D. Hunt

J. Bowmaker, D. Hunt, J. Cowing, 2004, Photochemical & photobiological sciences : Official journal of the European Photochemistry Association and the European Society for Photobiology.

The molecular mechanism for the spectral shifts between vertebrate ultraviolet- and violet-sensitive cone visual pigments.

J. Bowmaker, D. Hunt, P. Robinson, 2002, The Biochemical journal.

Evolution of Visual and Non-visual Pigments

D. Hunt, S. Collin, M. Hankins, 2014, Springer Series in Vision Research.

The visual pigments of the bottlenose dolphin (Tursiops truncatus)

D M Hunt, T W Cronin, T. Cronin, 1998, Visual Neuroscience.

The Genetics of Color Vision and Congenital Color Deficiencies

Livia S. Carvalho, D. Hunt, 2016 .

Retinal photoreceptor arrangement, SWS1 and LWS opsin sequence, and electroretinography in the South American marsupial Thylamys elegans (Waterhouse, 1839)

L. Peichl, D. Hunt, A. Palacios, 2010, The Journal of comparative neurology.

Hybridization in North American Asclepias. II. Flavonoid Evidence

D. Hunt, R. Wyatt, 1991 .

How parrots see their colours: novelty in the visual pigments of Platycercus elegans

Livia S. Carvalho, J. Bowmaker, D. Hunt, 2013, Journal of Experimental Biology.

Visual opsin diversity in sharks and rays.

T. Lamb, D. Hunt, S. Collin, 2019, Molecular biology and evolution.

Identification and characterization of visual pigments in caecilians (Amphibia: Gymnophiona), an order of limbless vertebrates with rudimentary eyes

J. Bowmaker, W. Himstedt, D. Hunt, 2010, Journal of Experimental Biology.

Shortwave visual sensitivity in tree and flying squirrels reflects changes in lifestyle

Livia S. Carvalho, J. Bowmaker, D. Hunt, 2006, Current Biology.

The Cone Visual Pigments of Two Australian Marsupials, the Honey Possum and the Fat–Tailed Dunnart, With the Potential For Trichromacy

D. Hunt, L. Beazley, J. Cowing, 2005 .

Molecular biology of photoreceptor spectral sensitivity

J. Bowmaker, D. Hunt, 1999 .

The evolution of early vertebrate photoreceptors

D. Hunt, S. Collin, N. Hart, 2009, Philosophical Transactions of the Royal Society B: Biological Sciences.

Spectral Tuning in the Eyes of Deep-Sea Lanternfishes (Myctophidae): A Novel Sexually Dimorphic Intra-Ocular Filter

D. Hunt, S. Collin, N. Hart, 2015, Brain, Behavior and Evolution.

Disease mechanism for retinitis pigmentosa (RP11) caused by mutations in the splicing factor gene PRPF31.

D. Hunt, S. Bhattacharya, E. Vithana, 2002, Human molecular genetics.

Anion sensitivity and spectral tuning of middle- and long-wavelength-sensitive (MWS/LWS) visual pigments

D. Hunt, M. Hankins, J. Cowing, 2012, Cellular and Molecular Life Sciences.

Clustering and frequency of mutations in the retinal guanylate cyclase (GUCY2D) gene in patients with dominant cone-rod dystrophies

D. Hunt, A. Bird, S. Bhattacharya, 2001, Journal of medical genetics.

Enhanced retinal longwave sensitivity using a chlorophyll-derived photosensitiser in Malacosteus niger, a deep-sea dragon fish with far red bioluminescence

R. Douglas, J. Partridge, K. Dulai, 1999, Vision Research.

The rhodopsin gene of the cuttlefish Sepia officinalis: sequence and spectral tuning.

D M Hunt, D. Hunt, J. Bellingham, 1998, The Journal of experimental biology.

The molecular basis of a spectral shift in the rhodopsins of two species of squid from different photic environments

J. Bowmaker, D. Hunt, A. Morris, 1993, Proceedings of the Royal Society of London. Series B: Biological Sciences.

The molecular basis for spectral tuning of rod visual pigments in deep-sea fish.

D M Hunt, J. Bowmaker, J. Partridge, 2001, The Journal of experimental biology.

Sertoli cell expression of the cystic fibrosis transmembrane conductance regulator.

