A novel dysferlin mutant pseudoexon bypassed with antisense oligonucleotides

por Dominov, Janice A, Uyan, Özgün, Sapp, Peter C, McKenna-Yasek, Diane, Nallamilli, Babi R R, Hegde, Madhuri, Brown, Robert H
Publicado 2014

Reply to comment on: A novel dysferlin mutant pseudoexon bypassed with antisense oligonucleotides

por Dominov, Janice A, Uyan, Özgün, Sapp, Peter C, McKenna-Yasek, Diane, Nallamilli, Babi Ramesh Reddy, Hegde, Madhuri, Brown, Robert H
Publicado 2015

Discovery, Validation and Characterization of Erbb4 and Nrg1 Haplotypes Using Data from Three Genome-Wide Association Studies of Schizophrenia

por Agim, Zeynep Sena, Esendal, Melda, Briollais, Laurent, Uyan, Ozgun, Meschian, Mehran, Martinez, Luis Antonio Mendoza, Ding, Yongmei, Basak, A. Nazli, Ozcelik, Hilmi
Publicado 2013

ATXN2 and Its Neighbouring Gene SH2B3 Are Associated with Increased ALS Risk in the Turkish Population

por Lahut, Suna, Ömür, Özgür, Uyan, Özgün, Ağım, Zeynep Sena, Özoğuz, Aslihan, Parman, Yeşim, Deymeer, Feza, Oflazer, Piraye, Koç, Filiz, Özçelik, Hilmi, Auburger, Georg, Başak, A. Nazlı
Publicado 2012

Genome-Wide Copy Number Variation in Sporadic Amyotrophic Lateral Sclerosis in the Turkish Population: Deletion of EPHA3 Is a Possible Protective Factor

por Uyan, Özgün, Ömür, Özgür, Ağım, Zeynep Sena, Özoğuz, Aslıhan, Li, Hong, Parman, Yeşim, Deymeer, Feza, Oflazer, Piraye, Koç, Filiz, Tan, Ersin, Özçelik, Hilmi, Başak, A. Nazlı
Publicado 2013

Inner nuclear protein Matrin-3 coordinates cell differentiation by stabilizing chromatin architecture

por Cha, Hye Ji, Uyan, Özgün, Kai, Yan, Liu, Tianxin, Zhu, Qian, Tothova, Zuzana, Botten, Giovanni A., Xu, Jian, Yuan, Guo-Cheng, Dekker, Job, Orkin, Stuart H.
Publicado 2021

Imaging Net Retrograde Axonal Transport In Vivo: A Physiological Biomarker

por Lee, Pin‐Tsun Justin, Kennedy, Zachary, Wang, Yuzhen, Lu, Yimeng, Cefaliello, Carolina, Uyan, Özgün, Song, Chun‐Qing, Godinho, Bruno Miguel da Cruz, Xu, Zuoshang, Rusckowski, Mary, Xue, Wen, Brown, Robert H.
Publicado 2022

Correction of pseudoexon splicing caused by a novel intronic dysferlin mutation

por Dominov, Janice A., Uyan, Özgün, McKenna‐Yasek, Diane, Nallamilli, Babi Ramesh Reddy, Kergourlay, Virginie, Bartoli, Marc, Levy, Nicolas, Hudson, Judith, Evangelista, Teresinha, Lochmuller, Hanns, Krahn, Martin, Rufibach, Laura, Hegde, Madhuri, Brown, Robert H.
Publicado 2019