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.
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
4.
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
5.
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
6.
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
7.
Exome sequencing identifies recurring FLT3 N676K mutations in core-binding factor leukemia.
Blood
; 122(10): 1761-9, 2013 Sep 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-23878140
8.
Inactivation of TP53 correlates with disease progression and low miR-34a expression in previously treated chronic lymphocytic leukemia patients.
Blood
; 121(18): 3650-7, 2013 May 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-23525797
9.
DNA Repair and Chromosomal Translocations.
Recent Results Cancer Res
; 200: 1-37, 2015.
Artigo
em Inglês
| MEDLINE | ID: mdl-26376870
10.
The FLT3ITD mRNA level has a high prognostic impact in NPM1 mutated, but not in NPM1 unmutated, AML with a normal karyotype.
Blood
; 119(19): 4383-6, 2012 May 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-22374696
11.
GATA2 zinc finger 1 mutations associated with biallelic CEBPA mutations define a unique genetic entity of acute myeloid leukemia.
Blood
; 120(2): 395-403, 2012 Jul 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-22649106
12.
Acute myeloid leukemia is propagated by a leukemic stem cell with lymphoid characteristics in a mouse model of CALM/AF10-positive leukemia.
Cancer Cell
; 10(5): 363-74, 2006 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-17097559
13.
Biallelic ATP2B1 variants as a likely cause of a novel neurodevelopmental malformation syndrome with primary hypoparathyroidism.
Eur J Hum Genet
; 32(1): 125-129, 2024 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-37926713
14.
RUNX1 mutations in cytogenetically normal acute myeloid leukemia are associated with a poor prognosis and up-regulation of lymphoid genes.
Haematologica
; 97(12): 1909-15, 2012 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-22689681
15.
Monoallelic CEBPA mutations in normal karyotype acute myeloid leukemia: independent favorable prognostic factor within NPM1 mutated patients.
Ann Hematol
; 91(7): 1051-63, 2012 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-22362118
16.
Age-dependent frequencies of NPM1 mutations and FLT3-ITD in patients with normal karyotype AML (NK-AML).
Ann Hematol
; 91(1): 9-18, 2012 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-21744003
17.
Expression analysis of genes located in the minimally deleted regions of 13q14 and 11q22-23 in chronic lymphocytic leukemia-unexpected expression pattern of the RHO GTPase activator ARHGAP20.
Genes Chromosomes Cancer
; 50(7): 546-58, 2011 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-21500311
18.
Global reduction of the epigenetic H3K79 methylation mark and increased chromosomal instability in CALM-AF10-positive leukemias.
Blood
; 114(3): 651-8, 2009 Jul 16.
Artigo
em Inglês
| MEDLINE | ID: mdl-19443658
19.
Laboratory quality assessment of candidate gene panel testing for acute myeloid leukaemia: a joint ALLG / RCPAQAP initiative.
Pathology
; 53(4): 487-492, 2021 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-33272691
20.
Rapid and sensitive screening for CEBPA mutations in acute myeloid leukaemia.
Br J Haematol
; 143(2): 230-9, 2008 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-18752591