D. Hunt, F. R. Boockfor, K. Walsh, 1998, American journal of physiology. Cell physiology.

Restoration of photoreceptor ultrastructure and function in retinal degeneration slow mice by gene therapy

D. Hunt, S. Bhattacharya, S. Fauser, 2000, Nature Genetics.

Negro alpha-thalassaemia is caused by deletion of a single alpha-globin gene.

D. Hunt, J. Clegg, D. Weatherall, 1979, Lancet.

NEGRO α-THALASSÆMIA IS CAUSED BY DELETION OF A SINGLE α-GLOBIN GENE

D. Hunt, J. Clegg, D. Weatherall, 1979, The Lancet.

Evaluation of the X-linked high-grade myopia locus (MYP1) with cone dysfunction and color vision deficiencies.

Yi-Ju Li, S. Züchner, D. Hunt, 2009, Investigative ophthalmology & visual science.

Progressive cone and cone-rod dystrophies: phenotypes and underlying molecular genetic basis.

D. Hunt, M. Michaelides, A. Moore, 2006, Survey of ophthalmology.

The cone dysfunction syndromes

D. Hunt, M. Michaelides, A. Moore, 2004, British Journal of Ophthalmology.

Mapping of a novel locus for achromatopsia (ACHM4) to 1p and identification of a germline mutation in the α subunit of cone transducin (GNAT2)

D. Hunt, T. Forshew, R. Trembath, 2002, Journal of medical genetics.

Molecular evolution of the cottoid fish endemic to Lake Baikal deduced from nuclear DNA evidence.

D M Hunt, J. Bowmaker, K. Dulai, 1997, Molecular phylogenetics and evolution.

Spectral tuning and molecular evolution of rod visual pigments in the species flock of cottoid fish in Lake Baikal

D. Hunt, J. Fitzgibbon, S. J. Slobodyanyuk, 1996, Vision Research.

The rhodopsin-encoding gene of bony fish lacks introns.

J. Bowmaker, D. Hunt, J. Fitzgibbon, 1995, Gene.

Sequence divergence, polymorphism and evolution of the middle-wave and long-wave visual pigment genes of great apes and old world monkeys

J. Mollon, J. Bowmaker, K. Dulai, 1994, Vision Research.

Visual opsin expression and morphological characterization of retinal photoreceptors in the pouched lamprey (Geotria australis, Gray)

D. Hunt, I. Potter, J. Hemmi, 2020, The Journal of comparative neurology.

Chromosomal localization, genomic organization and evolution of the genes encoding human phosphatidylinositol transfer protein membrane-associated (PITPNM) 1, 2 and 3

D. Hunt, S. Halford, C. Spalluto, 2004, Cytogenetic and Genome Research.

Expression of PRPF31 mRNA in patients with autosomal dominant retinitis pigmentosa: a molecular clue for incomplete penetrance?

D. Hunt, A. Bird, S. Bhattacharya, 2003, Investigative ophthalmology & visual science.

Validating Fluorescent Chrnb4.EGFP Mouse Models for the Study of Cone Photoreceptor Degeneration

Livia S. Carvalho, D. Hunt, R. Rashwan, 2020, Translational vision science & technology.

SPLICE: a technique for generating in vitro spliced coding sequences from genomic DNA.

D. Hunt, W. L. Davies, Livia S. Carvalho, 2007, BioTechniques.

Genetic linkage of cone–rod retinal dystrophy to chromosome 19q and evidence for segregation distortion

D. Hunt, S. Bhattacharya, C. Inglehearn, 1994, Nature Genetics.

Retinal Amino Acid Neurochemistry of the Southern Hemisphere Lamprey, Geotria australis

D. Hunt, M. Kalloniatis, I. Potter, 2013, PloS one.

Pyrimidine biosynthesis in the dumpy mutants of Drosophila melanogaster

D. Hunt, D. Blass, 2004, Molecular and General Genetics MGG.

Functional characterization, tuning, and regulation of visual pigment gene expression in an anadromous lamprey

Livia S. Carvalho, D. Hunt, I. Potter, 2007, FASEB journal : official publication of the Federation of American Societies for Experimental Biology.

The influence of ontogeny and light environment on the expression of visual pigment opsins in the retina of the black bream, Acanthopagrus butcheri

Livia S. Carvalho, L. Balmer, D. Hunt, 2008, Journal of Experimental Biology.

