Detalhe da pesquisa
1.
Patients and mice with deficiency in the SNARE protein SYNTAXIN-11 have a secondary B cell defect.
J Exp Med
; 221(7)2024 Jul 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-38722309
2.
Antibody-mediated cellular responses are dysregulated in Multisystem Inflammatory Syndrome in Children (MIS-C).
bioRxiv
; 2024 Apr 18.
Artigo
em Inglês
| MEDLINE | ID: mdl-38659969
3.
Rare predicted loss-of-function variants of type I IFN immunity genes are associated with life-threatening COVID-19.
Genome Med
; 15(1): 22, 2023 04 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-37020259
4.
Respiratory viral infections in otherwise healthy humans with inherited IRF7 deficiency.
J Exp Med
; 219(7)2022 07 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-35670811
5.
Rare predicted loss-of-function variants of type I IFN immunity genes are associated with life-threatening COVID-19.
medRxiv
; 2022 Oct 25.
Artigo
em Inglês
| MEDLINE | ID: mdl-36324795
6.
Rodent and fly models in behavioral neuroscience: An evaluation of methodological advances, comparative research, and future perspectives.
Neurosci Biobehav Rev
; 120: 1-12, 2021 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-33242563
7.
Hobit identifies tissue-resident memory T cell precursors that are regulated by Eomes.
Sci Immunol
; 6(62)2021 08 20.
Artigo
em Inglês
| MEDLINE | ID: mdl-34417257
8.
Correction: Patients and mice with deficiency in the SNARE protein SYNTAXIN-11 have a secondary B cell defect.
J Exp Med
; 221(7)2024 Jul 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-38771261
9.
Correction: Rare predicted loss-of-function variants of type I IFN immunity genes are associated with life-threatening COVID-19.
Genome Med
; 16(1): 6, 2024 Jan 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-38184654
10.
Correction: Respiratory viral infections in otherwise healthy humans with inherited IRF7 deficiency.
J Exp Med
; 219(12)2022 Dec 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-36342405
11.
Multidisciplinary investigation links backward-speech trait and working memory through genetic mutation.
Sci Rep
; 6: 20369, 2016 Feb 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-26838027
12.
Genome-wide analysis identifies a role for common copy number variants in specific language impairment.
Eur J Hum Genet
; 23(10): 1370-7, 2015 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-25585696
13.
Genome-Wide Studies of Specific Language Impairment.
Curr Behav Neurosci Rep
; 1(4): 242-250, 2014.
Artigo
em Inglês
| MEDLINE | ID: mdl-25411653