Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Sezen Güntekin Ergün"'
Autor:
Fulya Yaylacıoğlu Tuncay, Kübra Serbest Ceylanoğlu, Sezen Güntekin Ergün, Berçin Tarlan, Onur Konuk
Publikováno v:
Türk Oftalmoloji Dergisi, Vol 54, Iss 4, Pp 247-250 (2024)
Externí odkaz:
https://doaj.org/article/7988d6150a6a414785dc355b752d41fa
Autor:
Fulya Yaylacıoğlu Tuncay, Kübra Serbest Ceylanoğlu, Sezen Güntekin Ergün, Berçin Tarlan, Onur Konuk
Publikováno v:
Türk Oftalmoloji Dergisi, Vol 54, Iss 2, Pp 69-75 (2024)
Objectives: Forkhead box P3 (FOXP3) gene polymorphisms have been evaluated in many autoimmune diseases, including Graves’ disease (GD), in different populations. However, those polymorphisms have not been analyzed in GD or Graves’ ophthalmopathy
Externí odkaz:
https://doaj.org/article/51fb76cfb6e647f48940c957a6e9b6e0
Autor:
Burcu Yazıcıoğlu, Zühre Kaya, Sezen Güntekin Ergün, Ferda Perçin, Ülker Koçak, İdil Yenicesu, Türkiz Gürsel
Publikováno v:
Turkish Journal of Hematology, Vol 34, Iss 2, Pp 143-150 (2017)
Objective: High-dose methotrexate (HD-MTX) is widely used in the consolidation phase of childhood acute lymphoblastic leukemia (ALL), but the roles that polymorphisms in folate-related genes (FRGs) play in HD-MTX toxicity and prognosis in children wi
Externí odkaz:
https://doaj.org/article/1cfd80f6663942e996c0af4fb15e4b7e
Autor:
Sümeyye Turanlı, Esra Nalbat, Deniz Lengerli, Kübra İbiş, Sezen Güntekin Ergün, Ece Akhan Güzelcan, Mesut Muyan, Rengul Cetin-Atalay, Burcu Çalışkan, Erden Banoglu
Publikováno v:
ACS Omega. 7:36206-36226
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1e99320e112c0a9b1f9d0a50abff0514
https://doi.org/10.1021/acsomega.2c03405
https://doi.org/10.1021/acsomega.2c03405
Autor:
Guyem Kolbaşı Demircioğlu, Sezen Güntekin Ergün, Kıvılcım Gücüyener, Ferda Perçin, Mehmet Ergün
Publikováno v:
Journal of Istanbul Faculty of Medicine / İstanbul Tıp Fakültesi Dergisi.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::472dddd0571b4fc7d71bc1a2721d2de2
https://doi.org/10.26650/iuitfd.1164334
https://doi.org/10.26650/iuitfd.1164334
Autor:
Sezen Güntekin, Ergün, Burcu Baloş, Tuncer, Mehmet Ali, Ergün, Guyem, Kolbaşı, Metin, Orhan, Ferda E, Perçin
Publikováno v:
Oral healthpreventive dentistry. 18(1)
The aim of this study was to assess the genetic evaluation of a three-generation consanguineous family with isolated oligodontia.A 16-year-old male patient who had been referred for orthodontic treatment due to the presence of oligodontia, and his fa
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::f042c86ba9c81fbf4f8b0656dbecdda7
https://pubmed.ncbi.nlm.nih.gov/32618450
https://pubmed.ncbi.nlm.nih.gov/32618450
Autor:
Mohammed Hawash, Deniz Cansen Kahraman, Sezen Guntekin Ergun, Rengul Cetin-Atalay, Sultan Nacak Baytas
Publikováno v:
BMC Chemistry, Vol 15, Iss 1, Pp 1-14 (2021)
Abstract Background Liver cancer is predicted to be the sixth most diagnosed cancer globally and fourth leading cause of cancer deaths. In this study, a series of indole-3-isoxazole-5-carboxamide derivatives were designed, synthesized, and evaluated
Externí odkaz:
https://doaj.org/article/5babdee60f4d4b078a7393ea07b9214d
Autor:
Murat Erdem, İbrahim Ozgul, Didem Naz Dioken, Irmak Gurcuoglu, Sezen Guntekin Ergun, Rengul Cetin-Atalay, Tolga Can, Ayse Elif Erson-Bensan
Publikováno v:
Scientific Reports, Vol 11, Iss 1, Pp 1-15 (2021)
Abstract Roles of HNRNPA1 are beginning to emerge in cancers; however, mechanisms causing deregulation of HNRNPA1 function remain elusive. Here, we describe an isoform switch between the 3′-UTR isoforms of HNRNPA1 in breast cancers. We show that th
Externí odkaz:
https://doaj.org/article/bd105dc456f04a9b967fd9a19f1e036d
A new method for analysis of whole exome sequencing data (SELIM) depending on variant prioritization
Publikováno v:
Informatics in Medicine Unlocked, Vol 8, Iss , Pp 51-53 (2017)
Background: After the first genome had been sequenced in 2003 with an international project, Human Genome Project, the 1000 Genomes Project also revealed the analysis of 1092 and 2504 genomes respectively. Whole exome sequencing of human samples was
Externí odkaz:
https://doaj.org/article/a5fe0ba422c1400f9c9c0522e86ddd47