Guven GS - Search Results

1

DNA repair gene XRCC1 and XPD polymorphisms and their association with coronary artery disease risks and micronucleus frequency.

Guven M, Guven GS, Oz E, Ozaydin A, Batar B, Ulutin T, Hacihanefioglu S, Domanic N. Guven M, et al. Among authors: guven gs. Heart Vessels. 2007 Nov;22(6):355-60. doi: 10.1007/s00380-007-0986-9. Epub 2007 Nov 26. Heart Vessels. 2007. PMID: 18043991

2

Decreased DNA repair gene XRCC1 expression is associated with radiotherapy-induced acute side effects in breast cancer patients.

Batar B, Guven G, Eroz S, Bese NS, Guven M. Batar B, et al. Gene. 2016 May 10;582(1):33-7. doi: 10.1016/j.gene.2016.01.040. Epub 2016 Jan 27. Gene. 2016. PMID: 26826460

3

Polymorphisms of the DNA repair genes XPD and XRCC1 and the risk of age-related macular degeneration.

Görgün E, Güven M, Unal M, Batar B, Güven GS, Yenerel M, Tatlipinar S, Seven M, Yüksel A. Görgün E, et al. Among authors: guven gs, guven m. Invest Ophthalmol Vis Sci. 2010 Sep;51(9):4732-7. doi: 10.1167/iovs.09-4842. Epub 2010 Apr 7. Invest Ophthalmol Vis Sci. 2010. PMID: 20375340

4

DNA repair XRCC1 Arg399Gln polymorphism is associated with the risk of development of end-stage renal disease.

Trabulus S, Guven GS, Altiparmak MR, Batar B, Tun O, Yalin AS, Tunckale A, Guven M. Trabulus S, et al. Among authors: guven gs, guven m. Mol Biol Rep. 2012 Jun;39(6):6995-7001. doi: 10.1007/s11033-012-1529-8. Mol Biol Rep. 2012. PMID: 22302399

5

Enhanced sensitivity to oxidant-induced micronucleus frequency in elderly individuals is not associated with glutathione S-transferase M1 (GSTM1) null genotype in lymphocytes.

Guven GS, Guven M, Onaran I, Tunckale A, Hacihanefioglu S, Ulutin T. Guven GS, et al. Among authors: guven m. Gerontology. 2005 Jan-Feb;51(1):29-33. doi: 10.1159/000081431. Gerontology. 2005. PMID: 15591753

6

Glutathione S-transferase M1, GSTT1 and GSTP1 genetic polymorphisms and the risk of age-related macular degeneration.

Güven M, Görgün E, Ünal M, Yenerel M, Batar B, Küçümen B, Dinç UA, Güven GS, Ulus T, Yüksel A. Güven M, et al. Among authors: guven gs. Ophthalmic Res. 2011;46(1):31-7. doi: 10.1159/000321940. Epub 2011 Jan 5. Ophthalmic Res. 2011. PMID: 21212706

7

Relationship between genomic damage and clinical features in dialysis patients.

Guven GS, Altiparmak MR, Trabulus S, Yalin AS, Batar B, Tunckale A, Guven M. Guven GS, et al. Among authors: guven m. Genet Test Mol Biomarkers. 2013 Mar;17(3):202-6. doi: 10.1089/gtmb.2012.0301. Epub 2013 Jan 9. Genet Test Mol Biomarkers. 2013. PMID: 23301554

8

The influence of GSTM1 null genotype on susceptibility to in vitro oxidative stress.

Onaran I, Güven G, Ozaydin A, Ulutin T. Onaran I, et al. Toxicology. 2001 Jan 26;157(3):195-205. doi: 10.1016/s0300-483x(00)00358-9. Toxicology. 2001. PMID: 11164984

9

Expression of aphidicolin, FUdR and caffeine-induced fragile sites in lymphocytes of healthy Turkish individuals.

Güven GS, Hacihanefioğlu S, Cenani A. Güven GS, et al. Genetica. 1999;105(1):109-16. doi: 10.1023/a:1003799927024. Genetica. 1999. PMID: 10483096

10

Joubert syndrome co-existing with partial Xp trisomy: review of the literature.

Güven GS, Fenerci EY, Deviren A, Ozkiliç A, Yüksel A, Hacihanefioğlu S. Güven GS, et al. Genet Couns. 2004;15(3):321-8. Genet Couns. 2004. PMID: 15517825 Review.

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