Developmental dynamics of cone photoreceptors in the eel

J. Bowmaker, D. Hunt, G. Jeffery, 2009, BMC Developmental Biology.

An early-onset autosomal dominant macular dystrophy (MCDR3) resembling North Carolina macular dystrophy maps to chromosome 5.

D. Hunt, G. Holder, C. Bellmann, 2003, Investigative ophthalmology & visual science.

Focus on molecules: retinol dehydrogenase 12 (RDH12).

D. Hunt, A. Moore, D. Mackay, 2008, Experimental eye research.

Autosomal dominant cone-rod retinal dystrophy (CORD6) from heterozygous mutation of GUCY2D, which encodes retinal guanylate cyclase.

J D Mollon, D M Hunt, F W Fitzke, 2000, Ophthalmology.

Colour vision and speciation in Lake Victoria cichlids of the genus Pundamilia

J. Bowmaker, D. Hunt, O. Seehausen, 2005, Molecular ecology.

A detailed study of the phenotype of an autosomal dominant cone-rod dystrophy (CORD7) associated with mutation in the gene for RIM1

D M Hunt, F W Fitzke, A C Bird, 2005, British Journal of Ophthalmology.

Genomic organisation and alternative splicing of human RIM1, a gene implicated in autosomal dominant cone-rod dystrophy (CORD7).

D. Hunt, S. Halford, A. Moore, 2003, Genomics.

Eel visual pigments revisited: The fate of retinal cones during metamorphosis

J. Bowmaker, D. Hunt, G. Jeffery, 2008, Visual Neuroscience.

Spectral Diversification and Trans-Species Allelic Polymorphism during the Land-to-Sea Transition in Snakes

J. Partridge, D. Hunt, D. Gower, 2020, Current Biology.

Evolution of the eyes of vipers with and without infrared-sensing pit organs

L. Peichl, R. Douglas, J. Partridge, 2019, Biological Journal of the Linnean Society.

Differential stability of variant OPN1LW gene transcripts in myopic patients

D. Mackey, D. Hunt, L. Griffiths, 2019, Molecular vision.

Clinical characterization and genetic mapping of North Carolina macular dystrophy

D. Hunt, Z. Tong, A. Moore, 2008, Vision Research.

An autosomal dominant bull's-eye macular dystrophy (MCDR2) that maps to the short arm of chromosome 4.

D. Hunt, C. Bellmann, M. Michaelides, 2003, Investigative ophthalmology & visual science.

Assessment of the interphotoreceptor matrix proteoglycan-1 (IMPG1) gene localised to 6q13-q15 in autosomal dominant Stargardt-like disease (ADSTGD), progressive bifocal chorioretinal atrophy (PBCRA), and North Carolina macular dystrophy (MCDR1).

U. Felbor, D. Hunt, A. Gehrig, 1998, Journal of medical genetics.

Mutations in HPRP3, a third member of pre-mRNA splicing factor genes, implicated in autosomal dominant retinitis pigmentosa.

M. Hims, D. Hunt, T. Rosenberg, 2002, Human molecular genetics.

Disease mechanism for retinitis pigmentosa (RP11) caused by missense mutations in the splicing factor gene PRPF31

D. Hunt, S. Bhattacharya, V. Vaclavik, 2008, Molecular vision.

Ultraviolet-sensitive vision in long-lived birds

Livia S. Carvalho, D. Hunt, A. Bennett, 2011, Proceedings of the Royal Society B: Biological Sciences.

The molecular evolution of avian ultraviolet- and violet-sensitive visual pigments.

Livia S. Carvalho, J. Bowmaker, D. Hunt, 2007, Molecular biology and evolution.

Avian Visual Pigments: Characteristics, Spectral Tuning, and Evolution

D. Hunt, N. Hart, 2007, The American Naturalist.

Visual pigments and oil droplets in the retina of a passerine bird, the canary Serinus canaria: microspectrophotometry and opsin sequences

J. Bowmaker, D. Hunt, S. Wilkie, 1999, Vision Research.

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).

J. Bowmaker, D. Hunt, S. Wilkie, 1998, The Biochemical journal.

Morphological Characterization and Topographic Analysis of Multiple Photoreceptor Types in the Retinae of Mesopelagic Hatchetfishes with Tubular Eyes

D. Hunt, S. Collin, Lauren M. Biagioni, 2016, Front. Ecol. Evol..

The visual pigments of a deep-sea teleost, the pearl eye Scopelarchus analis

Livia S. Carvalho, J. Bowmaker, D. Hunt, 2007, Journal of Experimental Biology.

