Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Arash Adamnejad Ghafour"'
Autor:
Seref Bugra Tuncer, Betul Celik, Seda Kılıc Erciyas, Ozge Sukruoglu Erdogan, Ozge Pasin, Mukaddes Avsar, Busra Kurt Gultaslar, Arash Adamnejad Ghafour, Gamze Uyaroglu, Demet Akdeniz Odemis, Hulya Yazıcı
Publikováno v:
Heliyon, Vol 10, Iss 1, Pp e23876- (2024)
Ovarian cancer (OC) ranks as the eighth most prevalent malignancy among women globally. The short non-coding RNA molecules, microRNAs (miRNAs) target multiple mRNAs and regulate the gene expression. Here in this study, we aimed to validate miR-3135b
Externí odkaz:
https://doaj.org/article/60b24459e37e449ea70a87a538bfaffb
Autor:
Arash Adamnejad Ghafour, Demet Akdeniz Odemis, Seref Bugra Tuncer, Busra Kurt, Mukaddes Avsar Saral, Seda Kilic Erciyas, Ozge Sukruoglu Erdogan, Betul Celik, Pinar Saip, Hulya Yazici
Publikováno v:
Journal of Ovarian Research, Vol 14, Iss 1, Pp 1-15 (2021)
Abstract The most common gynecologic cancers detected in women in Turkey are uterine cancer, ovarian cancer, and cervical cancer. These data reported that a mean of 3800 individuals were diagnosed with uterine cancer, 2790 were diagnosed with ovarian
Externí odkaz:
https://doaj.org/article/2d639461c5bb4ba083e9ea1a2dc2ae0c
Autor:
Demet Akdeniz Odemis, Betul Celik, Seda Kilic Erciyas, Ozge Sukruoglu Erdogan, Seref Bugra Tuncer, Busra Kurt Gultaslar, Arash Adamnejad Ghafour, Pinar Saip, Hulya Yazici
Publikováno v:
Turkish Journal of Biochemistry. 47:588-594
Objectives To find BRCA1/2 test selection criteria unique to the Turkish population, as well as to provide the BRCA1/2 gene mutation distributions of patient population to the literature. Methods Genetic counseling was given to 2,373 cases with a fam
Autor:
SEREF BUGRA TUNCER, Betul Celik, Seda Kılıc Erciyas, Ozge Sukruoglu Erdogan, Demet Akdeniz Odemis, Büşra Kurt Gültaslar, Arash Adamnejad Ghafour, Mualla Pınar Saip, Hulya Yazici
Purpose: Ovarian cancer is the seventh most frequent cancer in women worldwide and the eighth leading cause of death from cancer. Approximately 5–10% of all diagnosed cancer cases are caused by hereditary cancer risk syndromes. The aim of this stud
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::652129eed087e075a0e9c18eeef5a920
https://doi.org/10.21203/rs.3.rs-1241858/v1
https://doi.org/10.21203/rs.3.rs-1241858/v1
Autor:
Hulya Yazici, Betul Celik, Demet Akdeniz Odemis, Pinar Saip, Seda Kilic Erciyas, Seref Bugra Tuncer, Busra Kurt, Arash Adamnejad Ghafour, Ozge Sukruoglu Erdogan, Mukaddes Avsar Saral
Publikováno v:
Journal of Ovarian Research, Vol 14, Iss 1, Pp 1-15 (2021)
Journal of Ovarian Research
Journal of Ovarian Research
The most common gynecologic cancers detected in women in Turkey are uterine cancer, ovarian cancer, and cervical cancer. These data reported that a mean of 3800 individuals were diagnosed with uterine cancer, 2790 were diagnosed with ovarian cancer,
Autor:
Pinar Saip, Demet Akdeniz Odemis, Mukaddes Avsar Sarali, Betul Celik, Busra Kurt, Hulya Yazici, Seref Bugra Tuncer, Seda Kilic, Ozge Sukruoglu Erdogan, Arash Adamnejad Ghafour
MicroRNAs (miRNAs), are endogenous noncoding single strand RNA molecules with approximate length of 22 nucleotides. Ovarian cancer is a heterogenous disease which includes different biologic behaviors in the clinical, and molecular level. miRNAs have
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::10f17e787fd235d835e57f9dd76b3153
https://doi.org/10.21203/rs.3.rs-84141/v1
https://doi.org/10.21203/rs.3.rs-84141/v1
Autor:
Sema Buyukkapu Bay, Samuray Tuncer, Arash Adamnejad Ghafour, Betul Celik, Yasemin Gider, Hulya Yazici, Rejin Kebudi, Khariga Jabbarli, Mukaddes Avsar, Seref Bugra Tuncer, Gozde Kuru Turkcan, Seda Kilic Erciyas, Demet Akdeniz Odemis, Ozge Sukruoglu Erdogan
Publikováno v:
Journal of Oncology, Vol 2020 (2020)
Journal of Oncology
Journal of Oncology
Purpose. Various molecular variations are known to result in different gene variants in the FGFR4 gene, known for its oncogenic transformation activity. The goal of this study was to investigate the FGFR4 p.Gly388Arg variant that plays role in the pr