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pro vyhledávání: '"A N, Başak"'
Akademický článek
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Autor:
Tecellioğlu, M.1 (AUTHOR), Türkmen, N. Başak2 (AUTHOR) nesebasak86@gmail.com, Ciftçi, O.3 (AUTHOR), Taşlıdere, A.4 (AUTHOR), Ekmekyapar, T.5 (AUTHOR), Yüce, H.2 (AUTHOR), Öztanır, M. N.6 (AUTHOR), Özcan, C.7 (AUTHOR)
Publikováno v:
Journal of Evolutionary Biochemistry & Physiology. Jul2022, Vol. 58 Issue 4, p1041-1054. 14p.
Autor:
Ö, Öztop-Çakmak, G, Şimşir, Ş, Tekgül, M S, Aygün, O, Gökler, B, Kahyaoğlu, Z E, Kaya, R, Palvadeau, A N, Başak, S, Ertan
Publikováno v:
Revue Neurologique. 178:907-913
VPS13D is a recently described gene. Worldwide, only 15 families with 23 affected individuals have been reported with a VPS13D-based disease. Mutated VPS13D causes a complex phenotype with a hyperkinetic movement disorder and ataxia, especially in ch
Publikováno v:
Journal of Evolutionary Biochemistry and Physiology. 58:1819-1833
The objective of this study was to evaluate the biological activities of chrysin (CRY), curcumin (CUR), and ellagic acid (EA) by comparing the anti-proliferative, anti-migration effects, and apoptotic gene expressions between the three human cancer c
Autor:
M. Tecellioğlu, N. Başak Türkmen, O. Ciftçi, A. Taşlıdere, T. Ekmekyapar, H. Yüce, M. N. Öztanır, C. Özcan
Multiple sclerosis (MS) is a disease of the central nervous system of unknown cause and limited therapeutical treatments. In this study we analyzed the effects of resveratrol (RSV), a polyphenolic compound with well-known neuroprotective effects, on
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f6dfdd3cb1127548a2d6d7499f37824f
https://hdl.handle.net/11499/50422
https://hdl.handle.net/11499/50422
Autor:
Ö, Uyanık, Ş, Gürbüz, O, Çiftci, H, Oğuztürk, M, Aydın, A, Çetin, N, Başak, M, Gökhan Turtay, N, Yücel
Publikováno v:
European review for medical and pharmacological sciences. 25(23)
Irinotecan (IR/CPT-11) is a semisynthetic, water-soluble derivative of the alkaloid camptothecin. It is a topoisomerase I group antineoplastic drug commonly used for the treatment of many cancer types, although it has side effects in tissues such as
Publikováno v:
In Expert Systems With Applications March 2009 36(2) Part 1:1337-1354
Akademický článek
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Publikováno v:
Turkish journal of haematology : official journal of Turkish Society of Haematology. 18(2)
A three-year old Turkish girl having both homozygous ß-thalassemia and hereditary spherocytosis and her family have been studied. The molecular defect causing thalassemia in the family was of the frame shift codon 8 (-AA) mutation type. The diagnosi
Publikováno v:
Turkish journal of haematology : official journal of Turkish Society of Haematology. 18(3)
We report here a ß- thalassemia major case (homozygous IVS-1-110 G-A) associated with Familial Mediterranean Fever (FMF) (homozygous 694 Met-Val). Our patient's clinical course revealed a possible synergistic effect between colchicine and desferriox