Güven GS - Search Results

1

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

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

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

4

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

5

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

6

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

7

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

8

A new syndrome presenting with dysmorphic facies, oculocutaneous albinism, glaucoma, cryptorchidism and mental retardation.

Seven M, Yosunkaya E, Yilmaz SB, Karaca E, Guven G, Yuksel A. Seven M, et al. Genet Couns. 2011;22(1):25-34. Genet Couns. 2011. PMID: 21614985

9

Sudden vision loss in a mucopolysaccharidosis I patient receiving enzyme replacement therapy.

Yosunkaya E, Karaca E, Yilmaz SB, Gezdirici A, Guven G, Seven M, Yuksel A. Yosunkaya E, et al. Genet Couns. 2011;22(4):371-6. Genet Couns. 2011. PMID: 22303797

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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