Detalhe da pesquisa
1.
Homozygous DBF4 mutation as a cause of severe congenital neutropenia.
J Allergy Clin Immunol
; 152(1): 266-277, 2023 07.
Artigo
Inglês
| MEDLINE | ID: mdl-36841265
2.
Murine myeloproliferative disorder as a consequence of impaired collaboration between dendritic cells and CD4 T cells.
Blood
; 133(4): 319-330, 2019 01 24.
Artigo
Inglês
| MEDLINE | ID: mdl-30333120
3.
Defective Sec61α1 underlies a novel cause of autosomal dominant severe congenital neutropenia.
J Allergy Clin Immunol
; 146(5): 1180-1193, 2020 11.
Artigo
Inglês
| MEDLINE | ID: mdl-32325141
4.
Early-onset stroke and vasculopathy associated with mutations in ADA2.
N Engl J Med
; 370(10): 911-20, 2014 Mar 06.
Artigo
Inglês
| MEDLINE | ID: mdl-24552284
5.
Peptide library-based evaluation of T-cell receptor breadth detects defects in global and regulatory activation in human immunologic diseases.
Proc Natl Acad Sci U S A
; 110(20): 8164-9, 2013 May 14.
Artigo
Inglês
| MEDLINE | ID: mdl-23637345
6.
Diminished allergic disease in patients with STAT3 mutations reveals a role for STAT3 signaling in mast cell degranulation.
J Allergy Clin Immunol
; 132(6): 1388-96, 2013 Dec.
Artigo
Inglês
| MEDLINE | ID: mdl-24184145
7.
Disrupted Ca2+ homeostasis and immunodeficiency in patients with functional IP3 receptor subtype 3 defects.
Cell Mol Immunol
; 20(1): 11-25, 2023 01.
Artigo
Inglês
| MEDLINE | ID: mdl-36302985
8.
Elevated IgE and atopy in patients treated for early-onset ADA-SCID.
J Allergy Clin Immunol
; 132(6): 1444-6, 2013 Dec.
Artigo
Inglês
| MEDLINE | ID: mdl-23895897
9.
Author Correction: Disrupted Ca2+ homeostasis and immunodeficiency in patients with functional IP3 receptor subtype 3 defects.
Cell Mol Immunol
; 20(1): 114, 2023 Jan.
Artigo
Inglês
| MEDLINE | ID: mdl-36471115
10.
PD-L1 up-regulation restrains Th17 cell differentiation in STAT3 loss- and STAT1 gain-of-function patients.
J Exp Med
; 214(9): 2523-2533, 2017 Sep 04.
Artigo
Inglês
| MEDLINE | ID: mdl-28710273