Myelodysplastic syndromes and acute myeloid leukemia with mutations of the tumor suppressor gene TP53
The result's identifiers
Result code in IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00023736%3A_____%2F24%3A00013692" target="_blank" >RIV/00023736:_____/24:00013692 - isvavai.cz</a>
Result on the web
<a href="https://novapublishers.com/shop/advances-in-genetics-research-volume-22/" target="_blank" >https://novapublishers.com/shop/advances-in-genetics-research-volume-22/</a>
DOI - Digital Object Identifier
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Alternative languages
Result language
angličtina
Original language name
Myelodysplastic syndromes and acute myeloid leukemia with mutations of the tumor suppressor gene TP53
Original language description
TP53 gene mutations were detected in 10-20% of patients with de novo myelodysplastic syndromes (MDS) or acute myeloid leukemia (AML). The TP53 mutation is a common molecular abnormality in MDS and is associated with poor outcomes. These outcomes depend on the type of TP53 mutation and variant allele frequency (VAF).
Czech name
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Czech description
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Classification
Type
C - Chapter in a specialist book
CEP classification
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OECD FORD branch
30205 - Hematology
Result continuities
Project
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Continuities
I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace
Others
Publication year
2024
Confidentiality
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů
Data specific for result type
Book/collection name
Advances in genetics research: volume 22
ISBN
979-8-89113-693-9
Number of pages of the result
29
Pages from-to
37-65
Number of pages of the book
259
Publisher name
Nova Science
Place of publication
New York
UT code for WoS chapter
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