Detalhe da pesquisa
1.
FLT3L governs the development of partially overlapping hematopoietic lineages in humans and mice.
Cell;
2024 May 02.
Artigo
em Inglês
| MEDLINE
| ID: mdl-38701783
2.
Human inherited CCR2 deficiency underlies progressive polycystic lung disease.
Cell;
187(2): 390-408.e23, 2024 01 18.
Artigo
em Inglês
| MEDLINE
| ID: mdl-38157855
3.
Human MCTS1-dependent translation of JAK2 is essential for IFN-γ immunity to mycobacteria.
Cell;
186(23): 5114-5134.e27, 2023 11 09.
Artigo
em Inglês
| MEDLINE
| ID: mdl-37875108
4.
Human IRF1 governs macrophagic IFN-γ immunity to mycobacteria.
Cell;
186(3): 621-645.e33, 2023 02 02.
Artigo
em Inglês
| MEDLINE
| ID: mdl-36736301
5.
Human T-bet Governs Innate and Innate-like Adaptive IFN-γ Immunity against Mycobacteria.
Cell;
183(7): 1826-1847.e31, 2020 12 23.
Artigo
em Inglês
| MEDLINE
| ID: mdl-33296702
6.
Genome-wide association study of resistance to Mycobacterium tuberculosis infection identifies a locus at 10q26.2 in three distinct populations.
PLoS Genet;
17(3): e1009392, 2021 03.
Artigo
em Inglês
| MEDLINE
| ID: mdl-33661925
7.
Clinical, Immunological, and Genetic Findings in Iranian Patients with MHC-II Deficiency: Confirmation of c.162delG RFXANK Founder Mutation in the Iranian Population.
J Clin Immunol;
43(8): 1941-1952, 2023 Nov.
Artigo
em Inglês
| MEDLINE
| ID: mdl-37584719
8.
Common homozygosity for predicted loss-of-function variants reveals both redundant and advantageous effects of dispensable human genes.
Proc Natl Acad Sci U S A;
117(24): 13626-13636, 2020 06 16.
Artigo
em Inglês
| MEDLINE
| ID: mdl-32487729
9.
Taking population stratification into account by local permutations in rare-variant association studies on small samples.
Genet Epidemiol;
45(8): 821-829, 2021 12.
Artigo
em Inglês
| MEDLINE
| ID: mdl-34402542
10.
Homozygosity for TYK2 P1104A underlies tuberculosis in about 1% of patients in a cohort of European ancestry.
Proc Natl Acad Sci U S A;
116(21): 10430-10434, 2019 05 21.
Artigo
em Inglês
| MEDLINE
| ID: mdl-31068474
11.
Neutralizing IFN-γ autoantibodies are rare and pathogenic in HLA-DRB1*15:02 or 16:02 individuals.
J Clin Invest;
134(8)2024 Mar 12.
Artigo
em Inglês
| MEDLINE
| ID: mdl-38470480
12.
Human inherited PD-L1 deficiency is clinically and immunologically less severe than PD-1 deficiency.
J Exp Med;
221(6)2024 Jun 03.
Artigo
em Inglês
| MEDLINE
| ID: mdl-38634869
13.
Helper T cell immunity in humans with inherited CD4 deficiency.
J Exp Med;
221(5)2024 May 06.
Artigo
em Inglês
| MEDLINE
| ID: mdl-38557723
14.
The immunopathological landscape of human pre-TCRα deficiency: From rare to common variants.
Science;
383(6686): eadh4059, 2024 03.
Artigo
em Inglês
| MEDLINE
| ID: mdl-38422122
15.
Inborn errors of OAS-RNase L in SARS-CoV-2-related multisystem inflammatory syndrome in children.
Science;
379(6632): eabo3627, 2023 02 10.
Artigo
em Inglês
| MEDLINE
| ID: mdl-36538032
16.
Inherited human ITK deficiency impairs IFN-γ immunity and underlies tuberculosis.
J Exp Med;
220(1)2023 01 02.
Artigo
em Inglês
| MEDLINE
| ID: mdl-36326697
17.
Human IL-23 is essential for IFN-γ-dependent immunity to mycobacteria.
Sci Immunol;
8(80): eabq5204, 2023 02 17.
Artigo
em Inglês
| MEDLINE
| ID: mdl-36763636
18.
Encephalitis and poor neuronal death-mediated control of herpes simplex virus in human inherited RIPK3 deficiency.
Sci Immunol;
8(82): eade2860, 2023 04 21.
Artigo
em Inglês
| MEDLINE
| ID: mdl-37083451
19.
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
20.
Impaired IL-23-dependent induction of IFN-γ underlies mycobacterial disease in patients with inherited TYK2 deficiency.
J Exp Med;
219(10)2022 10 03.
Artigo
em Inglês
| MEDLINE
| ID: mdl-36094518