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Page 1
Hereditary spastic paraplegia with recessive trait caused by mutation in KLC4 gene.
Bayrakli F, Poyrazoglu HG, Yuksel S, Yakicier C, Erguner B, Sagiroglu MS, Yuceturk B, Ozer B, Doganay S, Tanrikulu B, Seker A, Akbulut F, Ozen A, Per H, Kumandas S, Altuner Torun Y, Bayri Y, Sakar M, Dagcinar A, Ziyal I. Bayrakli F, et al. Among authors: yuceturk b. J Hum Genet. 2015 Dec;60(12):763-8. doi: 10.1038/jhg.2015.109. Epub 2015 Oct 1. J Hum Genet. 2015. PMID: 26423925 Clinical Trial.
Novel POC1A mutation in primordial dwarfism reveals new insights for centriole biogenesis.
Koparir A, Karatas OF, Yuceturk B, Yuksel B, Bayrak AO, Gerdan OF, Sagiroglu MS, Gezdirici A, Kirimtay K, Selcuk E, Karabay A, Creighton CJ, Yuksel A, Ozen M. Koparir A, et al. Among authors: yuceturk b. Hum Mol Genet. 2015 Oct 1;24(19):5378-87. doi: 10.1093/hmg/ddv261. Epub 2015 Jul 10. Hum Mol Genet. 2015. PMID: 26162852 Review.
The altered promoter methylation of oxytocin receptor gene in autism.
Elagoz Yuksel M, Yuceturk B, Karatas OF, Ozen M, Dogangun B. Elagoz Yuksel M, et al. Among authors: yuceturk b. J Neurogenet. 2016 Sep-Dec;30(3-4):280-284. doi: 10.1080/01677063.2016.1202951. Epub 2016 Aug 5. J Neurogenet. 2016. PMID: 27309964
Role of miR-145 in human laryngeal squamous cell carcinoma.
Karatas OF, Yuceturk B, Suer I, Yilmaz M, Cansiz H, Solak M, Ittmann M, Ozen M. Karatas OF, et al. Among authors: yuceturk b. Head Neck. 2016 Feb;38(2):260-6. doi: 10.1002/hed.23890. Epub 2015 Jun 16. Head Neck. 2016. PMID: 26083661
11 results