Identification of a locus on chromosome 1q44 for familial cold urticaria.
about
Mutation of a new gene encoding a putative pyrin-like protein causes familial cold autoinflammatory syndrome and Muckle-Wells syndromePYPAF1, a PYRIN-containing Apaf1-like protein that assembles with ASC and regulates activation of NF-kappa BThe tumor-necrosis-factor receptor-associated periodic syndrome: new mutations in TNFRSF1A, ancestral origins, genotype-phenotype studies, and evidence for further genetic heterogeneity of periodic fevers.New mutations of CIAS1 that are responsible for Muckle-Wells syndrome and familial cold urticaria: a novel mutation underlies both syndromesNALPs: a novel protein family involved in inflammationThe PYRIN connection: novel players in innate immunity and inflammation.IL-1 blockade in autoinflammatory syndromes.Unusual urticarias.The histone deacetylase inhibitor ITF2357 reduces production of pro-inflammatory cytokines in vitro and systemic inflammation in vivoPharmacokinetics, safety and inducible cytokine responses during a phase 1 trial of the oral histone deacetylase inhibitor ITF2357 (givinostat).Familial cold autoinflammatory syndrome: phenotype and genotype of an autosomal dominant periodic feverClinical characteristics in subjects with NLRP3 V198M diagnosed at a single UK center and a review of the literature.Developments in the scientific and clinical understanding of autoinflammatory disordersCanakinumab for treatment of cryopyrin-associated periodic syndrome.Genetic and molecular basis of inflammasome-mediated disease.Clinical immunology review series: An approach to the patient with a periodic fever syndrome.Gene hunting in autoinflammation.Recurrent Fevers for the Pediatric Immunologist: It's Not All Immunodeficiency.Autoinflammatory Syndromes in Children.Interleukin-1 antagonists in the treatment of autoinflammatory syndromes, including cryopyrin-associated periodic syndrome.What do we know about the inflammasome in humans?Muckle-Wells syndrome: clinical and histological skin findings compatible with cold air urticaria in a large kindred.Association of mutations in the NALP3/CIAS1/PYPAF1 gene with a broad phenotype including recurrent fever, cold sensitivity, sensorineural deafness, and AA amyloidosis.Long term management of patients with cryopyrin-associated periodic syndromes (CAPS): focus on rilonacept (IL-1 Trap).Rationale for IL-1beta-targeted therapy to minimize hypoxic-ischemic encephalopathy.A conformational analysis of mouse Nalp3 domain structures by molecular dynamics simulations, and binding site analysis
P2860
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P2860
Identification of a locus on chromosome 1q44 for familial cold urticaria.
description
2000 nî lūn-bûn
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Identification of a locus on chromosome 1q44 for familial cold urticaria
@nl
Identification of a locus on chromosome 1q44 for familial cold urticaria.
@ast
Identification of a locus on chromosome 1q44 for familial cold urticaria.
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label
Identification of a locus on chromosome 1q44 for familial cold urticaria
@nl
Identification of a locus on chromosome 1q44 for familial cold urticaria.
@ast
Identification of a locus on chromosome 1q44 for familial cold urticaria.
@en
prefLabel
Identification of a locus on chromosome 1q44 for familial cold urticaria
@nl
Identification of a locus on chromosome 1q44 for familial cold urticaria.
@ast
Identification of a locus on chromosome 1q44 for familial cold urticaria.
@en
P2093
P2860
P356
P1476
Identification of a locus on chromosome 1q44 for familial cold urticaria.
@en
P2093
A A Wanderer
D H Broide
F A Wright
H M Hoffman
R D Kolodner
P2860
P304
P356
10.1086/302874
P407
P577
2000-03-30T00:00:00Z