Zobrazeno 1 - 10
of 16
pro vyhledávání: '"Nagehan Ersoy Tunali"'
Autor:
Nagehan Ersoy Tunali, Ezgi Keske
Publikováno v:
D: Wet biomarkers.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::be382fa1895bc0ba13d22982c740b874
https://doi.org/10.1136/jnnp-2022-ehdn.67
https://doi.org/10.1136/jnnp-2022-ehdn.67
Autor:
Gülçin Özkara, Nagehan Ersoy Tunali
Publikováno v:
Molecular Biology Reports. 48:4073-4081
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 sperm production and testicular
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::391c415f6a9d4c2362f2c39f6fa44cd7
https://doi.org/10.1007/s11033-021-06417-7
https://doi.org/10.1007/s11033-021-06417-7
Publikováno v:
Alzheimer's & Dementia. 17
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::76c343de5cfef6bc1fb643360aa5e930
https://doi.org/10.1002/alz.057854
https://doi.org/10.1002/alz.057854
Autor:
Fatma Sağır, Erdem Tüzün, Temel Tombul, Recai Turkoglu, Gizem Koral, Nagehan Ersoy Tunali, Vuslat Yilmaz, Selen Çırak
Publikováno v:
Genetic testing and molecular biomarkers. 25(11)
Introduction: 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 to factors regu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::af905f4bd3197d28a46f8ff3073f4c7b
https://pubmed.ncbi.nlm.nih.gov/34788141
https://pubmed.ncbi.nlm.nih.gov/34788141
Autor:
Serdar Aykan, Engin Kandirali, Nagehan Ersoy Tunali, Gunal Bilek, Omer Onur Cakir, Suat Hayri Kucuk, Necip Ozan Tiryakioglu, Atilla Semerciöz, Mustafa Zafer Temiz
Publikováno v:
Biomarkers in Medicine. 13:59-68
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: Diagnostic performances of PSA and Zn/PSA were inves
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::19d5cac07ce5260a72f1b7f852eaac6e
https://doi.org/10.2217/bmm-2018-0260
https://doi.org/10.2217/bmm-2018-0260
Autor:
Gülçin, Özkara, Nagehan, Ersoy Tunali
Publikováno v:
Molecular biology reports. 48(5)
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 sperm production and testicular
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::a0ceae770cba32d22689fa2e5947a8b3
https://pubmed.ncbi.nlm.nih.gov/34057684
https://pubmed.ncbi.nlm.nih.gov/34057684
Publikováno v:
Pathogenic mechanisms.
Background N-methyl-d-aspartic acid receptor (NMDA) mediated excitotoxic destruction of striatal neurons is one of the models proposed for the pathogenesis of Huntington’s disease. Polyamines (putrescine, spermidine and spermine) may be involved in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d1c51f34ed56d2292e1550fceb4d95a7
https://doi.org/10.1136/jnnp-2018-ehdn.24
https://doi.org/10.1136/jnnp-2018-ehdn.24
Autor:
Gupse Adali, Ilyas Tuncer, Nagehan Ersoy Tunali, Elif Yorulmaz, Feruze Yilmaz Enc, Sibel Güray Mungan, Celal Ulasoglu, Necip Ozan Tiryakioglu
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 related to mucosal
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5be7dad5be327c8a89a8caac904a2650
http://hdl.handle.net/11363/780
http://hdl.handle.net/11363/780
Autor:
Nagehan Ersoy Tunali
Publikováno v:
Huntington's Disease-Molecular Pathogenesis and Current Models
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::46fe894c6bd9f4471d7cb083338f275a
https://doi.org/10.5772/62999
https://doi.org/10.5772/62999
Autor:
Ferdinando Palmieri, N. Ozan Tiryakioglu, Giuseppe Punzi, Hasan Önal, Carlo M.T. Marobbio, Seha Saygili, Nagehan Ersoy Tunali
Publikováno v:
Molecular Genetics and Metabolism
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 the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e28b5c361ecfffeddfcde4bc6026ce5c
http://europepmc.org/articles/PMC4015418
http://europepmc.org/articles/PMC4015418