Laminin α1 reduces muscular dystrophy in dy 2J mice-Reference-Cited by-同舟云学术

登录注册会员服务联系我们

Laminin α1 reduces muscular dystrophy in dy 2J mice

Published:2018-09 Issue: Volume:70 Page:36-49
ISSN:0945-053X
Container-title:Matrix Biology
language:en
Short-container-title:Matrix Biology

Author:

Gawlik Kinga I.,Harandi Vahid M.,Cheong Rachel Y.,Petersén Åsa,Durbeej Madeleine

Funder

Anna and Edwin Berger Foundation

Association Française contre les Myopathies

Crafoord Foundation

Greta and Johan Kock Foundation

Jane and Dan Olsson Foundation

Olle Engkvist Byggmästare Foundation

Royal Physiographic Society in Lund

The Swedish Research Council

Tore Nilsson Foundation

Österlund Foundation

Publisher

Elsevier BV

Subject

Molecular Biology

Reference54 articles.

1. Merosin-deficient congenital muscular dystrophy, autosomal recessive (MDC1A, MIM#156225, LAMA2 gene coding for alpha2 chain of laminin);Allamand;Eur. J. Hum. Genet.,2002

2. LAMA2-related muscular dystrophy;Quijano-Roy,1993

3. Laminin-deficient muscular dystrophy: molecular pathogenesis and structural repair strategies;Yurchenco;Matrix Biol.,2017

4. Laminin-alpha2 chain-deficient congenital muscular dystrophy: pathophysiology and development of treatment;Durbeej;Curr. Top. Membr.,2015

5. The nature and biology of basement membranes;Pozzi;Matrix Biol.,2017

Cited by 18 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. Efficient and durable gene activation by Cas9-mediated epigenome editing in vivo;2024-05-05

2. The Interaction of LAMA2 and Duration of Illness Affects the Thickness of the Right Transverse Temporal Gyrus in Major Depressive Disorder;Neuropsychiatric Disease and Treatment;2023-12

3. Vemurafenib improves muscle histopathology in a mouse model of LAMA2-related congenital muscular dystrophy;Disease Models & Mechanisms;2023-05-10

4. CRISPRa-induced upregulation of humanLAMA1compensates forLAMA2-deficiency in Merosin-deficient congenital muscular dystrophy;2023-03-07

5. Flavonoids and Omega3 Prevent Muscle and Cardiac Damage in Duchenne Muscular Dystrophy Animal Model;Cells;2021-10-28

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