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ST6Gal-I regulates macrophage apoptosis via α2-6 sialylation of the TNFR1 death receptor
scientific journal article
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instance of
scholarly article
1 reference
stated in
PubMed
PubMed ID
21930713
retrieved
31 January 2017
title
ST6Gal-I regulates macrophage apoptosis via α2-6 sialylation of the TNFR1 death receptor
(English)
1 reference
stated in
PubMed
PubMed ID
21930713
retrieved
31 January 2017
main subject
macrophage
0 references
apoptotic process
0 references
protein sialylation
1 reference
stated in
Gene Ontology release 2020-05-02
Gene Ontology ID
GO:1990743
author name string
Zhongyu Liu
series ordinal
1
1 reference
stated in
PubMed
PubMed ID
21930713
retrieved
31 January 2017
Amanda F. Swindall
series ordinal
2
1 reference
stated in
PubMed
PubMed ID
21930713
retrieved
31 January 2017
Robert A. Kesterson
series ordinal
3
1 reference
stated in
PubMed
PubMed ID
21930713
retrieved
31 January 2017
Trenton R. Schoeb
series ordinal
4
1 reference
stated in
PubMed
PubMed ID
21930713
retrieved
31 January 2017
Daniel C. Bullard
series ordinal
5
1 reference
stated in
PubMed
PubMed ID
21930713
retrieved
31 January 2017
Susan L. Bellis
series ordinal
6
1 reference
stated in
PubMed
PubMed ID
21930713
retrieved
31 January 2017
language of work or name
English
0 references
publication date
11 November 2011
1 reference
stated in
PubMed
PubMed ID
21930713
retrieved
31 January 2017
published in
Journal of Biological Chemistry
1 reference
stated in
PubMed
PubMed ID
21930713
retrieved
31 January 2017
volume
286
1 reference
stated in
PubMed
PubMed ID
21930713
retrieved
31 January 2017
issue
45
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stated in
PubMed
PubMed ID
21930713
retrieved
31 January 2017
page(s)
39654–39662
1 reference
stated in
PubMed
PubMed ID
21930713
retrieved
31 January 2017
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Sialylation of the Fas death receptor by ST6Gal-I provides protection against Fas-mediated apoptosis in colon carcinoma cells
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The ST6Gal I sialyltransferase selectively modifies N-glycans on CD45 to negatively regulate galectin-1-induced CD45 clustering, phosphatase modulation, and T cell death
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Hyposialylation of integrins stimulates the activity of myeloid fibronectin receptors
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Cell surface sialylation plays a role in modulating sensitivity towards APO-1-mediated apoptotic cell death.
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Proteolytic shedding of ST6Gal-I by BACE1 regulates the glycosylation and function of alpha4beta1 integrins
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27 November 2018
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27 November 2018
A protein kinase C/Ras/ERK signaling pathway activates myeloid fibronectin receptors by altering beta1 integrin sialylation
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The histone deacetylase inhibitor sodium butyrate interacts synergistically with phorbol myristate acetate (PMA) to induce mitochondrial damage and apoptosis in human myeloid leukemia cells through a tumor necrosis factor-alpha-mediated process
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Macrophage lineage cells in inflammation: characterization by colony-stimulating factor-1 (CSF-1) receptor (c-Fms), ER-MP58, and ER-MP20 (Ly-6C) expression.
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Identification of Two Forms (31-33 and 48 kD) of the Urinary Soluble p55 Tumor Necrosis Factor Receptor That Are Differentially N- and O-Glycosylated
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Activation of murine CD4+ and CD8+ T lymphocytes leads to dramatic remodeling of N-linked glycans
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retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Identifiers
DOI
10.1074/JBC.M111.276063
1 reference
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
4757681
OpenCitations bibliographic resource ID
4757681
1 reference
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
4757681
PMCID
3234788
1 reference
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
4757681
PubMed ID
21930713
1 reference
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
4757681
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