Fukutin is prerequisite to ameliorate muscular dystrophic phenotype by myofiber-selective LARGE expression-Reference-Cited by-同舟云学术

登录注册会员服务联系我们

Fukutin is prerequisite to ameliorate muscular dystrophic phenotype by myofiber-selective LARGE expression

Published:2015-02-09 Issue:1 Volume:5 Page:
ISSN:2045-2322
Container-title:Scientific Reports
language:en
Short-container-title:Sci Rep

Author:

Ohtsuka Yoshihisa,Kanagawa Motoi,Yu Chih-Chieh,Ito Chiyomi,Chiyo Tomoko,Kobayashi Kazuhiro,Okada Takashi,Takeda Shin'ichi,Toda Tatsushi

Publisher

Springer Science and Business Media LLC

Subject

Multidisciplinary

Link

http://www.nature.com/articles/srep08316.pdf

Reference53 articles.

1. Toda, T. et al. Fukuyama-type congenital muscular dystrophy (FCMD) and alpha-dystroglycanopathy. Congenit. Anom. (Kyoto). 43, 97–104 (2003).

2. Michele, D. E. & Campbell, K. P. Dystrophin-glycoprotein complex: post-translational processing and dystroglycan function. J. Biol. Chem. 278, 15457–15460 (2003).

3. Beltrán-Valero de Bernabé, D. et al. Mutations in the O-mannosyltransferase gene POMT1 give rise to the severe neuronal migration disorder Walker-Warburg syndrome. Am. J. Hum. Genet. 71, 1033–1043 (2002).

4. van Reeuwijk, J. et al. POMT2 mutations cause alpha-dystroglycan hypoglycosylation and Walker-Warburg syndrome. J. Med. Genet. 42, 907–912 (2005).

5. Yoshida, A. et al. Muscular dystrophy and neuronal migration disorder caused by mutations in a glycosyltransferase, POMGnT1. Dev. Cell 1, 717–724 (2001).

Cited by 22 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. Laminin α5_CD239_Spectrin is a candidate association that compensates the linkage between the basement membrane and cytoskeleton in skeletal muscle fibers;Matrix Biology Plus;2022-08

2. The role of protein glycosylation in muscle diseases;Molecular Biology Reports;2022-04-15

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

4. PCYT2 synthesizes CDP-glycerol in mammals and reduced PCYT2 enhances the expression of functionally glycosylated α-dystroglycan;The Journal of Biochemistry;2021-07-13

5. A Japanese family with POMT2-related limb girdle muscular dystrophy;Rinsho Shinkeigaku;2021

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