Ozkul Y - Search Results

1

Serum micro-rna profiles in patients with autosomal dominant polycystic kidney disease according to hypertension and renal function.

Kocyigit I, Taheri S, Sener EF, Eroglu E, Ozturk F, Unal A, Korkmaz K, Zararsiz G, Sipahioglu MH, Ozkul Y, Tokgoz B, Oymak O, Ecder T, Axelsson J. Kocyigit I, et al. Among authors: ozkul y. BMC Nephrol. 2017 May 30;18(1):179. doi: 10.1186/s12882-017-0600-z. BMC Nephrol. 2017. PMID: 28558802 Free PMC article.

2

An overview of the genetic aspects of hair loss and its connection with nutrition.

Gokce N, Basgoz N, Kenanoglu S, Akalin H, Ozkul Y, Ergoren MC, Beccari T, Bertelli M, Dundar M. Gokce N, et al. Among authors: ozkul y. J Prev Med Hyg. 2022 Oct 17;63(2 Suppl 3):E228-E238. doi: 10.15167/2421-4248/jpmh2022.63.2S3.2765. eCollection 2022 Jun. J Prev Med Hyg. 2022. PMID: 36479473 Free PMC article. Review.

3

Apolipoprotein E3/E3 genotype decreases the risk of pituitary dysfunction after traumatic brain injury due to various causes: preliminary data.

Tanriverdi F, Taheri S, Ulutabanca H, Caglayan AO, Ozkul Y, Dundar M, Selcuklu A, Unluhizarci K, Casanueva FF, Kelestimur F. Tanriverdi F, et al. Among authors: ozkul y. J Neurotrauma. 2008 Sep;25(9):1071-7. doi: 10.1089/neu.2007.0456. J Neurotrauma. 2008. PMID: 18707245

4

Methylation status of CpG islands at sites -59 to +96 in exon 1 of the BRCA2 gene varies in mammary tissue among women with sporadic breast cancer.

Cucer N, Taheri S, Ok E, Ozkul Y. Cucer N, et al. Among authors: ozkul y. J Genet. 2008 Aug;87(2):155-8. doi: 10.1007/s12041-008-0023-5. J Genet. 2008. PMID: 18776644 No abstract available.

5

Expression of WT1 gene in multiple myeloma patients at diagnosis: is WT1 gene expression a useful marker in multiple myeloma?

Saatci C, Caglayan AO, Kocyigit I, Akalin H, Kaynar LG, Altuntas F, Eser B, Demir M, Cetin M, Ozkul Y. Saatci C, et al. Among authors: ozkul y. Hematology. 2010 Feb;15(1):39-42. doi: 10.1179/102453310X12583347009496. Hematology. 2010. PMID: 20132661 Free article.

6

A molecular analysis of familial Mediterranean fever disease in a cohort of Turkish patients.

Dundar M, Kiraz A, Emirogullari EF, Saatci CE, Taheri S, Baskol M, Polat S, Ozkul Y. Dundar M, et al. Among authors: ozkul y. Ann Saudi Med. 2012 Jul-Aug;32(4):343-8. doi: 10.5144/0256-4947.2012.343. Ann Saudi Med. 2012. PMID: 22705602 Free PMC article.

7

Do thrombophilic gene mutations have a role on thromboembolic events in cancer patients?

Ozkan M, Sivgin S, Kocyigit I, Emirogullari F, Dikilitas M, Kaynar L, Ozkul Y, Er O. Ozkan M, et al. Among authors: ozkul y. Asia Pac J Clin Oncol. 2012 Sep;8(3):e34-41. doi: 10.1111/j.1743-7563.2012.01536.x. Epub 2012 May 15. Asia Pac J Clin Oncol. 2012. PMID: 22898008

8

Association of TNF-α -308 G > A and ACE I/D gene polymorphisms in hemodialysis patients with arteriovenous fistula thrombosis.

Sener EF, Taheri S, Korkmaz K, Zararsiz G, Serhatlioglu F, Unal A, Emirogullari ON, Ozkul Y. Sener EF, et al. Among authors: ozkul y. Int Urol Nephrol. 2014 Jul;46(7):1419-25. doi: 10.1007/s11255-013-0580-2. Epub 2013 Oct 15. Int Urol Nephrol. 2014. PMID: 24126814

9

The role of endothelial nitric oxide synthase gene G894T and intron 4 VNTR polymorphisms in hemodialysis patients with vascular access thrombosis.

Şener EF, Emiroğulları ÖN, Serhatlıoğlu F, Özkul Y. Şener EF, et al. Among authors: ozkul y. Anadolu Kardiyol Derg. 2014 May;14(3):239-43. doi: 10.5152/akd.2013.4779. Anadolu Kardiyol Derg. 2014. PMID: 24936541

10

MTHFR Gene C677T Polymorphism in Autism Spectrum Disorders.

Sener EF, Oztop DB, Ozkul Y. Sener EF, et al. Among authors: ozkul y. Genet Res Int. 2014;2014:698574. doi: 10.1155/2014/698574. Epub 2014 Nov 6. Genet Res Int. 2014. PMID: 25431675 Free PMC article.

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