Detalhe da pesquisa
1.
Multibatch Cytometry Data Integration for Optimal Immunophenotyping.
J Immunol
; 206(1): 206-213, 2021 01 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-33229441
2.
STAT5B restrains human B-cell differentiation to maintain humoral immune homeostasis.
J Allergy Clin Immunol
; 150(4): 931-946, 2022 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-35469842
3.
A Novel TRAF3IP2 Mutation Causing Chronic Mucocutaneous Candidiasis.
J Clin Immunol
; 41(6): 1376-1379, 2021 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-33825088
4.
Biallelic TRAF3IP2 variants causing chronic mucocutaneous candidiasis in a child harboring a STAT1 variant.
Pediatr Allergy Immunol
; 32(8): 1804-1812, 2021 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-34289170
5.
Activating mutations in PIK3CD disrupt the differentiation and function of human and murine CD4+ T cells.
J Allergy Clin Immunol
; 144(1): 236-253, 2019 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-30738173
6.
Cytokine-Mediated Regulation of Human Lymphocyte Development and Function: Insights from Primary Immunodeficiencies.
J Immunol
; 199(6): 1949-1958, 2017 09 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-28874415
7.
NK cells are required for dendritic cell-based immunotherapy at the time of tumor challenge.
J Immunol
; 192(5): 2514-21, 2014 Mar 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-24477907
8.
Monogenic mutations differentially affect the quantity and quality of T follicular helper cells in patients with human primary immunodeficiencies.
J Allergy Clin Immunol
; 136(4): 993-1006.e1, 2015 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-26162572
9.
Inherited human ITK deficiency impairs IFN-γ immunity and underlies tuberculosis.
J Exp Med
; 220(1)2023 01 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-36326697
10.
Elucidating the effects of disease-causing mutations on STAT3 function in autosomal-dominant hyper-IgE syndrome.
J Allergy Clin Immunol
; 138(4): 1210-1213.e5, 2016 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-27315770
11.
Human STAT3 variants underlie autosomal dominant hyper-IgE syndrome by negative dominance.
J Exp Med
; 218(8)2021 08 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-34137790
12.
Inherited PD-1 deficiency underlies tuberculosis and autoimmunity in a child.
Nat Med
; 27(9): 1646-1654, 2021 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-34183838
13.
X-linked recessive TLR7 deficiency in ~1% of men under 60 years old with life-threatening COVID-19.
Sci Immunol
; 6(62)2021 08 19.
Artigo
em Inglês
| MEDLINE | ID: mdl-34413140
14.
Biochemically deleterious human NFKB1 variants underlie an autosomal dominant form of common variable immunodeficiency.
J Exp Med
; 218(11)2021 11 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-34473196
15.
Signal Transducer and Activator of Transcription 3 Control of Human T and B Cell Responses.
Front Immunol
; 9: 168, 2018.
Artigo
em Inglês
| MEDLINE | ID: mdl-29472924
16.
A recessive form of hyper-IgE syndrome by disruption of ZNF341-dependent STAT3 transcription and activity.
Sci Immunol
; 3(24)2018 06 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-29907691
17.
Multi-target chimaeric VLP as a therapeutic vaccine in a model of colorectal cancer.
J Immunother Cancer
; 5(1): 69, 2017 08 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-28806910
18.
Antigen delivery by virus-like particles for immunotherapeutic vaccination.
Ther Deliv
; 5(11): 1223-40, 2014 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-25491672