Effects of altered sialic acid biosynthesis on N-linked glycan branching and cell surface interactions (Q33781368)

28424265

29 July 2017

title

Effects of altered sialic acid biosynthesis on N-linked glycan branching and cell surface interactions (English)

1 reference

29 July 2017

1

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:28424265%20AND%20SRC:MED&resulttype=core&format=json

7 June 2020

Jennifer J. Kohler

8

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7 June 2020

Anne Dell

6

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Paola Grassi

5

object named as

Paola Grassi

1 reference

7 June 2020

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2

Poh-Choo Pang

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7 June 2020

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Soumya Krishnamurthy

3

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7 June 2020

Amberlyn M Wands

4

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7 June 2020

Stuart M Haslam

7

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7 June 2020

language of work or name

English

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publication date

19 April 2017

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28424265

29 July 2017

number of pages

15

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Journal of Biological Chemistry

inferred from page(s)

published in

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volume

292

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7 June 2020

issue

23

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7 June 2020

page(s)

9637-9651

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:28424265%20AND%20SRC:MED&resulttype=core&format=json

Golgi self-correction generates bioequivalent glycans to preserve cellular homeostasis.

7 June 2020

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4 July 2018

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4 July 2018

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4 July 2018

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N- and O-glycans modulate galectin-1 binding, CD45 signaling, and T cell death

4 July 2018

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4 July 2018

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Prophylactic treatment with sialic acid metabolites precludes the development of the myopathic phenotype in the DMRV-hIBM mouse model

4 July 2018

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Galectin-glycan lattices regulate cell-surface glycoprotein organization and signalling

4 July 2018

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CD45 glycosylation controls T-cell life and death

4 July 2018

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4 July 2018

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4 July 2018

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

4 July 2018

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Complex N-glycan number and degree of branching cooperate to regulate cell proliferation and differentiation.

4 July 2018

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4 July 2018

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4 July 2018

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4 July 2018

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4 July 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

4 July 2018

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4 July 2018

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4 July 2018

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4 July 2018

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4 July 2018

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4 July 2018

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4 July 2018

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4 July 2018

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4 July 2018

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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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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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A Japanese patient with distal myopathy with rimmed vacuoles: missense mutations in the epimerase domain of the UDP-N-acetylglucosamine 2-epimerase/N-acetylmannosamine kinase (GNE) gene accompanied by hyposialylation of skeletal muscle glycoproteins

21 January 2018

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Metabolic homeostasis and tissue renewal are dependent on beta1,6GlcNAc-branched N-glycans.

21 January 2018

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Epigenetically mediated loss of UDP-GlcNAc 2-epimerase/ManNAc kinase expression in hyposialylated cell lines

21 January 2018

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Sialic acid metabolism is involved in the regulation of gene expression during neuronal differentiation of PC12 cells

21 January 2018

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Lessons from GNE-deficient embryonic stem cells: sialic acid biosynthesis is involved in proliferation and gene expression

21 January 2018

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Characterization of the cellular uptake and metabolic conversion of acetylated N-acetylmannosamine (ManNAc) analogues to sialic acids

21 January 2018

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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

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The key enzyme of sialic acid biosynthesis (GNE) promotes neurite outgrowth of PC12 cells

21 January 2018

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Galectin-1 induces skeletal muscle differentiation in human fetal mesenchymal stem cells and increases muscle regeneration

21 January 2018

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21 January 2018

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Apoptosis of T cells mediated by galectin-1.

21 January 2018

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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

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Fluorometric high-performance liquid chromatography of N-acetyl- and N-glycolylneuraminic acids and its application to their microdetermination in human and animal sera, glycoproteins, and glycolipids

21 January 2018

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12 December 2020

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

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12 December 2020

Lack of galectin-1 results in defects in myoblast fusion and muscle regeneration

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Production and titration of lentiviral vectors

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Normal development of mice carrying a null mutation in the gene encoding the L14 S-type lectin

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Identifiers

DOI

10.1074/JBC.M116.764597

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:28424265%20AND%20SRC:MED&resulttype=core&format=json

7 June 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:28424265%20AND%20SRC:MED&resulttype=core&format=json

7 June 2020

28424265

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