Detalhe da pesquisa
1.
Interfering with Interferons: A Critical Mechanism for Critical COVID-19 Pneumonia.
Annu Rev Immunol
; 41: 561-585, 2023 04 26.
Artigo
em Inglês
| MEDLINE | ID: mdl-37126418
2.
Migration-induced cell shattering due to DOCK8 deficiency causes a type 2-biased helper T cell response.
Nat Immunol
; 21(12): 1528-1539, 2020 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-33020661
3.
Dual proteolytic pathways govern glycolysis and immune competence.
Cell
; 159(7): 1578-90, 2014 Dec 18.
Artigo
em Inglês
| MEDLINE | ID: mdl-25525876
4.
Insights into immunity from clinical and basic science studies of DOCK8 immunodeficiency syndrome.
Immunol Rev
; 287(1): 9-19, 2019 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-30565250
5.
Hyper-IgE Syndrome due to an Elusive Novel Intronic Homozygous Variant in DOCK8.
J Clin Immunol
; 42(1): 119-129, 2022 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-34657245
6.
IFIH1 loss-of-function variants contribute to very early-onset inflammatory bowel disease.
Hum Genet
; 140(9): 1299-1312, 2021 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-34185153
7.
Magnesium transporter 1 (MAGT1) deficiency causes selective defects in N-linked glycosylation and expression of immune-response genes.
J Biol Chem
; 294(37): 13638-13656, 2019 09 13.
Artigo
em Inglês
| MEDLINE | ID: mdl-31337704
8.
New immunodeficiency syndromes that help us understand the IFN-mediated antiviral immune response.
Curr Opin Pediatr
; 31(6): 815-820, 2019 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-31693592
9.
Recent Advances in DOCK8 Immunodeficiency Syndrome.
J Clin Immunol
; 36(5): 441-9, 2016 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-27207373
10.
Somatic reversion in dedicator of cytokinesis 8 immunodeficiency modulates disease phenotype.
J Allergy Clin Immunol
; 133(6): 1667-75, 2014 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-24797421
11.
Autosomal recessive phosphoglucomutase 3 (PGM3) mutations link glycosylation defects to atopy, immune deficiency, autoimmunity, and neurocognitive impairment.
J Allergy Clin Immunol
; 133(5): 1400-9, 1409.e1-5, 2014 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-24589341
12.
Prostaglandin E2 induces matrix metalloproteinase 9 expression in dendritic cells through two independent signaling pathways leading to activator protein 1 (AP-1) activation.
J Biol Chem
; 286(45): 38913-23, 2011 Nov 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-21940623
13.
Additional diverse findings expand the clinical presentation of DOCK8 deficiency.
J Clin Immunol
; 32(4): 698-708, 2012 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-22476911
14.
Combined immunodeficiency associated with DOCK8 mutations.
N Engl J Med
; 361(21): 2046-55, 2009 Nov 19.
Artigo
em Inglês
| MEDLINE | ID: mdl-19776401
15.
Recessive inborn errors of type I IFN immunity in children with COVID-19 pneumonia.
J Exp Med
; 219(8)2022 08 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-35708626
16.
Inborn errors of TLR3- or MDA5-dependent type I IFN immunity in children with enterovirus rhombencephalitis.
J Exp Med
; 218(12)2021 12 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-34726731
17.
Dissecting molecular steps in chromatin domain activation during hematopoietic differentiation.
Mol Cell Biol
; 27(12): 4551-65, 2007 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-17438135
18.
Vaccine strain varicella-zoster virus-induced central nervous system vasculopathy as the presenting feature of DOCK8 deficiency.
J Allergy Clin Immunol
; 133(4): 1225-1227, 2014 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-24418481
19.
Distinct functions of dispersed GATA factor complexes at an endogenous gene locus.
Mol Cell Biol
; 26(19): 7056-67, 2006 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-16980610
20.
Life-threatening influenza pneumonitis in a child with inherited IRF9 deficiency.
J Exp Med
; 215(10): 2567-2585, 2018 10 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-30143481