(Q34447217)

25385754

2 August 2017

title

An inherited mutation in NLRC4 causes autoinflammation in human and mice (English)

1 reference

2 August 2017

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25385754%20AND%20SRC:MED&resulttype=core&format=json

8 June 2020

author name string

Akiko Kitamura

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25385754%20AND%20SRC:MED&resulttype=core&format=json

8 June 2020

Yuki Sasaki

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25385754%20AND%20SRC:MED&resulttype=core&format=json

8 June 2020

Takaya Abe

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25385754%20AND%20SRC:MED&resulttype=core&format=json

8 June 2020

Hirotsugu Kano

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25385754%20AND%20SRC:MED&resulttype=core&format=json

8 June 2020

language of work or name

English

0 references

publication date

10 November 2014

1 reference

25385754

Journal of Experimental Medicine

2 August 2017

published in

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25385754%20AND%20SRC:MED&resulttype=core&format=json

8 June 2020

volume

211

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25385754%20AND%20SRC:MED&resulttype=core&format=json

8 June 2020

issue

12

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25385754%20AND%20SRC:MED&resulttype=core&format=json

8 June 2020

page(s)

2385-2396

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25385754%20AND%20SRC:MED&resulttype=core&format=json

describes a project that uses

8 June 2020

ImageQuant

1 reference

11 June 2022

https://www.ebi.ac.uk/europepmc/webservices/rest/PMC4235634/fullTextXML

based on heuristic

inferred from PubMed Central ID database lookup

cites work

Mutation of NLRC4 causes a syndrome of enterocolitis and autoinflammation

1 reference

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An activating NLRC4 inflammasome mutation causes autoinflammation with recurrent macrophage activation syndrome

6 July 2018

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Treating inflammation by blocking interleukin-1 in humans

6 July 2018

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Cutting edge: Mouse NAIP1 detects the type III secretion system needle protein

6 July 2018

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Human NAIP and mouse NAIP1 recognize bacterial type III secretion needle protein for inflammasome activation

6 July 2018

1 reference

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Crystal structure of NLRC4 reveals its autoinhibition mechanism

6 July 2018

1 reference

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Lighting the fires within: the cell biology of autoinflammatory diseases

6 July 2018

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Measles virus V protein inhibits NLRP3 inflammasome-mediated interleukin-1β secretion

6 July 2018

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Mutations in proteasome subunit β type 8 cause chronic atypical neutrophilic dermatosis with lipodystrophy and elevated temperature with evidence of genetic and phenotypic heterogeneity.

6 July 2018

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A mutation in the immunoproteasome subunit PSMB8 causes autoinflammation and lipodystrophy in humans

6 July 2018

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Innate immune recognition of bacterial ligands by NAIPs determines inflammasome specificity

6 July 2018

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Genetics of monogenic autoinflammatory diseases: past successes, future challenges

6 July 2018

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Identification and functional consequences of a recurrent NLRP12 missense mutation in periodic fever syndromes.

6 July 2018

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The inflammasome NLRs in immunity, inflammation, and associated diseases

6 July 2018

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PSMB8 encoding the β5i proteasome subunit is mutated in joint contractures, muscle atrophy, microcytic anemia, and panniculitis-induced lipodystrophy syndrome

6 July 2018

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Sterile inflammation: sensing and reacting to damage

6 July 2018

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Caspase-1-induced pyroptosis is an innate immune effector mechanism against intracellular bacteria.

6 July 2018

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A mutation in the Nlrp3 gene causing inflammasome hyperactivation potentiates Th17 cell-dominant immune responses

6 July 2018

1 reference

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6 July 2018

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6 July 2018

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6 July 2018

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Mutation of a new gene encoding a putative pyrin-like protein causes familial cold autoinflammatory syndrome and Muckle-Wells syndrome

6 July 2018

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6 July 2018

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Crossref

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Germline mutations in the extracellular domains of the 55 kDa TNF receptor, TNFR1, define a family of dominantly inherited autoinflammatory syndromes.

21 January 2018

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A cassette vector for high-level reporter expression driven by a hybrid invariant chain promoter in transgenic mice

21 January 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/25385754

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Polymorphisms in NACHT-LRR (NLR) genes in atopic dermatitis

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/25385754

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1084/JEM.20141091

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25385754%20AND%20SRC:MED&resulttype=core&format=json

8 June 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25385754%20AND%20SRC:MED&resulttype=core&format=json

8 June 2020

25385754

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25385754%20AND%20SRC:MED&resulttype=core&format=json