Zobrazeno 1 - 10
of 11
pro vyhledávání: '"Erol Eyupoglu"'
Autor:
Tolga T. Olmez, Esra Yuca, Erol Eyupoglu, Hazal B. Catalak, Ozgur Sahin, Urartu Ozgur Safak Seker
Publikováno v:
ACS Omega, Vol 3, Iss 1, Pp 585-594 (2018)
Externí odkaz:
https://doaj.org/article/a4865fef5b364e28bdbe98e9bbf24c14
Autor:
Erol Eyupoglu, Ozge Saatci, Ozgur Sahin, Yasser Riazalhosseini, Pouria Jandaghi, Nevin Belder, Unal Metin Tokat, Suhail A. Ansari, Aysegul Uner, Caglar Cekic, Pelin Gülizar Ersan, Merve Kayhan, Rasmi Rekha Mishra, Hilal Bal, Stefan Wiemann, Umar Raza
Publikováno v:
Clinical Cancer Research
Purpose: Tamoxifen remains an important hormonal therapy for ER-positive breast cancer; however, development of resistance is a major obstacle in clinics. Here, we aimed to identify novel mechanisms of tamoxifen resistance and provide actionable drug
Autor:
Yasser Riazalhosseini, Jose Guevara-Coto, Jose Molina-Mora, Dennis Jimenez-Vargas, Rodrigo Mora-Rodriguez, Erol Eyupoglu, Man Sai Acon, Ozgur Sahin
Publikováno v:
IWOBI
2018 IEEE International Work Conference on Bioinspired Intelligence (IWOBI)
2018 IEEE International Work Conference on Bioinspired Intelligence (IWOBI)
Chemotherapeutic drugs have been used as important strategies in cancer treatment. However, chemotherapy-resistant tumors arise especially in relapsing and progressive disease. Understanding of mechanisms underlaying Cisplatin-CDDP chemotherapy resis
Publikováno v:
Journal of Molecular Medicine
MicroRNAs (miRNAs) are 20-22-nucleotide small endogenous non-coding RNAs which regulate gene expression at post-transcriptional level. In the last two decades, identification of almost 2600 miRNAs in human and their potential to be modulated opened a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c9bc7f8960495740144736cce00c70c9
https://hdl.handle.net/11693/38109
https://hdl.handle.net/11693/38109
Autor:
Pelin Gülizar Ersan, Stefan Uhlmann, M. K. Altundag, Erol Eyupoglu, Suhail A. Ansari, Umar Raza, Merve Mutlu, Ozgur Sahin, Emre Yurdusev, Hayriye Tatlı Doğan, Gulnur Guler, Ozge Saatci, Jitao David Zhang
Publikováno v:
Oncotarget
// Umar Raza 1 , Ozge Saatci 1 , Stefan Uhlmann 2 , Suhail A Ansari 1 , Erol Eyupoglu 1 , Emre Yurdusev 1 , Merve Mutlu 1 , Pelin Gulizar Ersan 1 , Mustafa Kadri Altundag 3 , Jitao David Zhang 4 , Hayriye Tatli Dogan 5 , Gulnur Guler 5 , Ozgur Sahin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9e58fa84814a05d32ee6efaaa426f2e0
http://hdl.handle.net/11655/15398
http://hdl.handle.net/11655/15398
Autor:
Umar Raza, Ozgur Sahin, Daniel Gautheret, Can Alkan, Pelin Gülizar Ersan, Erol Eyupoglu, Denis Thieffry, Unal Metin Tokat, Yasser Riazalhosseini
Publikováno v:
Cancer Research. 77:2848-2848
Introduction: Triple negative breast cancer (TNBC), the most aggressive breast cancer subtype, has high incidence rate of lung metastasis. Not only protein coding transcripts, but also non-coding transcriptome, such as microRNAs (miRNAs) and long non
Publikováno v:
Cancer Research. 76:1912-1912
PI3K/Akt and MAPK signaling pathways, regulating cancer cell proliferation, apoptosis and metastasis, are among the top most deregulated pathways in cancer. Current kinase inhibitors used in clinics have limited success since one of these pathways ge
Publikováno v:
European Journal of Cancer. 61:S121
Öz bulunamadı.
Publikováno v:
Atlas of Genetics and Cytogenetics in Oncology and Haematology.
Review on MIR200C (microRNA 200c), with data on DNA, on the protein encoded, and where the gene is implicated.
Autor:
Bernd Wollnik, Ersan Kalay, Hanka Venselaar, Wasim Ahmad, Angelien Heister, Elif Bahat, Ahmet Karagüzel, Gert Vriend, Kwanghyuk Lee, Saima Riazuddin, Yun Li, Frans P.M. Cremers, Refik Caylan, Muhammad Tariq, Bert van der Zwaag, Muhammad Ansar, Han G. Brunner, Jaap Oostrik, Selçuk Arslan, Sheikh Riazuddin, Rob W.J. Collin, Theo A. Peters, Henk A. Spierenburg, Hannie Kremer, Erol Eyupoglu, Zubair M. Ahmed, Thomas B. Friedman, Suzanne M. Leal, Cor W. R. J. Cremers
Publikováno v:
American Journal of Human Genetics, 82, 125-38
American Journal of Human Genetics, 82, 1, pp. 125-38
American Journal of Human Genetics, 82, 1, pp. 125-38
SummaryIn a large consanguineous family of Turkish origin, genome-wide homozygosity mapping revealed a locus for recessive nonsyndromic hearing impairment on chromosome 14q24.3–q34.12. Fine mapping with microsatellite markers defined the critical l
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d5e455e4b6e3d95ed5ba68e4dd90b769
https://europepmc.org/articles/PMC2253958/
https://europepmc.org/articles/PMC2253958/