Animal models of amyotrophic lateral sclerosis: A comparison of model validity von Morrice, Jessica, Gregory-Evans, Cheryl, Shaw, Christopher

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Photoreceptor precursor cell integration into rodent retina after treatment with novel glycopeptide PKX‐001 von Viringipurampeer, Ishaq A., Yanai, Anat, Nizamudheen, Vahitha S., Gregory‐Evans, Cheryl Y., Gregory‐Evans, Kevin

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Modeling Environmentally-Induced Motor Neuron Degeneration in Zebrafish von Morrice, Jessica R., Gregory-Evans, Cheryl Y., Shaw, Christopher A.

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Necroptosis in amyotrophic lateral sclerosis and other neurological disorders von Morrice, Jessica R., Gregory-Evans, Cheryl Y., Shaw, Christopher A.

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Focused Magnetic Stem Cell Targeting to the Retina Using Superparamagnetic Iron Oxide Nanoparticles von Yanai, Anat, Häfeli, Urs O., Metcalfe, Andrew L., Soema, Peter, Addo, Lois, Gregory-Evans, Cheryl Y., Po, Kelvin, Shan, Xianghong, Moritz, Orson L., Gregory-Evans, Kevin

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Efficacy of Postnatal In Vivo Nonsense Suppression Therapy in a Pax6 Mouse Model of Aniridia von Wang, Xia, Gregory-Evans, Kevin, Wasan, Kishor M., Sivak, Olena, Shan, Xianghong, Gregory-Evans, Cheryl Y.

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Mutations in LRP5 or FZD4 Underlie the Common Familial Exudative Vitreoretinopathy Locus on Chromosome 11q von Toomes, Carmel, Bottomley, Helen M., Jackson, Richard M., Towns, Katherine V., Scott, Sheila, Mackey, David A., Craig, Jamie E., Jiang, Li, Yang, Zhenglin, Trembath, Richard, Woodruff, Geoffrey, Gregory-Evans, Cheryl Y., Gregory-Evans, Kevin, Parker, Michael J., Black, Graeme C.M., Downey, Louise M., Zhang, Kang, Inglehearn, Chris F.

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Discovery and characterization of small molecules targeting the DNA-binding ETS domain of ERG in prostate cancer von Butler, Miriam S, Roshan-Moniri, Mani, Hsing, Michael, Lau, Desmond, Kim, Ari, Yen, Paul, Mroczek, Marta, Nouri, Mannan, Lien, Scott, Axerio-Cilies, Peter, Dalal, Kush, Yau, Clement, Ghaidi, Fariba, Guo, Yubin, Yamazaki, Takeshi, Lawn, Sam, Gleave, Martin E, Gregory-Evans, Cheryl Y, McIntosh, Lawrence P, Cox, Michael E, Rennie, Paul S, Cherkasov, Artem

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An update on the genetics of ocular coloboma von ALSomiry, Aisha S., Gregory-Evans, Cheryl Y., Gregory-Evans, Kevin

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Foxf2: a novel locus for anterior segment dysgenesis adjacent to the Foxc1 gene von McKeone, Richard, Vieira, Helena, Gregory-Evans, Kevin, Gregory-Evans, Cheryl Y, Denny, Paul

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Postnatal manipulation of Pax6 dosage reverses congenital tissue malformation defects von Gregory-Evans, Cheryl Y, Wang, Xia, Wasan, Kishor M, Zhao, Jinying, Metcalfe, Andrew L, Gregory-Evans, Kevin

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Nonsense suppression therapies in ocular genetic diseases von Wang, Xia, Gregory-Evans, Cheryl Y

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NLRP3 inflammasome activation drives bystander cone photoreceptor cell death in a P23H rhodopsin model of retinal degeneration von Viringipurampeer, Ishaq A, Metcalfe, Andrew L, Bashar, Abu E, Sivak, Olena, Yanai, Anat, Mohammadi, Zeinabsadat, Moritz, Orson L, Gregory-Evans, Cheryl Y, Gregory-Evans, Kevin

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A mouse model of aniridia reveals the in vivo downstream targets of Pax6 driving iris and ciliary body development in the eye von Wang, Xia, Shan, Xianghong, Gregory-Evans, Cheryl Y.

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Prospects and modalities for the treatment of genetic ocular anomalies von Gregory-Evans, Cheryl Y., Wang, Xia, Gregory-Evans, Kevin

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Differentiation of Human Embryonic Stem Cells Using Size-Controlled Embryoid Bodies and Negative Cell Selection in the Production of Photoreceptor Precursor Cells von Yanai, Anat, Laver, Christopher R.J., Joe, Aaron W., Viringipurampeer, Ishaq A., Wang, Xia, Gregory-Evans, Cheryl Y., Gregory-Evans, Kevin

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Molecular genetic diagnostics for inherited retinal dystrophies in the clinical setting von Kolawole, Olubayo U., Huang, Albert, Gregory-Evans, Cheryl Y., Shunmugam, Maheshver, Weaver, Travers, Gregory-Evans, Kevin

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Novel pathogenic variants in Tubulin Tyrosine Like 5 ( TTLL5) associated with cone-dominant retinal dystrophies and an abnormal optical coherence tomography phenotype von Kolawole, Olubayo U, Gregory-Evans, Cheryl Y, Bikoo, Riyaz, Huang, Albert Z, Gregory-Evans, Kevin

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Loss-of-function mutations in KIF14 cause severe microcephaly and kidney development defects in humans and zebrafish von Reilly, Madeline Louise, Stokman, Marijn F, Magry, Virginie, Jeanpierre, Cecile, Alves, Marine, Paydar, Mohammadjavad, Hellinga, Jacqueline, Delous, Marion, Pouly, Daniel, Failler, Marion, Martinovic, Jelena, Loeuillet, Laurence, Leroy, Brigitte, Tantau, Julia, Roume, Joelle, Gregory-Evans, Cheryl Y, Shan, Xianghong, Filges, Isabel, Allingham, John S, Kwok, Benjamin H, Saunier, Sophie, Giles, Rachel H, Benmerah, Alexandre

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Cone-Rod Dystrophy Due to Mutations in a Novel Photoreceptor-Specific Homeobox Gene ( CRX) Essential for Maintenance of the Photoreceptor von Freund, Carol L, Gregory-Evans, Cheryl Y, Furukawa, Takahisa, Papaioannou, Myrto, Looser, Jens, Ploder, Lynda, Bellingham, James, Ng, David, Herbrick, Jo-Anne S, Duncan, Alessandra, Scherer, Stephen W, Tsui, Lap-Chee, Loutradis-Anagnostou, Aphrodite, Jacobson, Samuel G, Cepko, Constance L, Bhattacharya, Shomi S, McInnes, Roderick R

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