Kurum Yazarı "Güzel, Ali İrfan" PubMed İndeksli Yayınlar Koleksiyonu İçin Listeleme
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Are there fetal stem cells in the maternal brain?
Demirhan, Osman; Çekin, Necmi; Taştemir, Deniz; Tunç, Erdal; Güzel, Ali İrfan; Meral, Demet; Demirbek, Bülent (Wolters Kluwer Medknow Publications, 2013)Fetal cells can enter maternal blood during pregnancy but whether they can also cross the blood-brain barrier to enter the maternal brain remains poorly understood. Previous results suggest that fetal cells are summoned ... -
Association of paraoxonase-1 L55M and Q192R polymorphisms with PCOS risk and potential risk factors for atherosclerosis
Nalkıran, Hatice Sevim; Şahin, Serap Baydur; Ayaz, Teslime; Nalkıran, İhsan; Güzel, Ali İrfan; Eldeş, Tuğba; Yıldız, Yasin (Future Medicine Ltd, 2019)Aim: To examine the PON1-L55M and-Q192R polymorphisms for polycystic ovary syndrome (PCOS) risk in relation with atherosclerosis risk markers. Methods: Blood samples were collected from 203 women (PCOS [n = 151], control ... -
Clodronate changes neurobiological effects of pulsed magnetic field on diabetic rats with peripheral neuropathy
Mert, Tufan; Öçal, Işıl; Güzel, Ali İrfan; Günay, İsmail (Taylor & Francis Ltd., 2013)Several studies have reported that pulsed magnetic fields (PMFs) can be a choice of therapy for diabetic peripheral neuropathy. However, the exact underlying mechanism of PMF is still not known. The purpose of this study ... -
Determination of genotypic and phenotypic characteristics of friedreich's ataxia and autosomal dominant spinocerebellar ataxia types 1, 2, 3, and 6
Boz, Pınar Bengi; Koç, Filiz; Sel, Sabriye Kocatürk; Güzel, Ali İrfan; Kasap, Halil (Aves, 2016)Introduction: This study aimed to analyze the genotypic characteristics of Friedreich's ataxia (FA) and autosomal dominant ataxias [such as spinocerebellar ataxia (SCA) types 1, 2, 3, and 6] using molecular and biological ... -
The first report described as an important study: The association of mannose-binding lectin gene 2 polymorphisms in children with down syndrome
Background: Mannose-binding lectin gene 2 (MBL2) plays a very important role in the first line of host immune response in Down syndrome (DS). The importance of MBL2 gene polymorphisms in children with DS is unclear, and ... -
Genetic variations in OLR1 gene associated with PCOS and atherosclerotic risk factors
Şahin, Serap Baydur; Nalkıran, İhsan; Ayaz, Teslime; Güzel, Ali İrfan; Eldeş, Tuğba; Calapoğlu, Tuğba; Nalkıran, Hatice Sevim (Sage Publications, 2023)Polycystic ovary syndrome (PCOS) is the most common endocrinopathy in women of reproductive age. The aim of this study was to investigate the association of oxidized low-density lipoprotein receptor 1 (OLR1) gene variations ... -
Pelvic radiation-induced testicular damage: an experimental study at 1 gray
Rakıcı, Sema Yılmaz; Güzel, Ali İrfan; Tümkaya, Levent; Nalkıran, Hatice Sevim; Mercantepe, Tolga (Taylor & Francis Inc, 2020)Therapeutic radiation of the pelvic region has been shown to cause damage to testicular germ cells. in this study we aimed to evaluate the effects of a low therapeutic dose of 1 Gy on the induction of cellular and histological ... -
Rapid detection of fetal aneuploidies by quantitative fluorescent- polymerase chain reaction for prenatal diagnosis in the turkish population
Güzel, Ali İrfan; Yilmaz, M.B.; Demirhan, O.; Pazarbasi, A.; Kocaturk-Sel, S.; Erkoc, M.A.; Sariturk, C. (0-Belirlenecek, 2012)Prenatal diagnosis is testing for diseases or conditions in a fetus or embryo before it is born. It employs a variety of techniques to determine the health and condition of an unborn fetus. The main goal of this process ... -
The reliability of maternal serum triple test in prenatal diagnosis of fetal chromosomal abnormalities of pregnant Turkish women
Demirhan, Osman; Pazarbaşı, Ayfer; Güzel, Ali İrfan; Taştemir, Deniz; Yılmaz, Bertan; Kasap, Mülkiye; Özgünen, Fatma Tuncay; Evrüke, Cüneyt; Demir, Cansun; Tunç, Erdal; Kocatürk-Sel, Sabriye; Onatoǧlu-Aríkan, Dilge (2011)Aim: The purpose of this article was to evaluate the reliability of maternal serum triple marker screening of alpha-fetoprotein, human chorionic gonadotropin, and unconjugated estriol for the prenatal diagnosis of fetal ... -
Variants in taste genes on caries risk and caries activity status
Telatar, Gül Yıldız; Saydam, Faruk; Güzel, Ali İrfan; Telatar, Barış Can (Springer Japan Kk, 2020)The aim of this study was to evaluate the role of taste-related gene polymorphisms (CA6,TAS1R1,TAS1R3, TLR2,andTLR4)on dental caries and caries activity in adults. Individuals aged 25-44 years included in the study were ...