The X-linked retinitis pigmentosa protein RP2 facilitates G protein traffic. by Schwarz, N, Novoselova, T, Wait, R, Hardcastle, A, Cheetham, M

Novel retinal and cone photoreceptor transcripts revealed by human macular expression profiling. by Hornan, D, Peirson, S, Hardcastle, A, Molday, R, Cheetham, M, Webster, A

Modulation of Sub-RPE deposits in vitro: a potential model for age-related macular degeneration. by Amin, S, Chong, N, Bailey, T, Zhang, J, Knupp, C, Cheetham, M, Greenwood, J, Luthert, P

Isolation and characterization of murine Cds (CDP-diacylglycerol synthase) 1 and 2. by Inglis-Broadgate, S, Ocaka, L, Banerjee, R, Gaasenbeek, M, Chapple, J, Cheetham, M, Clark, B, Hunt, D, Halford, S

Differential expression of two distinct functional isoforms of melanopsin (Opn4) in the mammalian retina. by Pires, S, Hughes, S, Turton, M, Melyan, Z, Peirson, S, Zheng, L, Kosmaoglou, M, Bellingham, J, Cheetham, M, Lucas, R, Foster, R, Hankins, M, Halford, S

Identification of novel mutations in the carbohydrate sulfotransferase gene (CHST6) causing macular corneal dystrophy. by El-Ashry, M, El-Aziz, A, Wilkins, S, Cheetham, M, Wilkie, SE, Hardcastle, A, Halford, S, Bayoumi, A, Ficker, L, Tuft, S, Bhattacharya, S, Ebenezer, N

POLCAM: instant molecular orientation microscopy for the life sciences by Bruggeman, E, Zhang, O, Needham, L, Körbel, M, Daly, S, Cheetham, M, Peters, R, Wu, T, Klymchenko, AS, Davis, SJ, Paluch, EK, Klenerman, D, Lew, MD, O’Holleran, K, Lee, SF

Novel homozygous splicing mutations in ARL2BP cause autosomal recessive retinitis pigmentosa by Fiorentino, A, Yu, J, Arno, G, Pontikos, N, Halford, S, Broadgate, S, Michaelides, M, Carss, K, Raymond, F, Cheetham, M, Webster, A, Downes, S, Hardcastle, A, NIHR-BioResource Rare Diseases Consortium, UK Inherited Retinal Dystrophy Consortium

EYS, encoding an ortholog of Drosophila spacemaker, is mutated in autosomal recessive retinitis pigmentosa. by El-Aziz, A, Barragan, I, O'Driscoll, C, Goodstadt, L, Prigmore, E, Borrego, S, Mena, M, Pieras, J, El-Ashry, M, Safieh, L, Shah, A, Cheetham, M, Carter, N, Chakarova, C, Ponting, C, Bhattacharya, S, Antinolo, G

Leber congenital amaurosis associated with AIPL1: challenges in ascribing disease causation, clinical findings, and implications for gene therapy. by Tan, M, Mackay, D, Cowing, J, Tran, H, Smith, A, Wright, G, Dev-Borman, A, Henderson, R, Moradi, P, Russell-Eggitt, I, Maclaren, R, Robson, A, Cheetham, M, Thompson, D, Webster, A, Michaelides, M, Ali, R, Moore, A

Autosomal-dominant corneal endothelial dystrophies CHED1 and PPCD1 are allelic disorders caused by non-coding mutations in the promoter of OVOL2 by Davidson, A, Liskova, P, Evans, C, Dudakova, L, Nosková, L, Pontikos, N, Hartmannová, H, Hodaňová, K, Stránecký, V, Kozmík, Z, Levis, H, Idigo, N, Sasai, N, Maher, G, Bellingham, J, Veli, N, Ebenezer, N, Cheetham, M, Daniels, J, Thaung, C, Jirsova, K, Plagnol, V, Filipec, M, Kmoch, S, Tuft, S, Hardcastle, A