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Innate immune recognition of bacterial ligands by NAIPs determines inflammasome specificity
scientific journal article
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Statements
instance of
scholarly article
1 reference
stated in
PubMed
PubMed ID
21874021
retrieved
24 January 2017
title
Innate immune recognition of bacterial ligands by NAIPs determines inflammasome specificity
(English)
1 reference
stated in
PubMed
PubMed ID
21874021
retrieved
24 January 2017
main subject
NLR family, apoptosis inhibitory protein 6
1 reference
stated in
GOA release 2020-03-11
Caspase 1
1 reference
stated in
GOA release 2020-03-11
NLR family, apoptosis inhibitory protein 5
1 reference
stated in
GOA release 2020-03-11
NLR family, apoptosis inhibitory protein 2
1 reference
stated in
GOA release 2020-03-11
NLR family, CARD domain containing 4
1 reference
stated in
GOA release 2020-03-11
inflammasome complex
1 reference
based on heuristic
inferred from title
author name string
Eric M. Kofoed
series ordinal
1
1 reference
stated in
PubMed
PubMed ID
21874021
retrieved
24 January 2017
Russell E. Vance
series ordinal
2
1 reference
stated in
PubMed
PubMed ID
21874021
retrieved
24 January 2017
language of work or name
English
0 references
publication date
28 August 2011
1 reference
stated in
PubMed
PubMed ID
21874021
retrieved
24 January 2017
published in
Nature
1 reference
stated in
PubMed
PubMed ID
21874021
retrieved
24 January 2017
volume
477
1 reference
stated in
PubMed
PubMed ID
21874021
retrieved
24 January 2017
page(s)
592–595
1 reference
stated in
PubMed
PubMed ID
21874021
retrieved
24 January 2017
issue
7366
1 reference
stated in
PubMed
PubMed ID
21874021
retrieved
24 January 2017
cites work
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PubMed Central
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19 March 2017
The inflammasomes
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PubMed Central
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19 March 2017
Silica crystals and aluminum salts activate the NALP3 inflammasome through phagosomal destabilization
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PubMed Central
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19 March 2017
Repeated recruitment of LTR retrotransposons as promoters by the anti-apoptotic locus NAIP during mammalian evolution
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PubMed Central
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19 March 2017
Cytoplasmic flagellin activates caspase-1 and secretion of interleukin 1beta via Ipaf
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Cytosolic flagellin requires Ipaf for activation of caspase-1 and interleukin 1beta in salmonella-infected macrophages
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19 March 2017
Flagellin-deficient Legionella mutants evade caspase-1- and Naip5-mediated macrophage immunity
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19 March 2017
Nucleotide binding to CARD12 and its role in CARD12-mediated caspase-1 activation
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PubMed Central
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19 March 2017
Heterotypic interactions among NACHT domains: implications for regulation of innate immune responses
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PubMed Central
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19 March 2017
The inflammasome: a molecular platform triggering activation of inflammatory caspases and processing of proIL-beta
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PubMed Central
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19 March 2017
Thioredoxin-interacting protein links oxidative stress to inflammasome activation
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PubMed Central
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Host-microbe interactions: shaping the evolution of the plant immune response
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Analysis of molecular masses and oligomeric states of protein complexes by blue native electrophoresis and isolation of membrane protein complexes by two-dimensional native electrophoresis
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Innate immune detection of the type III secretion apparatus through the NLRC4 inflammasome
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Critical function for Naip5 in inflammasome activation by a conserved carboxy-terminal domain of flagellin
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Cytosolic recognition of flagellin by mouse macrophages restricts Legionella pneumophila infection
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High-resolution genetic and physical map of the Lgn1 interval in C57BL/6J implicates Naip2 or Naip5 in Legionella pneumophila pathogenesis
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Differential requirements for NAIP5 in activation of the NLRC4 inflammasome
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2 June 2018
Naip5 affects host susceptibility to the intracellular pathogen Legionella pneumophila.
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Birc1e is the gene within the Lgn1 locus associated with resistance to Legionella pneumophila.
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A phenylalanine clamp catalyzes protein translocation through the anthrax toxin pore
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The Birc1e cytosolic pattern-recognition receptor contributes to the detection and control of Legionella pneumophila infection
1 reference
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PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/21874021
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Identifiers
DOI
10.1038/NATURE10394
1 reference
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
331774
Dimensions Publication ID
1009302090
0 references
OpenCitations bibliographic resource ID
331774
1 reference
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
331774
PMCID
3184209
1 reference
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
331774
PubMed ID
21874021
1 reference
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
331774
ResearchGate publication ID
51602045
0 references
Springer Nature article ID
10.1038/nature10394
0 references
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