HspB8, a small heat shock protein mutated in human neuromuscular disorders, has in vivo chaperone activity in cultured cells. (Q46477704)

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11 January 2020

title

HspB8, a small heat shock protein mutated in human neuromuscular disorders, has in vivo chaperone activity in cultured cells (English)

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11 January 2020

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1

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11 January 2020

author name string

Mitchel Sivilotti

2

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11 January 2020

Aura T Chávez Zobel

3

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11 January 2020

Herman Lambert

4

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11 January 2020

Jacques Landry

5

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11 January 2020

publication date

6 May 2005

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11 January 2020

published in

Human Molecular Genetics

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11 January 2020

volume

14

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11 January 2020

page(s)

1659-1669

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11 January 2020

issue

12

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Inherent toxicity of aggregates implies a common mechanism for protein misfolding diseases

11 January 2020

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Molecular chaperones in the cytosol: from nascent chain to folded protein

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Mechanisms for regulation of Hsp70 function by Hsp40

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CHIP: a link between the chaperone and proteasome systems

21 January 2018

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The sperm outer dense fiber protein is the 10th member of the superfamily of mammalian small stress proteins

21 January 2018

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The human genome encodes 10 alpha-crystallin-related small heat shock proteins: HspB1-10

21 January 2018

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Crystal structure of a small heat-shock protein

21 January 2018

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Alpha-crystallin can function as a molecular chaperone

21 January 2018

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A small heat shock protein stably binds heat-denatured model substrates and can maintain a substrate in a folding-competent state

21 January 2018

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Polyglutamine length-dependent interaction of Hsp40 and Hsp70 family chaperones with truncated N-terminal huntingtin: their role in suppression of aggregation and cellular toxicity

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Polyglutamine-expanded androgen receptors form aggregates that sequester heat shock proteins, proteasome components and SRC-1, and are suppressed by the HDJ-2 chaperone

21 January 2018

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Chaperone suppression of alpha-synuclein toxicity in a Drosophila model for Parkinson's disease

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Molecular chaperones enhance the degradation of expanded polyglutamine repeat androgen receptor in a cellular model of spinal and bulbar muscular atrophy

21 January 2018

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Huntingtin-encoded polyglutamine expansions form amyloid-like protein aggregates in vitro and in vivo

21 January 2018

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Hsp70 and hsp40 chaperones can inhibit self-assembly of polyglutamine proteins into amyloid-like fibrils

21 January 2018

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Alpha B-crystallin is expressed in non-lenticular tissues and accumulates in Alexander's disease brain

21 January 2018

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Polyglutamine fibrillogenesis: the pathway unfolds

21 January 2018

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Formic acid dissolves aggregates of an N-terminal huntingtin fragment containing an expanded polyglutamine tract: applying to quantification of protein components of the aggregates

21 January 2018

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Androgen receptor gene mutations in X-linked spinal and bulbar muscular atrophy

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21 January 2018

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From the cradle to the grave: molecular chaperones that may choose between folding and degradation

21 January 2018

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