about
Cloning, chromosomal localization and functional expression of the gene encoding the alpha-subunit of the cGMP-gated channel in human cone photoreceptorsThe classical human phosphoglucomutase (PGM1) isozyme polymorphism is generated by intragenic recombinationIdentification of regulatory targets of tissue-specific transcription factors: application to retina-specific gene regulation.Constitutively active rhodopsin and retinal diseaseMultiple phosphorylated isoforms of NRL are expressed in rod photoreceptorsChemistry of the retinoid (visual) cycleMolecular study of the rhodopsin gene in retinitis pigmentosa patients in the Basque Country.Recent advances in the gene map of inherited eye disorders: primary hereditary diseases of the retina, choroid, and vitreous.Site-directed mutagenesis of highly conserved amino acids in the first cytoplasmic loop of Drosophila Rh1 opsin blocks rhodopsin synthesis in the nascent stateElectrostatic compensation restores trafficking of the autosomal recessive retinitis pigmentosa E150K opsin mutant to the plasma membrane.New aspects of an old theme: the genetic basis of human color vision.Conservation of molecular interactions stabilizing bovine and mouse rhodopsin.Defective intracellular transport is the molecular basis of rhodopsin-dependent dominant retinal degenerationA study of unusual Rayleigh matches in deutan deficiency.Color discrimination in the tufted capuchin monkey, Sapajus spp.Membrane receptors and transporters involved in the function and transport of vitamin A and its derivatives.A novel mechanistic spectrum underlies glaucoma-associated chromosome 6p25 copy number variation.Molecular genetics of infantile-onset retinal dystrophies.Nanoparticles for retinal gene therapy.Novel thiazole derivatives: a patent review (2008 - 2012. Part 2).Photoreceptor Cilia and Retinal Ciliopathies.Reduced Discrimination in the Tritanopic Confusion Line for Congenital Color Deficiency Adults.Retinitis pigmentosa and related disorders: phenotypes of rhodopsin and peripherin/RDS mutations.Light-dependent activation of rod transducin by pineal opsin.Evolutionary analysis of rhodopsin and cone pigments: connecting the three-dimensional structure with spectral tuning and signal transferCopy-number variation is an important contributor to the genetic causality of inherited retinal degenerations.Sex-related differences in chromatic sensitivity.Analysis of the short wavelength-sensitive ("blue") cone mosaic in the primate retina: comparison of New World and Old World monkeys.The transcription factor Nr2e3 functions in retinal progenitors to suppress cone cell generation.Regulation of adenylyl cyclase in LTP
P2860
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P2860
description
1992 nî lūn-bûn
@nan
1992年の論文
@ja
1992年論文
@yue
1992年論文
@zh-hant
1992年論文
@zh-hk
1992年論文
@zh-mo
1992年論文
@zh-tw
1992年论文
@wuu
1992年论文
@zh
1992年论文
@zh-cn
name
Molecular genetics of human visual pigments.
@ast
Molecular genetics of human visual pigments.
@en
type
label
Molecular genetics of human visual pigments.
@ast
Molecular genetics of human visual pigments.
@en
prefLabel
Molecular genetics of human visual pigments.
@ast
Molecular genetics of human visual pigments.
@en
P2093
P1476
Molecular genetics of human visual pigments.
@en
P2093
P304
P356
10.1146/ANNUREV.GE.26.120192.002155
P577
1992-01-01T00:00:00Z