HEK293S Cells Have Functional Retinoid Processing Machinery
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[1] H. Stieve,et al. Direct correlation between the R2 component of the early receptor potential and the formation of Metarhodopsin II in the excised bovine retina , 2004, Biophysics of structure and mechanism.
[2] K. Palczewski,et al. Crystal Structure of Rhodopsin: A G‐Protein‐Coupled Receptor , 2002, Chembiochem : a European journal of chemical biology.
[3] P. Sieving,et al. Mutations in the gene encoding lecithin retinol acyltransferase are associated with early-onset severe retinal dystrophy , 2001, Nature Genetics.
[4] J. M. Sullivan,et al. All-trans-retinal forms a visible-absorbing pigment with human rod opsin. , 2001, Biochemistry.
[5] J. Hurley,et al. Visual Cycle Impairment in Cellular Retinaldehyde Binding Protein (CRALBP) Knockout Mice Results in Delayed Dark Adaptation , 2001, Neuron.
[6] K. Prof,et al. Crystal structure of rhodopsin: a G protein-coupled receptor. Palczewski K,*(1) kumasaka T, hori T, behnke CA, motoshima H, fox BA, trong IL, teller DC, okada T, stenkamp RE, yamamoto M, miyano M. Science 2000;289:739-745 , 2002, American journal of ophthalmology.
[7] D. Bok,et al. Esterification of all-trans-retinol in normal human epithelial cell strains and carcinoma lines from oral cavity, skin and breast: reduced expression of lecithin:retinol acyltransferase in carcinoma lines. , 2000, Carcinogenesis.
[8] Y. Miyake,et al. A high association with cone dystrophy in Fundus albipunctatus caused by mutations of the RDH5 gene. , 2000, Investigative ophthalmology & visual science.
[9] Y. Tano,et al. Mutations in the 11-cis retinol dehydrogenase gene in Japanese patients with Fundus albipunctatus. , 2000, Investigative ophthalmology & visual science.
[10] K. Palczewski,et al. Isomerization of all-trans-retinol to cis-retinols in bovine retinal pigment epithelial cells: dependence on the specificity of retinoid-binding proteins. , 2000, Biochemistry.
[11] K. Palczewski,et al. Stereoisomeric specificity of the retinoid cycle in the vertebrate retina. , 2000, The Journal of biological chemistry.
[12] T. Aleman,et al. Rod and cone visual cycle consequences of a null mutation in the 11-cis-retinol dehydrogenase gene in man , 2000, Visual Neuroscience.
[13] K. Palczewski,et al. X-Ray diffraction analysis of three-dimensional crystals of bovine rhodopsin obtained from mixed micelles. , 2000, Journal of structural biology.
[14] A. Romert,et al. Gene structure, expression analysis, and membrane topology of RDH4. , 2000, Experimental cell research.
[15] A. Adler,et al. Human interphotoreceptor matrix contains serum albumin and retinol-binding protein. , 2000, Experimental eye research.
[16] J. M. Sullivan,et al. Electrical approach to study rhodopsin activation in single cells with early receptor current assay. , 2000, Methods in enzymology.
[17] J. Sullivan,et al. Development of stable cell lines expressing high levels of point mutants of human opsin for biochemical and biophysical studies. , 2000, Methods in enzymology.
[18] W. Blaner,et al. Biochemical properties, tissue expression, and gene structure of a short chain dehydrogenase/ reductase able to catalyze cis-retinol oxidation. , 1999, Journal of lipid research.
[19] J. M. Sullivan,et al. Normal and Mutant Rhodopsin Activation Measured with the Early Receptor Current in a Unicellular Expression System , 1999, The Journal of general physiology.
[20] J. M. Sullivan,et al. Time-resolved rhodopsin activation currents in a unicellular expression system. , 1999, Biophysical journal.
[21] R. Crouch,et al. Identification of RPE65 in transformed kidney cells1 , 1999, FEBS letters.
[22] J. Storch,et al. Differential Mechanisms of Retinoid Transfer from Cellular Retinol Binding Proteins Types I and II to Phospholipid Membranes* , 1999, The Journal of Biological Chemistry.
[23] M. Gelb,et al. Preferential Release of 11-cis-retinol from Retinal Pigment Epithelial Cells in the Presence of Cellular Retinaldehyde-binding Protein* , 1999, Journal of Biological Chemistry.
[24] U. Eriksson,et al. Activity of human 11-cis-retinol dehydrogenase (Rdh5) with steroids and retinoids and expression of its mRNA in extra-ocular human tissue. , 1999, The Biochemical journal.
[25] D. Bok,et al. Molecular and Biochemical Characterization of Lecithin Retinol Acyltransferase* , 1999, The Journal of Biological Chemistry.
[26] D. Bok,et al. Rpe65 is necessary for production of 11-cis-vitamin A in the retinal visual cycle , 1998, Nature Genetics.
[27] Jack M. Sullivan,et al. Low-cost monochromatic microsecond flash microbeam apparatus for single-cell photolysis of rhodopsin or other photolabile pigments , 1998 .
