Adaptive optics retinal imaging reveals S-cone dystrophy in tritan color-vision deficiency

scientific article

Adaptive optics retinal imaging reveals S-cone dystrophy in tritan color-vision deficiency is …
instance of (P31):
scholarly articleQ13442814

External links are
P356DOI10.1364/JOSAA.24.001438
P932PMC publication ID2082754
P698PubMed publication ID17429491

P50authorMaureen NeitzQ80856434
Rigmor C. BaraasQ50854568
David H. FosterQ51135433
David R. WilliamsQ56650695
P2093author name stringJoseph Carroll
Mina Chung
Karen L Gunther
P2860cites workMutation spectrum of the rhodopsin gene among patients with autosomal dominant retinitis pigmentosaQ24560214
Rhodopsin mutations in autosomal dominant retinitis pigmentosaQ24564252
Human tritanopia associated with a third amino acid substitution in the blue-sensitive visual pigmentQ24670034
Human tritanopia associated with two amino acid substitutions in the blue-sensitive opsinQ24675989
Identification of novel rhodopsin mutations associated with retinitis pigmentosa by GC-clamped denaturing gradient gel electrophoresisQ24678541
A novel mutation in the short-wavelength-sensitive cone pigment gene associated with a tritan color vision defectQ28262688
Further studies supporting the identity of congenital tritanopia and hereditary dominant optic atrophyQ71148298
Visual pigment gene structure and the severity of color vision defectsQ71669073
Luminance noise and the rapid determination of discrimination ellipses in colour deficiencyQ72041858
Aging of the human photoreceptor mosaic: evidence for selective vulnerability of rods in central retinaQ72569235
Modeling cat retinal beta-cell arraysQ73633156
Supernormal vision and high-resolution retinal imaging through adaptive opticsQ73900804
Modelling the mosaic organization of rod and cone photoreceptors with a minimal-spacing ruleQ74673084
THE INHERITANCE OF CONGENITAL TRITANOPIA WITH THE REPORT OF AN EXTENSIVE PEDIGREEQ76748375
Red, green, and red-green hybrid pigments in the human retina: correlations between deduced protein sequences and psychophysically measured spectral sensitivitiesQ77581236
Relating color discrimination to photopigment genes in deutan observersQ77809832
Tertiary structure and spectral tuning of UV and violet pigments in vertebratesQ28749199
The arrangement of the three cone classes in the living human eye.Q33852770
Molecular genetics of color vision and color vision defectsQ33920947
Human photoreceptor topographyQ34034782
New Farnsworth-Munsell 100 hue test norms of normal observers for each year of age 5-22 and for age decades 30-70Q34160341
Functional photoreceptor loss revealed with adaptive optics: an alternate cause of color blindnessQ34321474
Distribution and morphology of human cone photoreceptors stained with anti-blue opsinQ34601678
Photoreceptor degeneration and dysfunction in aging and age-related maculopathyQ34688056
Crystal structure of rhodopsin: a template for cone visual pigments and other G protein-coupled receptors.Q34985056
Preretinopic changes in the colour vision of juvenile diabeticsQ35306956
Structure and function in rhodopsin: packing of the helices in the transmembrane domain and folding to a tertiary structure in the intradiscal domain are coupledQ36588880
The mosaic of nerve cells in the mammalian retinaQ39193004
Human visual pigments: microspectrophotometric results from the eyes of seven personsQ40092643
A novel amino acid substitution is responsible for spectral tuning in a rodent violet-sensitive visual pigmentQ40543001
Neural bases of visual deficits during agingQ40808710
The morphological development of the human foveaQ41429281
A qualitative and quantitative analysis of the human fovea during developmentQ42525565
Dynamics of the eye's wave aberrationQ43551856
Packing arrangement of the three cone classes in primate retinaQ43588716
Photoreceptor inner segments in monkey and human retina: mitochondrial density, optics, and regional variationQ44268744
Estimates of L:M cone ratio from ERG flicker photometry and geneticsQ44392227
The reflectance of single cones in the living human eye.Q44595317
The locus of fixation and the foveal cone mosaicQ46758766
Organization of the human trichromatic cone mosaic.Q46764062
The genetics of tritan disturbancesQ50335619
The familial distribution of congenital tritanopia, with some remarks on some similar conditionsQ50335620
The characteristics of tritanopiaQ50335622
Spectral tuning in the human blue cone pigment.Q50516392
Differential diagnosis of congenital tritanopia and dominantly inherited juvenile optic atrophy.Q50914096
Color-axis determination on the Farnsworth-Munsell 100-hue test.Q50915201
Color matching in autosomal dominant tritan defect.Q50937391
Cone spacing and the visual resolution limit.Q52591288
Aging of the human retina. Differential loss of neurons and retinal pigment epithelial cellsQ53709826
Psychophysical estimate of extrafoveal cone spacing.Q54334092
Ophthalmological findings in the tritans, described by Wright and KalmusQ66887648
Evidence of photoreceptor migration during early foveal development: a quantitative analysis of human fetal retinaeQ68126315
Congenital tritanopia without neuroretinal diseaseQ69118540
P4510describes a project that usesImageJQ1659584
P433issue5
P921main subjectadaptive opticsQ506922
P1104number of pages10
P304page(s)1438-1447
P577publication date2007-05-01
P1433published inJournal of the Optical Society of AmericaQ6296174
P1476titleAdaptive optics retinal imaging reveals S-cone dystrophy in tritan color-vision deficiency
P478volume24