Number of the records: 1  

Frequent Chromatin Rearrangements in Myelodysplastic Syndromes - What Stands Behind?

  1. 1.
    SYSNO ASEP0435477
    Document TypeJ - Journal Article
    R&D Document TypeJournal Article
    Subsidiary JČlánek ve WOS
    TitleFrequent 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) RID
    Number of authors8
    Source TitleFolia Biologica. - : Univerzita Karlova v Praze - ISSN 0015-5500
    Roč. 60, č. 2014 (2014), s. 1-7
    Number of pages8 s.
    Publication formPrint - P
    Languageeng - English
    CountryCZ - Czech Republic
    Keywordsmyelodysplastic syndromes ; chromosomal rearrangements ; chromosome 5 deletions
    Subject RIVBO - Biophysics
    R&D ProjectsGBP302/12/G157 GA ČR - Czech Science Foundation (CSF)
    EE2.3.30.0030 GA MŠMT - Ministry of Education, Youth and Sports (MEYS)
    Institutional supportBFU-R - RVO:68081707
    UT WOS000343275800001
    AnnotationMyelodysplastic 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.
    WorkplaceInstitute of Biophysics
    ContactJana Poláková, polakova@ibp.cz, Tel.: 541 517 244
    Year of Publishing2015
Number of the records: 1  

  This site uses cookies to make them easier to browse. Learn more about how we use cookies.