Biblio
Evaluating the expression of oct4 as a prognostic tumor marker in bladder cancer. Iran J Basic Med Sci. 2012;15(6):1154-61.
. A novel in vitro model for cancer stem cell culture using ectopically expressed piwil2 stable cell line. Cell J. 2013;15(3):250-7.
. . Potential roles of 5´ UTR and 3´ UTR regions in post-trans-criptional regulation of mouse Oct4 gene in BMSC and P19 cells. Iran J Basic Med Sci. 2014;17(7):490-496.
. Comparing The Effects of Small Molecules BIX-01294, Bay K8644, RG-108 and Valproic Acid, and Their Different Combinations on Induction of Pluripotency Marker-Genes by Oct4 in The Mouse Brain. Cell J. 2015;16(4):416-25.
. Enrichment of A Rare Subpopulation of miR-302-Expressing Glioma Cells by Serum Deprivation. Cell J. 2015;16(4):494-505.
. Evaluation of the expressions pattern of miR-10b, 21, 200c, 373 and 520c to find the correlation between epithelial-to-mesenchymal transition and melanoma stem cell potential in isolated cancer stem cells. Cell Mol Biol Lett. 2015;20(3):448-465.
. Verification of ALDH Activity as a Biomarker in Colon Cancer Stem Cells-Derived HT-29 Cell Line. Iran J Cancer Prev. 2015;8(5):e3446.
. CD133 Is Not Suitable Marker for Isolating Melanoma Stem Cells from D10 Cell Line. Cell J. 2016;18(1):21-7.
. Differential Expression of OCT4 Pseudogenes in Pluripotent and Tumor Cell Lines. Cell J. 2016;18(1):28-36.
. Generation of a human iPSC line harboring a biallelic large deletion at the INK4 locus (HMGUi001-A-5). Stem Cell Res. 2020;47:101927.
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