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Journal Abstract Search

277 related items for PubMed ID: 26738566

  • 1. Modeling autosomal dominant optic atrophy using induced pluripotent stem cells and identifying potential therapeutic targets.
    Chen J, Riazifar H, Guan MX, Huang T.
    Stem Cell Res Ther; 2016 Jan 07; 7():2. PubMed ID: 26738566
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  • 2. Modelling autosomal dominant optic atrophy associated with OPA1 variants in iPSC-derived retinal ganglion cells.
    Sladen PE, Jovanovic K, Guarascio R, Ottaviani D, Salsbury G, Novoselova T, Chapple JP, Yu-Wai-Man P, Cheetham ME.
    Hum Mol Genet; 2022 Oct 10; 31(20):3478-3493. PubMed ID: 35652445
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  • 3. Creation of an Isogenic Human iPSC-Based RGC Model of Dominant Optic Atrophy Harboring the Pathogenic Variant c.1861C>T (p.Gln621Ter) in the OPA1 Gene.
    García-López M, Jiménez-Vicente L, González-Jabardo R, Dorado H, Gómez-Manjón I, Martín MÁ, Ayuso C, Arenas J, Gallardo ME.
    Int J Mol Sci; 2024 Jun 30; 25(13):. PubMed ID: 39000346
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  • 5. Influence of Opa1 Mutation on Survival and Function of Retinal Ganglion Cells.
    González-Menéndez I, Reinhard K, Tolivia J, Wissinger B, Münch TA.
    Invest Ophthalmol Vis Sci; 2015 Jul 30; 56(8):4835-45. PubMed ID: 26218912
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  • 9. Opa1 deficiency in a mouse model of autosomal dominant optic atrophy impairs mitochondrial morphology, optic nerve structure and visual function.
    Davies VJ, Hollins AJ, Piechota MJ, Yip W, Davies JR, White KE, Nicols PP, Boulton ME, Votruba M.
    Hum Mol Genet; 2007 Jun 01; 16(11):1307-18. PubMed ID: 17428816
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  • 10. Increased steroidogenesis promotes early-onset and severe vision loss in females with OPA1 dominant optic atrophy.
    Sarzi E, Seveno M, Angebault C, Milea D, Rönnbäck C, Quilès M, Adrian M, Grenier J, Caignard A, Lacroux A, Lavergne C, Reynier P, Larsen M, Hamel CP, Delettre C, Lenaers G, Müller A.
    Hum Mol Genet; 2016 Jun 15; 25(12):2539-2551. PubMed ID: 27260406
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  • 12. The molecular mechanisms of OPA1-mediated optic atrophy in Drosophila model and prospects for antioxidant treatment.
    Yarosh W, Monserrate J, Tong JJ, Tse S, Le PK, Nguyen K, Brachmann CB, Wallace DC, Huang T.
    PLoS Genet; 2008 Jan 15; 4(1):e6. PubMed ID: 18193945
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  • 13. Genomics combined with a protein informatics platform to assess a novel pathogenic variant c.1024 A>G (p.K342E) in OPA1 in a patient with autosomal dominant optic atrophy.
    Ahuja AS, Selvam P, Vadlamudi C, Chopra H, Richter JE, Macklin SK, Samreen A, Helmi H, Mohammaad AN, Hines S, Davila MC, Atwal PS, Caulfield TR.
    Ophthalmic Genet; 2020 Dec 15; 41(6):563-569. PubMed ID: 32940104
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  • 14. Analysis of opa1 isoforms expression and apoptosis regulation in autosomal dominant optic atrophy (ADOA) patients with mutations in the opa1 gene.
    Formichi P, Radi E, Giorgi E, Gallus GN, Brunetti J, Battisti C, Rufa A, Dotti MT, Franceschini R, Bracci L, Federico A.
    J Neurol Sci; 2015 Apr 15; 351(1-2):99-108. PubMed ID: 25796301
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  • 19. Opa1 deficiency in a mouse model of dominant optic atrophy leads to retinal ganglion cell dendropathy.
    Williams PA, Morgan JE, Votruba M.
    Brain; 2010 Oct 15; 133(10):2942-51. PubMed ID: 20817698
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