi Izumikawa, Yuko Nobe, Harunori Yoshikawa, et al.
Neuropathology and Applied Neurobiology|September 5, 2014
Accumulation of dipeptide repeat proteins predates that of TDP-43 in frontotemporal lobar degeneration associated with hexanucleotide repeat expansions in C9ORF72 geneAtik Baborie, Timothy D Griffiths, Evelyn Jaros, et al.
Journal of the Neurological Sciences|June 12, 2016
TDP-43 in the hypoglossal nucleus identifies amyotrophic lateral sclerosis in behavioral variant frontotemporal dementiaGlenda M Halliday, Matthew C Kiernan, Jillian J Kril, et al.
Acta Neuropathologica Communications|August 29, 2020
Unclassified four-repeat tauopathy associated with familial parkinsonism and progressive respiratory failureMasayoshi Nakano, Yuichi Riku, Kenya Nishioka, et al.
Acta Neuropathologica|August 13, 2025
Biallelic variants in DNAJC7 cause familial amyotrophic lateral sclerosis with the TDP-43 pathologyToru Yamashita, Osamu Yokota, Daiki Ousaka, et al.
Pageof 29