Hereditary immunologic disorders caused by pyrin and cryopyrin (Q31121756)

29 June 2017

title

Hereditary immunologic disorders caused by pyrin and cryopyrin (English)

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29 June 2017

Hal M Hoffman

1

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29 June 2017

publication date

1 September 2007

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Current Allergy and Asthma Reports

29 June 2017

published in

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29 June 2017

volume

7

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29 June 2017

issue

5

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29 June 2017

page(s)

323-330

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Cutting edge: CATERPILLER: a large family of mammalian genes containing CARD, pyrin, nucleotide-binding, and leucine-rich repeat domains

29 June 2017

cites work

1 reference

Crossref

https://api.crossref.org/works/10.1007%2FS11882-007-0049-4

IL-converting enzyme/caspase-1 inhibitor VX-765 blocks the hypersensitive response to an inflammatory stimulus in monocytes from familial cold autoinflammatory syndrome patients

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1007%2FS11882-007-0049-4

Familial Mediterranean fever: the genetics of inflammation

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1007%2FS11882-007-0049-4

Fine structure mapping of CIAS1: identification of an ancestral haplotype and a common FCAS mutation, L353P.

21 January 2018

1 reference

12 December 2020

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

1 reference

12 December 2020

Genetic control of MHC class II expression

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12 December 2020

Familial autoinflammatory diseases: genetics, pathogenesis and treatment

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12 December 2020

Inborn and acquired abnormalities of the complement system of man.

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

Prevention of cold-associated acute inflammation in familial cold autoinflammatory syndrome by interleukin-1 receptor antagonist

1 reference

12 December 2020

Inflammasome adaptors and sensors: intracellular regulators of infection and inflammation

1 reference

12 December 2020

NALPs: a novel protein family involved in inflammation

1 reference

12 December 2020

The Toll-like receptors: analysis by forward genetic methods

1 reference

12 December 2020

The clinical continuum of cryopyrinopathies: novel CIAS1 mutations in North American patients and a new cryopyrin model

1 reference

12 December 2020

Neonatal-onset multisystem inflammatory disease responsive to interleukin-1beta inhibition

1 reference

12 December 2020

NODs: intracellular proteins involved in inflammation and apoptosis

1 reference

12 December 2020

Are innate immune signaling pathways in plants and animals conserved?

1 reference

12 December 2020

PYPAF1, a PYRIN-containing Apaf1-like protein that assembles with ASC and regulates activation of NF-kappa B

1 reference

12 December 2020

Intrafamilial variable phenotypic expression of a CIAS1 mutation: from Muckle-Wells to chronic infantile neurological cutaneous and articular syndrome

1 reference

12 December 2020

Primary immunodeficiencies: a flurry of new genes

1 reference

12 December 2020

Disease-associated mutations in CIAS1 induce cathepsin B-dependent rapid cell death of human THP-1 monocytic cells

1 reference

12 December 2020

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

1 reference

12 December 2020

SGT1 is essential for Nod1 activation

1 reference

12 December 2020

NALP1 in vitiligo-associated multiple autoimmune disease

1 reference

12 December 2020

Structural, expression, and evolutionary analysis of mouse CIAS1

1 reference

12 December 2020

A human homologue of the Drosophila Toll protein signals activation of adaptive immunity

1 reference

12 December 2020

Interleukin-1-receptor antagonist in the Muckle-Wells syndrome.

1 reference

12 December 2020

Spectrum of clinical features in Muckle-Wells syndrome and response to anakinra

1 reference

12 December 2020

Inflammasome components NALP 1 and 3 show distinct but separate expression profiles in human tissues suggesting a site-specific role in the inflammatory response

1 reference

12 December 2020

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

1 reference

12 December 2020

Pharmacological characterization of ATP- and LPS-induced IL-1beta release in human monocytes

1 reference

12 December 2020

Familial Mediterranean fever and the other autoinflammatory syndromes: evaluation of the patient with recurrent fever.

1 reference

12 December 2020

NOD-like receptors and human diseases.

1 reference

12 December 2020

The 'Muckle–Wells' syndrome

1 reference

12 December 2020

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

1 reference

12 December 2020

Chronic granulomatous disease

1 reference

12 December 2020

Familial cold autoinflammatory syndrome: phenotype and genotype of an autosomal dominant periodic fever

1 reference

12 December 2020

Plant disease resistance protein signaling: NBS-LRR proteins and their partners

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12 December 2020

NLRs join TLRs as innate sensors of pathogens

1 reference

12 December 2020

1 reference

12 December 2020

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

1 reference

12 December 2020

De novo CIAS1 mutations, cytokine activation, and evidence for genetic heterogeneity in patients with neonatal-onset multisystem inflammatory disease (NOMID): a new member of the expanding family of pyrin-associated autoinflammatory diseases

1 reference

12 December 2020

Identification of bacterial muramyl dipeptide as activator of the NALP3/cryopyrin inflammasome.

1 reference

12 December 2020

Expression and regulation of cryopyrin and related proteins in rheumatoid arthritis synovium

1 reference

12 December 2020

The PYRIN domain: a novel motif found in apoptosis and inflammation proteins

1 reference

12 December 2020

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

1 reference

12 December 2020

A chronic, infantile, neurological, cutaneous and articular (CINCA) syndrome. A specific entity analysed in 30 patients

1 reference

12 December 2020

CATERPILLERs, pyrin and hereditary immunological disorders

1 reference

12 December 2020

The systemic autoinflammatory diseases: inborn errors of the innate immune system.

1 reference

12 December 2020

MHC2TA is associated with differential MHC molecule expression and susceptibility to rheumatoid arthritis, multiple sclerosis and myocardial infarction

1 reference

12 December 2020

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

1 reference

12 December 2020

MDP-induced interleukin-1beta processing requires Nod2 and CIAS1/NALP3.

1 reference

12 December 2020

A candidate gene for familial Mediterranean fever

1 reference

12 December 2020

2. Update on primary immunodeficiency diseases

1 reference

12 December 2020

10.1007/S11882-007-0049-4

Identifiers

DOI

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Dimensions Publication ID

29 June 2017

1036062936

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Fatcat ID

release_draz6iab4jcnzcbc44sqir7tzi

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/draz6iab4jcnzcbc44sqir7tzi

24 November 2022

mapped directly with Wikidata item

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