Ustek D - Search Results

1

Mitochondrial DNA profiling via genomic analysis in mesial temporal lobe epilepsy patients with hippocampal sclerosis.

Gurses C, Azakli H, Alptekin A, Cakiris A, Abaci N, Arikan M, Kursun O, Gokyigit A, Ustek D. Gurses C, et al. Among authors: ustek d. Gene. 2014 Apr 1;538(2):323-7. doi: 10.1016/j.gene.2014.01.030. Epub 2014 Jan 16. Gene. 2014. PMID: 24440288

2

Whole mitochondrial DNA variations in hippocampal surgical specimens and blood samples with high-throughput sequencing: a case of mesial temporal lobe epilepsy with hippocampal sclerosis.

Azakli H, Gurses C, Arikan M, Aydoseli A, Aras Y, Sencer A, Gokyigit A, Bilgic B, Ustek D. Azakli H, et al. Among authors: ustek d. Gene. 2013 Oct 15;529(1):190-4. doi: 10.1016/j.gene.2013.06.077. Epub 2013 Jul 18. Gene. 2013. PMID: 23872536

3

A genome-wide analysis of lentivector integration sites using targeted sequence capture and next generation sequencing technology.

Ustek D, Sirma S, Gumus E, Arikan M, Cakiris A, Abaci N, Mathew J, Emrence Z, Azakli H, Cosan F, Cakar A, Parlak M, Kursun O. Ustek D, et al. Infect Genet Evol. 2012 Oct;12(7):1349-54. doi: 10.1016/j.meegid.2012.05.001. Epub 2012 May 14. Infect Genet Evol. 2012. PMID: 22613802

4

Whole mitochondrial genome analysis of a family with NARP/MILS caused by m.8993T>C mutation in the MT-ATP6 gene.

Kara B, Arıkan M, Maraş H, Abacı N, Cakıris A, Ustek D. Kara B, et al. Among authors: ustek d. Mol Genet Metab. 2012 Nov;107(3):389-93. doi: 10.1016/j.ymgme.2012.06.013. Epub 2012 Jul 10. Mol Genet Metab. 2012. PMID: 22819295

5

Mitochondrial mutations in patients with congenital heart defects by next generation sequencing technology.

Abaci N, Arıkan M, Tansel T, Sahin N, Cakiris A, Pacal F, Sırma Ekmekci S, Gök E, Üstek D. Abaci N, et al. Among authors: ustek d. Cardiol Young. 2015 Apr;25(4):705-11. doi: 10.1017/S1047951114000754. Epub 2014 Jun 10. Cardiol Young. 2015. PMID: 24912974

6

Role of the line probe assay INNO-LiPA HBV DR and ultradeep pyrosequencing in detecting resistance mutations to nucleoside/nucleotide analogues in viral samples isolated from chronic hepatitis B patients.

Mese S, Arikan M, Cakiris A, Abaci N, Gumus E, Kursun O, Onel D, Ustek D, Kaymakoglu S, Badur S, Yenen OS, Bozkaya E. Mese S, et al. Among authors: ustek d. J Gen Virol. 2013 Dec;94(Pt 12):2729-2738. doi: 10.1099/vir.0.053041-0. Epub 2013 Sep 17. J Gen Virol. 2013. PMID: 24045109

7

Analysis of potential antiviral resistance mutation profiles within the HBV reverse transcriptase in untreated chronic hepatitis B patients using an ultra-deep pyrosequencing method.

Ciftci S, Keskin F, Cakiris A, Akyuz F, Pinarbasi B, Abaci N, Dincer E, Badur S, Kaymakoglu S, Ustek D. Ciftci S, et al. Among authors: ustek d. Diagn Microbiol Infect Dis. 2014 May;79(1):25-30. doi: 10.1016/j.diagmicrobio.2014.01.005. Epub 2014 Jan 14. Diagn Microbiol Infect Dis. 2014. PMID: 24630522

8

Association of familial Mediterranean fever-related MEFV variations with ankylosing spondylitis.

Cosan F, Ustek D, Oku B, Duymaz-Tozkir J, Cakiris A, Abaci N, Ocal L, Aral O, Gül A. Cosan F, et al. Among authors: ustek d. Arthritis Rheum. 2010 Nov;62(11):3232-6. doi: 10.1002/art.27683. Arthritis Rheum. 2010. PMID: 20669279 Free article.

9

MEFV gene 3'-UTR Alu repeat polymorphisms in patients with familial Mediterranean fever.

Ustek D, Ekmekçi C, Oku B, Coşan F, Cakiris A, Abaci N, Celik S, Kamali S, Hatemi G, Kasapçopur O, Ozdoğan H, Gül A. Ustek D, et al. Clin Exp Rheumatol. 2008 Jul-Aug;26(4 Suppl 50):S72-6. Clin Exp Rheumatol. 2008. PMID: 19026119

10

No association of the TLR2 gene Arg753Gln polymorphism with rheumatic heart disease and Behçet's disease.

Coşan F, Oku B, Cakiris A, Duymaz-Tozkir J, Mercanoğlu F, Saruhan-Direskeneli G, Ustek D, Gül A. Coşan F, et al. Among authors: ustek d. Clin Rheumatol. 2009 Dec;28(12):1385-8. doi: 10.1007/s10067-009-1252-6. Epub 2009 Aug 21. Clin Rheumatol. 2009. PMID: 19693643

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