Detalles de la búsqueda
1.
The Dicentric Chromosome dic(20;22) Is a Recurrent Abnormality in Myelodysplastic Syndromes and Is a Product of Telomere Fusion.
Cytogenet Genome Res
; 150(3-4): 262-272, 2016.
Artículo
en Inglés
| MEDLINE | ID: mdl-28259884
2.
The paradox of 20q11.21 amplification in a subset of cases of myeloid malignancy with chromosome 20 deletion.
Genes Chromosomes Cancer
; 49(11): 998-1013, 2010 Nov.
Artículo
en Inglés
| MEDLINE | ID: mdl-20645416
3.
Detailed molecular cytogenetic characterisation of the myeloid cell line U937 reveals the fate of homologous chromosomes and shows that centromere capture is a feature of genome instability.
Mol Cytogenet
; 13(1): 50, 2020 Dec 14.
Artículo
en Inglés
| MEDLINE | ID: mdl-33317567
4.
BCL-XL inhibition by BH3-mimetic drugs induces apoptosis in models of Epstein-Barr virus-associated T/NK-cell lymphoma.
Blood Adv
; 4(19): 4775-4787, 2020 10 13.
Artículo
en Inglés
| MEDLINE | ID: mdl-33017468
5.
Hemopoietic Cell Kinase amplification with Protein Tyrosine Phosphatase Receptor T depletion leads to polycythemia, aberrant marrow erythoid maturation, and splenomegaly.
Sci Rep
; 9(1): 7050, 2019 05 07.
Artículo
en Inglés
| MEDLINE | ID: mdl-31065022
6.
Analysis of Chromothripsis by Combined FISH and Microarray Analysis.
Methods Mol Biol
; 1769: 53-77, 2018.
Artículo
en Inglés
| MEDLINE | ID: mdl-29564818
7.
MACROD2 Haploinsufficiency Impairs Catalytic Activity of PARP1 and Promotes Chromosome Instability and Growth of Intestinal Tumors.
Cancer Discov
; 8(8): 988-1005, 2018 08.
Artículo
en Inglés
| MEDLINE | ID: mdl-29880585
8.
ETV6 deletion is a common additional abnormality in patients with myelodysplastic syndromes or acute myeloid leukemia and monosomy 7.
Haematologica
; 97(12): 1933-6, 2012 Dec.
Artículo
en Inglés
| MEDLINE | ID: mdl-22875624
9.
Active centromere and chromosome identification in fixed cell lines.
Mol Cytogenet
; 9: 28, 2016.
Artículo
en Inglés
| MEDLINE | ID: mdl-27011768
10.
A comparison of two contrasting recurrent isochromosomes 20 found in myelodysplastic syndromes suggests that retention of proximal 20q is a significant factor in myeloid malignancies.
Cancer Genet Cytogenet
; 163(2): 176-9, 2005 Dec.
Artículo
en Inglés
| MEDLINE | ID: mdl-16337864
11.
Recurrent duplication of Xq27-qter in hematological malignancies revealed by multicolor fluorescence in situ hybridization and multicolor banding.
Cancer Genet Cytogenet
; 161(2): 125-9, 2005 Sep.
Artículo
en Inglés
| MEDLINE | ID: mdl-16102582
12.
Src family kinases and their role in hematological malignancies.
Leuk Lymphoma
; 56(3): 577-86, 2015 Mar.
Artículo
en Inglés
| MEDLINE | ID: mdl-24898666
13.
Chromothripsis under the microscope: a cytogenetic perspective of two cases of AML with catastrophic chromosome rearrangement.
Cancer Genet
; 206(6): 238-51, 2013 Jun.
Artículo
en Inglés
| MEDLINE | ID: mdl-23911237
14.
Genome organization and the role of centromeres in evolution of the erythroleukaemia cell line HEL.
Evol Med Public Health
; 2013(1): 225-40, 2013 Jan.
Artículo
en Inglés
| MEDLINE | ID: mdl-24481202
15.
CGH and SNP array using DNA extracted from fixed cytogenetic preparations and long-term refrigerated bone marrow specimens.
Mol Cytogenet
; 5: 10, 2012 Feb 02.
Artículo
en Inglés
| MEDLINE | ID: mdl-22300816
16.
The use of M-FISH and M-BAND to define chromosome abnormalities.
Methods Mol Biol
; 730: 203-18, 2011.
Artículo
en Inglés
| MEDLINE | ID: mdl-21431644
17.
The role of dicentric chromosome formation and secondary centromere deletion in the evolution of myeloid malignancy.
Genet Res Int
; 2011: 643628, 2011.
Artículo
en Inglés
| MEDLINE | ID: mdl-22567363
18.
Unbalanced translocations of 20q in AML and MDS often involve interstitial rather than terminal deletions of 20q.
Cancer Genet
; 204(3): 153-61, 2011 Mar.
Artículo
en Inglés
| MEDLINE | ID: mdl-21504715
19.
A cryptic deletion in 5q31.2 provides further evidence for a minimally deleted region in myelodysplastic syndromes.
Cancer Genet
; 204(4): 187-94, 2011 Apr.
Artículo
en Inglés
| MEDLINE | ID: mdl-21536236
20.
A FISH comparison of variant derivatives of the recurrent dic(17;20) of myelodysplastic syndromes and acute myeloid leukemia: Obligatory retention of genes on 17p and 20q may explain the formation of dicentric chromosomes.
Genes Chromosomes Cancer
; 46(1): 27-36, 2007 Jan.
Artículo
en Inglés
| MEDLINE | ID: mdl-17048234