Unfolded protein response and activated degradative pathways regulation in GNE myopathy (Q36659841)

15 August 2017

Unfolded protein response and activated degradative pathways regulation in GNE myopathy (English)

1 reference

15 August 2017

Honghao Li

1

1 reference

15 August 2017

Qi Chen

2

1 reference

15 August 2017

Fuchen Liu

3

1 reference

15 August 2017

Xuemei Zhang

4

1 reference

15 August 2017

Wei Li

5

1 reference

15 August 2017

Shuping Liu

6

1 reference

15 August 2017

Yuying Zhao

7

1 reference

15 August 2017

Yaoqin Gong

8

1 reference

15 August 2017

Chuanzhu Yan

9

1 reference

15 August 2017

language of work or name

English

0 references

publication date

5 March 2013

1 reference

15 August 2017

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15 August 2017

8

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15 August 2017

e58116

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15 August 2017

3

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Creative Commons Attribution 4.0 International

15 August 2017

start time

5 March 2013

1 reference

April 2022 Public Data File from Crossref

copyright status

copyrighted

0 references

cites work

Mechanisms of cross-talk between the ubiquitin-proteasome and autophagy-lysosome systems

1 reference

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Sorting, recognition and activation of the misfolded protein degradation pathways through macroautophagy and the proteasome

30 September 2017

1 reference

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HDAC6 at the intersection of autophagy, the ubiquitin-proteasome system and neurodegeneration

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3589370

HDAC6 rescues neurodegeneration and provides an essential link between autophagy and the UPS

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3589370

p62/SQSTM1 forms protein aggregates degraded by autophagy and has a protective effect on huntingtin-induced cell death

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3589370

Roles of heat shock protein gp96 in the ER quality control: redundant or unique function?

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3589370

Proteasome inhibition and aggresome formation in sporadic inclusion-body myositis and in amyloid-beta precursor protein-overexpressing cultured human muscle fibers

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3589370

Distal myopathy with rimmed vacuoles: impaired O-glycan formation in muscular glycoproteins

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3589370

Endoplasmic reticulum stress and unfolded protein response in inclusion body myositis muscle.

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3589370

A subset of chaperones and folding enzymes form multiprotein complexes in endoplasmic reticulum to bind nascent proteins

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3589370

Inclusion-body myositis and myopathies: different etiologies, possibly similar pathogenic mechanisms

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3589370

Inclusion body myositis-like phenotype induced by transgenic overexpression of beta APP in skeletal muscle

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3589370

Nonaka myopathy is caused by mutations in the UDP-N-acetylglucosamine-2-epimerase/N-acetylmannosamine kinase gene (GNE)

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3589370

Protein dislocation from the ER requires polyubiquitination and the AAA-ATPase Cdc48.

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3589370

AAA-ATPase p97/Cdc48p, a cytosolic chaperone required for endoplasmic reticulum-associated protein degradation

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3589370

The UDP-N-acetylglucosamine 2-epimerase/N-acetylmannosamine kinase gene is mutated in recessive hereditary inclusion body myopathy

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3589370

A regulatory link between ER-associated protein degradation and the unfolded-protein response

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3589370

Functional and genomic analyses reveal an essential coordination between the unfolded protein response and ER-associated degradation

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3589370

A bifunctional enzyme catalyzes the first two steps in N-acetylneuraminic acid biosynthesis of rat liver. Molecular cloning and functional expression of UDP-N-acetyl-glucosamine 2-epimerase/N-acetylmannosamine kinase

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3589370

Familial distal myopathy with rimmed vacuole and lamellar (myeloid) body formation

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3589370

Sialic acids as ligands in recognition phenomena.

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3589370

"Rimmed vacuole myopathy" sparing the quadriceps. A unique disorder in Iranian Jews

30 September 2017

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0058116

Reduction of UDP-N-acetylglucosamine 2-epimerase/N-acetylmannosamine kinase activity and sialylation in distal myopathy with rimmed vacuoles

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0058116

Hypoglycosylation of alpha-dystroglycan in patients with hereditary IBM due to GNE mutations.

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0058116

Clinical and molecular genetic analysis in Chinese patients with distal myopathy with rimmed vacuoles

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0058116

Characterization of hereditary inclusion body myopathy myoblasts: possible primary impairment of apoptotic events

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0058116

Autophagy in a mouse model of distal myopathy with rimmed vacuoles or hereditary inclusion body myopathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0058116

Amyloid-beta42 is preferentially accumulated in muscle fibers of patients with sporadic inclusion-body myositis

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0058116

Abnormalities of NBR1, a novel autophagy-associated protein, in muscle fibers of sporadic inclusion-body myositis

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0058116

p62/SQSTM1 is overexpressed and prominently accumulated in inclusions of sporadic inclusion-body myositis muscle fibers, and can help differentiating it from polymyositis and dermatomyositis.

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0058116

A Gne knockout mouse expressing human GNE D176V mutation develops features similar to distal myopathy with rimmed vacuoles or hereditary inclusion body myopathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0058116

Expression of the lysosome-associated membrane proteins in myopathies with rimmed vacuoles

21 January 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/23472144

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

alpha-Dystroglycan does not play a major pathogenic role in autosomal recessive hereditary inclusion-body myopathy

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/23472144

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Proteasomes in distal myopathy with rimmed vacuoles

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/23472144

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1371/JOURNAL.PONE.0058116

1 reference

15 August 2017

0 references

1 reference

15 August 2017

1 reference