Protein Aggregation in Congenital Myopathies
Author:
Publisher
Elsevier BV
Subject
Clinical Neurology,Pediatrics, Perinatology, and Child Health
Reference31 articles.
1. Autosomal dominant distal myopathy: Further evidence of a chromosome 14 locus;Voit;Neuromuscul Disord,2001
2. Laing early onset distal myopathy: Slow myosin defect with variable abnormalities on muscle biopsy;Lamont;J Neurol Neurosurg Psychiatry,2006
3. Inclusion-body myositis: A myodegenerative conformational disorder associated with Abeta, protein misfolding, and proteasome inhibition;Askanas;Neurology,2006
4. Mutation in BAG3 causes severe dominant childhood muscular dystrophy;Selcen;Ann Neurol,2009
5. Severe infantile-onset cardiomyopathy associated with a homozygous deletion in desmin;Piñol-Ripoll;Neuromuscul Disord,2009
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. Functional Characterization of a Novel Genetic Variant in Desmin (p.Glu353dup) Causing Myofibrillar Myopathy and Generation of Patient-Derived Induced Pluripotent Stem Cells for Disease Modeling;2023-12-28
2. Mutual dependence between tropomodulin and tropomyosin in the regulation of sarcomeric actin assembly in Caenorhabditis elegans striated muscle;European Journal of Cell Biology;2022-04
3. Increased remodeling and impaired adaption to endurance exercise in desminopathy;2021-10-03
4. Generation of desminopathy in rats using CRISPR‐Cas9;Journal of Cachexia, Sarcopenia and Muscle;2020-09-07
5. The MTM1–UBQLN2–HSP complex mediates degradation of misfolded intermediate filaments in skeletal muscle;Nature Cell Biology;2018-01-22
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