Detalhe da pesquisa
1.
Abnormal biomarkers predict complex FAS or FADD defects missed by exome sequencing.
J Allergy Clin Immunol
; 153(1): 297-308.e12, 2024 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-37979702
2.
Human RIPK1 deficiency causes combined immunodeficiency and inflammatory bowel diseases.
Proc Natl Acad Sci U S A
; 116(3): 970-975, 2019 01 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-30591564
3.
Distinct molecular response patterns of activating STAT3 mutations associate with penetrance of lymphoproliferation and autoimmunity.
Clin Immunol
; 210: 108316, 2020 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-31770611
4.
Activated PI3Kδ syndrome type 2: Two patients, a novel mutation, and review of the literature.
Pediatr Allergy Immunol
; 27(6): 640-4, 2016 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-27116393
5.
A distinct CD38+CD45RA+ population of CD4+, CD8+, and double-negative T cells is controlled by FAS.
J Exp Med
; 218(2)2021 02 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-33170215
6.
High-throughput detection of nuclear factor-kappaB activity using a sensitive oligo-based chemiluminescent enzyme-linked immunosorbent assay.
Int J Cancer
; 127(2): 404-11, 2010 Jul 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-19924814
7.
Long-term robustness of a T-cell system emerging from somatic rescue of a genetic block in T-cell development.
EBioMedicine
; 59: 102961, 2020 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-32841837