about
Ultrasonographic assessment reveals detailed distribution of synovial inflammation in Blau syndrome.Revisiting Crohn's disease as a primary immunodeficiency of macrophagesRecent Insights Into the Genetics of Inflammatory Bowel DiseaseInnate immunity in inflammatory bowel disease: a disease hypothesisMutation 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 BChronic infantile neurological cutaneous and articular syndrome is caused by mutations in CIAS1, a gene highly expressed in polymorphonuclear cells and chondrocytesBlau syndrome polymorphisms in NOD2 identify nucleotide hydrolysis and helical domain 1 as signalling regulatorsMutations in NALP12 cause hereditary periodic fever syndromesEvaluation of Nod-like receptor (NLR) effector domain interactionsDe 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 diseasesControl of NOD2 and Rip2-dependent innate immune activation by GEF-H1A role for Erbin in the regulation of Nod2-dependent NF-kappaB signalingThe CATERPILLER protein monarch-1 is an antagonist of toll-like receptor-, tumor necrosis factor alpha-, and Mycobacterium tuberculosis-induced pro-inflammatory signalsHeterotypic interactions among NACHT domains: implications for regulation of innate immune responsesDeep resequencing of GWAS loci identifies independent rare variants associated with inflammatory bowel diseaseNew mutations of CIAS1 that are responsible for Muckle-Wells syndrome and familial cold urticaria: a novel mutation underlies both syndromesThe inflammasome: in memory of Dr. Jurg TschoppHorror autoinflammaticus: the molecular pathophysiology of autoinflammatory disease (*)The NLR gene family: a standard nomenclatureFunction of Nod-like receptors in microbial recognition and host defenseATP binding by monarch-1/NLRP12 is critical for its inhibitory functionChronic inflammation: importance of NOD2 and NALP3 in interleukin-1beta generationHigh-resolution physical map for chromosome 16q12.1-q13, the Blau syndrome locus.NOD-Like Receptors in Infection, Immunity, and DiseasesAutoinflammatory granulomatous diseases: from Blau syndrome and early-onset sarcoidosis to NOD2-mediated disease and Crohn's diseaseLighting the fires within: the cell biology of autoinflammatory diseasesPyrin- and CARD-only Proteins as Regulators of NLR FunctionsPrimary immunodeficiencies of pattern recognition receptorsBeyond the NLRP3 inflammasome: autoinflammatory diseases reach adolescenceStructures of the HIN Domain:DNA Complexes Reveal Ligand Binding and Activation Mechanisms of the AIM2 Inflammasome and IFI16 ReceptorReview of autoinflammatory diseases, with a special focus on periodic fever, aphthous stomatitis, pharyngitis and cervical adenitis syndromeGenetics of inflammatory bowel disease from multifactorial to monogenic formsNALPs: a novel protein family involved in inflammationRecent advances in the genetics of autoimmune diseaseNOD2: ethnic and geographic differencesCentaurin beta1 down-regulates nucleotide-binding oligomerization domains 1- and 2-dependent NF-kappaB activationCARD15/NOD2 mutations in Crohn's diseaseThe PYRIN domain in signal transductionThe Nod-like receptor (NLR) family: a tale of similarities and differences
P2860
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P2860
description
2001 nî lūn-bûn
@nan
2001 թուականի Սեպտեմբերին հրատարակուած գիտական յօդուած
@hyw
2001 թվականի սեպտեմբերին հրատարակված գիտական հոդված
@hy
2001年の論文
@ja
2001年学术文章
@wuu
2001年学术文章
@zh-cn
2001年学术文章
@zh-hans
2001年学术文章
@zh-my
2001年学术文章
@zh-sg
2001年學術文章
@yue
name
CARD15 mutations in Blau syndrome.
@ast
CARD15 mutations in Blau syndrome.
@en
CARD15 mutations in Blau syndrome.
@nl
type
label
CARD15 mutations in Blau syndrome.
@ast
CARD15 mutations in Blau syndrome.
@en
CARD15 mutations in Blau syndrome.
@nl
prefLabel
CARD15 mutations in Blau syndrome.
@ast
CARD15 mutations in Blau syndrome.
@en
CARD15 mutations in Blau syndrome.
@nl
P2093
P356
P1433
P1476
CARD15 mutations in Blau syndrome.
@en
P2093
Chamaillard M
Manouvrier-Hanu S
Miceli-Richard C
P2888
P356
10.1038/NG720
P407
P577
2001-09-01T00:00:00Z