Detalhe da pesquisa
1.
Multiplexed Functional Assessment of Genetic Variants in CARD11.
Am J Hum Genet
; 107(6): 1029-1043, 2020 12 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-33202260
2.
Gain-of-function mutations in CARD11 promote enhanced aggregation and idiosyncratic signalosome assembly.
Cell Immunol
; 353: 104129, 2020 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-32473470
3.
Hypomorphic caspase activation and recruitment domain 11 (CARD11) mutations associated with diverse immunologic phenotypes with or without atopic disease.
J Allergy Clin Immunol
; 143(4): 1482-1495, 2019 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-30170123
4.
Sensitivity to Restimulation-Induced Cell Death Is Linked to Glycolytic Metabolism in Human T Cells.
J Immunol
; 198(1): 147-155, 2017 01 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-27852741
5.
SAP facilitates recruitment and activation of LCK at NTB-A receptors during restimulation-induced cell death.
J Immunol
; 192(9): 4202-9, 2014 May 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-24688028
6.
Germline CARD11 Mutation in a Patient with Severe Congenital B Cell Lymphocytosis.
J Clin Immunol
; 35(1): 32-46, 2015 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-25352053
7.
Contemporaneous sample data tracking for the generation of genome edited cell lines.
Sci Rep
; 12(1): 21359, 2022 12 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-36494450
8.
Mild B-cell lymphocytosis in patients with a CARD11 C49Y mutation.
J Allergy Clin Immunol
; 136(3): 819-821.e1, 2015 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-25930198
9.
A Unique Heterozygous CARD11 Mutation Combines Pathogenic Features of Both Gain- and Loss-of-Function Patients in a Four-Generation Family.
Front Immunol
; 9: 2944, 2018.
Artigo
em Inglês
| MEDLINE | ID: mdl-30619304
10.
Germline hypomorphic CARD11 mutations in severe atopic disease.
Nat Genet
; 49(8): 1192-1201, 2017 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-28628108
11.
Corrigendum: Germline hypomorphic CARD11 mutations in severe atopic disease.
Nat Genet
; 49(11): 1661, 2017 10 27.
Artigo
em Inglês
| MEDLINE | ID: mdl-29074947
12.
Congenital B cell lymphocytosis explained by novel germline CARD11 mutations.
J Exp Med
; 209(12): 2247-61, 2012 Nov 19.
Artigo
em Inglês
| MEDLINE | ID: mdl-23129749