Ataxic phenotype with altered CaV3.1 channel property in a mouse model for spinocerebellar ataxia 42-Reference-Cited by-同舟云学术

Ataxic phenotype with altered CaV3.1 channel property in a mouse model for spinocerebellar ataxia 42

Published:2019-10 Issue: Volume:130 Page:104516
ISSN:0969-9961
Container-title:Neurobiology of Disease
language:en
Short-container-title:Neurobiology of Disease

Author:

Hashiguchi Shunta,Doi Hiroshi,Kunii Misako,Nakamura Yukihiro,Shimuta Misa,Suzuki Etsuko,Koyano Shigeru,Okubo Masaki,Kishida Hitaru,Shiina Masaaki,Ogata Kazuhiro,Hirashima Fumiko,Inoue Yukichi,Kubota Shun,Hayashi Noriko,Nakamura Haruko,Takahashi Keita^ORCID,Katsumoto Atsuko,Tada Mikiko,Tanaka Kenichi,Sasaoka Toshikuni,Miyatake Satoko,Miyake Noriko,Saitsu Hirotomo^ORCID,Sato Nozomu,Ozaki Kokoro^ORCID,Ohta Kiyobumi,Yokota Takanori,Mizusawa Hidehiro,Mitsui Jun,Ishiura Hiroyuki,Yoshimura Jun,Morishita Shinichi,Tsuji Shoji,Takeuchi Hideyuki^ORCID,Ishikawa Kinya,Matsumoto Naomichi,Ishikawa Taro,Tanaka Fumiaki^ORCID

Funder

Grants-in-Aid for Scientific Research

Japan Society for the Promotion of Science

Grants-in-Aid for Young Scientists

AMED

Health and Labor Sciences Research Grant

Ministry of Health, Labor and Welfare, Japan

Collaborative Research Project

Niigata University

Takeda Science Foundation

Wakaba Research Fund

Yokohama Foundation for Advanced Medical Science