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CD36 gene transfer confers capacity for phagocytosis of cells undergoing apoptosis
scientific journal article
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instance of
scholarly article
1 reference
stated in
PubMed
PubMed ID
7536797
retrieved
6 February 2017
title
CD36 gene transfer confers capacity for phagocytosis of cells undergoing apoptosis
(English)
1 reference
stated in
PubMed
PubMed ID
7536797
retrieved
6 February 2017
main subject
apoptotic process
0 references
phagocytosis
1 reference
based on heuristic
inferred from title
author name string
Y. Ren
series ordinal
1
1 reference
stated in
PubMed
PubMed ID
7536797
retrieved
6 February 2017
R. L. Silverstein
series ordinal
2
1 reference
stated in
PubMed
PubMed ID
7536797
retrieved
6 February 2017
J. Allen
series ordinal
3
1 reference
stated in
PubMed
PubMed ID
7536797
retrieved
6 February 2017
J. Savill
series ordinal
4
1 reference
stated in
PubMed
PubMed ID
7536797
retrieved
6 February 2017
language of work or name
English
0 references
publication date
1 May 1995
1 reference
stated in
PubMed
PubMed ID
7536797
retrieved
6 February 2017
published in
Journal of Experimental Medicine
1 reference
stated in
PubMed
PubMed ID
7536797
retrieved
6 February 2017
volume
181
1 reference
stated in
PubMed
PubMed ID
7536797
retrieved
6 February 2017
issue
5
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stated in
PubMed
PubMed ID
7536797
retrieved
6 February 2017
page(s)
1857–1862
1 reference
stated in
PubMed
PubMed ID
7536797
retrieved
6 February 2017
cites work
Cloning of a rat adipocyte membrane protein implicated in binding or transport of long-chain fatty acids that is induced during preadipocyte differentiation. Homology with human CD36
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PubMed Central
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CD36 is a receptor for oxidized low density lipoprotein
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PubMed Central
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PubMed Central
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Identification of glycoprotein IV (CD36) as a primary receptor for platelet-collagen adhesion
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PubMed Central
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17 March 2017
Isolation of the thrombospondin membrane receptor
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PubMed Central
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17 March 2017
Exposure of phosphatidylserine on the surface of apoptotic lymphocytes triggers specific recognition and removal by macrophages
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Cell death: the significance of apoptosis
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PubMed Central
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7 April 2017
Phagocyte recognition of cells undergoing apoptosis
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PubMed Central
reference URL
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3 June 2018
bcl-2 modulation of apoptosis induced by anticancer drugs: resistance to thymidylate stress is independent of classical resistance pathways.
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PubMed Central
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3 June 2018
Apoptosis and disease.
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PubMed Central
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Lethal effect of the anti-Fas antibody in mice
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Oxidized LDL binds to CD36 on human monocyte-derived macrophages and transfected cell lines. Evidence implicating the lipid moiety of the lipoprotein as the binding site
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PubMed Central
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3 June 2018
Macrophage phagocytosis of aging neutrophils in inflammation. Programmed cell death in the neutrophil leads to its recognition by macrophages
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Phagocytosis of aged human neutrophils by macrophages is mediated by a novel "charge-sensitive" recognition mechanism
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The osteoclast functional antigen, implicated in the regulation of bone resorption, is biochemically related to the vitronectin receptor
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CD36 directly mediates cytoadherence of Plasmodium falciparum parasitized erythrocytes.
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Identification of a platelet membrane glycoprotein as a falciparum malaria sequestration receptor
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Monoclonal antibodies that recognize calcium-dependent structures of human thrombospondin. Characterization and mapping of their epitopes
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Selective inhibition of integrin function by antibodies specific for ligand-occupied receptor conformers.
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3 June 2018
Human monocytes CD36 and CD16 are signaling molecules. Evidence from studies using antibody-induced chemiluminescence as a tool to probe signal transduction
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Genome digestion is a dispensable consequence of physiological cell death mediated by cytotoxic T lymphocytes
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PubMed Central
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3 June 2018
Thrombospondin cooperates with CD36 and the vitronectin receptor in macrophage recognition of neutrophils undergoing apoptosis
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2192004
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3 June 2018
CD36 peptides enhance or inhibit CD36-thrombospondin binding. A two-step process of ligand-receptor interaction
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Membrane glycoprotein CD36: a review of its roles in adherence, signal transduction, and transfusion medicine
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PubMed Central
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Sense and antisense cDNA transfection of CD36 (glycoprotein IV) in melanoma cells. Role of CD36 as a thrombospondin receptor
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The specific recognition by macrophages of CD8+,CD45RO+ T cells undergoing apoptosis: a mechanism for T cell clearance during resolution of viral infections
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stated in
PubMed Central
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27 November 2018
Resolution of acute inflammation and the role of apoptosis in the tissue fate of granulocytes
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PubMed Central
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27 November 2018
Monoclonal anti-human monocyte antibodies OKM1 and OKM5 possess distinctive tissue distributions including differential reactivity with vascular endothelium
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/7536797
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Vitronectin receptor-mediated phagocytosis of cells undergoing apoptosis
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/7536797
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Different populations of macrophages use either the vitronectin receptor or the phosphatidylserine receptor to recognize and remove apoptotic cells
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/7536797
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
T-cell apoptosis detected in situ during positive and negative selection in the thymus
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/7536797
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Monoclonal antibodies specific for platelet glycoproteins react with human monocytes
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/7536797
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Identifiers
DOI
10.1084/JEM.181.5.1857
1 reference
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
3158246
OpenCitations bibliographic resource ID
3158246
1 reference
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
3158246
PMCID
2192004
1 reference
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
3158246
PubMed ID
7536797
1 reference
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
3158246
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