[28] L. Lebioda,et al. Molecular Characterization of a Novel Short-chain Dehydrogenase/Reductase That Reduces All-trans-retinal* , 1998, The Journal of Biological Chemistry.
[29] N. Noy,et al. Cellular Retinaldehyde-binding Protein Ligand Interactions , 1998, The Journal of Biological Chemistry.
[30] K. Palczewski,et al. Reduction of all-trans-retinal limits regeneration of visual pigment in mice , 1998, Vision Research.
[31] A. Romert,et al. The identification of a 9-cis retinol dehydrogenase in the mouse embryo reveals a pathway for synthesis of 9-cis retinoic acid. , 1998, Proceedings of the National Academy of Sciences of the United States of America.
[32] A. Fulton,et al. Mutations in the RPE65 gene in patients with autosomal recessive retinitis pigmentosa or leber congenital amaurosis. , 1998, Proceedings of the National Academy of Sciences of the United States of America.
[33] G. Willsky,et al. Renal drug metabolism. , 1998, Pharmacological reviews.
[34] R. Rando,et al. Regulation of isomerohydrolase activity in the visual cycle. , 1998, Biochemistry.
[35] A. Fulton,et al. Mutations in the RPE 65 gene in patients with autosomal recessive retinitis pigmentosa or Leber congenital amaurosis , 1998 .
[36] D. Higgins,et al. Coexpression of the mRNAs encoding retinol dehydrogenase isozymes and cellular retinol‐binding protein , 1997, Journal of cellular physiology.
[37] E. Zrenner,et al. Mutations in RPE65 cause Leber's congenital amaurosis , 1997, Nature Genetics.
[38] Birgit Lorenz,et al. Mutations in RPE65 cause autosomal recessive childhood–onset severe retinal dystrophy , 1997, Nature Genetics.
[39] J. Crabb,et al. Mutation of the gene encoding cellular retinaldehyde–binding protein in autosomal recessive retinitis pigmentosa , 1997, Nature Genetics.
[40] R. Blomhoff,et al. Retinol-binding Protein and Asialo-orosomucoid Are Taken Up by Different Pathways in Liver Cells (*) , 1995, The Journal of Biological Chemistry.
[41] U. Hellman,et al. The Retinal Pigment Epithelial-specific 11-cis Retinol Dehydrogenase Belongs to the Family of Short Chain Alcohol Dehydrogenases (*) , 1995, The Journal of Biological Chemistry.
[42] B. Sakmann,et al. Single-Channel Recording , 1995, Springer US.
[43] N. Noy,et al. Control of substrate flow at a branch in the visual cycle. , 1994, Biochemistry.
[44] J. Mcdowell. 7 - Preparing Rod Outer Segment Membranes, Regenerating Rhodopsin, and Determining Rhodopsin Concentration , 1993 .
[45] R. Rando. MOLECULAR MECHANISMS IN VISUAL PIGMENT REGENERATION , 1992, Photochemistry and photobiology.
[46] D. Baylor,et al. Rapid charge movements and photosensitivity of visual pigments in salamander rods and cones. , 1991, The Journal of physiology.
[47] R. Rando. Membrane phospholipids as an energy source in the operation of the visual cycle. , 1991, Biochemistry.
[48] K. Nakanishi,et al. Substrate specificities and mechanism in the enzymatic processing of vitamin A into 11-cis-retinol. , 1990, Biochemistry.
[49] P. Gouras,et al. Synthesis of retinoids by human retinal epithelium and transfer to rod outer segments. , 1990, The Biochemical journal.
[50] N. Noy,et al. Thermodynamic parameters of the binding of retinol to binding proteins and to membranes. , 1990, Biochemistry.
[51] J. Nathans,et al. Production of bovine rhodopsin by mammalian cell lines expressing cloned cDNA: Spectrophotometry and subcellular localization , 1989, Vision Research.
[52] G. Chader,et al. Interphotoreceptor retinoid-binding protein: role in delivery of retinol to the pigment epithelium. , 1989, Experimental eye research.
[53] F. Cañada,et al. Solubilization and partial purification of retinyl ester synthetase and retinoid isomerase from bovine ocular pigment epithelium. , 1989, The Journal of biological chemistry.
[54] K. Donner,et al. Low retinal noise in animals with low body temperature allows high visual sensitivity , 1988, Nature.
[55] P. Gouras,et al. Retinoid metabolism in cultured human retinal pigment epithelium. , 1988, The Biochemical journal.
[56] P. Bernstein,et al. Biochemical characterization of the retinoid isomerase system of the eye. , 1987, The Journal of biological chemistry.
[57] R. Rando,et al. Biosynthesis of 11-cis-retinoids and retinyl esters by bovine pigment epithelium membranes. , 1987, Biochemistry.
[58] P. Bernstein,et al. Mechanism of action of aromatic amines that short-circuit the visual cycle. , 1986, Biochemistry.
