About: Frequent Chromatin Rearrangements in Myelodysplastic Syndromes - What Stands Behind?     Goto   Sponge   NotDistinct   Permalink

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  • 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.
  • 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. (en)
Title
  • Frequent Chromatin Rearrangements in Myelodysplastic Syndromes - What Stands Behind?
  • Frequent Chromatin Rearrangements in Myelodysplastic Syndromes - What Stands Behind? (en)
skos:prefLabel
  • Frequent Chromatin Rearrangements in Myelodysplastic Syndromes - What Stands Behind?
  • Frequent Chromatin Rearrangements in Myelodysplastic Syndromes - What Stands Behind? (en)
skos:notation
  • RIV/68081707:_____/14:00435477!RIV15-GA0-68081707
http://linked.open...avai/riv/aktivita
http://linked.open...avai/riv/aktivity
  • I, P(EE2.3.30.0030), P(GBP302/12/G157)
http://linked.open...iv/cisloPeriodika
  • 2014
http://linked.open...vai/riv/dodaniDat
http://linked.open...aciTvurceVysledku
http://linked.open.../riv/druhVysledku
http://linked.open...iv/duvernostUdaju
http://linked.open...titaPredkladatele
http://linked.open...dnocenehoVysledku
  • 17517
http://linked.open...ai/riv/idVysledku
  • RIV/68081707:_____/14:00435477
http://linked.open...riv/jazykVysledku
http://linked.open.../riv/klicovaSlova
  • myelodysplastic syndromes; chromosomal rearrangements; chromosome 5 deletions (en)
http://linked.open.../riv/klicoveSlovo
http://linked.open...odStatuVydavatele
  • CZ - Česká republika
http://linked.open...ontrolniKodProRIV
  • [5BEF539795D6]
http://linked.open...i/riv/nazevZdroje
  • Folia Biologica
http://linked.open...in/vavai/riv/obor
http://linked.open...ichTvurcuVysledku
http://linked.open...cetTvurcuVysledku
http://linked.open...vavai/riv/projekt
http://linked.open...UplatneniVysledku
http://linked.open...v/svazekPeriodika
  • 60
http://linked.open...iv/tvurceVysledku
  • Kozubek, Stanislav
  • Lukášová, Emilie
  • Pagáčová, Eva
  • Falk, Martin
  • Oltová, A.
  • Falková, Iva
  • Michalová, K.
  • Raška, I.
http://linked.open...ain/vavai/riv/wos
  • 000343275800001
issn
  • 0015-5500
number of pages
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