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Naoki Atsuta

Showing results (101-110 of 114) with videos related to

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BMJ Open|October 26, 2024
Protocol for a phase 2 study of bosutinib for amyotrophic lateral sclerosis using real-world data: induced pluripotent stem cell-based drug repurposing for amyotrophic lateral sclerosis medicine (iDReAM) studyKeiko Imamura, Yuishin Izumi, Naohiro Egawa, et al.
PNAS Nexus|August 12, 2024
CHCHD2 P14L, found in amyotrophic lateral sclerosis, exhibits cytoplasmic mislocalization and alters Ca<sup>2+</sup> homeostasisAya Ikeda, Hongrui Meng, Daisuke Taniguchi, et al.
Journal of Neurology|January 20, 2020
Cognitive and behavioral status in Japanese ALS patients: a multicenter studyYasuhiro Watanabe, Joost Raaphorst, Yuishin Izumi, et al.
Neurobiology of Aging|January 18, 2022
Mutation screening of the DNAJC7 gene in Japanese patients with sporadic amyotrophic lateral sclerosisGenki Tohnai, Ryoichi Nakamura, Naoki Atsuta, et al.
JMIR Research Protocols|December 23, 2018
The Japanese Early-Stage Trial of High-Dose Methylcobalamin for Amyotrophic Lateral Sclerosis (JETALS): Protocol for a Randomized Controlled TrialRyosuke Oki, Yuishin Izumi, Hiroyuki Nodera, et al.
Human Molecular Genetics|June 14, 2011
A functional variant in ZNF512B is associated with susceptibility to amyotrophic lateral sclerosis in JapaneseAritoshi Iida, Atsushi Takahashi, Michiaki Kubo, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|January 10, 2016
A rapid functional decline type of amyotrophic lateral sclerosis is linked to low expression of TTNHazuki Watanabe, Naoki Atsuta, Akihiro Hirakawa, et al.
Neurobiology of Aging|February 6, 2018
Frequency and characteristics of the TBK1 gene variants in Japanese patients with sporadic amyotrophic lateral sclerosisGenki Tohnai, Ryoichi Nakamura, Jun Sone, et al.
The Lancet Regional Health. Western Pacific|September 29, 2025
Pan-Asian consortium for treatment and research in ALS (PACTALS) guidelines for management of amyotrophic lateral sclerosisSteve Vucic, Nortina Shahrizaila, Osamu Kano, et al.
American Journal of Human Genetics|October 15, 2013
ERBB4 mutations that disrupt the neuregulin-ErbB4 pathway cause amyotrophic lateral sclerosis type 19Yuji Takahashi, Yoko Fukuda, Jun Yoshimura, et al.
Pageof 12

Showing results (101-110 of 114) with videos related to

Sort By:
Pageof 12
BMJ Open|October 26, 2024
Protocol for a phase 2 study of bosutinib for amyotrophic lateral sclerosis using real-world data: induced pluripotent stem cell-based drug repurposing for amyotrophic lateral sclerosis medicine (iDReAM) studyKeiko Imamura, Yuishin Izumi, Naohiro Egawa, et al.
PNAS Nexus|August 12, 2024
CHCHD2 P14L, found in amyotrophic lateral sclerosis, exhibits cytoplasmic mislocalization and alters Ca<sup>2+</sup> homeostasisAya Ikeda, Hongrui Meng, Daisuke Taniguchi, et al.
Journal of Neurology|January 20, 2020
Cognitive and behavioral status in Japanese ALS patients: a multicenter studyYasuhiro Watanabe, Joost Raaphorst, Yuishin Izumi, et al.
Neurobiology of Aging|January 18, 2022
Mutation screening of the DNAJC7 gene in Japanese patients with sporadic amyotrophic lateral sclerosisGenki Tohnai, Ryoichi Nakamura, Naoki Atsuta, et al.
JMIR Research Protocols|December 23, 2018
The Japanese Early-Stage Trial of High-Dose Methylcobalamin for Amyotrophic Lateral Sclerosis (JETALS): Protocol for a Randomized Controlled TrialRyosuke Oki, Yuishin Izumi, Hiroyuki Nodera, et al.
Human Molecular Genetics|June 14, 2011
A functional variant in ZNF512B is associated with susceptibility to amyotrophic lateral sclerosis in JapaneseAritoshi Iida, Atsushi Takahashi, Michiaki Kubo, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|January 10, 2016
A rapid functional decline type of amyotrophic lateral sclerosis is linked to low expression of TTNHazuki Watanabe, Naoki Atsuta, Akihiro Hirakawa, et al.
Neurobiology of Aging|February 6, 2018
Frequency and characteristics of the TBK1 gene variants in Japanese patients with sporadic amyotrophic lateral sclerosisGenki Tohnai, Ryoichi Nakamura, Jun Sone, et al.
The Lancet Regional Health. Western Pacific|September 29, 2025
Pan-Asian consortium for treatment and research in ALS (PACTALS) guidelines for management of amyotrophic lateral sclerosisSteve Vucic, Nortina Shahrizaila, Osamu Kano, et al.
American Journal of Human Genetics|October 15, 2013
ERBB4 mutations that disrupt the neuregulin-ErbB4 pathway cause amyotrophic lateral sclerosis type 19Yuji Takahashi, Yoko Fukuda, Jun Yoshimura, et al.
Pageof 12