Detalhe da pesquisa
1.
Human immune diversity: from evolution to modernity.
Nat Immunol
; 22(12): 1479-1489, 2021 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-34795445
2.
Antiapoptotic Mcl-1 is critical for the survival and niche-filling capacity of Foxp3⺠regulatory T cells.
Nat Immunol
; 14(9): 959-65, 2013 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-23852275
3.
A Pathology-based Case Series of Influenza- and COVID-19-associated Pulmonary Aspergillosis: The Proof Is in the Tissue.
Am J Respir Crit Care Med
; 208(3): 301-311, 2023 08 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-37311243
4.
DNA replication-associated inborn errors of immunity.
J Allergy Clin Immunol
; 151(2): 345-360, 2023 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-36395985
5.
Homozygous DBF4 mutation as a cause of severe congenital neutropenia.
J Allergy Clin Immunol
; 152(1): 266-277, 2023 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-36841265
6.
"IL-2 immunotherapy for targeting regulatory T cells in autoimmunity".
Genes Immun
; 24(5): 248-262, 2023 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-37741949
7.
CTLA4-Ig Effectively Controls Clinical Deterioration and Immune Condition in a Murine Model of Foxp3 Deficiency.
J Clin Immunol
; 43(6): 1393-1402, 2023 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-37156988
8.
Human Autosomal Recessive DNA Polymerase Delta 3 Deficiency Presenting as Omenn Syndrome.
J Clin Immunol
; 44(1): 2, 2023 12 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-38099988
9.
Regulatory T-cell stability and functional plasticity in health and disease.
Immunol Cell Biol
; 101(2): 112-129, 2023 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-36479949
10.
A Novel Homozygous Stop Mutation in IL23R Causes Mendelian Susceptibility to Mycobacterial Disease.
J Clin Immunol
; 42(8): 1638-1652, 2022 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-35829840
11.
Phenotypic analysis of pyrin-associated autoinflammation with neutrophilic dermatosis patients during treatment.
Rheumatology (Oxford)
; 60(11): 5436-5446, 2021 11 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-33693560
12.
Murine myeloproliferative disorder as a consequence of impaired collaboration between dendritic cells and CD4 T cells.
Blood
; 133(4): 319-330, 2019 01 24.
Artigo
em Inglês
| MEDLINE | ID: mdl-30333120
13.
Defective Sec61α1 underlies a novel cause of autosomal dominant severe congenital neutropenia.
J Allergy Clin Immunol
; 146(5): 1180-1193, 2020 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-32325141
14.
IFN-γ and CD25 drive distinct pathologic features during hemophagocytic lymphohistiocytosis.
J Allergy Clin Immunol
; 143(6): 2215-2226.e7, 2019 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-30578871
15.
Machine learning identifies an immunological pattern associated with multiple juvenile idiopathic arthritis subtypes.
Ann Rheum Dis
; 78(5): 617-628, 2019 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-30862608
16.
NFIL3 mutations alter immune homeostasis and sensitise for arthritis pathology.
Ann Rheum Dis
; 78(3): 342-349, 2019 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-30552177
17.
Multiple sclerosis risk variants alter expression of co-stimulatory genes in B cells.
Brain
; 141(3): 786-796, 2018 03 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-29361022
18.
Abnormal differentiation of B cells and megakaryocytes in patients with Roifman syndrome.
J Allergy Clin Immunol
; 142(2): 630-646, 2018 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-29391254
19.
Genetic ablation of IP3 receptor 2 increases cytokines and decreases survival of SOD1G93A mice.
Hum Mol Genet
; 25(16): 3491-3499, 2016 08 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-27378687
20.
Defective germinal center B-cell response and reduced arthritic pathology in microRNA-29a-deficient mice.
Cell Mol Life Sci
; 74(11): 2095-2106, 2017 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-28124096