Works by Kanuga, Naheed


Results: 16
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    Three Different Cone Opsin Gene Array Mutational Mechanisms with Genotype-Phenotype Correlation and Functional Investigation of Cone Opsin Variants.

    Published in:
    Human Mutation, 2014, v. 35, n. 11, p. 1354, doi. 10.1002/humu.22679
    By:
    • Gardner, Jessica C.;
    • Liew, Gerald;
    • Quan, Ying‐Hua;
    • Ermetal, Burcu;
    • Ueyama, Hisao;
    • Davidson, Alice E.;
    • Schwarz, Nele;
    • Kanuga, Naheed;
    • Chana, Ravinder;
    • Maher, Eamonn R.;
    • Webster, Andrew R.;
    • Holder, Graham E.;
    • Robson, Anthony G.;
    • Cheetham, Michael E.;
    • Liebelt, Jan;
    • Ruddle, Jonathan B.;
    • Moore, Anthony T.;
    • Michaelides, Michel;
    • Hardcastle, Alison J.
    Publication type:
    Article
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    Rescue of mutant rhodopsin traffic by metformin-induced AMPK activation accelerates photoreceptor degeneration.

    Published in:
    Human Molecular Genetics, 2017, v. 26, n. 2, p. 305, doi. 10.1093/hmg/ddw387
    By:
    • Athanasiou, Dimitra;
    • Aguila, Monica;
    • Opefi, Chikwado A.;
    • South, Kieron;
    • Bellingham, James;
    • Bevilacqua, Dalila;
    • Munro, Peter M.;
    • Kanuga, Naheed;
    • Mackenzie, Francesca E.;
    • Dubis, Adam M.;
    • Georgiadis, Anastasios;
    • Graca, Anna B.;
    • Pearson, Rachael A.;
    • Ali, Robin R.;
    • Sakami, Sanae;
    • Palczewski, Krzysztof;
    • Sherman, Michael Y.;
    • Reeves, Philip J.;
    • Cheetham, Michael E.
    Publication type:
    Article
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    Hsp90 inhibition protects against inherited retinal degeneration.

    Published in:
    Human Molecular Genetics, 2014, v. 23, n. 8, p. 2164
    By:
    • Aguilà, Mònica;
    • Bevilacqua, Dalila;
    • McCulley, Caroline;
    • Schwarz, Nele;
    • Athanasiou, Dimitra;
    • Kanuga, Naheed;
    • Novoselov, Sergey S.;
    • Lange, Clemens A.K.;
    • Ali, Robin R.;
    • Bainbridge, James W.;
    • Gias, Carlos;
    • Coffey, Peter J.;
    • Garriga, Pere;
    • Cheetham, Michael E.
    Publication type:
    Article
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    Deep intronic mutation in OFD1, identified by targeted genomic next-generation sequencing, causes a severe form of X-linked retinitis pigmentosa (RP23).

    Published in:
    Human Molecular Genetics, 2012, v. 21, n. 16, p. 3647, doi. 10.1093/hmg/dds194
    By:
    • Webb, Tom R.;
    • Parfitt, David A.;
    • Gardner, Jessica C.;
    • Martinez, Ariadna;
    • Bevilacqua, Dalila;
    • Davidson, Alice E.;
    • Zito, Ilaria;
    • Thiselton, Dawn L.;
    • Ressa, Jacob H.C.;
    • Apergi, Marina;
    • Schwarz, Nele;
    • Kanuga, Naheed;
    • Michaelides, Michel;
    • Cheetham, Michael E.;
    • Gorin, Michael B.;
    • Hardcastle, Alison J.
    Publication type:
    Article
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    X-linked cataract and Nance-Horan syndrome are allelic disorders.

    Published in:
    Human Molecular Genetics, 2009, v. 18, n. 14, p. 2643, doi. 10.1093/hmg/ddp206
    By:
    • Coccia, Margherita;
    • Brooks, Simon P.;
    • Webb, Tom R.;
    • Christodoulou, Katja;
    • Wozniak, Izabella O.;
    • Murday, Victoria;
    • Balicki, Martha;
    • Yee, Harris A.;
    • Wangensteen, Teresia;
    • Riise, Ruth;
    • Saggar, Anand K.;
    • Park, Soo-Mi;
    • Kanuga, Naheed;
    • Francis, Peter J.;
    • Maher, Eamonn R.;
    • Moore, Anthony T.;
    • Russell-Eggitt, Isabelle M.;
    • Hardcastle, Alison J.
    Publication type:
    Article
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