Gorukmez O - Search Results

1

Association of the ACE I/D gene polymorphisms with JAK2V617F-positive polycythemia vera and essential thrombocythemia.

Gorukmez O, Sag ŞO, Gorukmez Ö, Ture M, Topak A, Sahinturk S, Ozkaya G, Gulten T, Ali R, Yakut T. Gorukmez O, et al. Genet Test Mol Biomarkers. 2015 Jun;19(6):303-8. doi: 10.1089/gtmb.2014.0334. Epub 2015 May 8. Genet Test Mol Biomarkers. 2015. PMID: 25955555

2

Lack of association of ACE gene I/D polymorphism with obstructive sleep apnea syndrome in Turkish patients.

Yakut T, Karkucak M, Ursavas A, Gulten T, Burgazlioglu B, Gorukmez O, Karadag M. Yakut T, et al. Among authors: gorukmez o. Genet Mol Res. 2010 Apr 20;9(2):734-8. doi: 10.4238/vol9-2gmr755. Genet Mol Res. 2010. PMID: 20449805 Free article.

3

Lack of association of genetic polymorphisms of angiotensin-converting enzyme gene I/D and glutathione-S-transferase enzyme T1 and M1 with retinopathy of prematures.

Yildiz M, Karkucak M, Yakut T, Gorukmez O, Ozmen A. Yildiz M, et al. Among authors: gorukmez o. Genet Mol Res. 2010 Oct 26;9(4):2131-9. doi: 10.4238/vol9-4gmr887. Genet Mol Res. 2010. PMID: 21038299 Free article.

4

Evaluation of the JAK2-V617F gene mutation in Turkish patients with essential thrombocythemia and polycythemia vera.

Karkucak M, Yakut T, Ozkocaman V, Ozkalemkas F, Ali R, Bayram M, Gorukmez O, Ocakoglu G. Karkucak M, et al. Among authors: gorukmez o. Mol Biol Rep. 2012 Sep;39(9):8663-7. doi: 10.1007/s11033-012-1721-x. Epub 2012 Jun 22. Mol Biol Rep. 2012. PMID: 22722988

5

Effect of cyclin [corrected] D1 (CCND1) gene polymorphism on tumor formation and behavior in patients with prolactinoma.

Cander S, Ertürk E, Karkucak M, Oz Gül O, Görükmez O, Yakut T, Unal OK, Ersoy C, Tuncel E, Imamoğlu S. Cander S, et al. Among authors: gorukmez o. Gene. 2012 Nov 1;509(1):158-63. doi: 10.1016/j.gene.2012.07.056. Epub 2012 Aug 8. Gene. 2012. PMID: 22967707

6

Cathecol-O-methyl transferase Val158Met genotype is not a risk factor for conversion disorder.

Armagan E, Almacıoglu ML, Yakut T, Köse A, Karkucak M, Köksal O, Görükmez O. Armagan E, et al. Among authors: gorukmez o. Genet Mol Res. 2013 Mar 19;12(1):852-8. doi: 10.4238/2013.March.19.1. Genet Mol Res. 2013. PMID: 23613193 Free article.

7

Another small supernumerary marker chromosome derived from chromosome 9 in a Klinefelter patient.

Gulten T, Gorukmez O, Gorukmez O, Karkucak M, Ture M, Yakut T. Gulten T, et al. Among authors: gorukmez o. West Indian Med J. 2012 Dec;61(9):924-7. doi: 10.7727/wimj.2012.027. West Indian Med J. 2012. PMID: 24020236

8

MMP2 gene-735 C/T and MMP9 gene -1562 C/T polymorphisms in JAK2V617F positive myeloproliferative disorders.

Sag SO, Gorukmez O, Ture M, Gorukmez O, Topak A, Sahinturk S, Ocakoglu G, Gulten T, Ali R, Yakut T. Sag SO, et al. Among authors: gorukmez o. Asian Pac J Cancer Prev. 2015;16(2):443-9. doi: 10.7314/apjcp.2015.16.2.443. Asian Pac J Cancer Prev. 2015. PMID: 25684469 Free article.

9

De novo partial trisomy distal 4q: a case report.

Gorukmez O, Sag SO, Gorukmez O, Ture M, Gulten T, Yakut T. Gorukmez O, et al. Genet Couns. 2014;25(4):423-8. Genet Couns. 2014. PMID: 25804022

10

A novel mutation in the FRAS1 gene in a patient with Fraser syndrome.

Ozemri Sag S, Gorukmez O, Gorukmez O, Ture M, Sahinturk S, Topak A, Gulten T, Schanze D, Yakut T, Zenker M. Ozemri Sag S, et al. Among authors: gorukmez o. Genet Couns. 2015;26(1):21-7. Genet Couns. 2015. PMID: 26043503

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