Detalhe da pesquisa
1.
Time-resolved systems immunology reveals a late juncture linked to fatal COVID-19.
Cell
; 184(7): 1836-1857.e22, 2021 04 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-33713619
2.
SASH3 variants cause a novel form of X-linked combined immunodeficiency with immune dysregulation.
Blood
; 138(12): 1019-1033, 2021 09 23.
Artigo
em Inglês
| MEDLINE | ID: mdl-33876203
3.
Dominant activating RAC2 mutation with lymphopenia, immunodeficiency, and cytoskeletal defects.
Blood
; 133(18): 1977-1988, 2019 05 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-30723080
4.
Cutaneous barrier leakage and gut inflammation drive skin disease in Omenn syndrome.
J Allergy Clin Immunol
; 146(5): 1165-1179.e11, 2020 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-32311393
5.
X-linked carriers of chronic granulomatous disease: Illness, lyonization, and stability.
J Allergy Clin Immunol
; 141(1): 365-371, 2018 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-28528201
6.
Cytoskeletal abnormalities and neutrophil dysfunction in WDR1 deficiency.
Blood
; 128(17): 2135-2143, 2016 10 27.
Artigo
em Inglês
| MEDLINE | ID: mdl-27557945
7.
CARD9-Dependent Neutrophil Recruitment Protects against Fungal Invasion of the Central Nervous System.
PLoS Pathog
; 11(12): e1005293, 2015 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-26679537
8.
Anakinra-Associated Systemic Amyloidosis.
Arthritis Rheumatol
; 76(1): 100-106, 2024 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-37488949
9.
B-cell activating factor (BAFF) is elevated in chronic granulomatous disease.
Clin Immunol
; 148(2): 258-64, 2013 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-23773925
10.
Inherited ARPC5 mutations cause an actinopathy impairing cell motility and disrupting cytokine signaling.
Nat Commun
; 14(1): 3708, 2023 06 22.
Artigo
em Inglês
| MEDLINE | ID: mdl-37349293
11.
Constitutively active Lyn kinase causes a cutaneous small vessel vasculitis and liver fibrosis syndrome.
Nat Commun
; 14(1): 1502, 2023 03 17.
Artigo
em Inglês
| MEDLINE | ID: mdl-36932076
12.
Characterization of the antispike IgG immune response to COVID-19 vaccines in people with a wide variety of immunodeficiencies.
Sci Adv
; 9(41): eadh3150, 2023 10 13.
Artigo
em Inglês
| MEDLINE | ID: mdl-37824621
13.
Autosomal dominant and sporadic monocytopenia with susceptibility to mycobacteria, fungi, papillomaviruses, and myelodysplasia.
Blood
; 115(8): 1519-29, 2010 Feb 25.
Artigo
em Inglês
| MEDLINE | ID: mdl-20040766
14.
Preclinical Evaluation of Foamy Virus Vector-Mediated Gene Addition in Human Hematopoietic Stem/Progenitor Cells for Correction of Leukocyte Adhesion Deficiency Type 1.
Hum Gene Ther
; 33(23-24): 1293-1304, 2022 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-36094106
15.
Immunopathological signatures in multisystem inflammatory syndrome in children and pediatric COVID-19.
Nat Med
; 28(5): 1050-1062, 2022 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-35177862
16.
Multicenter analysis of neutrophil extracellular trap dysregulation in adult and pediatric COVID-19.
JCI Insight
; 7(16)2022 08 22.
Artigo
em Inglês
| MEDLINE | ID: mdl-35852866
17.
Phase I Study of Zotiraciclib in Combination with Temozolomide for Patients with Recurrent High-grade Astrocytomas.
Clin Cancer Res
; 27(12): 3298-3306, 2021 06 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-33785481
18.
An immune-based biomarker signature is associated with mortality in COVID-19 patients.
JCI Insight
; 6(1)2021 01 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-33232303
19.
Patients with Idiopathic Pulmonary Nontuberculous Mycobacterial Disease Have Normal Th1/Th2 Cytokine Responses but Diminished Th17 Cytokine and Enhanced Granulocyte-Macrophage Colony-Stimulating Factor Production.
Open Forum Infect Dis
; 6(12): ofz484, 2019 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-31807607
20.
NCF1 (p47phox)-deficient chronic granulomatous disease: comprehensive genetic and flow cytometric analysis.
Blood Adv
; 3(2): 136-147, 2019 01 22.
Artigo
em Inglês
| MEDLINE | ID: mdl-30651282