Number of the records: 1
Frequent Chromatin Rearrangements in Myelodysplastic Syndromes - What Stands Behind?
- 1.
SYSNO ASEP 0435477 Document Type J - Journal Article R&D Document Type Journal Article Subsidiary J Článek ve WOS Title Frequent Chromatin Rearrangements in Myelodysplastic Syndromes - What Stands Behind? Author(s) Pagáčová, Eva (BFU-R) ORCID
Falk, Martin (BFU-R) RID, ORCID
Falková, Iva (BFU-R) ORCID
Lukášová, Emilie (BFU-R) RID, ORCID
Michalová, K. (CZ)
Oltová, A. (CZ)
Raška, I. (CZ)
Kozubek, Stanislav (BFU-R) RIDNumber of authors 8 Source Title Folia Biologica. - : Univerzita Karlova v Praze - ISSN 0015-5500
Roč. 60, č. 2014 (2014), s. 1-7Number of pages 8 s. Publication form Print - P Language eng - English Country CZ - Czech Republic Keywords myelodysplastic syndromes ; chromosomal rearrangements ; chromosome 5 deletions Subject RIV BO - Biophysics R&D Projects GBP302/12/G157 GA ČR - Czech Science Foundation (CSF) EE2.3.30.0030 GA MŠMT - Ministry of Education, Youth and Sports (MEYS) Institutional support BFU-R - RVO:68081707 UT WOS 000343275800001 Annotation Myelodysplastic syndromes (MDS) represent a clinically and genetically heterogeneous group of clonal haematopoietic diseases characterized by a short survival and high rate of transformation to acute myeloid leukaemia (AML). In spite of this variability, MDS is associated with typical recurrent non-random cytogenetic defects. Chromosomal abnormalities are detected in the malignant bone-marrow cells of approximately 40-80 % of patients with primary or secondary MDS. The most frequent chromosomal rearrangements involve chromosomes 5, 7 and 8. MDS often shows presence of unbalanced chromosomal changes, especially large deletions [del(5), del(7q), del(12p), del(18q), del(20q)] or losses of whole chromosomes (7 and Y). The most typical cytogenetic abnormality is a partial or complete deletion of 5q- that occurs in roughly 30 % of all MDS cases either as the sole abnormality or in combination with other aberrations as a part of frequently complex karyotypes. The mechanisms responsible for the formation of MDS-associated recurrent trans-locations and complex karyotypes are unknown. Workplace Institute of Biophysics Contact Jana Poláková, polakova@ibp.cz, Tel.: 541 517 244 Year of Publishing 2015
Number of the records: 1