Mutations in HspB1 and hereditary neuropathies
Author:
Publisher
Springer Science and Business Media LLC
Subject
Cell Biology,Biochemistry
Link
https://link.springer.com/content/pdf/10.1007/s12192-020-01099-9.pdf
Reference90 articles.
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2. Alderson TR et al (2019) Local unfolding of the HSP27 monomer regulates chaperone activity. Nat Commun 10:1068. https://doi.org/10.1038/s41467-019-08557-8
3. Almeida-Souza L et al (2010) Increased monomerization of mutant HSPB1 leads to protein hyperactivity in Charcot-Marie-Tooth neuropathy. J Biol Chem 285:12778–12786. https://doi.org/10.1074/jbc.M109.082644
4. Almeida-Souza L et al (2011a) Small heat-shock protein HSPB1 mutants stabilize microtubules in Charcot-Marie-Tooth neuropathy. J Neurosci 31:15320–15328. https://doi.org/10.1523/JNEUROSCI.3266-11.2011
5. Almeida-Souza L, Timmerman V, Janssens S (2011b) Microtubule dynamics in the peripheral nervous system: a matter of balance. Bioarchitecture 1:267–270. https://doi.org/10.4161/bioa.1.6.191982011BIOARCHITECTURE0049R
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