MUSILOVÁ, Milena, Filip RÁZGA, Tomáš JURČEK, Ivana JEŽÍŠKOVÁ, Marek BORSKÝ, Veronika NÉMETHOVÁ, Daniela ŽÁČKOVÁ, Martin ČULEN, Dana DVOŘÁKOVÁ, Jiří MAYER and Zdeněk RÁČIL. BCR-ABL1 kinase domain mutational analysis of CD34+ stem/progenitor cells in newly diagnosed CML patients by next-generation sequencing. American Journal of Hematology. Wiley-Blackwell, 2014, vol. 89, No 10, p. 1016-1017. ISSN 0361-8609. Available from: https://dx.doi.org/10.1002/ajh.23794.
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Basic information
Original name BCR-ABL1 kinase domain mutational analysis of CD34+ stem/progenitor cells in newly diagnosed CML patients by next-generation sequencing
Authors MUSILOVÁ, Milena (203 Czech Republic, belonging to the institution), Filip RÁZGA (703 Slovakia, belonging to the institution), Tomáš JURČEK (203 Czech Republic, belonging to the institution), Ivana JEŽÍŠKOVÁ (203 Czech Republic), Marek BORSKÝ (203 Czech Republic), Veronika NÉMETHOVÁ (703 Slovakia), Daniela ŽÁČKOVÁ (203 Czech Republic, belonging to the institution), Martin ČULEN (703 Slovakia, belonging to the institution), Dana DVOŘÁKOVÁ (203 Czech Republic, belonging to the institution), Jiří MAYER (203 Czech Republic, belonging to the institution) and Zdeněk RÁČIL (203 Czech Republic, guarantor, belonging to the institution).
Edition American Journal of Hematology, Wiley-Blackwell, 2014, 0361-8609.
Other information
Original language English
Type of outcome Article in a journal
Field of Study 30200 3.2 Clinical medicine
Country of publisher United States of America
Confidentiality degree is not subject to a state or trade secret
Impact factor Impact factor: 3.798
RIV identification code RIV/00216224:14110/14:00078340
Organization unit Faculty of Medicine
Doi http://dx.doi.org/10.1002/ajh.23794
UT WoS 000342689200021
Keywords in English BCR-ABL; CD34+; CML; next generation sequencing
Tags EL OK, podil, RIV, WOS
Tags International impact, Reviewed
Changed by Changed by: Soňa Böhmová, učo 232884. Changed: 13/3/2015 14:14.
Abstract
Mutations in the BCR-ABL1 kinase domain (KD) represent one of the most important causes of resistance to tyrosine kinase inhibitors (TKIs) treatment in patients with chronic myeloid leukemia (CML). The resistance-causing mutations are hypothesized to expand directly from the stem and/or progenitor cells and are present in CD341 cells significantly earlier than they occur in bone marrow or peripheral blood. Thus, early detection of these mutations is of great importance, since it can affect the subsequent TKI therapy.
Links
EE2.3.30.0037, research and development projectName: Zaměstnáním nejlepších mladých vědců k rozvoji mezinárodní spolupráce
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