Implications of TP53 allelic state for genome stability, clinical presentation and outcomes in myelodysplastic syndromes
The result's identifiers
Result code in IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00023736%3A_____%2F20%3A00013056" target="_blank" >RIV/00023736:_____/20:00013056 - isvavai.cz</a>
Result on the web
<a href="https://doi.org/10.1038/s41591-020-1008-z" target="_blank" >https://doi.org/10.1038/s41591-020-1008-z</a>
DOI - Digital Object Identifier
<a href="http://dx.doi.org/10.1038/s41591-020-1008-z" target="_blank" >10.1038/s41591-020-1008-z</a>
Alternative languages
Result language
angličtina
Original language name
Implications of TP53 allelic state for genome stability, clinical presentation and outcomes in myelodysplastic syndromes
Original language description
Tumor protein p53 (TP53) is the most frequently mutated gene in cancer. In patients with myelodysplastic syndromes (MDS), TP53 mutations are associated with high-risk disease, rapid transformation to acute myeloid leukemia (AML), resistance to conventional therapies and dismal outcomes. Consistent with the tumor-suppressive role of TP53, patients harbor both mono- and biallelic mutations. However, the biological and clinical implications of TP53 allelic state have not been fully investigated in MDS or any other cancer type.
Czech name
—
Czech description
—
Classification
Type
J<sub>ost</sub> - Miscellaneous article in a specialist periodical
CEP classification
—
OECD FORD branch
30205 - Hematology
Result continuities
Project
—
Continuities
I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace
Others
Publication year
2020
Confidentiality
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů
Data specific for result type
Name of the periodical
Nature Medicine
ISSN
1078-8956
e-ISSN
—
Volume of the periodical
26
Issue of the periodical within the volume
10
Country of publishing house
US - UNITED STATES
Number of pages
8
Pages from-to
1549-1556
UT code for WoS article
000616468700001
EID of the result in the Scopus database
2-s2.0-85088857953