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Dermal fibroblast transcriptome indicates contribution of WNT signaling pathways in the pathogenesis of Apert syndrome.
Çetinkaya A, Taşkıran E, Soyer T, Şimşek-Kiper PÖ, Utine GE, Tunçbilek G, Boduroğlu K, Alikaşifoğlu M. Çetinkaya A, et al. Among authors: tuncbilek g. Turk J Pediatr. 2017;59(6):619-624. doi: 10.24953/turkjped.2017.06.001. Turk J Pediatr. 2017. PMID: 30035392 Free article.
Cetinkaya A, Taskiran E, Soyer T, Simsek-Kiper PO, Utine GE, Tuncbilek G, Boduroglu K, Alikasifoglu M. Dermal fibroblast transcriptome indicates contribution of WNT signaling pathways in the pathogenesis of Apert syndrome. ...
Cetinkaya A, Taskiran E, Soyer T, Simsek-Kiper PO, Utine GE, Tuncbilek G, Boduroglu K, Alikasifoglu M. Dermal fibroblast trans …
ALX4 dysfunction disrupts craniofacial and epidermal development.
Kayserili H, Uz E, Niessen C, Vargel I, Alanay Y, Tuncbilek G, Yigit G, Uyguner O, Candan S, Okur H, Kaygin S, Balci S, Mavili E, Alikasifoglu M, Haase I, Wollnik B, Akarsu NA. Kayserili H, et al. Among authors: tuncbilek g. Hum Mol Genet. 2009 Nov 15;18(22):4357-66. doi: 10.1093/hmg/ddp391. Epub 2009 Aug 19. Hum Mol Genet. 2009. PMID: 19692347
Disruption of ALX1 causes extreme microphthalmia and severe facial clefting: expanding the spectrum of autosomal-recessive ALX-related frontonasal dysplasia.
Uz E, Alanay Y, Aktas D, Vargel I, Gucer S, Tuncbilek G, von Eggeling F, Yilmaz E, Deren O, Posorski N, Ozdag H, Liehr T, Balci S, Alikasifoglu M, Wollnik B, Akarsu NA. Uz E, et al. Among authors: tuncbilek g. Am J Hum Genet. 2010 May 14;86(5):789-96. doi: 10.1016/j.ajhg.2010.04.002. Epub 2010 May 6. Am J Hum Genet. 2010. PMID: 20451171 Free PMC article.
Effects of iloprost on calvarial sutures.
Tunçbilek G, Korkusuz P, Ozgür F. Tunçbilek G, et al. J Craniofac Surg. 2008 Nov;19(6):1472-80. doi: 10.1097/SCS.0b013e318188a31b. J Craniofac Surg. 2008. PMID: 19098535
63 results