Zobrazeno 1 - 10
of 23
pro vyhledávání: '"Sener Tasdemir"'
Publikováno v:
Eurasian Journal of Medicine, Vol 51, Iss 2, Pp 177-185 (2019)
Externí odkaz:
https://doaj.org/article/f15a6d34460a44db8b516b5481080a5a
Publikováno v:
Eurasian Journal of Medicine, Vol 51, Iss 2, Pp 177-185 (2019)
Objective In this study, we investigated the frequency of Epidermal growth factor receptor (EGFR) gene mutations, the level of EGFR mRNA and protein expressions in Turkish population for indicating substantial differences in the frequency of EGFR mut
Publikováno v:
American Journal of Medical Genetics Part A. 170:220-225
Vici syndrome (OMIM 242840) is a rare syndrome and since its initial description by Vici et al. [1988], only 29 cases have been reported. We describe two brothers from healthy consanguineous Turkish parents with psychomotor delay, congenital bilatera
Autor:
Mehmet Yilmaz, Haktan Bağış Erdem, Abdulgani Tatar, Ragip Atakan Al, Ibrahim Sahin, Metin Ingec, Sener Tasdemir
Publikováno v:
Perinatal Journal. 22:138-141
Objective: In our clinic, 1429 patients who underwent amniocen- tesis and cordocentesis for prenatal diagnosis were evaluated retro- spectively. Methods: The cell culture success, prenatal diagnosis indications, detected chromosomal anomalies and the
Publikováno v:
NeuroMolecular Medicine. 16:587-593
WOS: 000340096700006 PubMed: 24845269 Migraine is a common neurological disorder characterized by recurrent attacks, unilateral head pain, and related symptoms. The aim of this study was to investigate three endothelial nitric oxide synthase (eNOS) p
Autor:
Aysegul Ozanturk, Sener Tasdemir, Avni Kaya, Hakan Doneray, Zerrin Orbak, Fatih Bingöl, Atilla Cayir
Publikováno v:
Pediatrics. 133:e780-e783
Alström syndrome (Online Mendelian Inheritance in Man ALMS #203800) is a rare hereditary disorder caused by mutations in the gene ALMS1. This rare disorder’s characteristics are cone-rod dystrophy resulting in blindness in childhood, insulin-resis
Publikováno v:
Biochemical genetics. 54(4)
The aim of this study was to research carbonic anhydrase (CA) VI one single-nucleotide polymorphism (SNP) and its potential association with dental-oral health status (dental caries, Plaque Index (PI) and Gingival Index (GI)) and salivary parameters
Autor:
Recep Eröz, Murat Kara, Sener Tasdemir, Haktan Bağış Erdem, Hasan Turkez, Ragip Ismail Engin, Hasan Dogan, Ibrahim Sahin
Publikováno v:
Genetic testing and molecular biomarkers. 20(4)
Dogan, Hasan/0000-0002-5232-4336 WOS: 000373932400008 PubMed: 26866305 Aims: Nucleolar organizer regions, also known as argyrophilic nucleolar organizer regions, are associated with ribosomal genes. The main function of the nucleolus is the rapid pro
Publikováno v:
Central nervous system agents in medicinal chemistry. 17(2)
Thymol (THY), which is a monocyclic monoterpene, is one of the major constituent of the essential oils of thyme and origanum. To date, although various biological activities of THY have been demonstrated, its neurotoxicity has never been explored. We
Autor:
Haktan Bağış Erdem, Sener Tasdemir, Gökhan Özdemir, Lütfi Özel, Recep Eröz, Ibrahim Sahin, Abdulgani Tatar
WOS: 000377435300004 PubMed: 26951304 An important type of arterial thrombosis, ischemic stroke is associated with increased mortality risk, severe disability and life quality impairment. In this study, we analyzed mean platelet volume, platelet coun
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::78bf6ec9a1aec349f0870009343f8ffe
https://hdl.handle.net/20.500.12684/3256
https://hdl.handle.net/20.500.12684/3256