Detalhe da pesquisa
1.
Author Correction: DOCK8 functions as an adaptor that links TLR-MyD88 signaling to B cell activation.
Nat Immunol
; 23(5): 815, 2022 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-35332329
2.
DOCK8 functions as an adaptor that links TLR-MyD88 signaling to B cell activation.
Nat Immunol
; 13(6): 612-20, 2012 May 13.
Artigo
em Inglês
| MEDLINE | ID: mdl-22581261
3.
The opposing effects of two gene defects in STX11 and SLP76 on the disease in a patient with an inborn error of immunity.
J Allergy Clin Immunol
; 152(6): 1597-1606, 2023 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-37595757
4.
Severe allergic dysregulation due to a gain of function mutation in the transcription factor STAT6.
J Allergy Clin Immunol
; 152(1): 182-194.e7, 2023 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-36758835
5.
A novel homozygous mutation in RASGRP1 that predisposes to immune dysregulation and immunodeficiency associated with uncontrolled Epstein-Barr virus-induced B cell proliferation.
Clin Immunol
; 257: 109813, 2023 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-37898412
6.
Challenges in glioblastoma immunotherapy: mechanisms of resistance and therapeutic approaches to overcome them.
Br J Cancer
; 127(6): 976-987, 2022 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-35662275
7.
Hypomorphic variants in AK2 reveal the contribution of mitochondrial function to B-cell activation.
J Allergy Clin Immunol
; 146(1): 192-202, 2020 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-31862378
8.
Wiskott-Aldrich Syndrome in four male siblings from a consanguineous family from Lebanon.
Clin Immunol
; 219: 108573, 2020 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-32814211
9.
Mechanisms of genotype-phenotype correlation in autosomal dominant anhidrotic ectodermal dysplasia with immune deficiency.
J Allergy Clin Immunol
; 141(3): 1060-1073.e3, 2018 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-28629746
10.
DNA recombination defects in Kuwait: Clinical, immunologic and genetic profile.
Clin Immunol
; 187: 68-75, 2018 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-29051008
11.
Inherited DOCK2 Deficiency in Patients with Early-Onset Invasive Infections.
N Engl J Med
; 372(25): 2409-22, 2015 Jun 18.
Artigo
em Inglês
| MEDLINE | ID: mdl-26083206
12.
DOCK8 Deficiency Presenting as an IPEX-Like Disorder.
J Clin Immunol
; 37(8): 811-819, 2017 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-29058101
13.
The Rho GTPase Cdc42 Is Essential for the Activation and Function of Mature B Cells.
J Immunol
; 194(10): 4750-8, 2015 May 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-25870239
14.
Recurrent viral infections associated with a homozygous CORO1A mutation that disrupts oligomerization and cytoskeletal association.
J Allergy Clin Immunol
; 137(3): 879-88.e2, 2016 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-26476480
15.
Hematopoietic stem cell transplantation outcomes for 11 patients with dedicator of cytokinesis 8 deficiency.
J Allergy Clin Immunol
; 138(3): 852-859.e3, 2016 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-27130861
16.
Combined immunodeficiency due to a homozygous mutation in ORAI1 that deletes the C-terminus that interacts with STIM 1.
Clin Immunol
; 166-167: 100-2, 2016 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-27063589
17.
Mutations in pyrin masquerading as a primary immunodeficiency.
Clin Immunol
; 171: 65-66, 2016 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-27538774
18.
Regulatory T-cell deficiency and immune dysregulation, polyendocrinopathy, enteropathy, X-linked-like disorder caused by loss-of-function mutations in LRBA.
J Allergy Clin Immunol
; 135(1): 217-27, 2015 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-25468195
19.
The extended clinical phenotype of 64 patients with dedicator of cytokinesis 8 deficiency.
J Allergy Clin Immunol
; 136(2): 402-12, 2015 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-25724123
20.
Mutations in Recombination Activating Gene 1 and 2 in patients with severe combined immunodeficiency disorders in Egypt.
Clin Immunol
; 158(2): 167-73, 2015 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-25869295