Behavioral and histological analyses of the mouse

Bassoon behavioral analysis histological analysis model mouse progressive supranuclear palsy-like syndrome

Journal

Frontiers in neuroscience
ISSN: 1662-4548
Titre abrégé: Front Neurosci
Pays: Switzerland
ID NLM: 101478481

Informations de publication

Date de publication:
2024
Historique:
received: 08 04 2024
accepted: 11 07 2024
medline: 12 8 2024
pubmed: 12 8 2024
entrez: 12 8 2024
Statut: epublish

Résumé

Tauopathy is known to be a major pathognomonic finding in important neurodegenerative diseases such as progressive supranuclear palsy (PSP) and corticobasal degeneration. However, the mechanism by which tauopathy is triggered remains to be elucidated. We previously identified the point mutation c.11596C > G, p.Pro3866Ala in the

Identifiants

DOI: 10.3389/fnins.2024.1414145 PMID: 39130376 PMC: PMC11310129
pubmed: 39130376
doi: 10.3389/fnins.2024.1414145
pmc: PMC11310129
doi:

Types de publication

Journal Article

Langues

eng

Pagination

1414145

Informations de copyright

Copyright © 2024 Tanaka, Yaguchi, Yoshizaki, Kudo, Mori, Nomura, Pan, Miki, Takahashi, Hara, Wakabayashi and Yabe.

Déclaration de conflit d'intérêts

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Auteurs

Daiki Tanaka (D)

Department of Neurology, Faculty of Medicine and Graduate School of Medicine, Hokkaido University, Sapporo, Japan.

Hiroaki Yaguchi (H)

Department of Neurology, Faculty of Medicine and Graduate School of Medicine, Hokkaido University, Sapporo, Japan.

Kaichi Yoshizaki (K)

Department of Disease Model, Aichi Developmental Disability Center, Kasugai, Japan.
Integrated Analysis of Bioresource and Health Care, Future Medical Sciences, Kobe University Graduate School of Medicine, Kobe, Japan.

Akihiko Kudo (A)

Department of Neurology, Faculty of Medicine and Graduate School of Medicine, Hokkaido University, Sapporo, Japan.

Fumiaki Mori (F)

Department of Neuropathology, Hirosaki University Graduate School of Medicine, Hirosaki, Japan.

Taichi Nomura (T)

Department of Neurology, Faculty of Medicine and Graduate School of Medicine, Hokkaido University, Sapporo, Japan.

Jing Pan (J)

Department of Neurology, Faculty of Medicine and Graduate School of Medicine, Hokkaido University, Sapporo, Japan.

Yasuo Miki (Y)

Department of Neuropathology, Hirosaki University Graduate School of Medicine, Hirosaki, Japan.

Hidehisa Takahashi (H)

Department of Molecular Biology, Yokohama City University Graduate School of Medicine, Yokohama, Japan.

Taichi Hara (T)

Laboratory of Food and Life Science, Faculty of Human Sciences, Waseda University, Tokyo, Japan.

Koichi Wakabayashi (K)

Department of Neuropathology, Hirosaki University Graduate School of Medicine, Hirosaki, Japan.

Ichiro Yabe (I)

Department of Neurology, Faculty of Medicine and Graduate School of Medicine, Hokkaido University, Sapporo, Japan.

Classifications MeSH