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Results: 1-8 |
Results: 8
Vision in the ultraviolet
Authors: Hunt, DM Wilkie, SE Bowmaker, JK Poopalasundaram, S
Citation: Dm. Hunt et al., Vision in the ultraviolet, CELL MOL L, 58(11), 2001, pp. 1583-1598
The destabilization of human GCAP1 by a proline to leucine mutation might cause cone-rod dystrophy
Authors: Newbold, RJ Deery, EC Walker, CE Wilkie, SE Srinivasan, N Hunt, DM Bhattacharya, SS Warren, MJ
Citation: Rj. Newbold et al., The destabilization of human GCAP1 by a proline to leucine mutation might cause cone-rod dystrophy, HUM MOL GEN, 10(1), 2001, pp. 47-54
A novel keratocan mutation causing autosomal recessive cornea plana
Authors: Lehmann, OJ El-Ashry, MF Ebenezer, ND Ocaka, L Francis, PJ Wilkie, SE Patel, RJ Ficker, L Jordan, T Khaw, PT Bhattacharya, SS
Citation: Oj. Lehmann et al., A novel keratocan mutation causing autosomal recessive cornea plana, INV OPHTH V, 42(13), 2001, pp. 3118-3122
Interactions within the coiled-coil domain of RetGC-1 guanylyl cyclase areoptimized for regulation rather than for high affinity
Authors: Ramamurthy, V Tucker, C Wilkie, SE Daggett, V Hunt, DM Hurley, JB
Citation: V. Ramamurthy et al., Interactions within the coiled-coil domain of RetGC-1 guanylyl cyclase areoptimized for regulation rather than for high affinity, J BIOL CHEM, 276(28), 2001, pp. 26218-26229
Identification and functional consequences of a new mutation (E155G) in the gene for GCAP1 that causes autosomal dominant cone dystrophy
Authors: Wilkie, SE Li, Y Deery, EC Newbold, RJ Garibaldi, D Bateman, JB Zhang, H Lin, W Zack, DJ Bhattacharya, SS Warren, MJ Hunt, DM Zhang, K
Citation: Se. Wilkie et al., Identification and functional consequences of a new mutation (E155G) in the gene for GCAP1 that causes autosomal dominant cone dystrophy, AM J HU GEN, 69(3), 2001, pp. 471-480
Functional characterization of missense mutations at codon 838 in retinal guanylate cyclase correlates with disease severity in patients with autosomal dominant cone-rod dystrophy
Authors: Wilkie, SE Newbold, RJ Deery, E Walker, CE Stinton, I Ramamurthy, V Hurley, JB Bhattacharya, SS Warren, MJ Hunt, DM
Citation: Se. Wilkie et al., Functional characterization of missense mutations at codon 838 in retinal guanylate cyclase correlates with disease severity in patients with autosomal dominant cone-rod dystrophy, HUM MOL GEN, 9(20), 2000, pp. 3065-3073
Spectral tuning of avian violet- and ultraviolet-sensitive visual pigments
Authors: Wilkie, SE Robinson, PR Cronin, TW Poopalasundaram, S Bowmaker, JK Hunt, DM
Citation: Se. Wilkie et al., Spectral tuning of avian violet- and ultraviolet-sensitive visual pigments, BIOCHEM, 39(27), 2000, pp. 7895-7901
Visual pigments and oil droplets in the retina of a passerine bird, the canary Serinus canaria: microspectrophotometry and opsin sequences
Authors: Das, D Wilkie, SE Hunt, DM Bowmaker, JK
Citation: D. Das et al., Visual pigments and oil droplets in the retina of a passerine bird, the canary Serinus canaria: microspectrophotometry and opsin sequences, VISION RES, 39(17), 1999, pp. 2801-2815
Risultati: 1-8 |