This is a Demo Server. Data inside this system is only for test purpose.

Veri Setleri

Permanent URI for this collectionhttp://65.108.157.135:4000/handle/123456789/17

Browse

Browsing Veri Setleri by Author "Erdoğan, İpek"

Filter results by typing the first few letters
Now showing 1 - 2 of 2
  • Thumbnail Image
    Data Paper
    Small RNA data set that includes tRNA-derived fragments from Jurkat cells treated with camptothecin
    (Elsevier Ltd., 2018-04) Coşacak, Mehmet İlyas; Akgül, Bünyamin; Erdoğan, İpek; Nalbant, Ayten; Akgül, Bünyamin
    In this article, we report a small RNA data set obtained from human T cell acute leukemia Jurkat cells, which were treated with the universal apoptotic agent camptothecin. Based on the Annexin-V labeling pattern, we sorted two Jurkat subpopulations in treated cells: one that is sensitive to the drug and the other being relatively more resistant. We report new original data that include the frequency of tRNA-derived fragments (tRF) in drug-sensitive and resistant cells. We also present partially analyzed data to show the origin of reads on tRNAs as well as the borders of the fragments. We believe that this data can benefit the science community working in the field of tRF and/or apoptosis.
  • Thumbnail Image
    Data Paper
    Citation Count: 0
    Small RNA data set that includes tRNA-derived fragments from Jurkat cells treated with camptothecin
    (Elsevier Ltd., 2018-04) Coşacak, Mehmet İlyas; Akgül, Bünyamin; Erdoğan, İpek; Nalbant, Ayten; Akgül, Bünyamin
    In this article, we report a small RNA data set obtained from human T cell acute leukemia Jurkat cells, which were treated with the universal apoptotic agent camptothecin. Based on the Annexin-V labeling pattern, we sorted two Jurkat subpopulations in treated cells: one that is sensitive to the drug and the other being relatively more resistant. We report new original data that include the frequency of tRNA-derived fragments (tRF) in drug-sensitive and resistant cells. We also present partially analyzed data to show the origin of reads on tRNAs as well as the borders of the fragments. We believe that this data can benefit the science community working in the field of tRF and/or apoptosis.