Gulten T - Search Results

1

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: gulten t. 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.

2

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. Among authors: gulten t. 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

3

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: gulten t. Genet Mol Res. 2010 Apr 20;9(2):734-8. doi: 10.4238/vol9-2gmr755. Genet Mol Res. 2010. PMID: 20449805 Free article.

4

Spectrum of EGFR gene mutations and ALK rearrangements in lung cancer patients in Turkey.

Sag SO, Gorukmez O, Ture M, Gorukmez O, Deligonul A, Sahinturk S, Topak A, Gulten T, Kurt E, Yakut T. Sag SO, et al. Among authors: gulten t. Springerplus. 2016 Apr 19;5:482. doi: 10.1186/s40064-016-2150-4. eCollection 2016. Springerplus. 2016. PMID: 27217997 Free PMC article.

5

Qualitative and quantitative evaluation of the BCR-ABL fusion gene in chronic myelogenous leukemia by flourescence in situ hybridization and molecular genetic methods.

Ozemri Sag S, Yakut T, Gorukmez O, Gorukmez O, Ture M, Karkucak M, Gulten T, Ali R. Ozemri Sag S, et al. Among authors: gulten t. Genet Test Mol Biomarkers. 2015 Oct;19(10):584-8. doi: 10.1089/gtmb.2015.0056. Epub 2015 Aug 26. Genet Test Mol Biomarkers. 2015. PMID: 26308792

6

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. West Indian Med J. 2012 Dec;61(9):924-7. doi: 10.7727/wimj.2012.027. West Indian Med J. 2012. PMID: 24020236

7

The variant translocation of ABL1 gene t(2;9)(q21;q34) in a childhood T-cell acute lymphoblastic leukemia.

Karkucak M, Yakut T, Baytan B, Gulten T, Gunes AM. Karkucak M, et al. Among authors: gulten t. Bratisl Lek Listy. 2012;113(1):19-20. doi: 10.4149/bll_2012_004. Bratisl Lek Listy. 2012. PMID: 22380496

8

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: gulten t. Genet Couns. 2015;26(1):21-7. Genet Couns. 2015. PMID: 26043503

9

AML1 amplification and 17q25 deletion in a case of childhood acute lymphoblastic leukemia.

Gulten T, Yakut T, Karkucak M, Baytan B, Guneş AM. Gulten T, et al. J Clin Lab Anal. 2009;23(6):368-71. doi: 10.1002/jcla.20343. J Clin Lab Anal. 2009. PMID: 19927343 Free PMC article.

10

TURNER SYNDROME WITH 45,X/46,X,I(Xq)/47,X,I(Xq),I(Xq) KARYOTYPE.

Gorukmez O, Sag SO, Gulten T, Gorukmez, Ture M, Yakut T. Gorukmez O, et al. Among authors: gulten t. Genet Couns. 2015;26(2):267-9. Genet Couns. 2015. PMID: 26349201 No abstract available.

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