Form of presentation | Articles in international journals and collections |
Year of publication | 2013 |
Язык | английский |
|
Martynova Ekaterina Vladimirovna, author
Rizvanov Albert Anatolevich, author
Salafutdinov Ilnur Ildusovich, author
Soloveva Valeriya Vladimirovna, author
Khaybullina Svetlana Francevna, author
|
Bibliographic description in the original language |
Solovyeva V.V. Human Adipose Derived Stem Cells Do Not Alter Cytokine Secretion in Response To The Genetic Modification With pEGFP-N2 Plasmid DNA / V.V. Solovyeva, I.I. Salafutdinov, E.V. Martynova, S.F. Khaiboullina, A.A. Rizvanov // World Applied Sciences Journal. – 2013. – Vol.26, No.7. – P.968-972. |
Annotation |
Adipose tissue contain progenitor cells with regenerative (angiogenic, neuroprotection, trophic etc.) potential and treatment based on adipose tissue-derived stem cells (ADSCs) transplantation may constitute a promising therapy. Genetic modification of stem cells with genes encoding growth factors and other biologically active molecules might further increase therapeutic efficiency. However, there is a question about the advantages and disadvantages of such gene/stem cell therapy. For a better understanding of the mechanisms occurring in organism after cell transplantation we should first study cell behavior
in vitro. Here we report results of ADSCs transfection with plasmid DNA pEGFP-N2 and subsequent study of cytokines and chemokines secretion using Luminex technology. |
Keywords |
Plasmid, pEGFP-N2, Cytokines, Chemokines, Human Adipose Derived Stem Cells, Transfection |
The name of the journal |
World Applied Sciences Journal
|
URL |
http://www.idosi.org/wasj/wasj26%287%2913/21.pdf |
Please use this ID to quote from or refer to the card |
https://repository.kpfu.ru/eng/?p_id=94046&p_lang=2 |
Full metadata record |
Field DC |
Value |
Language |
dc.contributor.author |
Martynova Ekaterina Vladimirovna |
ru_RU |
dc.contributor.author |
Rizvanov Albert Anatolevich |
ru_RU |
dc.contributor.author |
Salafutdinov Ilnur Ildusovich |
ru_RU |
dc.contributor.author |
Soloveva Valeriya Vladimirovna |
ru_RU |
dc.contributor.author |
Khaybullina Svetlana Francevna |
ru_RU |
dc.date.accessioned |
2013-01-01T00:00:00Z |
ru_RU |
dc.date.available |
2013-01-01T00:00:00Z |
ru_RU |
dc.date.issued |
2013 |
ru_RU |
dc.identifier.citation |
Solovyeva V.V. Human Adipose Derived Stem Cells Do Not Alter Cytokine Secretion in Response To The Genetic Modification With pEGFP-N2 Plasmid DNA / V.V. Solovyeva, I.I. Salafutdinov, E.V. Martynova, S.F. Khaiboullina, A.A. Rizvanov // World Applied Sciences Journal. – 2013. – Vol.26, No.7. – P.968-972. |
ru_RU |
dc.identifier.uri |
https://repository.kpfu.ru/eng/?p_id=94046&p_lang=2 |
ru_RU |
dc.description.abstract |
World Applied Sciences Journal |
ru_RU |
dc.description.abstract |
Adipose tissue contain progenitor cells with regenerative (angiogenic, neuroprotection, trophic etc.) potential and treatment based on adipose tissue-derived stem cells (ADSCs) transplantation may constitute a promising therapy. Genetic modification of stem cells with genes encoding growth factors and other biologically active molecules might further increase therapeutic efficiency. However, there is a question about the advantages and disadvantages of such gene/stem cell therapy. For a better understanding of the mechanisms occurring in organism after cell transplantation we should first study cell behavior
in vitro. Here we report results of ADSCs transfection with plasmid DNA pEGFP-N2 and subsequent study of cytokines and chemokines secretion using Luminex technology. |
ru_RU |
dc.language.iso |
ru |
ru_RU |
dc.subject |
Plasmid |
ru_RU |
dc.subject |
pEGFP-N2 |
ru_RU |
dc.subject |
Cytokines |
ru_RU |
dc.subject |
Chemokines |
ru_RU |
dc.subject |
Human Adipose Derived Stem Cells |
ru_RU |
dc.subject |
Transfection |
ru_RU |
dc.title |
Human Adipose Derived Stem Cells Do Not Alter Cytokine Secretion in Response To The Genetic Modification With pEGFP-N2 Plasmid DNA |
ru_RU |
dc.type |
Articles in international journals and collections |
ru_RU |
|