Detalhe da pesquisa
1.
Partial RAG deficiency in humans induces dysregulated peripheral lymphocyte development and humoral tolerance defect with accumulation of T-bet+ B cells.
Nat Immunol
; 23(8): 1256-1272, 2022 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-35902638
2.
Clinical and Treatment History of Patients with Partial DiGeorge Syndrome and Autoimmune Cytopenia at Multiple Centers.
J Clin Immunol
; 44(2): 42, 2024 Jan 17.
Artigo
em Inglês
| MEDLINE | ID: mdl-38231436
3.
Lineage Reconstruction of In Vitro Identified Antigen-Specific Autoreactive B Cells from Adaptive Immune Receptor Repertoires.
Int J Mol Sci
; 24(1)2022 Dec 23.
Artigo
em Inglês
| MEDLINE | ID: mdl-36613668
4.
Correction to: Clinical and Treatment History of Patients with Partial DiGeorge Syndrome and Autoimmune Cytopenia at Multiple Centers.
J Clin Immunol
; 44(3): 72, 2024 Feb 29.
Artigo
em Inglês
| MEDLINE | ID: mdl-38421526
5.
Reduced numbers of circulating group 2 innate lymphoid cells in patients with common variable immunodeficiency.
Eur J Immunol
; 47(11): 1959-1969, 2017 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-28718914
6.
Ligase-4 Deficiency Causes Distinctive Immune Abnormalities in Asymptomatic Individuals.
J Clin Immunol
; 36(4): 341-53, 2016 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-27063650
7.
PRKDC mutations associated with immunodeficiency, granuloma, and autoimmune regulator-dependent autoimmunity.
J Allergy Clin Immunol
; 135(6): 1578-88.e5, 2015 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-25842288
8.
Identification of patients with RAG mutations previously diagnosed with common variable immunodeficiency disorders.
J Clin Immunol
; 35(2): 119-24, 2015 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-25516070
9.
Decline of FOXN1 gene expression in human thymus correlates with age: possible epigenetic regulation.
Immun Ageing
; 12: 18, 2015.
Artigo
em Inglês
| MEDLINE | ID: mdl-26516334
10.
Prevalence and clinical challenges among adults with primary immunodeficiency and recombination-activating gene deficiency.
J Allergy Clin Immunol
; 141(6): 2303-2306, 2018 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-29477728
11.
Adult-Onset Myopathy in a Patient with Hypomorphic RAG2 Mutations and Combined Immune Deficiency.
J Clin Immunol
; 38(6): 642-645, 2018 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-30159811
12.
Evolving Approach to Clinical Cytometry for Immunodeficiencies and Other Immune Disorders.
Clin Lab Med
; 43(3): 467-483, 2023 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-37481324
13.
B cell abnormalities and autoantibody production in patients with partial RAG deficiency.
Front Immunol
; 14: 1155380, 2023.
Artigo
em Inglês
| MEDLINE | ID: mdl-37475856
14.
Tissue transglutaminase contributes to the all-trans-retinoic acid-induced differentiation syndrome phenotype in the NB4 model of acute promyelocytic leukemia.
Blood
; 116(19): 3933-43, 2010 Nov 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-20739659
15.
Corrigendum: Case report: Initial treatment adjustments and complications in ovarian cancer patient with inborn error of immunity.
Front Oncol
; 12: 1007616, 2022.
Artigo
em Inglês
| MEDLINE | ID: mdl-36226071
16.
Dysregulated stem cell niches and altered lymphocyte recirculation cause B and T cell lymphopenia in WHIM syndrome.
Sci Immunol
; 7(75): eabo3170, 2022 09 23.
Artigo
em Inglês
| MEDLINE | ID: mdl-36149943
17.
Cellular Mechanisms Underlying B Cell Abnormalities in Patients With Gain-of-Function Mutations in the PIK3CD Gene.
Front Immunol
; 13: 890073, 2022.
Artigo
em Inglês
| MEDLINE | ID: mdl-35799777
18.
Impaired receptor editing and heterozygous RAG2 mutation in a patient with systemic lupus erythematosus and erosive arthritis.
J Allergy Clin Immunol
; 135(1): 272-3, 2015 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-25312763
19.
Asymptomatic Infant With Atypical SCID and Novel Hypomorphic RAG Variant Identified by Newborn Screening: A Diagnostic and Treatment Dilemma.
Front Immunol
; 11: 1954, 2020.
Artigo
em Inglês
| MEDLINE | ID: mdl-33117328
20.
Combined Immunodeficiency With Late-Onset Progressive Hypogammaglobulinemia and Normal B Cell Count in a Patient With RAG2 Deficiency.
Front Pediatr
; 7: 122, 2019.
Artigo
em Inglês
| MEDLINE | ID: mdl-31058115