Specific binding of collagen Q to the neuromuscular junction is exploited to cure congenital myasthenia and to explore bases of myasthenia gravis-Reference-Cited by-同舟云学术

登录注册会员服务联系我们

Specific binding of collagen Q to the neuromuscular junction is exploited to cure congenital myasthenia and to explore bases of myasthenia gravis

Published:2013-03 Issue:1 Volume:203 Page:335-340
ISSN:0009-2797
Container-title:Chemico-Biological Interactions
language:en
Short-container-title:Chemico-Biological Interactions

Author:

Ohno Kinji,Ito Mikako,Kawakami Yu,Krejci Eric,Engel Andrew G.

Funder

MEXT and MHLW of Japan

ANR maladies rares of France

NIH and the Muscular Dystrophy of the United States

Publisher

Elsevier BV

Subject

Toxicology,General Medicine

Reference14 articles.

1. Acetylcholinesterase clustering at the neuromuscular junction involves perlecan and dystroglycan;Peng;J. Cell Biol.,1999

2. Protein-anchoring strategy for delivering acetylcholinesterase to the neuromuscular junction;Ito;Mol. Ther.,2012

3. Anti-MuSK autoantibodies block binding of collagen Q to MuSK;Kawakami;Neurology,2011

4. Human endplate acetylcholinesterase deficiency caused by mutations in the collagen-like tail subunit (ColQ) of the asymmetric enzyme;Ohno;Proc. Natl. Acad. Sci. U.S.A.,1998

5. Mutation in the human acetylcholinesterase-associated collagen gene, COLQ, is responsible for congenital myasthenic syndrome with end-plate acetylcholinesterase deficiency (Type Ic);Donger;Am. J. Hum. Genet.,1998

Cited by 16 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. Congenital myasthenic syndromes: increasingly complex;Current Opinion in Neurology;2024-07-25

2. Myasthenia gravis: Molecular mechanisms and promising therapeutic strategies;Biochemical Pharmacology;2023-12

3. Perlecan, A Multi-Functional, Cell-Instructive, Matrix-Stabilizing Proteoglycan With Roles in Tissue Development Has Relevance to Connective Tissue Repair and Regeneration;Frontiers in Cell and Developmental Biology;2022-04-01

4. Myasthenia Gravis;Acquired Neuromuscular Disorders;2022

5. Mechanisms of Congenital Myasthenia Caused by Three Mutations in the COLQ Gene;Frontiers in Pediatrics;2021-11-29

同舟云学术

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"同舟云学术"是以全球学者为主线，采集、加工和组织学术论文而形成的新型学术文献查询和分析系统，可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容，当前同舟云学术共收录了国内外主流学术期刊6万余种，收集的期刊论文及会议论文总量共计约1.5亿篇，并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询！咨询电话：010-8811{复制后删除}0370

www.globalauthorid.com

TOP

Copyright © 2019-2024 北京同舟云网络信息技术有限公司
京公网安备11010802033243号京ICP备18003416号-3