Shedding Light on Serpent Sight: The Visual Pigments of Henophidian Snakes

Livia S. Carvalho, D. Hunt, D. Gower, 2009, The Journal of Neuroscience.

Into the blue: gene duplication and loss underlie color vision adaptations in a deep-sea chimaera, the elephant shark Callorhinchus milii.

David M Hunt, Livia S. Carvalho, Byrappa Venkatesh, 2008, Genome research.

Mechanisms of wavelength tuning in the rod opsins of deep-sea fishes

J. Partridge, K. Dulai, D. Hunt, 1997, Proceedings of the Royal Society of London. Series B: Biological Sciences.

Evolution of Vertebrate Phototransduction: Cascade Activation

T. Lamb, D. Hunt, S. Collin, 2016, Molecular biology and evolution.

Adaptive gene loss reflects differences in the visual ecology of basal vertebrates.

D. Hunt, S. Collin, W. L. Davies, 2009, Molecular biology and evolution.

Cone monochromacy and visual pigment spectral tuning in wobbegong sharks

D. Hunt, S. Collin, N. Hart, 2012, Biology Letters.

Multiple rod–cone and cone–rod photoreceptor transmutations in snakes: evidence from visual opsin gene expression

J. Partridge, D. Hunt, R. Fisher, 2016, Proceedings of the Royal Society B: Biological Sciences.

Abnormal spermiogenesis in two pink-eyed sterile mutants in the mouse.

D. Hunt, D. Johnson, 1971, Journal of embryology and experimental morphology.

Mix and Match Color Vision: Tuning Spectral Sensitivity by Differential Opsin Gene Expression in Lake Malawi Cichlids

David M. Hunt, Karen L. Carleton, J. Bowmaker, 2005, Current Biology.

Guanylate cyclase activating proteins, guanylate cyclase and disease.

D. Hunt, M. Warren, S. Wilkie, 2002, Advances in experimental medicine and biology.

A retGC-1 mutation in autosomal dominant cone-rod dystrophy.

A. Munnich, D. Hunt, E. Souied, 1998, American journal of human genetics.

Molecular, Cellular and Functional Changes in the Retinas of Young Adult Mice Lacking the Voltage-Gated K+ Channel Subunits Kv8.2 and K2.1

Livia S. Carvalho, J. Nerbonne, D. Hunt, 2021, International journal of molecular sciences.

The Role of the Voltage-Gated Potassium Channel Proteins Kv8.2 and Kv2.1 in Vision and Retinal Disease: Insights from the Study of Mouse Gene Knock-Out Mutations

David M. Hunt, Nathan S. Hart, Livia S. Carvalho, 2019, eNeuro.

Functional Analysis of Missense Mutations in Kv8.2 Causing Cone Dystrophy with Supernormal Rod Electroretinogram*

D. Hunt, M. Stocker, S. Wilkie, 2012, The Journal of Biological Chemistry.

“CONE DYSTROPHY WITH SUPERNORMAL ROD ELECTRORETINOGRAM”: A COMPREHENSIVE GENOTYPE/PHENOTYPE STUDY INCLUDING FUNDUS AUTOFLUORESCENCE AND EXTENSIVE ELECTROPHYSIOLOGY

D. Hunt, G. Holder, M. Michaelides, 2010, Retina.

Mutations in the gene KCNV2 encoding a voltage-gated potassium channel subunit cause "cone dystrophy with supernormal rod electroretinogram" in humans.

D. Hunt, A. Bird, G. Holder, 2006, American journal of human genetics.

Gene therapy for inherited retinal degeneration

R R Ali, M B Reichel, D M Hunt, 1997, The British journal of ophthalmology.

Biochemical observations on the cartilage of achondroplastic (can) mice.

D R Johnson, D M Hunt, D. Hunt, 1974, Journal of embryology and experimental morphology.

