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Journal of Virology
|
April 29, 2026
Pseudovirus-mediated proximity labeling identifies candidate host cell membrane proteins involved in viral attachment
Norihiro Kotani, Kensuke Iwasa, Tomoko Amimoto, et al.
Eneuro
|
May 6, 2022
Inhibition of Crmp1 Phosphorylation at Ser522 Ameliorates Motor Function and Neuronal Pathology in Amyotrophic Lateral Sclerosis Model Mice
Tetsuya Asano, Haruko Nakamura, Yuko Kawamoto, et al.
Acta Neuropathologica Communications
|
September 24, 2025
Facilitated α-synuclein oligomer sharing among glial cells by a centrally acting connexin inhibitor attenuates a rapidly progressive multiple system atrophy-cerebellar type model by reducing the neuronal α-synuclein burden
Masaya Harada, Katsuhisa Masaki, Tatsunori Tanaka, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
October 23, 2025
Differential <i>O</i>-glucose elongation on a specific EGF repeat within the canonical ligand-binding domain regulates DLL1/4-NOTCH1 signaling
Yohei Tsukamoto, Kazuhiro Aoki, Yuichi Kama, et al.
Multiple Sclerosis and Related Disorders
|
August 25, 2024
Clinical practice guidelines for multiple sclerosis, neuromyelitis optica spectrum disorder, and myelin oligodendrocyte glycoprotein antibody-associated disease 2023 in Japan
Masaaki Niino, Noriko Isobe, Manabu Araki, et al.
Annals of Neurology
|
December 8, 2023
RNA Foci in Two bi-Allelic RFC1 Expansion Carriers
Taishi Wada, Hiroshi Doi, Masaki Okubo, et al.
Journal of Human Genetics
|
February 7, 2018
Cerebellar ataxia-dominant phenotype in patients with ERCC4 mutations
Hiroshi Doi, Shigeru Koyano, Satoko Miyatake, et al.
Annals of Neurology
|
August 22, 2019
GGC Repeat Expansion of NOTCH2NLC in Adult Patients with Leukoencephalopathy
Masaki Okubo, Hiroshi Doi, Ryoko Fukai, et al.
Annals of Neurology
|
November 10, 2018
Biallelic COLGALT1 variants are associated with cerebral small vessel disease
Satoko Miyatake, Sacha Schneeberger, Norihisa Koyama, et al.
EMBO Molecular Medicine
|
November 4, 2016
A POGLUT1 mutation causes a muscular dystrophy with reduced Notch signaling and satellite cell loss
Emilia Servián-Morilla, Hideyuki Takeuchi, Tom V Lee, et al.
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Search research articles
Search
Showing results (201-210 of 214) with videos related to
Sort By:
Page
of 22
Journal of Virology
|
April 29, 2026
Pseudovirus-mediated proximity labeling identifies candidate host cell membrane proteins involved in viral attachment
Norihiro Kotani, Kensuke Iwasa, Tomoko Amimoto, et al.
Eneuro
|
May 6, 2022
Inhibition of Crmp1 Phosphorylation at Ser522 Ameliorates Motor Function and Neuronal Pathology in Amyotrophic Lateral Sclerosis Model Mice
Tetsuya Asano, Haruko Nakamura, Yuko Kawamoto, et al.
Acta Neuropathologica Communications
|
September 24, 2025
Facilitated α-synuclein oligomer sharing among glial cells by a centrally acting connexin inhibitor attenuates a rapidly progressive multiple system atrophy-cerebellar type model by reducing the neuronal α-synuclein burden
Masaya Harada, Katsuhisa Masaki, Tatsunori Tanaka, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
October 23, 2025
Differential <i>O</i>-glucose elongation on a specific EGF repeat within the canonical ligand-binding domain regulates DLL1/4-NOTCH1 signaling
Yohei Tsukamoto, Kazuhiro Aoki, Yuichi Kama, et al.
Multiple Sclerosis and Related Disorders
|
August 25, 2024
Clinical practice guidelines for multiple sclerosis, neuromyelitis optica spectrum disorder, and myelin oligodendrocyte glycoprotein antibody-associated disease 2023 in Japan
Masaaki Niino, Noriko Isobe, Manabu Araki, et al.
Annals of Neurology
|
December 8, 2023
RNA Foci in Two bi-Allelic RFC1 Expansion Carriers
Taishi Wada, Hiroshi Doi, Masaki Okubo, et al.
Journal of Human Genetics
|
February 7, 2018
Cerebellar ataxia-dominant phenotype in patients with ERCC4 mutations
Hiroshi Doi, Shigeru Koyano, Satoko Miyatake, et al.
Annals of Neurology
|
August 22, 2019
GGC Repeat Expansion of NOTCH2NLC in Adult Patients with Leukoencephalopathy
Masaki Okubo, Hiroshi Doi, Ryoko Fukai, et al.
Annals of Neurology
|
November 10, 2018
Biallelic COLGALT1 variants are associated with cerebral small vessel disease
Satoko Miyatake, Sacha Schneeberger, Norihisa Koyama, et al.
EMBO Molecular Medicine
|
November 4, 2016
A POGLUT1 mutation causes a muscular dystrophy with reduced Notch signaling and satellite cell loss
Emilia Servián-Morilla, Hideyuki Takeuchi, Tom V Lee, et al.
Page
of 22