Frequent alterations in messenger RNA splicing 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_____%2F18%3A00011943" target="_blank" >RIV/00023736:_____/18:00011943 - isvavai.cz</a>
Result on the web
<a href="https://www.novapublishers.com/catalog/product_info.php?products_id=63968" target="_blank" >https://www.novapublishers.com/catalog/product_info.php?products_id=63968</a>
DOI - Digital Object Identifier
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Alternative languages
Result language
angličtina
Original language name
Frequent alterations in messenger RNA splicing in myelodysplastic syndromes
Original language description
Author discusses splicing of pre-mRNAs coding for proteins. Since the discovery of frequent spliceosomal gene mutations which occur in about 65% of patients with myelodysplastic syndrome (MDS), we know that splicing factor gene mutations are the most frequent mutations found in MDS patients. Predominantly, four splicing factor genes (SF3B1, SRSF2, U2AF1, ZRSR2) are mutated in MDS and related malignancies.
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
V - Vyzkumna aktivita podporovana z jinych verejnych zdroju
Others
Publication year
2018
Confidentiality
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů
Data specific for result type
Book/collection name
mRNA: molecular biology, processing and function
ISBN
978-1-53613-168-0
Number of pages of the result
25
Pages from-to
97-122
Number of pages of the book
152
Publisher name
Nova Science
Place of publication
New York
UT code for WoS chapter
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