Zobrazeno 1 - 10
of 27
pro vyhledávání: '"Selin Unal"'
Autor:
Hakan Yavuzer, Isil Bavunoglu, Dilek Cuhadar Ercelebi, Aydın Tunçkale, Tuba Mutlu, Selin Unal, Yalcin Hacioglu, Serap Yavuzer, Bahadir Batar, Mahir Cengiz, Duygu Erhan, Mehmet Güven
Publikováno v:
Gene. 673
TMPRSS6 gene mutations can result in iron deficiency anemia (IDA) and cause an increased iron-regulatory hormone, hepcidin, levels. TMPRSS6 encodes a serine protease, matriptase-2, which functions as negative regulatory protein of hepcidin transcript
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e16ef632750c50731c1180a2ab78fccf
https://pubmed.ncbi.nlm.nih.gov/29928945
https://pubmed.ncbi.nlm.nih.gov/29928945
Autor:
Bahadir Batar, Ziya Ismailoglu, Mehmet Güven, Zeki Öngen, Bilgehan Karadag, İlhan Onaran, Selin Unal
Publikováno v:
Gene. 558:99-102
Coronary artery disease (CAD), being a multifactorial disease process, has been suggested to be associated by the interaction of both environmental and genetic risk factors. Toll-like receptors (TLRs) are related to the receptors of the innate immune
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::46fca10d8383c82c2e7e576ac1759c67
https://doi.org/10.1016/j.gene.2014.12.047
https://doi.org/10.1016/j.gene.2014.12.047
Publikováno v:
Molecular Biology Reports
One-third of all individuals with epilepsy are resistant to antiepileptic drug (AED) treatment. Antiepileptic treatment response has been suggested to be modulated by genetic polymorphisms of drug efflux transporters. Several polymorphic variants wit
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d17758470c10de30277c6e945f9e5ff0
https://doi.org/10.1007/s11033-013-2866-y
https://doi.org/10.1007/s11033-013-2866-y
Autor:
Mehmet Güven, Bahadir Batar, Safa Baris, Duygu Erhan, Selin Unal, Nihal Özdemir, Merve Bostancı, Tiraje Celkan
Publikováno v:
Meta Gene
The variations between different individuals in the xenobiotic metabolizing enzymes' activity were shown to modify susceptibility to childhood acute lymphoblastic leukemia (ALL). Polymorphisms associated with genes coding for the glutathione S-transf
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bcce8f6b3575c25321e00d5e55941c29
https://pubmed.ncbi.nlm.nih.gov/26137447
https://pubmed.ncbi.nlm.nih.gov/26137447
Publikováno v:
Molecular diagnosistherapy. 18(2)
Despite the availability of several antiepileptic drugs, drug resistance remains one of the major challenges in epilepsy therapy. Genetic factors are known to play a significant role in the prognosis and treatment of epilepsy. The aim of this study w
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2362b7b3f7c8f82a8619921f0a654b60
https://pubmed.ncbi.nlm.nih.gov/24338437
https://pubmed.ncbi.nlm.nih.gov/24338437
Autor:
Bahadir Batar, İlhan Onaran, Zeki Öngen, Mehmet Güven, Selin Unal, Bilgehan Karadag, Ziya Ismailoglu
Publikováno v:
Gene. 568:228
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::72a5547b16da38d9789f1e10268a1084
https://doi.org/10.1016/j.gene.2015.05.033
https://doi.org/10.1016/j.gene.2015.05.033
Publikováno v:
International Journal of Artificial Organs; Nov2024, Vol. 47 Issue 11, p810-815, 6p
Autor:
O'TOOLE, MOLLY (AUTHOR)
Publikováno v:
Newsweek Global. 12/28/2018, Vol. 171 Issue 20, p16-23. 8p. 9 Color Photographs.
Autor:
Salopek, Paul
Publikováno v:
National Geographic. Mar2015, Vol. 227 Issue 3, p48-71. 24p. 14 Color Photographs, 1 Map.
Autor:
O'TOOLE, MOLLY (AUTHOR)
Publikováno v:
Newsweek Mexico. 12/23/2018, Vol. 22 Issue 52, p30-35. 6p. 4 Color Photographs.