[59] P. Bernstein,et al. Short-circuiting the visual cycle with retinotoxic aromatic amines. , 1986, Proceedings of the National Academy of Sciences of the United States of America.
[60] B. Stillman,et al. Replication and supercoiling of simian virus 40 DNA in cell extracts from human cells , 1985, Molecular and cellular biology.
[61] F. Crescitelli. Some properties of solubilized human rhodopsin. , 1985, Experimental eye research.
[62] P. Bernstein,et al. Nonstereospecific biosynthesis of 11-cis-retinal in the eye. , 1985, Biochemistry.
[63] J. Horwitz,et al. Evidence for a common batho-intermediate in the bleaching of rhodopsin and isorhodopsin , 1984, Vision Research.
[64] P. Liebman,et al. Temperature and pH dependence of the metarhodopsin I-metarhodopsin II kinetics and equilibria in bovine rod disk membrane suspensions. , 1984, Biochemistry.
[65] A. Kini,et al. Seven new hindered isomeric rhodopsins: A reexamination of the stereospecificity of the binding site of bovine opsin , 1984 .
[66] R. Rando,et al. STUDIES ON THE CATALYZED INTERCONVERSIONS OF VITAMIN A DERIVATIVES , 1983 .
[67] Fred J. Sigworth,et al. Fitting and Statistical Analysis of Single-Channel Records , 1983 .
[68] J. C. Saari,et al. Identification of the endogenous retinoids associated with three cellular retinoid-binding proteins from bovine retina and retinal pigment epithelium. , 1982, The Journal of biological chemistry.
[69] J. C. Saari,et al. Enzymatic reduction of 11-cis-retinal bound to cellular retinal-binding protein. , 1982, Biochimica et biophysica acta.
[70] G. Groenendijk,et al. Dark isomerization of retinals in the presence of phosphatidylethanolamine. , 2005, European journal of biochemistry.
[71] D. Baylor,et al. Two components of electrical dark noise in toad retinal rod outer segments. , 1980, The Journal of physiology.
[72] D. Baylor,et al. Thermal activation of the visual transduction mechanism in retinal rods , 1979, Nature.
[73] T. Yoshizawa,et al. Recognition of opsin to the longitudinal length of retinal isomers in the formation of rhodopsin , 1978, Vision Research.
[74] D. Albert,et al. Cellular retinol- and retinoic acid-binding proteins in transformed mammalian cells. , 1978, Investigative ophthalmology & visual science.
[75] F. Graham,et al. Characteristics of a human cell line transformed by DNA from human adenovirus type 5. , 1977, The Journal of general virology.
[76] C. Bridges. Rhodopsin regeneration in rod outer segments: utilization of 11-cis retinal and retinol. , 1977, Experimental eye research.
[77] V. Ramamurthy,et al. Rhodopsin analogues from highly hindered 7-cis isomers of retinal , 1976, Nature.
[78] D. Page,et al. Retinoic acid binding protein: occurrence in human tumors , 1975, Science.
[79] J. Rotmans,et al. Biochemical aspects of the visual process. XXVII. Stereospecificity of ocular retinol dehydrogenases and the visual cycle. , 1970, Biochimica et biophysica acta.
[80] T. Williams,et al. Upper limits to the bleaching of rhodopsin by high intensity flashes. , 1974, Vision research.
[81] S. Futterman,et al. The stability of 11-cis-retinal and reactivity toward nucleophiles , 1974 .
[82] S. Futterman. Recent studies on a possible mechanism for visual pigment regeneration. , 1974, Experimental eye research.
[83] S. Futterman,et al. The catalytic isomerization of all-trans-retinal to 9-cis-retinal and 13-cis-retinal. , 1973, The Journal of biological chemistry.
[84] I. Ostapenko,et al. 9-Cis isomerization of all-trans retinal during in vitro regeneration of visual pigment. , 1973, Nature: New biology.
[85] J. Rotmans,et al. Biochemical aspects of the visual process. XIX. Formation of isorhodopsin from photolyzed rhodopsin by bacterial action. , 1972, Biochimica et biophysica acta.
[86] T. Ebrey. The thermal decay of the intermediates of rhodopsin in situ. , 1968, Vision research.
[87] R. Cone. Early Receptor Potential: Photoreversible Charge Displacement in Rhodopsin , 1967, Science.
[88] T. Williams,et al. Rhodopsin bleaching: relative effectiveness of high and low intensity flashes. , 1965, Vision research.
[89] T. Williams,et al. Photoreversal of Rhodopsin Bleaching , 1964, The Journal of general physiology.
[90] Hagins Wa. The quantum efficiency of bleaching of rhodopsin in situ. , 1955 .
[91] The quantum efficiency of bleaching of rhodopsin in situ. , 1955, The Journal of physiology.
[92] G. Wald,et al. CIS-TRANS ISOMERS OF VITAMIN A AND RETINENE IN THE RHODOPSIN SYSTEM , 1952, The Journal of general physiology.