Chaperonopathies: Spotlight on Hereditary Motor Neuropathies-Reference-Cited by-同舟云学术

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Chaperonopathies: Spotlight on Hereditary Motor Neuropathies

Published:2016-12-14 Issue: Volume:3 Page:
ISSN:2296-889X
Container-title:Frontiers in Molecular Biosciences
language:
Short-container-title:Front. Mol. Biosci.

Author:

Lupo Vincenzo,Aguado Carmen,Knecht Erwin,Espinós Carmen

Funder

Instituto de Salud Carlos III

Ministerio de Economía y Competitividad

Publisher

Frontiers Media SA

Subject

Biochemistry, Genetics and Molecular Biology (miscellaneous),Molecular Biology,Biochemistry

Reference78 articles.

1. A mutation in the small heat-shock protein HSPB1 leading to distal hereditary motor neuronopathy disrupts neurofilament assembly and the axonal transport of specific cellular cargoes;Ackerley;Hum. Mol. Genet.,2006

2. Small heat-shock protein HSPB1 mutants stabilize microtubules in Charcot-Marie-Tooth neuropathy;Almeida-Souza;J. Neurosci.,2011

3. Increased monomerization of mutant HSPB1 leads to protein hyperactivity in Charcot-Marie-Tooth neuropathy;Almeida-Souza;J. Biol. Chem.,2010

4. Application of targeted multi-gene panel testing for the diagnosis of inherited peripheral neuropathy provides a high diagnostic yield with unexpected phenotype-genotype variability;Antoniadi;BMC Med. Genet.,2015

5. Chaperone-assisted selective autophagy is essential for muscle maintenance;Arndt;Curr. Biol.,2010

Cited by 27 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. Proteostasis plays an important role in demyelinating Charcot Marie Tooth disease;Biochemical Pharmacology;2023-10

2. Distinctive chaperonopathy in skeletal muscle associated with the dominant variant in DNAJB4;Acta Neuropathologica;2022-12-13

3. DNAJB2 c.184C>T mutation associated with distal hereditary motor neuropathy with rimmed vacuolar myopathy;Clinical Neuropathology;2022-09-01

4. Distinctive chaperonopathy in skeletal muscle associated with the dominant variant in DNAJB4;2022-07-28

5. Genetic spectrum in a cohort of patients with distal hereditary motor neuropathy;Annals of Clinical and Translational Neurology;2022-03-17

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