(Q40146198)

English

The SPRY domain of Pyrin, mutated in familial Mediterranean fever patients, interacts with inflammasome components and inhibits proIL-1beta processing

scientific article published on 13 April 2007

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

17 September 2017

The SPRY domain of Pyrin, mutated in familial Mediterranean fever patients, interacts with inflammasome components and inhibits proIL-1beta processing (English)

1 reference

Europe PubMed Central

PubMed publication ID

17 September 2017

0 references

inflammasome complex

1 reference

based on heuristic

inferred from title

familial Mediterranean fever

1 reference

based on heuristic

inferred from title

4

1 reference

Europe PubMed Central

PubMed publication ID

17 September 2017

author name string

S Papin

1

1 reference

Europe PubMed Central

PubMed publication ID

17 September 2017

S Cuenin

2

1 reference

Europe PubMed Central

PubMed publication ID

17 September 2017

L Agostini

3

1 reference

Europe PubMed Central

PubMed publication ID

17 September 2017

S Werner

5

1 reference

Europe PubMed Central

PubMed publication ID

17 September 2017

H-D Beer

6

1 reference

Europe PubMed Central

PubMed publication ID

17 September 2017

C Grütter

7

1 reference

Europe PubMed Central

PubMed publication ID

17 September 2017

M Grütter

8

1 reference

Europe PubMed Central

PubMed publication ID

17 September 2017

J Tschopp

9

1 reference

Europe PubMed Central

PubMed publication ID

17 September 2017

publication date

13 April 2007

1 reference

Europe PubMed Central

PubMed publication ID

17 September 2017

Cell Death & Differentiation

1 reference

Europe PubMed Central

PubMed publication ID

17 September 2017

14

1 reference

Europe PubMed Central

PubMed publication ID

17 September 2017

8

1 reference

Europe PubMed Central

PubMed publication ID

17 September 2017

1457-1466

1 reference

Europe PubMed Central

PubMed publication ID

17 September 2017

The autoinflammatory syndromes

1 reference

https://api.crossref.org/works/10.1038%2FSJ.CDD.4402142

21 January 2018

Hereditary fevers

1 reference

https://api.crossref.org/works/10.1038%2FSJ.CDD.4402142

21 January 2018

Familial autoinflammatory diseases: genetics, pathogenesis and treatment

1 reference

https://api.crossref.org/works/10.1038%2FSJ.CDD.4402142

21 January 2018

NALP3 forms an IL-1beta-processing inflammasome with increased activity in Muckle-Wells autoinflammatory disorder

1 reference

https://api.crossref.org/works/10.1038%2FSJ.CDD.4402142

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1038%2FSJ.CDD.4402142

21 January 2018

Chronic infantile neurological cutaneous and articular syndrome is caused by mutations in CIAS1, a gene highly expressed in polymorphonuclear cells and chondrocytes

1 reference

https://api.crossref.org/works/10.1038%2FSJ.CDD.4402142

21 January 2018

Mutations in the gene encoding mevalonate kinase cause hyper-IgD and periodic fever syndrome. International Hyper-IgD Study Group.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.CDD.4402142

21 January 2018

Mutations in MVK, encoding mevalonate kinase, cause hyperimmunoglobulinaemia D and periodic fever syndrome

1 reference

https://api.crossref.org/works/10.1038%2FSJ.CDD.4402142

21 January 2018

Mutations in CD2BP1 disrupt binding to PTP PEST and are responsible for PAPA syndrome, an autoinflammatory disorder

1 reference

https://api.crossref.org/works/10.1038%2FSJ.CDD.4402142

21 January 2018

The TNF receptor-associated periodic syndrome (TRAPS): emerging concepts of an autoinflammatory disorder

1 reference

https://api.crossref.org/works/10.1038%2FSJ.CDD.4402142

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1038%2FSJ.CDD.4402142

21 January 2018

A candidate gene for familial Mediterranean fever

1 reference

https://api.crossref.org/works/10.1038%2FSJ.CDD.4402142

21 January 2018

Lipopolysaccharide-induced expression of multiple alternatively spliced MEFV transcripts in human synovial fibroblasts: a prominent splice isoform lacks the C-terminal domain that is highly mutated in familial Mediterranean fever

1 reference

https://api.crossref.org/works/10.1038%2FSJ.CDD.4402142

21 January 2018

Alternative splicing at the MEFV locus involved in familial Mediterranean fever regulates translocation of the marenostrin/pyrin protein to the nucleus

1 reference

https://api.crossref.org/works/10.1038%2FSJ.CDD.4402142

21 January 2018

The familial Mediterranean fever protein, pyrin, associates with microtubules and colocalizes with actin filaments

1 reference

https://api.crossref.org/works/10.1038%2FSJ.CDD.4402142

21 January 2018

Interaction between pyrin and the apoptotic speck protein (ASC) modulates ASC-induced apoptosis

