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Functional divergence of the two Elongator subcomplexes during neurodevelopment.
Gaik M, Kojic M, Stegeman MR, Öncü-Öner T, Kościelniak A, Jones A, Mohamed A, Chau PYS, Sharmin S, Chramiec-Głąbik A, Indyka P, Rawski M, Biela A, Dobosz D, Millar A, Chau V, Ünalp A, Piper M, Bellingham MC, Eichler EE, Nickerson DA, Güleryüz H, Abbassi NEH, Jazgar K, Davis MJ, Mercimek-Andrews S, Cingöz S, Wainwright BJ, Glatt S. Gaik M, et al. Among authors: unalp a. EMBO Mol Med. 2022 Jul 7;14(7):e15608. doi: 10.15252/emmm.202115608. Epub 2022 Jun 13. EMBO Mol Med. 2022. PMID: 35698786 Free PMC article.
GPR56 homozygous nonsense mutation p.R271* associated with phenotypic variability in bilateral frontoparietal polymicrogyria.
Öncü-Öner T, Ünalp A, Porsuk-Doru İ, Ağılkaya S, Güleryüz H, Saraç A, Ergüner B, Yüksel B, Hız-Kurul S, Cingöz S. Öncü-Öner T, et al. Among authors: unalp a. Turk J Pediatr. 2018;60(3):229-237. doi: 10.24953/turkjped.2018.03.001. Turk J Pediatr. 2018. PMID: 30511534 Free article.
Oncu-Oner T, Unalp A, Porsuk-Doru I, Agilkaya S, Guleryuz H, Sarac A, Erguner B, Yuksel B, Hiz-Kurul S, Cingoz S. ...Herein, we describe three siblings of consanguineous parents with a homozygous germline mutation (p.R271*) located in the seventh exon …
Oncu-Oner T, Unalp A, Porsuk-Doru I, Agilkaya S, Guleryuz H, Sarac A, Erguner B, Yuksel B, Hiz-Kurul S, Cingoz S. ...He …
Identification of PCDH19 Gene Mutations/Deletions in Patients with Early Onset Epilepsy.
Gursoy S, Ataman E, Baysal BT, Özyılmaz B, Gençpınar P, Hız AS, Yiş U, Ünalp A, Dündar NO, Ülgenalp A, Erçal D. Gursoy S, et al. Among authors: unalp a. Ann Indian Acad Neurol. 2020 Mar-Apr;23(2):206-210. doi: 10.4103/aian.AIAN_465_19. Epub 2020 Feb 25. Ann Indian Acad Neurol. 2020. PMID: 32189863 Free PMC article.
Investigation of the most common clinical and imaging findings and the role of tubulin genes in the etiology of malformations of cortical development.
Aksel Kiliçarslan Ö, Ataman E, Gürsoy S, Gürbüz G, Ünalp A, Gençpinar P, Olgaç Dündar N, Edizer S, Ülgenalp A, Giray Bozkaya Ö. Aksel Kiliçarslan Ö, et al. Among authors: unalp a. Turk J Med Sci. 2020 Oct 22;50(6):1573-1579. doi: 10.3906/sag-1901-170. Turk J Med Sci. 2020. PMID: 32718119 Free PMC article.
Childhood onset limb-girdle muscular dystrophies in the Aegean part of Turkey.
Yiş U, Diniz G, Hazan F, Daimagüler HS, Baysal BT, Baydan F, Akinci G, Ünalp A, Aktan G, Bayram E, Hiz S, Paketçi C, Okur D, Özer E, Danyeli AE, Polat M, Uyanik G, Çirak S. Yiş U, et al. Among authors: unalp a. Acta Myol. 2018 Sep 1;37(3):210-220. eCollection 2018 Sep. Acta Myol. 2018. PMID: 30838351 Free PMC article.
99 results