Temporal requirement of dystroglycan glycosylation during brain development and rescue of severe cortical dysplasia via gene delivery in the fetal stage

Author:

Sudo Atsushi1,Kanagawa Motoi1,Kondo Mai1,Ito Chiyomi1,Kobayashi Kazuhiro1,Endo Mitsuharu2,Minami Yasuhiro2,Aiba Atsu3,Toda Tatsushi14

Affiliation:

1. Division of Neurology/Molecular Brain Science, Kobe University Graduate School of Medicine, Kobe 650-0017, Japan

2. Division of Cell Physiology, Kobe University Graduate School of Medicine, Kobe 650-0017, Japan

3. Laboratory of Animal Resources, Center for Disease Biology and Integrative Medicine, The University of Tokyo, Tokyo 113-0033, Japan

4. Department of Neurology, Graduate School of Medicine, The University of Tokyo, Tokyo 113-0033, Japan

Funder

National Center of Neurology and Psychiatry

NCNP

Japan Agency for Medical Research and Development

AMED

Japan Society for the Promotion of Science

JSPS

Takeda Science Foundation

Publisher

Oxford University Press (OUP)

Subject

Genetics (clinical),Genetics,Molecular Biology,General Medicine

Cited by 21 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

1. Cortical Neuron Migration in Health and Disease;Neocortical Neurogenesis in Development and Evolution;2023-08-08

2. Germline C1GALT1C1 mutation causes a multisystem chaperonopathy;Proceedings of the National Academy of Sciences;2023-05-22

3. Multiple Functions of Fukutin, the Gene Responsible for Fukuyama Congenital Muscular Dystrophy, Especially in the Central Nervous System;Advances in Muscular Dystrophy Research - From Cellular and Molecular Basis to Therapies [Working Title];2022-10-17

4. Compound variants of FKTN , POMGNT1 , and LAMB1 gene identified by prenatal whole‐exome sequencing in three fetuses with congenital hydrocephalus;Journal of Obstetrics and Gynaecology Research;2022-07-17

5. CDP-ribitol prodrug treatment ameliorates ISPD-deficient muscular dystrophy mouse model;Nature Communications;2022-04-14

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