Detalhe da pesquisa
1.
FLT3L governs the development of partially overlapping hematopoietic lineages in humans and mice.
Cell
; 187(11): 2817-2837.e31, 2024 May 23.
Artigo
em Inglês
| MEDLINE | ID: mdl-38701783
2.
Clinical and functional spectrum of RAC2-related immunodeficiency.
Blood
; 143(15): 1476-1487, 2024 Apr 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-38194689
3.
Human kidney-derived hematopoietic stem cells can support long-term multilineage hematopoiesis.
Kidney Int
; 103(1): 70-76, 2023 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-36108807
4.
A combination of cyclophosphamide and interleukin-2 allows CD4+ T cells converted to Tregs to control scurfy syndrome.
Blood
; 137(17): 2326-2336, 2021 04 29.
Artigo
em Inglês
| MEDLINE | ID: mdl-33545713
5.
NHP2 deficiency impairs rRNA biogenesis and causes pulmonary fibrosis and Høyeraal-Hreidarsson syndrome.
Hum Mol Genet
; 29(6): 907-922, 2020 04 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-31985013
6.
A gain-of-function RAC2 mutation is associated with bone-marrow hypoplasia and an autosomal dominant form of severe combined immunodeficiency.
Haematologica
; 106(2): 404-411, 2021 02 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-31919089
7.
Reticular dysgenesis: international survey on clinical presentation, transplantation, and outcome.
Blood
; 129(21): 2928-2938, 2017 05 25.
Artigo
em Inglês
| MEDLINE | ID: mdl-28331055
8.
Plerixafor enables safe, rapid, efficient mobilization of hematopoietic stem cells in sickle cell disease patients after exchange transfusion.
Haematologica
; 103(5): 778-786, 2018 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-29472357
9.
X-linked primary immunodeficiency associated with hemizygous mutations in the moesin (MSN) gene.
J Allergy Clin Immunol
; 138(6): 1681-1689.e8, 2016 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-27405666
10.
Improving the diagnostic efficiency of primary immunodeficiencies with targeted next-generation sequencing.
J Allergy Clin Immunol
; 147(2): 734-737, 2021 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-32531373
11.
An in vivo genetic reversion highlights the crucial role of Myb-Like, SWIRM, and MPN domains 1 (MYSM1) in human hematopoiesis and lymphocyte differentiation.
J Allergy Clin Immunol
; 136(6): 1619-1626.e5, 2015 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-26220525
12.
The BLNK adaptor protein has a nonredundant role in human B-cell differentiation.
J Allergy Clin Immunol
; 134(1): 145-54, 2014 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-24582315
13.
Recombination-activating gene 1 (Rag1)-deficient mice with severe combined immunodeficiency treated with lentiviral gene therapy demonstrate autoimmune Omenn-like syndrome.
J Allergy Clin Immunol
; 133(4): 1116-23, 2014 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-24332219
14.
Generation of adult human T-cell progenitors for immunotherapeutic applications.
J Allergy Clin Immunol
; 141(4): 1491-1494.e4, 2018 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-29208547
15.
Comprehensive genetic profiling reveals frequent alterations of driver genes on the X chromosome in extranodal NK/T-cell lymphoma.
Cancer Res
; 2024 Apr 24.
Artigo
em Inglês
| MEDLINE | ID: mdl-38657099
16.
Gene-corrected human Munc13-4-deficient CD8+ T cells can efficiently restrict EBV-driven lymphoproliferation in immunodeficient mice.
Blood
; 128(24): 2859-2862, 2016 12 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-27799161
17.
Human T-lymphoid progenitors generated in a feeder-cell-free Delta-like-4 culture system promote T-cell reconstitution in NOD/SCID/γc(-/-) mice.
Stem Cells
; 30(8): 1771-80, 2012 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-22689616
18.
A neomorphic mutation in the interferon activation domain of IRF4 causes a dominant primary immunodeficiency.
J Exp Med
; 220(6)2023 06 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-36917008
19.
Severe hematopoietic stem cell inflammation compromises chronic granulomatous disease gene therapy.
Cell Rep Med
; 4(2): 100919, 2023 02 21.
Artigo
em Inglês
| MEDLINE | ID: mdl-36706754
20.
Adenylate kinase 2 expression and addiction in T-ALL.
Blood Adv
; 5(3): 700-710, 2021 02 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-33560378