1 reference

https://api.crossref.org/works/10.1038%2FSJ.CDD.4402142

21 January 2018

The PYRIN domain: a member of the death domain-fold superfamily

1 reference

https://api.crossref.org/works/10.1038%2FSJ.CDD.4402142

21 January 2018

Fire and death: the pyrin domain joins the death-domain superfamily

1 reference

https://api.crossref.org/works/10.1038%2FSJ.CDD.4402142

21 January 2018

The pyrin domain: a possible member of the death domain-fold family implicated in apoptosis and inflammation

1 reference

https://api.crossref.org/works/10.1038%2FSJ.CDD.4402142

21 January 2018

The inflammasome: a molecular platform triggering activation of inflammatory caspases and processing of proIL-beta

1 reference

https://api.crossref.org/works/10.1038%2FSJ.CDD.4402142

21 January 2018

Cryopyrin and pyrin activate caspase-1, but not NF-kappaB, via ASC oligomerization.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.CDD.4402142

21 January 2018

Regulation of cryopyrin/Pypaf1 signaling by pyrin, the familial Mediterranean fever gene product

1 reference

https://api.crossref.org/works/10.1038%2FSJ.CDD.4402142

21 January 2018

ASC is an activating adaptor for NF-kappa B and caspase-8-dependent apoptosis

1 reference

https://api.crossref.org/works/10.1038%2FSJ.CDD.4402142

21 January 2018

The tripartite motif family identifies cell compartments

1 reference

https://api.crossref.org/works/10.1038%2FSJ.CDD.4402142

21 January 2018

The cytoplasmic body component TRIM5alpha restricts HIV-1 infection in Old World monkeys

1 reference

https://api.crossref.org/works/10.1038%2FSJ.CDD.4402142

21 January 2018

Trim5alpha protein restricts both HIV-1 and murine leukemia virus

1 reference

https://api.crossref.org/works/10.1038%2FSJ.CDD.4402142

21 January 2018

The B30.2 domain of pyrin, the familial Mediterranean fever protein, interacts directly with caspase-1 to modulate IL-1beta production

1 reference

https://api.crossref.org/works/10.1038%2FSJ.CDD.4402142

21 January 2018

Targeted disruption of pyrin, the FMF protein, causes heightened sensitivity to endotoxin and a defect in macrophage apoptosis

1 reference

https://api.crossref.org/works/10.1038%2FSJ.CDD.4402142

21 January 2018

The estrogen-responsive B box protein: a novel enhancer of interleukin-1beta secretion

1 reference

https://api.crossref.org/works/10.1038%2FSJ.CDD.4402142

21 January 2018

Pyrin binds the PSTPIP1/CD2BP1 protein, defining familial Mediterranean fever and PAPA syndrome as disorders in the same pathway

1 reference

https://api.crossref.org/works/10.1038%2FSJ.CDD.4402142

21 January 2018

Isolation, genomic organization, and expression analysis of the mouse and rat homologs of MEFV, the gene for familial mediterranean fever

1 reference

https://api.crossref.org/works/10.1038%2FSJ.CDD.4402142

21 January 2018

Episodic evolution of pyrin in primates: human mutations recapitulate ancestral amino acid states

1 reference

https://api.crossref.org/works/10.1038%2FSJ.CDD.4402142

21 January 2018

Identification of CARDIAK, a RIP-like kinase that associates with caspase-1

1 reference

https://api.crossref.org/works/10.1038%2FSJ.CDD.4402142

21 January 2018

Ancient Missense Mutations in a New Member of the RoRet Gene Family Are Likely to Cause Familial Mediterranean Fever

1 reference

https://api.crossref.org/works/10.1038%2FSJ.CDD.4402142

7 January 2021

based on heuristic

inferred from DOI database lookup

Interaction of pyrin with 14.3.3 in an isoform-specific and phosphorylation-dependent manner regulates its translocation to the nucleus

1 reference

https://api.crossref.org/works/10.1038%2FSJ.CDD.4402142

7 January 2021

based on heuristic

inferred from DOI database lookup

Expression of apoptosis-associated speck-like protein containing a caspase recruitment domain, a pyrin N-terminal homology domain-containing protein, in normal human tissues

1 reference

https://api.crossref.org/works/10.1038%2FSJ.CDD.4402142

7 January 2021

based on heuristic

inferred from DOI database lookup

Familial Mediterranean fever at the millennium. Clinical spectrum, ancient mutations, and a survey of 100 American referrals to the National Institutes of Health.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.CDD.4402142

7 January 2021

based on heuristic

inferred from DOI database lookup

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10.1038/SJ.CDD.4402142

1 reference

Europe PubMed Central

PubMed publication ID

17 September 2017

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release_lj466mo3y5fuxhiye5pwcsirmu

1 reference

https://api.fatcat.wiki/v0/release/lj466mo3y5fuxhiye5pwcsirmu

24 November 2022

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mapped directly with Wikidata item

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

17 September 2017

ResearchGate publication ID

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