Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Nilgün Duman"'
Autor:
Ibrahim Boga, Sebnem Ozemri Sag, Nilgun Duman, Sevda Yesim Ozdemir, Mahmut Cerkez Ergoren, Kubilay Dalci, Cem Mujde, Cem Kaan Parsak, Cagla Rencuzogullari, Ozge Sonmezler, Orcun Yalav, Adem Alemdar, Lamiya Aliyeva, Ozlem Bozkurt, Sibel Cetintas, Erdem Cubukcu, Adem Deligonul, Berkcan Dogan, Cemre Ornek Erguzeloglu, Turkkan Evrensel, Sehsuvar Gokgoz, Kazim Senol, Sahsine Tolunay, Esra Akyurek, Neslihan Basgoz, Nuriye Gökçe, Bilge Dundar, Figen Ozturk, Duygu Taskin, Mercan Demirtas, Murat Cag, Omer Diker, Polat Olgun, Sevcan Tug Bozdogan, Munis Dundar, Atil Bisgin, Sehime Gulsun Temel
Publikováno v:
European Journal of Breast Health, Vol 19, Iss 3, Pp 235-252 (2023)
Objective:Breast cancer (BC) is the most common cancer type in women and may be inherited, mostly in an autosomal dominant pattern. The clinical diagnosis of BC relies on the published diagnostic criteria, and analysis of two genes, BRCA1 and BRCA2,
Externí odkaz:
https://doaj.org/article/a71c390801df4f9498bd73b6b92a7cb8
Autor:
Sukru Ozturk, Ugur Ozbek, Kivanc Cefle, Aris Cakiris, Sukru Palanduz, Meliha Nalcaci, Duran Ustek, Nilgün Duman, Melih Aktan
Publikováno v:
Genetic Testing and Molecular Biomarkers. 16:287-291
Polymorphisms of the x-ray repair cross-complementing group 1 (XRCC1) gene have been reported to be associated with various forms of cancer. We evaluated the possible effects of the Arg194Trp and the Arg399Gln polymorphisms on the risk for chronic ly
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::092c05a3f1807b567958faf0daad1659
https://doi.org/10.1089/gtmb.2011.0152
https://doi.org/10.1089/gtmb.2011.0152
Autor:
Alp Saruhanoglu, Kivanc Cefle, B Sevinç, Sukru Palanduz, Nilgün Duman, Saman Warnakulasuriya, H Tanyeri, Sevda Ozel, Savas Ozturk, Sertan Ergun
Publikováno v:
Oral Diseases. 15:499-504
Objective: The purpose of this study was to determine the genetic instability of peripheral blood lymphocytes from patients diagnosed with oral lichen planus (OLP) by investigation of frequencies of micronuclei (MN) and sister chromatid exchange (SCE
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0efd15d4a67d37ea442888ed93820d00
https://doi.org/10.1111/j.1601-0825.2009.01576.x
https://doi.org/10.1111/j.1601-0825.2009.01576.x
Autor:
Nilgun Duman, Zahraa ALzaidi, Busra Aynekin, Duygu Taskin, Busra Demirors, Abdulbaki Yildirim, Izem Olcay Sahin, Faik Bilgili, Eda Tahir Turanli, Tommaso Beccari, Matteo Bertelli, Munis Dundar
Publikováno v:
Journal of Pharmaceutical Analysis, Vol 11, Iss 6, Pp 675-682 (2021)
The pandemic caused by the worldwide spread of the coronavirus, which first appeared in 2019, has been named coronavirus disease 19 (COVID-19). More than 4.5 million deaths have been recorded due to the pandemic caused by severe acute respiratory syn
Externí odkaz:
https://doaj.org/article/e4f4106a59bc48d99dbb818c7061710f
Autor:
Sukru Ozturk, Kivanc Cefle, Nilgün Duman, Ferhan Mantar, Kerim Güler, Sukru Palanduz, Nilüfer Gözüm
Publikováno v:
Ophthalmic genetics. 28(3)
Bloom syndrome is an autosomal recessive disorder characterized by proportionate short stature, photosensitivity, immunodeficiency, hypogonadism and a tendency to develop various malignancies. The greatly increased frequency of sister chromatid excha
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::20b227bfc1bc0b5250ec6017aeb825d0
https://pubmed.ncbi.nlm.nih.gov/17896317
https://pubmed.ncbi.nlm.nih.gov/17896317
Autor:
Serap Nur Ergor, Mehmet Serdar Kutuk, Nilgun Duman, Can Yilmaz Yozgat, Hafize Otcu Temur, Murat Ugurlucan, Yilmaz Yozgat
Publikováno v:
Pediatrics and Neonatology, Vol 62, Iss 1, Pp 125-126 (2021)
Externí odkaz:
https://doaj.org/article/483f35b1512b44bf9d74eb80868edfea