Drosophila model to clarify the pathological significance of OPA1 in autosomal dominant optic atrophy by Yohei Nitta, Jiro Osaka, Ryuto Maki, Satoko Hakeda-Suzuki, Emiko Suzuki, Satoshi Ueki, Takashi Suzuki, Atsushi Sugie

Subjects: “…dominant optic atrophy…”
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The Influence of Mitochondrial Dynamics and Function on Retinal Ganglion Cell Susceptibility in Optic Nerve Disease by Nicole A. Muench, Sonia Patel, Margaret E. Maes, Ryan J. Donahue, Akihiro Ikeda, Robert W. Nickells

Subjects: “…dominant optic atrophy…”
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Identification of AFG3L2 dominant optic atrophy following reanalysis of clinical exome sequencing by Michael C. Brodsky, Rory J. Olson, Faizal Z. Asumda, Madeline Q.R. Lopour, Lisa A. Schimmenti, Eric W. Klee

Subjects: “…Dominant optic atrophy…”
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<i>OPA1</i> Dominant Optic Atrophy: Diagnostic Approach in the Pediatric Population by Natalia Arruti, Patricia Rodríguez-Solana, María Nieves-Moreno, Marta Guerrero-Carretero, Ángela del Pozo, Victoria E. F. Montaño, Fernando Santos-Simarro, Emi Rikeros-Orozco, Luna Delgado-Mora, Elena Vallespín, Susana Noval

Subjects: “…dominant optic atrophy…”
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OPA1: 516 unique variants and 831 patients registered in an updated centralized Variome database by Bastien Le Roux, Guy Lenaers, Xavier Zanlonghi, Patrizia Amati-Bonneau, Floris Chabrun, Thomas Foulonneau, Angélique Caignard, Stéphanie Leruez, Philippe Gohier, Vincent Procaccio, Dan Milea, Johan T. den Dunnen, Pascal Reynier, Marc Ferré

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Genetic underpinnings explored: OPA1 deletion and complex phenotypes on chromosome 3q29 by Ethan Hung-Hsi Wang, Pei-Hsuan Lin, Pei-Liang Wu, Eugene Yu-Chuan Kang, Laura Liu, Lung-Kun Yeh, Kuan-Jen Chen, Meng-Chang Hsiao, Nan-Kai Wang

Subjects: “…Autosomal dominant optic atrophy…”
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Optimized OPA1 Isoforms 1 and 7 Provide Therapeutic Benefit in Models of Mitochondrial Dysfunction by Daniel M. Maloney, Naomi Chadderton, Sophia Millington-Ward, Arpad Palfi, Ciara Shortall, James J. O’Byrne, James J. O’Byrne, Lorraine Cassidy, David Keegan, Peter Humphries, Paul Kenna, Paul Kenna, Gwyneth Jane Farrar

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Dominant Optic Atrophy (DOA): Modeling the Kaleidoscopic Roles of OPA1 in Mitochondrial Homeostasis by Valentina Del Dotto, Valerio Carelli, Valerio Carelli

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Disruption of mitochondrial homeostasis and permeability transition pore opening in OPA1 iPSC-derived retinal ganglion cells by Michael Whitehead, Joshua P. Harvey, Paul E. Sladen, Giada Becchi, Kritarth Singh, Yujiao Jennifer Sun, Thomas Burgoyne, Michael R. Duchen, Patrick Yu-Wai-Man, Michael E. Cheetham

Subjects: “…Dominant optic atrophy…”
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Ocular manifestations of mitochondrial disease by S. D. Mathebula

Subjects: “…dominant optic atrophy…”
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First submicroscopic inversion of the OPA1 gene identified in dominant optic atrophy – a case report by Nicole Weisschuh, Pascale Mazzola, Tilman Heinrich, Tobias Haack, Bernd Wissinger, Felix Tonagel, Carina Kelbsch

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Autosomal dominant optic atrophy: A novel treatment for OPA1 splice defects using U1 snRNA adaption by Christoph Jüschke, Thomas Klopstock, Claudia B. Catarino, Marta Owczarek-Lipska, Bernd Wissinger, John Neidhardt

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<i>Caenorhabditis elegans</i> as a Model System to Study Human Neurodegenerative Disorders by Antonis Roussos, Katerina Kitopoulou, Fivos Borbolis, Konstantinos Palikaras

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Generation of iPSC-Derived RGCs for Modeling Dominant Optic Atrophy by Marta García-López, M. Esther Gallardo

Subjects: “…dominant optic atrophy…”
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Establishing induced pluripotent stem cell lines from two dominant optic atrophy patients with distinct OPA1 mutations and clinical pathologies by Katherine A. Pohl, Katherine A. Pohl, Xiangmei Zhang, Anh H. Pham, Jane W. Chan, Alfredo A. Sadun, Xian-Jie Yang, Xian-Jie Yang

Subjects: “…dominant optic atrophy…”
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Dominant mutations in MIEF1 affect mitochondrial dynamics and cause a singular late onset optic neuropathy by Majida Charif, Yvette C. Wong, Soojin Kim, Agnès Guichet, Catherine Vignal, Xavier Zanlonghi, Philippe Bensaid, Vincent Procaccio, Dominique Bonneau, Patrizia Amati-Bonneau, Pascal Reynier, Dimitri Krainc, Guy Lenaers

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Neuro-ophthalmic manifestations of mitochondrial disorders and their management by Jane H Lock, Neha K Irani, Nancy J Newman

Subjects: “…dominant optic atrophy…”
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Derivation and Characterization of Isogenic <i>OPA1</i> Mutant and Control Human Pluripotent Stem Cell Lines by Katherine A. Pohl, Xiangmei Zhang, Johnny Jeonghyun Ji, Linsey Stiles, Alfredo A. Sadun, Xian-Jie Yang

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