Detalhe da pesquisa
1.
Persistent Hypogammaglobulinemia after Receiving Rituximab Post-HSCT Is Not Caused by an Intrinsic B Cell Defect.
Int J Mol Sci
; 24(21)2023 Nov 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-37958995
2.
Modeling altered T-cell development with induced pluripotent stem cells from patients with RAG1-dependent immune deficiencies.
Blood
; 128(6): 783-93, 2016 08 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-27301863
3.
Cysteine and hydrophobic residues in CDR3 serve as distinct T-cell self-reactivity indices.
J Allergy Clin Immunol
; 144(1): 333-336, 2019 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-31053347
4.
Abnormalities of T-cell receptor repertoire in CD4+ regulatory and conventional T cells in patients with RAG mutations: Implications for autoimmunity.
J Allergy Clin Immunol
; 140(6): 1739-1743.e7, 2017 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-28864286
5.
Advances in gene therapy for inborn errors of immunity.
Curr Opin Allergy Clin Immunol
; 23(6): 467-477, 2023 12 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-37846903
6.
Partial correction of immunodeficiency by lentiviral vector gene therapy in mouse models carrying Rag1 hypomorphic mutations.
Front Immunol
; 14: 1268620, 2023.
Artigo
em Inglês
| MEDLINE | ID: mdl-38022635
7.
Human JAK1 gain of function causes dysregulated myelopoeisis and severe allergic inflammation.
JCI Insight
; 7(24)2022 12 22.
Artigo
em Inglês
| MEDLINE | ID: mdl-36546480
8.
Perinatal Infections With Ureaplasma.
Pediatr Infect Dis J
; 40(5S): S26-S30, 2021 05 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-34042907
9.
EXTL3 mutations cause skeletal dysplasia, immune deficiency, and developmental delay.
J Exp Med
; 214(3): 623-637, 2017 03 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-28148688
10.
Natural Killer Cells from Patients with Recombinase-Activating Gene and Non-Homologous End Joining Gene Defects Comprise a Higher Frequency of CD56bright NKG2A+++ Cells, and Yet Display Increased Degranulation and Higher Perforin Content.
Front Immunol
; 8: 798, 2017.
Artigo
em Inglês
| MEDLINE | ID: mdl-28769923
11.
Corrigendum: Natural Killer Cells from Patients with Recombinase-Activating Gene and Non-Homologous End Joining Gene Defects Comprise a Higher Frequency of CD56bright NKG2A+++ Cells, and Yet Display Increased Degranulation and Higher Perforin Content.
Front Immunol
; 8: 1244, 2017.
Artigo
em Inglês
| MEDLINE | ID: mdl-29042861
12.
Rapid generation of novel models of RAG1 deficiency by CRISPR/Cas9-induced mutagenesis in murine zygotes.
Oncotarget
; 7(11): 12962-74, 2016 Mar 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-26887046
13.
Characterization of T and B cell repertoire diversity in patients with RAG deficiency.
Sci Immunol
; 1(6)2016 12 16.
Artigo
em Inglês
| MEDLINE | ID: mdl-28783691
14.
Novel Genome-Editing Tools to Model and Correct Primary Immunodeficiencies.
Front Immunol
; 6: 250, 2015.
Artigo
em Inglês
| MEDLINE | ID: mdl-26052330