Visual system evolution and the nature of the ancestral snake
Simões, B. F, Sampaio, F. L, Jared, C, Antoniazzi, M. M, Loew, E. R, Bowmaker, J. K, Rodriguez, A, Hart, N. S, Hunt, D. M, Partridge, J. C, Gower, D. J
Published in Journal of evolutionary biology (01.07.2015)
Published in Journal of evolutionary biology (01.07.2015)
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Journal Article
A novel connexin50 mutation associated with congenital nuclear pulverulent cataracts
Arora, A, Minogue, P J, Liu, X, Addison, P K, Russel-Eggitt, I, Webster, A R, Hunt, D M, Ebihara, L, Beyer, E C, Berthoud, V M, Moore, A T
Published in Journal of medical genetics (01.03.2008)
Published in Journal of medical genetics (01.03.2008)
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Journal Article
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
Mutations in the Retinal Guanylate Cyclase (RETGC-1) Gene in Dominant Cone-Rod Dystrophy
Kelsell, Rosemary E., Gregory-Evans, Kevin, Payne, Annette M., Perrault, Isabelle, Kaplan, Josseline, Yang, Ruey-Bing, Garbers, David L., Bird, Alan C., Moore, Anthony T., Hunt, David M.
Published in Human molecular genetics (01.07.1998)
Published in Human molecular genetics (01.07.1998)
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Journal Article
Systemic acquired resistance
Ryals, J.A. (Ciba-Geigy Corporation, Research Triangle Park, NC.), Neuenschwander, U.H, Willits, M.G, Molina, A, Steiner, H.Y, Hunt, M.D
Published in The Plant cell (01.10.1996)
Published in The Plant cell (01.10.1996)
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Journal Article
A detailed phenotypic study of “cone dystrophy with supernormal rod ERG”
Michaelides, M, Holder, G E, Webster, A R, Hunt, D M, Bird, A C, Fitzke, F W, Mollon, J D, Moore, A T
Published in British journal of ophthalmology (01.03.2005)
Published in British journal of ophthalmology (01.03.2005)
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Journal Article
Restoration of photoreceptor ultrastructure and function in retinal degeneration slow mice by gene therapy
Ali, Robin R, Sarra, Gian-Marco, Stephens, Clare, Alwis, Mahesh de, Bainbridge, James W.B, Munro, Peter M, Fauser, Sascha, Reichel, Martin B, Kinnon, Christine, Hunt, David M, Bhattacharya, Shomi S, Thrasher, Adrian J
Published in Nature genetics (01.07.2000)
Published in Nature genetics (01.07.2000)
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Journal Article
Blue cone monochromatism: a phenotype and genotype assessment with evidence of progressive loss of cone function in older individuals
MICHAELIDES, M, JOHNSON, S, SIMUNOVIC, M. P, BRADSHAW, K, HOLDER, G, MOLLON, J. D, MOORE, A. T, HUNT, D. M
Published in Eye (London) (01.01.2005)
Published in Eye (London) (01.01.2005)
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Journal Article
A novel GJA8 mutation is associated with autosomal dominant lamellar pulverulent cataract: further evidence for gap junction dysfunction in human cataract
Arora, A, Minogue, P J, Liu, X, Reddy, M A, Ainsworth, J R, Bhattacharya, S S, Webster, A R, Hunt, D M, Ebihara, L, Moore, A T, Beyer, E C, Berthoud, V M
Published in Journal of medical genetics (01.01.2006)
Published in Journal of medical genetics (01.01.2006)
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Journal Article
Achromatopsia caused by novel mutations in both CNGA3 and CNGB3
Johnson, S, Michaelides, M, Aligianis, I A, Ainsworth, J R, Mollon, J D, Maher, E R, Moore, A T, Hunt, D M
Published in Journal of medical genetics (01.02.2004)
Published in Journal of medical genetics (01.02.2004)
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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
An autosomal recessive cone–rod dystrophy associated with amelogenesis imperfecta
Michaelides, M, Bloch-Zupan, A, Holder, G E, Hunt, D M, Moore, A T
Published in Journal of medical genetics (01.06.2004)
Published in Journal of medical genetics (01.06.2004)
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Journal Article
Transphyseal reconstruction of the anterior cruciate ligament in prepubescent children
LIDDLE, A. D, IMBULDENIYA, A. M, HUNT, D. M
Published in Journal of bone and joint surgery. British volume (01.10.2008)
Published in Journal of bone and joint surgery. British volume (01.10.2008)
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Journal Article
Cone dystrophy phenotype associated with a frameshift mutation (M280fsX291) in the α-subunit of cone specific transducin (GNAT2)
Michaelides, M, Aligianis, I A, Holder, G E, Simunovic, M, Mollon, J D, Maher, E R, Hunt, D M, Moore, A T
Published in British journal of ophthalmology (01.11.2003)
Published in British journal of ophthalmology (01.11.2003)
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Journal Article
CAG repeat expansions and schizophrenia: association with disease in females and with early age-at-onset
Morris, A G, Gaitonde, E, McKenna, P J, Mollon, J D, Hunt, D M
Published in Human molecular genetics (01.10.1995)
Published in Human molecular genetics (01.10.1995)
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Journal Article
Oligocone trichromacy: a rare and unusual cone dysfunction syndrome
Michaelides, M, Holder, G E, Bradshaw, K, Hunt, D M, Mollon, J D, Moore, A T
Published in British journal of ophthalmology (01.04.2004)
Published in British journal of ophthalmology (01.04.2004)
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Journal Article