Hi, I am Yasemin Gulgun Isgor, My LiveDNA is 90.264
Dr. Yasemin Gulgun Isgor
Highest Degree: Ph.D. in Biochemistry from Ankara University, Ankara, Turkey
Institute: Gazi University, Ankara, Turkey
Area of Interest: Chemistry
  •   Mitogen Activated Protein Kinases (serine/threonine PK)
  •   Nonreceptor Tyrosine Kinases (Src Family)
  •   Mitochondrial molecular pathology and therapeutic Targeting
  •   Bioorganic Chemistry
URL: http://livedna.org/90.264
My SELECTED Publications
1:   Akbay, A., A. Bozbas, Y.G. Isgor, Y. Yavuz and S. Elgun, 2000. Serum dipeptidylpeptidase activity and tissue polypeptide specific antigen in patients with advanced cirrhosis: Preliminary results. Clin. Chim. Acta., 292: 181-185.
PubMed  |  Direct Link  |  
2:   Glover, C.J., A.A. Rabow, Y.G. Isgor, R.H. Shoemaker and D.G. Covell, 2007. Data mining of NCI's anticancer screening database reveals mitochondrial complex I inhibitors cytotoxic to leukemia cell lines. Biochem. Pharmacol., 73: 331-340.
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3:   Isgor, Y.G. and E.U. Akkaya, 1997. Chemosensing in deep red: A squaraine-based fluorescent chemosensor for pH. Tetrahedron Lett., 38: 7417-7420.
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4:   Isgor, Y.G., M. Iscan, H.S. Ozturk and I. Durak, 2008. Effects of water soluble garlic extract on human leukemia HL60 cell lines. Turk. J. Biochem., 33: 78-84.
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5:   Isgor, Y.G., Z. Kilic and S. Olgen, 2008. Novel aminomethylindole derivatives as inhibitors of pp60c-Src tyrosine kinase: Synthesis and biological activity. Chem. Biol. Drug. Des., 72: 599-604.
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6:   Kilic, Z., F. Sener, Y.G. Isgor, T. Coban and S. Olgen, 2010. N-substituted indole-3-imine derivatives and their amine congeners: antioxidant and Src kinase inhibitory effects. Z Naturforsch, 65: 347-354.
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7:   Kilic, Z., Y.G. Isgor and S. Olgen, 2009. Evaluation of new indole and bromoindole derivatives as pp60(c-Src) tyrosine kinase inhibitors. Chem. Biol. Drug. Des., 74: 397-404.
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8:   Kilic, Z., Y.G. Isgor and S. Olgen, 2009. Synthesis and pp60c-Src tyrosine kinase inhibitory activities of novel indole-3-imine and amine derivatives substituted at N1 and C5. Arch. Pharm. Chem. Life Sci., 342: 333-343.
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9:   Olgen, S., Y.G. Isgor and T. Coban, 2008. Synthesis and activity of novel 5-substituted pyrrolo[2,3-d]pyrimidine analogues as pp60(c-Src) tyrosine kinase inhibitors. Arch. Pharm. Chem. Life Sci., 341: 113-120.
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