A Molecular Genetic Investigation of Two Families With Macular Dysplasia in Association With Digit Abnormalities

D. Hunt, M. Michaelides, A. Webster, 2008 .

Detecting gene conversion: primate visual pigment genes

D. Balding, R. Nichols, D. Hunt, 1992, Proceedings of the Royal Society of London. Series B: Biological Sciences.

Early Prenatal Diagnosis of Hurler's Syndrome with Termination of Pregnancy and Confirmatory Findings on the Fetus

E. A. Wright, D. Hunt, D. Johnson, 1973, Journal of medical genetics.

Early Prenatal Diagnosis ofHurler's Syndrome with Termination ofPregnancy andConfirmatory Findings on theFetus

D. Hunt, D. Johnson, M. Dean, 1973 .

The number of triplet repeats in five brain-expressed loci with CAG repeats is not associated with schizophrenia

J. Mollon, P. McKenna, D. Hunt, 1997, Schizophrenia Research.

Molecular Genetics of Spectral Tuning in New World Monkey Color Vision

D. Hewett‐Emmett, S. Boissinot, S. Shyue, 1998, Journal of Molecular Evolution.

Spectral Sensitivity Tuning in the Deep-Sea

J. Bowmaker, R. Douglas, D. Hunt, 2003 .

Sequence divergence and copy number of the middle- and long-wave photopigment genes in old world monkeys

J. Mollon, J. Bowmaker, D. Hunt, 1992, Proceedings of the Royal Society of London. Series B: Biological Sciences.

Origin and Molecular Evolution of the X-linked Duplicate Color Vision Genes in Howler Monkeys

D. Hewett‐Emmett, S. Boissinot, Wen-Hsiung Li, 1997 .

Purple Secret: Genes, 'Madness' and the Royal Houses of Europe

D. Hunt, M. Warren, J. Röhl, 1998 .

Assessment of association of D3 dopamine receptor MscI polymorphism with schizophrenia: analysis of symptom ratings, family history, age at onset, and movement disorders.

J. Mollon, P. McKenna, D. Hunt, 1996, American journal of medical genetics.

X-linked cone dysfunction syndrome with myopia and protanopia.

J. Mollon, D. Hunt, G. Holder, 2005, Ophthalmology.

Localisation of the human blue cone pigment gene to chromosome band 7q31.3-32

D. Hunt, S. Gayther, J. Fitzgibbon, 2004, Human Genetics.

Autosomal dominant cone-rod dystrophy with mutations in the guanylate cyclase 2D gene encoding retinal guanylate cyclase-1.

D. Hunt, A. Bird, F. Fitzke, 2001, Archives of ophthalmology.

Identification and functional consequences of a new mutation (E155G) in the gene for GCAP1 that causes autosomal dominant cone dystrophy.

D. Zack, J. Bateman, D. Hunt, 2001, American journal of human genetics.

Dominant Cone-Rod Dystrophy: A Mouse Model Generated by Gene Targeting of the GCAP1/Guca1a Gene

E. L. West, D. Hunt, M. Michaelides, 2011, PloS one.

The rod opsin pigments from two marsupial species, the South American bare-tailed woolly opossum and the Australian fat-tailed dunnart.

J. Bowmaker, D. Hunt, L. Beazley, 2003, Gene.

Interactions within the Coiled-coil Domain of RetGC-1 Guanylyl Cyclase Are Optimized for Regulation Rather than for High Affinity*

V. Daggett, J. Hurley, D. Hunt, 2001, The Journal of Biological Chemistry.

The rod and green cone opsins of two avian species, the budgerigar, Melopsittacus undulatus, and the mallard duck, Anas platyrhynchus.

J. Bowmaker, D. Hunt, L. A. Heath, 1997, Gene.

Biochemical analysis of a dimerization domain mutation in RetGC-1 associated with dominant cone-rod dystrophy.

J. Hurley, D. Hunt, V. Ramamurthy, 1999, Proceedings of the National Academy of Sciences of the United States of America.

Abnormal epithelial transport in cystic fibrosis jejunum.

D. Hunt, E. O'Loughlin, K. Gaskin, 1991, The American journal of physiology.

Haemoglobin Constant Spring has an unstable alpha chain messenger RNA.

D. Hunt, J. Clegg, D. Weatherall, 1982, British journal of haematology.

Visual pigments and the photic environment: The cottoid fish of Lake Baikal

J. Bowmaker, D. Hunt, V. Govardovskii, 1994, Vision Research.

Clinical features of progressive bifocal chorioretinal atrophy: a retinal dystrophy linked to chromosome 6q.

