Visual pigments and oil droplets from six classes of photoreceptor in the retinas of birds
Bowmaker, J.K., Heath, L.A., Wilkie, S.E., Hunt, D.M.
Published in Vision research (Oxford) (01.08.1997)
Published in Vision research (Oxford) (01.08.1997)
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Journal Article
Vision in the ultraviolet
Hunt, D M, Wilkie, S E, Bowmaker, J K, Poopalasundaram, S
Published in Cellular and molecular life sciences : CMLS (01.10.2001)
Published in Cellular and molecular life sciences : CMLS (01.10.2001)
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Journal Article
Functional characterization of missense mutations at codon 838 in retinal guanylate cyclase correlates with disease severity in patients with autosomal dominant cone-rod dystrophy
WILKIE, Susan E, NEWBOLD, Richard J, DEERY, Evelyne, WALKER, Caroline E, STINTON, Inez, RAMAMURTHY, Visvanathan, HURLEY, James B, BHATTACHARYA, Shomi S, WARREN, Martin J, HUNT, David M
Published in Human molecular genetics (12.12.2000)
Published in Human molecular genetics (12.12.2000)
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Journal Article
Interactions within the Coiled-coil Domain of RetGC-1 Guanylyl Cyclase Are Optimized for Regulation Rather than for High Affinity
Ramamurthy, Visvanathan, Tucker, Chandra, Wilkie, Susan E., Daggett, Valerie, Hunt, David M., Hurley, James B.
Published in The Journal of biological chemistry (13.07.2001)
Published in The Journal of biological chemistry (13.07.2001)
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Journal Article
Spectral Tuning of Avian Violet- and Ultraviolet-Sensitive Visual Pigments
Wilkie, Susan E, Robinson, Phyllis R, Cronin, Thomas W, Poopalasundaram, Subathra, Bowmaker, James K, Hunt, David M
Published in Biochemistry (Easton) (11.07.2000)
Published in Biochemistry (Easton) (11.07.2000)
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Journal Article
Identification and Functional Consequences of a New Mutation (E155G) in the Gene for GCAP1 That Causes Autosomal Dominant Cone Dystrophy
Wilkie, Susan E., Li, Yang, Deery, Evelyne C., Newbold, Richard J., Garibaldi, Daniel, Bateman, J. Bronwyn, Zhang, Heidi, Lin, Wei, Zack, Donald J., Bhattacharya, Shomi S., Warren, Martin J., Hunt, David M., Zhang, Kang
Published in American journal of human genetics (01.09.2001)
Published in American journal of human genetics (01.09.2001)
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Journal Article
Characterisation of the ultraviolet-sensitive opsin gene in the honey bee, Apis mellifera
Bellingham, J, Wilkie, S.E, Morris, A.G, Bowmarker, J.K, Hunt, D.M
Published in European journal of biochemistry (01.02.1997)
Published in European journal of biochemistry (01.02.1997)
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Journal Article
The molecular basis for UV vision in birds: spectral characteristics, cDNA sequence and retinal localization of the UV-sensitive visual pigment of the budgerigar (Melopsittacus undulatus)
Wilkie, S E, Vissers, P M, Das, D, Degrip, W J, Bowmaker, J K, Hunt, D M
Published in Biochemical journal (15.02.1998)
Published in Biochemical journal (15.02.1998)
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Journal Article
A Novel Keratocan Mutation Causing Autosomal Recessive Cornea Plana
Lehmann, Ordan J, El-ashry, Mohamed F, Ebenezer, Neil D, Ocaka, Louise, Francis, Peter J, Wilkie, Susan E, Patel, Reshma J, Ficker, Linda, Jordan, Tim, Khaw, Peng T, Bhattacharya, Shomi S
Published in Investigative ophthalmology & visual science (01.12.2001)
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Published in Investigative ophthalmology & visual science (01.12.2001)
Journal Article
The destabilization of human GCAP1 by a proline to leucine mutation might cause cone-rod dystrophy
NEWBOLD, Richard J, DEERY, Evelyne C, WALKER, Caroline E, WILKIE, Susan E, SRINIVASAN, Narayanaswamy, HUNT, David M, BHATTACHARYA, Shomi S, WARREN, Martin J
Published in Human molecular genetics (2001)
Published in Human molecular genetics (2001)
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Journal Article
Polr3b heterozygosity in mice induces both beneficial and deleterious effects on health during ageing with no effect on lifespan
Borland, Gillian, Wilkie, Stephen E., Thomson, Jackie, Wang, Zhe, Tullet, Jennifer M. A., Alic, Nazif, Selman, Colin
Published in Aging cell (01.05.2024)
Published in Aging cell (01.05.2024)
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Journal Article
Genetic enhancement of cognition in a kindred with cone–rod dystrophy due to RIMS1 mutation
Sisodiya, Sanjay M, Thompson, Pamela J, Need, Anna, Harris, Sarah E, Weale, Michael E, Wilkie, Susan E, Michaelides, Michel, Free, Samantha L, Walley, Nicole, Gumbs, Curtis, Gerrelli, Dianne, Ruddle, Piers, Whalley, Lawrence J, Starr, John M, Hunt, David M, Goldstein, David B, Deary, Ian J, Moore, Anthony T
Published in Journal of medical genetics (01.06.2007)
Published in Journal of medical genetics (01.06.2007)
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Journal Article
Mutations in the Gene KCNV2 Encoding a Voltage-Gated Potassium Channel Subunit Cause “Cone Dystrophy with Supernormal Rod Electroretinogram” in Humans
Wu, Huimin, Cowing, Jill A., Michaelides, Michel, Wilkie, Susan E., Jeffery, Glen, Jenkins, Sharon A., Mester, Viktoria, Bird, Alan C., Robson, Anthony G., Holder, Graham E., Moore, Anthony T., Hunt, David M., Webster, Andrew R.
Published in American journal of human genetics (01.09.2006)
Published in American journal of human genetics (01.09.2006)
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