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of 58
pro vyhledávání: '"Nagehan Ersoy"'
Autor:
Nagehan Ersoy, A. Nazlı Başak
Publikováno v:
Türk Nöroloji Dergisi, Vol 11, Iss 1, Pp 27-44 (2005)
Huntington’s Disease (HD) is the most common among nine known polyglutamine disorders. Its prevalence is estimated to be 3-7/100 000 in populations of Western European descent. HD is an autosomal dominantly inherited neurodegenerative disorder o
Externí odkaz:
https://doaj.org/article/f797b75615fd4ea3ab985abee61da3da
Autor:
Nagehan Ersoy Tunali, Ezgi Keske
Publikováno v:
D: Wet biomarkers.
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
Publikováno v:
Alzheimer's & Dementia. 17
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
Akademický článek
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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
Autor:
Nagehan Ersoy Tunalı
Publikováno v:
Neurodegenerative Diseases-Molecular Mechanisms and Current Therapeutic Approaches ISBN: 9781838801496
Identification of polymorphic repeating units on DNA as a cause of many neurological disorders has introduced a new concept in molecular biology: Dynamic mutations. Many of the identified dynamic mutations involve expansion of trinucleotide repeats w
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5baf1681abd0a8c8bbbca27a94e8e8e3
https://doi.org/10.5772/intechopen.93508
https://doi.org/10.5772/intechopen.93508
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