Distinctive chaperonopathy in skeletal muscle associated with the dominant variant in DNAJB4-Reference-Cited by-同舟云学术

登录注册会员服务联系我们

Distinctive chaperonopathy in skeletal muscle associated with the dominant variant in DNAJB4

Published:2022-12-13 Issue:2 Volume:145 Page:235-255
ISSN:0001-6322
Container-title:Acta Neuropathologica
language:en
Short-container-title:Acta Neuropathol

Author:

Inoue Michio,Noguchi Satoru^ORCID,Inoue Yukiko U.,Iida Aritoshi,Ogawa Megumu,Bengoechea Rocio,Pittman Sara K.,Hayashi Shinichiro,Watanabe Kazuki,Hosoi Yasushi,Sano Terunori,Takao Masaki,Oya Yasushi,Takahashi Yuji,Miyajima Hiroaki,Weihl Conrad C.,Inoue Takayoshi,Nishino Ichizo

Funder

Intramural Research Grant for Neurological and Psychiatric 23 Disorders of the National Center of Neurology and Psychiatry

Japan Society for the Promotion of Science

Japan Agency for Medical Research and Development

National Institute of Arthritis and Musculoskeletal and Skin Diseases

National Institute on Aging

Publisher

Springer Science and Business Media LLC

Subject

Cellular and Molecular Neuroscience,Neurology (clinical),Pathology and Forensic Medicine

Link

https://link.springer.com/content/pdf/10.1007/s00401-022-02530-4.pdf

Reference74 articles.

1. Agbulut O, Destombes J, Thiesson D, Butler-Browne G (2000) Age-related appearance of tubular aggregates in the skeletal muscle of almost all male inbred mice. Histochem Cell Biol 114:477–481. https://doi.org/10.1007/s004180000211

2. Andley UP, Hamilton PD, Ravi N, Weihl CC (2011) A knock-in mouse model for the R120G mutation of alphaB-crystallin recapitulates human hereditary myopathy and cataracts. PLoS One 6:e17671. https://doi.org/10.1371/journal.pone.0017671

3. Anttonen A-K, Mahjneh I, Hämäläinen RH, Lagier-Tourenne C, Kopra O, Waris L et al (2005) The gene disrupted in Marinesco-Sjögren syndrome encodes SIL1, an HSPA5 cochaperone. Nat Genet 37:1309–1311. https://doi.org/10.1038/ng1677

4. Arndt V, Dick N, Tawo R, Dreiseidler M, Wenzel D, Hesse M et al (2010) Chaperone-assisted selective autophagy is essential for muscle maintenance. Curr Biol 20:143–148. https://doi.org/10.1016/j.cub.2009.11.022

5. Augusto V, Padovani CR, Campos GER (2004) Skeletal muscle fiber types in C57BL6J mice. J Morphol Sci 21:89–94

Cited by 5 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. GeneticSNUPNvariants cause spinocerebellar atrophy by disrupting global splicing in Purkinje cells;2024-07-12

2. Next Generation Sequencing and Electromyography Reveal the Involvement of the P2RX6 Gene in Myopathy;Current Issues in Molecular Biology;2024-01-29

3. Muscular Dystrophy: Underlying Cellular and Molecular Mechanisms and Various Nanotherapeutic Approaches for Muscular Dystrophy;Mechanism and Genetic Susceptibility of Neurological Disorders;2024

4. Loss and recovery of myocardial mitochondria in mice under different tail suspension time: Apoptosis and mitochondrial fission, fusion and autophagy;Experimental Physiology;2023-08-11

5. Extension of the DNAJB2a isoform in a dominant neuromyopathy family;Human Molecular Genetics;2023-04-18

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