Thrombopoietin receptor is required for the oncogenic function of CALR mutants
The result's identifiers
Result code in IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F65269705%3A_____%2F16%3A00065931" target="_blank" >RIV/65269705:_____/16:00065931 - isvavai.cz</a>
Alternative codes found
RIV/00216224:14110/16:00091729
Result on the web
<a href="http://www.nature.com/leu/journal/v30/n8/full/leu201632a.html" target="_blank" >http://www.nature.com/leu/journal/v30/n8/full/leu201632a.html</a>
DOI - Digital Object Identifier
<a href="http://dx.doi.org/10.1038/leu.2016.32" target="_blank" >10.1038/leu.2016.32</a>
Alternative languages
Result language
angličtina
Original language name
Thrombopoietin receptor is required for the oncogenic function of CALR mutants
Original language description
Myeloproliferative neoplasms (MPNs) are diseases characterized by the pathologic expansion of myeloid cells of the hematopoietic lineage. The three 'classical' MPNs include polycythemia vera (PV, increase in erythrocytes), essential thrombocythemia (ET, increase in platelets) and primary myelofibrosis (PMF, usually elevated platelet counts associated with fibrotic deposition in the bone marrow).1 MPNs are essentially clonal diseases driven by somatic mutations in hematopoietic stem and progenitor cells. So far, three genes have been identified that can drive the disease phenotype when mutated.2 Activating mutations in Janus Kinase 2 (JAK2) and the thrombopoietin receptor (MPL) have been known for close to a decade and their mechanism of action has been extensively studied.3-8 Recently, we and others identified somatic mutations in the CALR gene in 25-35% of ET and PMF patients.9,10
Czech name
—
Czech description
—
Classification
Type
J<sub>x</sub> - Unclassified - Peer-reviewed scientific article (Jimp, Jsc and Jost)
CEP classification
FD - Oncology and haematology
OECD FORD branch
—
Result continuities
Project
—
Continuities
I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace
Others
Publication year
2016
Confidentiality
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů
Data specific for result type
Name of the periodical
Leukemia
ISSN
0887-6924
e-ISSN
—
Volume of the periodical
30
Issue of the periodical within the volume
8
Country of publishing house
GB - UNITED KINGDOM
Number of pages
5
Pages from-to
1759-1763
UT code for WoS article
000380826400018
EID of the result in the Scopus database
—