Detalhe da pesquisa
1.
A Common Genetic Variant in TLR1 Enhances Human Neutrophil Priming and Impacts Length of Intensive Care Stay in Pediatric Sepsis.
J Immunol
; 196(3): 1376-86, 2016 Feb 01.
Artigo
Inglês
| MEDLINE | ID: mdl-26729809
2.
Inflammasome-independent IL-1ß mediates autoinflammatory disease in Pstpip2-deficient mice.
Proc Natl Acad Sci U S A
; 111(3): 1072-7, 2014 Jan 21.
Artigo
Inglês
| MEDLINE | ID: mdl-24395802
3.
The F-BAR protein PSTPIP1 controls extracellular matrix degradation and filopodia formation in macrophages.
Blood
; 123(17): 2703-14, 2014 Apr 24.
Artigo
Inglês
| MEDLINE | ID: mdl-24421327
4.
Mutations in extracellular matrix genes NID1 and LAMC1 cause autosomal dominant Dandy-Walker malformation and occipital cephaloceles.
Hum Mutat
; 34(8): 1075-9, 2013 Aug.
Artigo
Inglês
| MEDLINE | ID: mdl-23674478
5.
Exome sequencing reveals RAG1 mutations in a child with autoimmunity and sterile chronic multifocal osteomyelitis evolving into disseminated granulomatous disease.
J Clin Immunol
; 33(8): 1289-92, 2013 Nov.
Artigo
Inglês
| MEDLINE | ID: mdl-24122031
6.
Efficacy of anti-IL-1 treatment in Majeed syndrome.
Ann Rheum Dis
; 72(3): 410-3, 2013 Mar.
Artigo
Inglês
| MEDLINE | ID: mdl-23087183
7.
An autoinflammatory disease with deficiency of the interleukin-1-receptor antagonist.
N Engl J Med
; 360(23): 2426-37, 2009 Jun 04.
Artigo
Inglês
| MEDLINE | ID: mdl-19494218
8.
Recessive coding and regulatory mutations in FBLIM1 underlie the pathogenesis of chronic recurrent multifocal osteomyelitis (CRMO).
PLoS One
; 12(3): e0169687, 2017.
Artigo
Inglês
| MEDLINE | ID: mdl-28301468
9.
Correction: Recessive coding and regulatory mutations in FBLIM1 underlie the pathogenesis of chronic recurrent multifocal osteomyelitis (CRMO).
PLoS One
; 12(7): e0181222, 2017.
Artigo
Inglês
| MEDLINE | ID: mdl-28686717
10.
A missense mutation in pstpip2 is associated with the murine autoinflammatory disorder chronic multifocal osteomyelitis.
Bone
; 38(1): 41-7, 2006 Jan.
Artigo
Inglês
| MEDLINE | ID: mdl-16122996
11.
Dehydroepiandrosterone inhibits intracellular calcium release in beta-cells by a plasma membrane-dependent mechanism.
Steroids
; 71(8): 691-9, 2006 Aug.
Artigo
Inglês
| MEDLINE | ID: mdl-16725167
12.
Phenotypic Variability in Majeed Syndrome.
J Rheumatol
; 43(6): 1258-9, 2016 06.
Artigo
Inglês
| MEDLINE | ID: mdl-27252506
13.
Neutrophil dysfunction in a family with a SAPHO syndrome-like phenotype.
Arthritis Rheum
; 58(10): 3264-9, 2008 Oct.
Artigo
Inglês
| MEDLINE | ID: mdl-18821685
14.
Effect of treatment of diabetic rats with dehydroepiandrosterone on vascular and neural function.
Am J Physiol Endocrinol Metab
; 283(5): E1067-75, 2002 Nov.
Artigo
Inglês
| MEDLINE | ID: mdl-12376336