Molecular Chaperones in the Pathogenesis of Amyotrophic Lateral Sclerosis: The Role of HSPB1. (Q42369031)

28 October 2017

Molecular Chaperones in the Pathogenesis of Amyotrophic Lateral Sclerosis: The Role of HSPB1. (English)

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amyotrophic lateral sclerosis

28 October 2017

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2

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12 June 2020

Elias Adriaenssens

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Monica Bandettini di Poggio

12 June 2020

9

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12 June 2020

author name string

Simona Capponi

1

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12 June 2020

Alessandro Geroldi

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12 June 2020

Paola Origone

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12 June 2020

Simonetta Verdiani

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12 June 2020

Elena Cichero

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12 June 2020

Vicky De Winter

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12 June 2020

Marco Barberis

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12 June 2020

Paola Fossa

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12 June 2020

Paola Mandich

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12 June 2020

Emilia Bellone

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Vincent Timmerman

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12 June 2020

Adriano Chiò

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12 June 2020

publication date

5 August 2016

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28 October 2017

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12 June 2020

volume

37

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12 June 2020

issue

11

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12 June 2020

page(s)

1202-1208

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Truncated HSPB1 causes axonal neuropathy and impairs tolerance to unfolded protein stress

12 June 2020

cites work

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In silico evaluation of human small heat shock protein HSP27: homology modeling, mutation analyses and docking studies

29 May 2018

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Extrapyramidal and cognitive signs in amyotrophic lateral sclerosis: A population based cross-sectional study.

29 May 2018

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A first line of stress defense: small heat shock proteins and their function in protein homeostasis

29 May 2018

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29 May 2018

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Dissection of genetic factors associated with amyotrophic lateral sclerosis

29 May 2018

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The role of heat shock proteins in Amyotrophic Lateral Sclerosis: The therapeutic potential of Arimoclomol

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The small heat shock proteins αB-crystallin and Hsp27 suppress SOD1 aggregation in vitro

29 May 2018

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Mutations in UBQLN2 cause dominant X-linked juvenile and adult-onset ALS and ALS/dementia

29 May 2018

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29 May 2018

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Increased monomerization of mutant HSPB1 leads to protein hyperactivity in Charcot-Marie-Tooth neuropathy

29 May 2018

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Structural and functional diversities between members of the human HSPB, HSPH, HSPA, and DNAJ chaperone families.

29 May 2018

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29 May 2018

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Genetic variant in the HSPB1 promoter region impairs the HSP27 stress response

29 May 2018

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Mutant small heat-shock protein 27 causes axonal Charcot-Marie-Tooth disease and distal hereditary motor neuropathy

29 May 2018

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Protein misfolding, amyloid formation, and neurodegeneration: a critical role for molecular chaperones?

29 May 2018

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El Escorial revisited: revised criteria for the diagnosis of amyotrophic lateral sclerosis

29 May 2018

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29 May 2018

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29 May 2018

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17 August 2018

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17 August 2018

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17 August 2018

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Crossref

https://api.crossref.org/works/10.1002%2FHUMU.23062

Changes in oligomerization are essential for the chaperone activity of a small heat shock protein in vivo and in vitro

21 January 2018

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PubMed

https://pubmed.ncbi.nlm.nih.gov/27492805

12 December 2020

inferred from PubMed ID database lookup

Characterization of human small heat shock protein HspB1 that carries C-terminal domain mutations associated with hereditary motor neuron diseases

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/27492805

12 December 2020

inferred from PubMed ID database lookup

Mutations in the HSP27 (HSPB1) gene cause dominant, recessive, and sporadic distal HMN/CMT type 2

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/27492805

12 December 2020

inferred from PubMed ID database lookup

Production and titration of lentiviral vectors

1 reference

Crossref

https://api.crossref.org/works/10.1002%2FHUMU.23062

7 January 2021

inferred from DOI database lookup

Identifiers

DOI

10.1002/HUMU.23062

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:27492805%20AND%20SRC:MED&resulttype=core&format=json

12 June 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:27492805%20AND%20SRC:MED&resulttype=core&format=json

12 June 2020

PubMed publication ID

27492805

1 reference