Detalhe da pesquisa
1.
Class Switch Recombination Defects: impact on B cell maturation and antibody responses.
Clin Immunol
; 222: 108638, 2021 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-33276124
2.
Somatic Genetic Reversion of a Duplication Event in IL2RG in Siblings.
J Clin Immunol
; 43(8): 1747-1750, 2023 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-37481508
3.
A novel gain-of-function IKBA mutation underlies ectodermal dysplasia with immunodeficiency and polyendocrinopathy.
J Clin Immunol
; 33(6): 1088-99, 2013 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-23708964
4.
Comèl-Netherton syndrome defined as primary immunodeficiency.
J Allergy Clin Immunol
; 124(3): 536-43, 2009 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-19683336
5.
Novel signal transducer and activator of transcription 3 (STAT3) mutations, reduced T(H)17 cell numbers, and variably defective STAT3 phosphorylation in hyper-IgE syndrome.
J Allergy Clin Immunol
; 122(1): 181-7, 2008 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-18602572
6.
Heterozygous signal transducer and activator of transcription 3 mutations in hyper-IgE syndrome result in altered B-cell maturation.
J Allergy Clin Immunol
; 129(2): 559-62, 562.e1-2, 2012 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-22030463
7.
STAT3 mutation in the original patient with Job's syndrome.
N Engl J Med
; 357(16): 1667-8, 2007 Oct 18.
Artigo
em Inglês
| MEDLINE | ID: mdl-17942886