Detalhe da pesquisa
1.
A deep intronic splice mutation of STAT3 underlies hyper IgE syndrome by negative dominance.
Proc Natl Acad Sci U S A
; 116(33): 16463-16472, 2019 08 13.
Artigo
em Inglês
| MEDLINE | ID: mdl-31346092
2.
T-cell defects in patients with ARPC1B germline mutations account for combined immunodeficiency.
Blood
; 132(22): 2362-2374, 2018 11 29.
Artigo
em Inglês
| MEDLINE | ID: mdl-30254128
3.
Human STAT3 variants underlie autosomal dominant hyper-IgE syndrome by negative dominance.
J Exp Med
; 218(8)2021 08 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-34137790
4.
Activity inhibition and crystal polymorphism induced by active-site metal swapping.
Acta Crystallogr D Struct Biol
; 73(Pt 8): 641-649, 2017 Aug 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-28777079