Ganglioside GM3 levels are altered in a mouse model of HIBM: GM3 as a cellular marker of the disease (Q33552330)

28 July 2017

Ganglioside GM3 levels are altered in a mouse model of HIBM: GM3 as a cellular marker of the disease (English)

1 reference

28 July 2017

Thomas Paccalet

1

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author name string

Zoé Coulombe

series ordinal

2

1 reference

PubMed ID

20383336

28 July 2017

Jacques P Tremblay

series ordinal

3

1 reference

PubMed ID

20383336

28 July 2017

language of work or name

English

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publication date

7 April 2010

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28 July 2017

1 reference

28 July 2017

5

1 reference

28 July 2017

e10055

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28 July 2017

4

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Creative Commons Attribution 4.0 International

28 July 2017

start time

7 April 2010

1 reference

April 2022 Public Data File from Crossref

copyright status

copyrighted

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cites work

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UDP-N-acetylglucosamine 2-epimerase/N-acetylmannosamine kinase (GNE) binds to alpha-actinin 1: novel pathways in skeletal muscle?

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GNE protein expression and subcellular distribution are unaltered in HIBM.

21 June 2018

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Mutation in the key enzyme of sialic acid biosynthesis causes severe glomerular proteinuria and is rescued by N-acetylmannosamine

21 June 2018

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Reduced sialylation status in UDP-N-acetylglucosamine-2-epimerase/N-acetylmannosamine kinase (GNE)-deficient mice

21 June 2018

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The collapsin response mediator protein 1 (CRMP-1) and the promyelocytic leukemia zinc finger protein (PLZF) bind to UDP-N-acetylglucosamine 2-epimerase/N-acetylmannosamine kinase (GNE), the key enzyme of sialic acid biosynthesis

21 June 2018

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Ganglioside GM3 is involved in neuronal cell death

21 June 2018

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Cancer stem cells in the mammalian central nervous system

21 June 2018

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The ganglioside GD3 as the Greek goddess Hecate: several faces turned towards as many directions

21 June 2018

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Siglecs--the major subfamily of I-type lectins

21 June 2018

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Use of a cell-free system to determine UDP-N-acetylglucosamine 2-epimerase and N-acetylmannosamine kinase activities in human hereditary inclusion body myopathy

21 June 2018

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The homozygous M712T mutation of UDP-N-acetylglucosamine 2-epimerase/N-acetylmannosamine kinase results in reduced enzyme activities but not in altered overall cellular sialylation in hereditary inclusion body myopathy

21 June 2018

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Enhanced insulin sensitivity in mice lacking ganglioside GM3.

21 June 2018

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Evidence for a sialic acid salvaging pathway in lepidopteran insect cells

21 June 2018

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Sialylation is essential for early development in mice

21 June 2018

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

21 June 2018

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Plzf regulates limb and axial skeletal patterning

21 June 2018

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21 June 2018

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Immunohistochemical study of clathrin in distal myopathy with rimmed vacuoles.

21 June 2018

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A bifunctional enzyme catalyzes the first two steps in N-acetylneuraminic acid biosynthesis of rat liver. Purification and characterization of UDP-N-acetylglucosamine 2-epimerase/N-acetylmannosamine kinase

21 June 2018

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Sialic acids as ligands in recognition phenomena.

21 June 2018

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Hereditary inclusion body myopathy maps to chromosome 9p1-q1

21 June 2018

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Decrease of glomerular disialogangliosides in puromycin nephrosis of the rat

21 June 2018

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Biological roles of oligosaccharides: all of the theories are correct

21 June 2018

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Glycosphingolipids during skeletal muscle cell differentiation: comparison of normal and fusion-defective myoblasts

21 June 2018

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

21 June 2018

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A solvent partition method for microscale ganglioside purification.

21 June 2018

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Regulation of glycolipid synthesis during differentiation of clonal murine muscle cells

21 June 2018

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

21 June 2018

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Vacuolar myopathy sparing the quadriceps.

21 January 2018

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

21 January 2018

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Influence of UDP-GlcNAc 2-epimerase/ManNAc kinase mutant proteins on hereditary inclusion body myopathy.

21 January 2018

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

21 January 2018

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Hyposialylation of neprilysin possibly affects its expression and enzymatic activity in hereditary inclusion-body myopathy muscle

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0010055

No overall hyposialylation in hereditary inclusion body myopathy myoblasts carrying the homozygous M712T GNE mutation

21 January 2018

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Evidence for efficient uptake and incorporation of sialic acid by eukaryotic cells

21 January 2018

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

21 January 2018

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Localization of UDP-GlcNAc 2-epimerase/ManAc kinase (GNE) in the Golgi complex and the nucleus of mammalian cells

21 January 2018

1 reference

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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.

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0010055

Glycosphingolipid expression in human skeletal and heart muscle assessed by immunostaining thin-layer chromatography.

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0010055

Analysis of fluorescently labeled glycosphingolipid-derived oligosaccharides following ceramide glycanase digestion and anthranilic acid labeling

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0010055

Decreases of ganglioside GM3 in streptozotocin-induced diabetic glomeruli of rats

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0010055

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.0010055

Type I Gaucher disease, a glycosphingolipid storage disorder, is associated with insulin resistance

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0010055

Improved real-time RT-PCR method for high-throughput measurements using second derivative calculation and double correction.

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0010055

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.0010055

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0010055

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

21 January 2018

1 reference

12 December 2020

Glycosphingolipid biosynthesis during myogenesis of rat L6 cells in vitro

1 reference

12 December 2020

NCAM is hyposialylated in hereditary inclusion body myopathy due to GNE mutations

1 reference

12 December 2020

Glomerular Sialoprotein

1 reference

12 December 2020

Structure and function of renal glycosphingolipids.

1 reference

12 December 2020

A procedure for the quantitative isolation of brain gangliosides

1 reference

12 December 2020

Increased lysosome-related proteins in the skeletal muscles of distal myopathy with rimmed vacuoles

1 reference

12 December 2020

Immunohistological analyses of neutral glycosphingolipids and gangliosides in normal mouse skeletal muscle and in mice with neuromuscular diseases

1 reference

12 December 2020

Muscle sonography in six patients with hereditary inclusion body myopathy

1 reference

12 December 2020

Different distributions of glycosphingolipids in mouse and rabbit skeletal muscle demonstrated by biochemical and immunohistological analyses

1 reference

12 December 2020

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

1 reference

12 December 2020

Distal myopathy with rimmed vacuoles

1 reference

12 December 2020

Expression of neutral glycosphingolipids and gangliosides in human skeletal and heart muscle determined by indirect immunofluorescence staining

1 reference

12 December 2020

10.1371/JOURNAL.PONE.0010055

Identifiers

DOI

1 reference

release_nsfxtyzr7rdxfhswikij5vydpy

28 July 2017

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1 reference

Fatcat

https://api.fatcat.wiki/v0/release/nsfxtyzr7rdxfhswikij5vydpy

24 November 2022

mapped directly with Wikidata item

PMCID

2850932

1 reference

28 July 2017

1 reference

PubMed ID

20383336