Detalhe da pesquisa
1.
Mutations in MAP3K1 tilt the balance from SOX9/FGF9 to WNT/ß-catenin signaling.
Hum Mol Genet
; 23(4): 1073-83, 2014 Feb 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-24135036
2.
Loss-of-Function FANCL Mutations Associate with Severe Fanconi Anemia Overlapping the VACTERL Association.
Hum Mutat
; 36(5): 562-8, 2015 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-25754594
3.
Molecular mechanisms generating and stabilizing terminal 22q13 deletions in 44 subjects with Phelan/McDermid syndrome.
PLoS Genet
; 7(7): e1002173, 2011 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-21779178
4.
Variant Philadelphia translocations: molecular-cytogenetic characterization and prognostic influence on frontline imatinib therapy, a GIMEMA Working Party on CML analysis.
Blood
; 117(25): 6793-800, 2011 Jun 23.
Artigo
em Inglês
| MEDLINE | ID: mdl-21447834
5.
A novel, highly sensitive and rapid allele-specific loop-mediated amplification assay for the detection of the JAK2V617F mutation in chronic myeloproliferative neoplasms.
Haematologica
; 97(9): 1394-400, 2012 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-22315499
6.
Chronic myeloid leukemia: a prospective comparison of interphase fluorescence in situ hybridization and chromosome banding analysis for the definition of complete cytogenetic response: a study of the GIMEMA CML WP.
Blood
; 114(24): 4939-43, 2009 Dec 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-19797518
7.
Immature Immunoglobulin Gene Rearrangements Are Recurrent in B Precursor Adult Acute Lymphoblastic Leukemia Carrying TP53 Molecular Alterations.
Genes (Basel)
; 11(9)2020 08 20.
Artigo
em Inglês
| MEDLINE | ID: mdl-32825230
8.
Double homozygosity in CEP57 and DYNC2H1 genes detected by WES: Composite or expanded phenotype?
Mol Genet Genomic Med
; 8(3): e1064, 2020 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-31943948
9.
Frequent occurrence of non-malignant genetic alterations in clinical grade mesenchymal stromal cells expanded for cell therapy protocols.
Haematologica
; 99(6): e94-7, 2014 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-24682511
10.
Insertional translocation involving an additional nonchromothriptic chromosome in constitutional chromothripsis: Rule or exception?
Mol Genet Genomic Med
; 7(2): e00496, 2019 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-30565424
11.
Feasibility and outcome of tandem stem cell autotransplants in multiple myeloma.
Haematologica
; 90(12): 1643-9, 2005 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-16330437
12.
Prolonged administration of all-trans retinoic acid in combination with intensive chemotherapy and G-CSF for adult acute myelogenous leukemia: single-centre pilot study in different risk groups.
Hematol J
; 3(4): 193-200, 2002.
Artigo
em Inglês
| MEDLINE | ID: mdl-12189565
13.
Genomic quantitative real-time PCR proves residual disease positivity in more than 30% samples with negative mRNA-based qRT-PCR in Chronic Myeloid Leukemia.
Oncoscience
; 1(7): 510-21, 2014.
Artigo
em Inglês
| MEDLINE | ID: mdl-25594053
14.
The Polo-Like Kinase 1 (PLK1) inhibitor NMS-P937 is effective in a new model of disseminated primary CD56+ acute monoblastic leukaemia.
PLoS One
; 8(3): e58424, 2013.
Artigo
em Inglês
| MEDLINE | ID: mdl-23520509
15.
De novo balanced chromosome rearrangements in prenatal diagnosis.
Prenat Diagn
; 29(3): 257-65, 2009 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-19248039