The effect of clinically relevant doses of immunosuppressive drugs on human mesenchymal stem cells
The result's identifiers
Result code in IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F68378041%3A_____%2F18%3A00480546" target="_blank" >RIV/68378041:_____/18:00480546 - isvavai.cz</a>
Alternative codes found
RIV/00216208:11310/18:10385161
Result on the web
<a href="http://dx.doi.org/10.1016/j.biopha.2017.10.114" target="_blank" >http://dx.doi.org/10.1016/j.biopha.2017.10.114</a>
DOI - Digital Object Identifier
<a href="http://dx.doi.org/10.1016/j.biopha.2017.10.114" target="_blank" >10.1016/j.biopha.2017.10.114</a>
Alternative languages
Result language
angličtina
Original language name
The effect of clinically relevant doses of immunosuppressive drugs on human mesenchymal stem cells
Original language description
This paper is focused on the effects of a panel of immunosuppresive drugs on phenotype and function properties of human mesenchymal stem cells - MSC. It is shown that MSC are more resistant to a toxic effect of immunosuppressive drugs than are lymphocytes. Thus, during the immunotherapy, conbined application of immunosuppressive drugs and MSCs can be used.
Czech name
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Czech description
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Classification
Type
J<sub>imp</sub> - Article in a specialist periodical, which is included in the Web of Science database
CEP classification
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OECD FORD branch
10601 - Cell biology
Result continuities
Project
Result was created during the realization of more than one project. More information in the Projects tab.
Continuities
P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)
Others
Publication year
2018
Confidentiality
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů
Data specific for result type
Name of the periodical
Biomedicine & Pharmacotherapy
ISSN
0753-3322
e-ISSN
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Volume of the periodical
97
Issue of the periodical within the volume
jan
Country of publishing house
FR - FRANCE
Number of pages
10
Pages from-to
402-411
UT code for WoS article
000419041300051
EID of the result in the Scopus database
2-s2.0-85032286656