D. Hunt, A. Bird, K. Evans, 1996, Ophthalmology.

Genetic enhancement of cognition in a kindred with cone–rod dystrophy due to RIMS1 mutation

I. Deary, A. Need, D. Goldstein, 2007, Journal of Medical Genetics.

Phototactic tails: Evolution and molecular basis of a novel sensory trait in sea snakes

Alastair J. Ludington, J. Partridge, D. Hunt, 2019, Molecular ecology.

The destabilization of human GCAP1 by a proline to leucine mutation might cause cone-rod dystrophy.

D. Hunt, S. Bhattacharya, M. Warren, 2001, Human molecular genetics.

Evolution of the shut-off steps of vertebrate phototransduction

T. Lamb, D. Hunt, H. Patel, 2018, Open Biology.

Biogenic amines in Drosophila melanogaster selected for differences in larval feeding behavior.

D. Hunt, B. Burnet, D. Sewell, 1975, Behavioral biology.

Extended extraocular phenotype of PROM1 mutation in kindreds with known autosomal dominant macular dystrophy

I. Pavord, S. Sisodiya, D. Hunt, 2011, European Journal of Human Genetics.

The PROM1 mutation p.R373C causes an autosomal dominant bull's eye maculopathy associated with rod, rod-cone, and macular dystrophy.

D. Hunt, G. Holder, E. White, 2010, Investigative ophthalmology & visual science.

Postnatal development of colonic electrolyte transport in rabbits.

D. Hunt, E. O'Loughlin, D. Kreutzmann, 1990, American Journal of Physiology.

Localization of the gene encoding human phosphatidylinositol transfer protein (PITPN) to 17p13.3: a gene showing homology to the Drosophila retinal degeneration B gene (rdgB).

K. Dulai, D. Hunt, S. Gayther, 1994, Cytogenetics and cell genetics.

Purification, characterisation and intracellular localisation of aryl hydrocarbon interacting protein-like 1 (AIPL1) and effects of mutations associated with inherited retinal dystrophies.

D. Hunt, S. Bhattacharya, M. Warren, 2004, Biochimica et biophysica acta.

Evolution of the calcium feedback steps of vertebrate phototransduction

T. Lamb, D. Hunt, 2018, Open Biology.

Characterisation of two genes for guanylate cyclase activator protein (GCAP1 and GCAP2) in the Japanese pufferfish, Fugu rubripes.

D. Hunt, S. Bhattacharya, M. Warren, 2002, Biochimica et biophysica acta.

First record of the mandarin dogfish Cirrhigaleus barbifer (Chondrichthyes: Squalidae) from Western Australia

D. Hunt, S. Collin, R. Kempster, 2013 .

Anion sensitivity and spectral tuning of middle- and long-wavelength-sensitive (MWS/LWS) visual pigments

D. Hunt, M. Hankins, W. L. Davies, 2012, Cellular and Molecular Life Sciences.

Genetic differences in zinc and copper induction of liver metallothionein in inbred strains of the mouse

D. Hunt, C. Farr, 1989, Biochemical Genetics.

Genetic differences in zinc and copper induction of liver metallothionein in inbred strains of the mouse

D. Hunt, C. Farr, 1989, Biochemical Genetics.

Localisation of a gene for dominant cone-rod dystrophy (CORD6) to chromosome 17p.

D. Hunt, A. Bird, A. Moore, 1997, Human molecular genetics.

Evolution and Functional Characterisation of Melanopsins in a Deep-Sea Chimaera (Elephant Shark, Callorhinchus milii)

S. Brenner, B. Venkatesh, B. Tay, 2012, PloS one.

Cone visual pigments in two marsupial species: the fat-tailed dunnart (Sminthopsis crassicaudata) and the honey possum (Tarsipes rostratus)

D. Hunt, L. Beazley, W. L. Davies, 2008, Proceedings of the Royal Society B: Biological Sciences.

Enzyme Sequence and Its Relationship to Hyperbaric Stability of Artificial and Natural Fish Lactate Dehydrogenases

David J. Dunstan, David M. Hunt, Martin J. Warren, 2008, PloS one.

Characterisation of the ultraviolet-sensitive opsin gene in the honey bee, Apis mellifera.

D M Hunt, J. Bowmaker, D. Hunt, 1997, European journal of biochemistry.

Evolution of the vertebrate phototransduction cascade activation steps.

