Zobrazeno 1 - 10
of 22
pro vyhledávání: '"Mujgan Ozdemir Erdogan"'
Autor:
Mujgan Ozdemir Erdogan, Başak Gogus, Handan Yildiz, Sinan Kazan, Serdar Ceylaner, Alper Emre Kurt, Sena Ulu, Muhsin Elmas
Publikováno v:
Acta Scientific Medical Sciences. :10-25
Autor:
Mujgan Ozdemir Erdogan, Tülay Köken, Mustafa Solak, Muhsin Elmas, Mehmet Yaman, Saliha Handan Yildiz
Publikováno v:
Journal of Biochemical and Clinical Genetics. :3-6
Background: Multiple sclerosis (MS) is a demyelinating disease in which the insulating covers of nerve cells in the brain and spinal cord are damaged. In this study, we investigated the possible association of vitamin D levels and rs703842 in the CYP
Autor:
Mujgan Ozdemir Erdogan, Munevver Nisa Can, Cem Karaosmanoglu, Saliha Handan Yildiz, Mustafa Yildiz
Publikováno v:
Journal of Clinical and Experimental Investigations. 13:em00801
Autor:
Tevhide Fistik, Mujgan Ozdemir Erdogan, Muhsin Elmas, Saliha Handan Yildiz, Banu Değirmenci, Mustafa Solak
Publikováno v:
Meta Gene. 19:78-81
Objective The aim of our study is to determine the frequency of chromosome abnormalities and Y chromosome microdeletions which are the causes of primary infertility, in Afyonkarahisar. Materials and methods Cytogenetic analysis results of 504 inferti
Autor:
Kamuran Avci, Muhsin Elmas, Mustafa Solak, Mujgan Ozdemir Erdogan, Handan Yildiz, Basak Gogus
Publikováno v:
Molecular Biology Reports. 46:287-299
Whole-exome sequencing (WES) is an ideal method for the diagnosis of autosomal recessive diseases. The aim of this study was to evaluate the diagnostic power of WES in patients with autosomal recessive inheritance and to determine the relationship be
Autor:
Evrim Suna Arikan Terzi, Mustafa Solak, Zafer Söylemez, Nuray Varol, Mujgan Ozdemir Erdogan, Saliha Handan Yildiz, Kamuran Avci
Publikováno v:
Biotechnology & Biotechnological Equipment, Vol 32, Iss 6, Pp 1567-1574 (2018)
Obesity is a complex disorder with nearly epidemic proportions in many parts of the world. Genome-wide association studies have demonstrated high heritability for obesity and body mass, with associations of certain candidate genes and their variation
Autor:
Mustafa Solak, Evrim Suna Arikan Terzi, Mujgan Ozdemir Erdogan, Pınar Ozuğuz, Seval Doğruk Kaçar, Zafer Söylemez, Elvin Kuşku, Ayşen Yildirim, Saliha Handan Yildiz
Publikováno v:
Journal of Advances in Internal Medicine. 5:1-5
Vitiligo is a disease characterized by sharply limited white macular depigmentation as a result of melanocyte loss. Disease is divided into three types according to prevalence and localization as localized, general and universal. Etiology of vitiligo
Autor:
Saliha Handan Yildiz, Cem Karaosmanoğlu, Rahmi Duman, Nuray Varol, Müjgan Özdemir Erdoğan, Mustafa Solak, Reşat Duman, Muhsin Elmas
Publikováno v:
Egyptian Journal of Medical Human Genetics, Vol 24, Iss 1, Pp 1-8 (2023)
Abstract Background The human lens develops age-related cataracts (ARCs) because of the complicated effects of aging and stressful conditions. Under conditions involving oxidative stress, cells form stress granules (SGs). TDRD7 has been identified as
Externí odkaz:
https://doaj.org/article/987f359874d3420da439e51832492c37
Autor:
Kasım Demir, Şeref Yüksel, Mukremin Uysal, Memnune Sena Ulu, Ahmet Ahsen, Mujgan Ozdemir Erdogan, Gürsel Acartürk
Publikováno v:
Inflammation. 36:1357-1362
Familial Mediterranean fever (FMF), which is an autosomal recessive disease, is characterised by recurrent febrile episodes in association with peritonitis, pleuritis and arthritis and has ongoing subclinical inflammation during attack-free period. I
Autor:
Erman Bagcioglu, Burak Subasi, Asli Akilli, Mujgan Ozdemir Erdogan, Kerem Senol Coskun, Evrim Suna Arikan Terzi, Saliha Handan Yildiz, Ahmet Hamdi Alpaslan
Publikováno v:
Acta Neuropsychiatrica. 25:342-348
ObjectiveThe aim of this study is to investigate whether there were any associations between the T102C and 1438 A/G polymorphisms of the 5-HT2A receptor gene and schizophrenia. We conducted a case–control study of the T102C and 1438 A/G polymorphis