(Q58036292)

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Muscle weakness correlates with muscle atrophy and precedes the development of inclusion body or rimmed vacuoles in the mouse model of DMRV/hIBM

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scholarly article

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Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18628337%20AND%20SRC:MED&resulttype=core&format=json

10 January 2020

Muscle weakness correlates with muscle atrophy and precedes the development of inclusion body or rimmed vacuoles in the mouse model of DMRV/hIBM (English)

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18628337%20AND%20SRC:MED&resulttype=core&format=json

10 January 2020

muscle weakness

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based on heuristic

inferred from title

1 reference

based on heuristic

inferred from title

4

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18628337%20AND%20SRC:MED&resulttype=core&format=json

10 January 2020

author name string

Satoru Noguchi

2

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Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18628337%20AND%20SRC:MED&resulttype=core&format=json

10 January 2020

May Christine V Malicdan

1

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Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18628337%20AND%20SRC:MED&resulttype=core&format=json

10 January 2020

Yukiko K Hayashi

3

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Europe PubMed Central

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10 January 2020

publication date

15 July 2008

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Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18628337%20AND%20SRC:MED&resulttype=core&format=json

10 January 2020

Physiological Genomics

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Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18628337%20AND%20SRC:MED&resulttype=core&format=json

10 January 2020

35

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10 January 2020

1

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10 January 2020

106-115

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Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18628337%20AND%20SRC:MED&resulttype=core&format=json

10 January 2020

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

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOLGENOMICS.90219.2008

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOLGENOMICS.90219.2008

21 January 2018

Enhanced detection of congo-red-positive amyloid deposits in muscle fibers of inclusion body myositis and brain of Alzheimer's disease using fluorescence technique

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOLGENOMICS.90219.2008

21 January 2018

The E3 Ligase MuRF1 degrades myosin heavy chain protein in dexamethasone-treated skeletal muscle

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOLGENOMICS.90219.2008

21 January 2018

Ca(2+)-dependent proteolysis in muscle wasting.

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOLGENOMICS.90219.2008

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOLGENOMICS.90219.2008

21 January 2018

Concerted regulation of skeletal muscle contractility by oxygen tension and endogenous nitric oxide

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOLGENOMICS.90219.2008

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOLGENOMICS.90219.2008

21 January 2018

Autophagy in metazoans: cell survival in the land of plenty

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOLGENOMICS.90219.2008

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOLGENOMICS.90219.2008

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOLGENOMICS.90219.2008

21 January 2018

FoxO3 controls autophagy in skeletal muscle in vivo

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOLGENOMICS.90219.2008

21 January 2018

Distal myopathy with rimmed vacuoles is allelic to hereditary inclusion body myopathy

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOLGENOMICS.90219.2008

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOLGENOMICS.90219.2008

21 January 2018

Distal myopathy with rimmed vacuoles and hereditary inclusion body myopathy

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOLGENOMICS.90219.2008

21 January 2018

Nemaline myopathy: current concepts. The ENMC International Consortium and Nemaline Myopathy

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOLGENOMICS.90219.2008

21 January 2018

Loss of calpain 3 proteolytic activity leads to muscular dystrophy and to apoptosis-associated IkappaBalpha/nuclear factor kappaB pathway perturbation in mice.

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOLGENOMICS.90219.2008

21 January 2018

Rates of ubiquitin conjugation increase when muscles atrophy, largely through activation of the N-end rule pathway

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOLGENOMICS.90219.2008

21 January 2018

Pathogenic accumulation of APP in fast twitch muscle of IBM patients and a transgenic model

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOLGENOMICS.90219.2008

21 January 2018

Muscle wasting in a rat model of long-lasting sepsis results from the activation of lysosomal, Ca2+ -activated, and ubiquitin-proteasome proteolytic pathways.

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOLGENOMICS.90219.2008

21 January 2018

Roles for UDP-GlcNAc 2-epimerase/ManNAc 6-kinase outside of sialic acid biosynthesis: modulation of sialyltransferase and BiP expression, GM3 and GD3 biosynthesis, proliferation, and apoptosis, and ERK1/2 phosphorylation.

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOLGENOMICS.90219.2008

21 January 2018

Identifiers

10.1152/PHYSIOLGENOMICS.90219.2008

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18628337%20AND%20SRC:MED&resulttype=core&format=json

10 January 2020

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18628337%20AND%20SRC:MED&resulttype=core&format=json

10 January 2020

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