T. Lamb, D. Hunt, 2017, Developmental biology.

Sequence and evolution of the blue cone pigment gene in Old and New World primates.

J. Mollon, J. Bowmaker, D. Hunt, 1995, Genomics.

The rhodopsin gene of the cuttlefish, Sepia officinalis: cDNA sequence, gene structure and spectral tuning.

D. Hunt, J. Bellingham, A. Morris, 1998 .

Retinal ganglion cell responses in a dichromatic primate, Cebus apella.

Barry B. Lee, J. Kremers, D. Hunt, 1996 .

The origins of the full-field flash electroretinogram b-wave

Livia S. Carvalho, D. Hunt, Yashvi Bhatt, 2023, Frontiers in Molecular Neuroscience.

A human homolog of yeast pre-mRNA splicing gene, PRP31, underlies autosomal dominant retinitis pigmentosa on chromosome 19q13.4 (RP11).

D. Hunt, A. Bird, S. Bhattacharya, 2001, Molecular cell.

Localization of a gene (CORD7) for a dominant cone-rod dystrophy to chromosome 6q.

D. Hunt, A. Bird, M. Jay, 1998, American journal of human genetics.

Cone visual pigments in two species of South American marsupials.

Livia S. Carvalho, D. Hunt, L. Beazley, 2009, Gene.

Visual system evolution and the nature of the ancestral snake

J. Bowmaker, J. Partridge, D. Hunt, 2015, Journal of evolutionary biology.

Immune responses limit adenovirally mediated gene expression in the adult mouse eye

D. Hunt, S. Bhattacharya, D. Baker, 1998, Gene Therapy.

Bornholm Eye Disease Arises From a Specific Combination of Amino Acid Changes Encoded by Exon 3 of the L/M Cone Opsin Gene

D. Hunt, M. Neitz, M. McClements, 2010 .

Drug-resistant Drosophila indicate glutamate-gated chloride channels are targets for the antiparasitics nodulisporic acid and ivermectin.

D. Schmatz, D. Hunt, D. Cully, 2000, Proceedings of the National Academy of Sciences of the United States of America.

Two loci for Tuberous Sclerosis: one on 9q34 and one on 16p13

J. Attwood, J. Edwards, S. Povey, 1994, Annals of human genetics.

Genetic linkage analysis of a novel syndrome comprising North Carolina-like macular dystrophy and progressive sensorineural hearing loss

D. Hunt, B. Edmunds, P. Francis, 2003, The British journal of ophthalmology.

Vertebrate opsins belonging to different classes vary in constitutively active properties resulting from salt-bridge mutations.

D. Hunt, P. Robinson, J. Cowing, 2006, Biochemistry.

Clustering and frequency of mutations in the retinal guanylate cyclase ( GUCY2D ) gene in patients with dominant cone-rod dystrophies

D. Hunt, A. Bird, S. Bhattacharya, 2001 .

Mutant prominin 1 found in patients with macular degeneration disrupts photoreceptor disk morphogenesis in mice.

W. Huttner, D. Hunt, C. Lillo, 2008, The Journal of clinical investigation.

Ancient colour vision: multiple opsin genes in the ancestral vertebrates

M. A. Knight, D. Hunt, I. Potter, 2003, Current Biology.

The effect of cone opsin mutations on retinal structure and the integrity of the photoreceptor mosaic.

David Williams, A. Dubra, J. Neitz, 2012, Investigative ophthalmology & visual science.

Arctic reindeer extend their visual range into the ultraviolet

R. Douglas, D. Hunt, M. Neveu, 2011, Journal of Experimental Biology.

Spectral tuning of the long wavelength-sensitive cone pigment in four Australian marsupials.

D. Hunt, L. Beazley, C. Arrese, 2006, Gene.

Assignment1 of Claudin-1 (CLDN1) to human chromosome 3q28→q29 with somatic cell hybrids

D. Hunt, S. Halford, P. Adamson, 2000, Cytogenetic and Genome Research.

Disease mechanism for retinitis pigmentosa (RP11) caused by missense mutations in the splicing factor gene PRPF31

D. Hunt, S. Bhattacharya, V. Vaclavik, 2008, Molecular vision.

The cone dysfunction syndromes

D. Hunt, M. Michaelides, A. Moore, 2004, British Journal of Ophthalmology.