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Nagehan Ersoy Tunali

Explore the profile of Nagehan Ersoy Tunali including associated specialties, affiliations and a list of published articles. Areas
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Articles 7
Citations 32
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Recent Articles
1.
Sagir F, Ersoy Tunali N, Tombul T, Koral G, Cirak S, Yilmaz V, et al.
Genet Test Mol Biomarkers . 2021 Nov; 25(11):720-726. PMID: 34788141
Brain-derived neurotrophic factor (BDNF) levels are reduced in advanced stages of multiple sclerosis (MS) and may be associated with reduced regenerative capability in progressive MS. This has brought increased attention...
2.
Ozkara G, Ersoy Tunali N
Mol Biol Rep . 2021 May; 48(5):4073-4081. PMID: 34057684
Teratozoospermia is a condition related to poor morphologically normal sperm count below the lower reference limit, which could hinder natural conception. Single nucleotide polymorphisms (SNPs) in the genes involved in...
3.
Temiz M, Cakir O, Aykan S, Kucuk S, Tiryakioglu N, Bilek G, et al.
Biomark Med . 2019 Jan; 13(2):59-68. PMID: 30672309
Aim: To generate a combination of serum zinc (Zn) and prostate-specific antigen (PSA) in an attempt to provide better prediction of prostate biopsy outcomes with Zn/PSA ratios. Materials & Methods:...
4.
Adali G, Ersoy Tunali N, Yorulmaz E, Tiryakioglu N, Mungan S, Ulasoglu C, et al.
Turk J Gastroenterol . 2017 Jul; 28(4):254-259. PMID: 28699600
Background/aims: Ulcerative colitis (UC) and Crohn's disease are chronic inflammatory diseases. Genetic, immunologic, and microbial factors play an important role in their pathogenesis. Extracellular matrix protein 1 (ECM1), a gene...
5.
Ozan Tiryakioglu N, Ersoy Tunali N
Urol J . 2016 Apr; 13(2):2615-21. PMID: 27085562
Purpose: Polymorphisms in the genes coding for the carcinogen metabolizing enzymes may affect enzyme activities and alter the activation and detoxification rates of the carcinogens. AKR1C3 is one of the...
6.
Tiryakioglu N, Onal Z, Saygili S, Onal H, Ersoy Tunali N
Int J Dermatol . 2016 Feb; 56(1):106-108. PMID: 26889743
No abstract available.
7.
Ersoy Tunali N, Marobbio C, Ozan Tiryakioglu N, Punzi G, Saygili S, Onal H, et al.
Mol Genet Metab . 2014 Apr; 112(1):25-9. PMID: 24721342
The hyperornithinemia-hyperammonemia-homocitrullinuria syndrome is a rare autosomal recessive disorder caused by the functional deficiency of the mitochondrial ornithine transporter 1 (ORC1). ORC1 is encoded by the SLC25A15 gene and catalyzes...