Person: YÜCESAN, EMRAH
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Publication Metadata only Expression analysis of apoptosis related genes in human hippocampal sclerosis(2011-12-03T00:00:00Z) Yücesan, Emrah; YÜCESAN, EMRAHPublication Metadata only Paratiroit Hücre İzolasyonunda Enzimatik ve Mekanik İzolasyon Yöntemlerinin Karşılaştırılması(2018-05-04T00:00:00Z) Yücesan, Emrah; GÖNCÜ, BEYZA SERVET; YÜCESAN, EMRAHPublication Metadata only A comparative study of parathyroid transport solution and university of Wisconsin solution: effect on calcium-sensing receptor and vitamin-D receptor during cold ischemia in parathyroid tissue(2019-09-16T00:00:00Z) Yücesan, Emrah; GÖNCÜ, BEYZA SERVET; YÜCESAN, EMRAH; AKBAŞ, FAHRİ; KAZANCIOĞLU, RÜMEYZA; ERSOY, YELIZ EMINEPublication Metadata only Kalsiyum ve D Vitamini Metabolizmasında Görevli Transkripsiyon Faktörlerin Kültüre Edilen Paratiroit Dokularındaki Etkinliklerinin Paratiroit Nakil Sürecine Etkisi(2019-11-01T00:00:00Z) Yücesan, Emrah; YÜCESAN, EMRAH; GÖNCÜ, BEYZA SERVETPublication Metadata only Minor histocompatibility antigen sp110: an evolutionary trace for parathyroid tissue(2019-09-15T00:00:00Z) Yücesan, Emrah; GÖNCÜ, BEYZA SERVET; YÜCESAN, EMRAH; AKBAŞ, FAHRİ; ERSOY, YELIZ EMINEPublication Metadata only Paratiroit Hücrelerinin Mikroenkapsülasyonu ve Nakil Yöntemi(2018-11-29T00:00:00Z) Yücesan, Emrah; GÖNCÜ, BEYZA SERVET; YÜCESAN, EMRAHPublication Metadata only Mezyal Temporal Lob Epilepsisi Patogenezinde Sitokinlerin Rolü(2014-06-01T00:00:00Z) Bingol-Ozakpinar, Ozlem; Cikrikcioglu, Mehmet Ali; Erek-Toprak, Aybala; Karaca, Zeynep; Uras, Fikriye; Adeli, Khosrow; Uras, Ahmet Riza; Hursitoglu, Mehmet; YÜCESAN, EMRAHPublication Metadata only Uzamış Febril Nöbet Sonrası Süreçte Epileptogenezin Araştırılması(2019-05-21T00:00:00Z) Yücesan, Emrah; YÜCESAN, EMRAHPublication Metadata only New Transport Solution For Parathyroid Allotransplantation(2017-09-25T00:00:00Z) Yücesan, Emrah; AKBAŞ, FAHRİ; YÜCESAN, EMRAH; KAZANCIOĞLU, RÜMEYZAPublication Metadata only Whole genome SNP genotyping confirms segregation of Unverricht-Lundborg Disease (ULD) with a repeat expansion in CSTB on 21q in a large consanguineous family followed by a novel haplotype based approach identifying the parent of origin and carrier status in the child with Trisomy 21 under the age of onset for ULD.(2014-06-01T00:00:00Z) Yücesan, Emrah; YÜCESAN, EMRAH; İŞCAN, AKIN
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