Detalhe da pesquisa
1.
Plexin D1 negatively regulates zebrafish lymphatic development.
Development
; 149(21)2022 11 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-36205097
2.
Contribution of mutant HSC clones to immature and mature cells in MDS and CMML, and variations with AZA therapy.
Blood
; 141(11): 1316-1321, 2023 03 16.
Artigo
em Inglês
| MEDLINE | ID: mdl-36493342
3.
Deletion of Grin1 in mouse megakaryocytes reveals NMDA receptor role in platelet function and proplatelet formation.
Blood
; 139(17): 2673-2690, 2022 04 28.
Artigo
em Inglês
| MEDLINE | ID: mdl-35245376
4.
Molecular profiling of patients with cytogenetically normal acute myeloid leukemia and hyperleukocytosis.
Cancer
; 128(24): 4213-4222, 2022 12 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-36271776
5.
Mutations in HID1 Cause Syndromic Infantile Encephalopathy and Hypopituitarism.
Ann Neurol
; 90(1): 143-158, 2021 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-33999436
6.
Lysine acetyltransferase Tip60 is required for hematopoietic stem cell maintenance.
Blood
; 136(15): 1735-1747, 2020 10 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-32542325
7.
The cell of origin and the leukemia stem cell in acute myeloid leukemia.
Genes Chromosomes Cancer
; 58(12): 850-858, 2019 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-31471945
8.
Functional CRISPR and shRNA Screens Identify Involvement of Mitochondrial Electron Transport in the Activation of Evofosfamide.
Mol Pharmacol
; 95(6): 638-651, 2019 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-30979813
9.
Mutations in SEC24D, encoding a component of the COPII machinery, cause a syndromic form of osteogenesis imperfecta.
Am J Hum Genet
; 96(3): 432-9, 2015 Mar 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-25683121
10.
GPR56 identifies primary human acute myeloid leukemia cells with high repopulating potential in vivo.
Blood
; 127(16): 2018-27, 2016 Apr 21.
Artigo
em Inglês
| MEDLINE | ID: mdl-26834243
11.
Spectrum and prognostic relevance of driver gene mutations in acute myeloid leukemia.
Blood
; 128(5): 686-98, 2016 08 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-27288520
12.
Genetics of acute myeloid leukemia in the elderly: mutation spectrum and clinical impact in intensively treated patients aged 75 years or older.
Haematologica
; 103(11): 1853-1861, 2018 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-29903761
13.
A 29-gene and cytogenetic score for the prediction of resistance to induction treatment in acute myeloid leukemia.
Haematologica
; 103(3): 456-465, 2018 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-29242298
14.
A fluorescence in situ hybridization-based screen allows rapid detection of adverse cytogenetic alterations in patients with acute myeloid leukemia.
Genes Chromosomes Cancer
; 56(8): 632-638, 2017 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-28420034
15.
Acute myeloid leukemia with del(9q) is characterized by frequent mutations of NPM1, DNMT3A, WT1 and low expression of TLE4.
Genes Chromosomes Cancer
; 56(1): 75-86, 2017 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-27636548
16.
Adults with Philadelphia chromosome-like acute lymphoblastic leukemia frequently have IGH-CRLF2 and JAK2 mutations, persistence of minimal residual disease and poor prognosis.
Haematologica
; 102(1): 130-138, 2017 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-27561722
17.
Close correlation of copy number aberrations detected by next-generation sequencing with results from routine cytogenetics in acute myeloid leukemia.
Genes Chromosomes Cancer
; 55(7): 553-67, 2016 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-27015608
18.
A 4-gene expression score associated with high levels of Wilms Tumor-1 (WT1) expression is an adverse prognostic factor in acute myeloid leukaemia.
Br J Haematol
; 172(3): 401-11, 2016 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-26597595
19.
Isolated trisomy 13 defines a homogeneous AML subgroup with high frequency of mutations in spliceosome genes and poor prognosis.
Blood
; 124(8): 1304-11, 2014 Aug 21.
Artigo
em Inglês
| MEDLINE | ID: mdl-24923295
20.
A mutation in the 5'-UTR of IFITM5 creates an in-frame start codon and causes autosomal-dominant osteogenesis imperfecta type V with hyperplastic callus.
Am J Hum Genet
; 91(2): 349-57, 2012 Aug 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-22863195