Pathogenetic role of ETV6 fusion gene in leukemic transformation of myelodysplastic syndrome refractory anemia with excess blasts-1 with a new, rare translocation t(11;19)(q24.3;q13.12) and insertion ins(6;12)(p22.3p13)
The result's identifiers
Result code in IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F61989592%3A15110%2F14%3A33145790" target="_blank" >RIV/61989592:15110/14:33145790 - isvavai.cz</a>
Alternative codes found
RIV/00098892:_____/14:#0000661
Result on the web
<a href="http://dx.doi.org/10.3109/10428194.2013.814127" target="_blank" >http://dx.doi.org/10.3109/10428194.2013.814127</a>
DOI - Digital Object Identifier
<a href="http://dx.doi.org/10.3109/10428194.2013.814127" target="_blank" >10.3109/10428194.2013.814127</a>
Alternative languages
Result language
angličtina
Original language name
Pathogenetic role of ETV6 fusion gene in leukemic transformation of myelodysplastic syndrome refractory anemia with excess blasts-1 with a new, rare translocation t(11;19)(q24.3;q13.12) and insertion ins(6;12)(p22.3p13)
Original language description
Myelodysplastic syndrome (MDS) refers to a group of clonal disorders originating from hematopoietic stem cells, and is characterized by ineff ective diff erentiation of hematopoietic progenitors, bone marrow dysplasia, genetic instability and, often, a propensity to develop acute myeloid leukemia (AML). Th e molecular pathogenesis of MDS and the main cause for its progression to AML remain largely undefi ned. Early mutations in stem cells may cause diff erentiation arrest, leading to dysplasia, whereassubsequent defects aff ecting myeloid cell proliferation may cause the clonal expansion of aberrant cells and frank AML [1]. Although many chromosomal abnormalities have been detected in MDS, the genes involved in the pathogenesis have yet to be identified. According to a recently published new scoring system proposal, a total of fi ve prognostic subgroups were confi rmed, with 19 cytogenetic categories being defi ned [2]. With the exception of a complex karyotype, all detected chromoso
Czech name
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Czech description
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Classification
Type
J<sub>x</sub> - Unclassified - Peer-reviewed scientific article (Jimp, Jsc and Jost)
CEP classification
FD - Oncology and haematology
OECD FORD branch
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Result continuities
Project
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Continuities
I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace
Others
Publication year
2014
Confidentiality
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů
Data specific for result type
Name of the periodical
Leukemia & Lymphoma
ISSN
1042-8194
e-ISSN
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Volume of the periodical
55
Issue of the periodical within the volume
4
Country of publishing house
GB - UNITED KINGDOM
Number of pages
4
Pages from-to
950-953
UT code for WoS article
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EID of the result in the Scopus database
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