Detalhe da pesquisa
1.
Genome-wide association study identifies novel susceptibility loci for KIT D816V positive mastocytosis.
Am J Hum Genet
; 108(2): 284-294, 2021 02 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-33421400
2.
Monitoring Intracellular Oxygen Concentration: Implications for Hypoxia Studies and Real-Time Oxygen Monitoring.
Adv Exp Med Biol
; 876: 257-263, 2016.
Artigo
em Inglês
| MEDLINE | ID: mdl-26782220
3.
In trans early mosaic mutational escape and novel phenotypic features of germline SAMD9 mutation.
Br J Haematol
; 188(4): e53-e57, 2020 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-31900929
4.
Routine Screening for KIT M541L Is Not Warranted in the Diagnostic Work-Up of Patients with Hypereosinophilia.
Acta Haematol
; 139(2): 71-73, 2018.
Artigo
em Inglês
| MEDLINE | ID: mdl-29393093
5.
Ruxolitinib, a potent JAK1/JAK2 inhibitor, induces temporary reductions in the allelic burden of concurrent CSF3R mutations in chronic neutrophilic leukemia.
Haematologica
; 102(6): e238-e240, 2017 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-28302714
6.
Differential Requirement of Gata2a and Gata2b for Primitive and Definitive Myeloid Development in Zebrafish.
Front Cell Dev Biol
; 9: 708113, 2021.
Artigo
em Inglês
| MEDLINE | ID: mdl-34589480
7.
A versatile, automated and high-throughput drug screening platform for zebrafish embryos.
Biol Open
; 10(9)2021 09 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-34472582
8.
TLR7 ligation augments hematopoiesis in Rps14 (uS11) deficiency via paradoxical suppression of inflammatory signaling.
Blood Adv
; 5(20): 4112-4124, 2021 10 26.
Artigo
em Inglês
| MEDLINE | ID: mdl-34432872
9.
PRR14L mutations are associated with chromosome 22 acquired uniparental disomy, age-related clonal hematopoiesis and myeloid neoplasia.
Leukemia
; 33(5): 1184-1194, 2019 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-30573780
10.
Recurrent activating STAT5B N642H mutation in myeloid neoplasms with eosinophilia.
Leukemia
; 33(2): 415-425, 2019 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-30573779