Detalhe da pesquisa
1.
Mutations that prevent caspase cleavage of RIPK1 cause autoinflammatory disease.
Nature
; 577(7788): 103-108, 2020 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-31827281
2.
Old Dogs, New Tricks: Monogenic Autoinflammatory Disease Unleashed.
Annu Rev Genomics Hum Genet
; 17: 245-72, 2016 08 31.
Artigo
em Inglês
| MEDLINE | ID: mdl-27362340
3.
TLR2/TLR4-dependent exaggerated cytokine production in hyperimmunoglobulinaemia D and periodic fever syndrome.
Rheumatology (Oxford)
; 54(2): 363-8, 2015 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-25173351
4.
The discriminative capacity of soluble Toll-like receptor (sTLR)2 and sTLR4 in inflammatory diseases.
BMC Immunol
; 15: 55, 2014 Nov 19.
Artigo
em Inglês
| MEDLINE | ID: mdl-25406630
5.
MEFV mutations affecting pyrin amino acid 577 cause autosomal dominant autoinflammatory disease.
Ann Rheum Dis
; 73(2): 455-61, 2014 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-23505238
6.
Sustained efficacy of the monoclonal anti-interleukin-1 beta antibody canakinumab in a 9-month trial in Schnitzler's syndrome.
Ann Rheum Dis
; 72(10): 1634-8, 2013 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-23087179
7.
Mutations in the mevalonate kinase (MVK) gene cause nonsyndromic retinitis pigmentosa.
Ophthalmology
; 120(12): 2697-2705, 2013 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-24084495
8.
The influence of concentration/meditation on autonomic nervous system activity and the innate immune response: a case study.
Psychosom Med
; 74(5): 489-94, 2012 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-22685240
9.
Hyper-IgD syndrome or mevalonate kinase deficiency.
Curr Opin Rheumatol
; 23(5): 419-23, 2011 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-21760510
10.
Myeloid lineage-restricted somatic mosaicism of NLRP3 mutations in patients with variant Schnitzler syndrome.
J Allergy Clin Immunol
; 135(2): 561-4, 2015 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-25239704
11.
Sequence-Based Screening of Patients With Idiopathic Polyarteritis Nodosa, Granulomatosis With Polyangiitis, and Microscopic Polyangiitis for Deleterious Genetic Variants in ADA2.
Arthritis Rheumatol
; 73(3): 512-519, 2021 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-33021335
12.
Repulsion between Lys258 and upstream arginines explains the missorting of the AQP2 mutant p.Glu258Lys in nephrogenic diabetes insipidus.
Hum Mutat
; 30(10): 1387-96, 2009 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-19701945
13.
Mevalonate kinase deficiency nomenclature.
Rheumatol Int
; 34(2): 295-6, 2014 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-23921621
14.
Variable expression and treatment of PAPA syndrome.
Ann Rheum Dis
; 70(6): 1168-70, 2011 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-21325428
15.
Loss-of-function mutations in TNFAIP3 leading to A20 haploinsufficiency cause an early-onset autoinflammatory disease.
Nat Genet
; 48(1): 67-73, 2016 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-26642243
16.
ATP-Induced IL-1ß Specific Secretion: True Under Stringent Conditions.
Front Immunol
; 6: 54, 2015.
Artigo
em Inglês
| MEDLINE | ID: mdl-25729382
17.
The role of interleukin-1 beta in the pathophysiology of Schnitzler's syndrome.
Arthritis Res Ther
; 17: 187, 2015 Jul 22.
Artigo
em Inglês
| MEDLINE | ID: mdl-26198339
18.
Inflammasome-independent modulation of cytokine response by autophagy in human cells.
PLoS One
; 6(4): e18666, 2011 Apr 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-21490934
19.
The dectin-1/inflammasome pathway is responsible for the induction of protective T-helper 17 responses that discriminate between yeasts and hyphae of Candida albicans.
J Leukoc Biol
; 90(2): 357-66, 2011 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-21531876
20.
Mouse dendritic cells matured by ingestion of apoptotic blebs induce T cells to produce interleukin-17.
Arthritis Rheum
; 60(8): 2304-13, 2009 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-19644874