Origin of reproducibility in the responses of retinal rods to single photons.
暂无分享,去创建一个
[1] M. A. Erickson,et al. The effect of recombinant recoverin on the photoresponse of truncated rod photoreceptors. , 1998, Proceedings of the National Academy of Sciences of the United States of America.
[2] N. Engheta,et al. Kinetics of Recovery of the Dark-adapted Salamander Rod Photoresponse , 1998, The Journal of general physiology.
[3] Denis A. Baylor,et al. Prolonged photoresponses in transgenic mouse rods lacking arrestin , 1997, Nature.
[4] L. Lagnado,et al. G-protein deactivation is rate-limiting for shut-off of the phototransduction cascade , 1997, Nature.
[5] D. Baylor,et al. Molecular origin of continuous dark noise in rod photoreceptors. , 1996, Biophysical journal.
[6] H. Khorana,et al. Structural features and light-dependent changes in the cytoplasmic interhelical E-F loop region of rhodopsin: a site-directed spin-labeling study. , 1996, Biochemistry.
[7] W. G. Owen,et al. Dynamic, spatially nonuniform calcium regulation in frog rods exposed to light. , 1996, Journal of neurophysiology.
[8] T. Lamb,et al. Kinetics of desensitization induced by saturating flashes in toad and salamander rods. , 1996, The Journal of physiology.
[9] J. Hurley,et al. Responses of the phototransduction cascade to dim light. , 1996, Proceedings of the National Academy of Sciences of the United States of America.
[10] Y. Koutalos,et al. Regulation of sensitivity in vertebrate rod photoreceptors by calcium , 1996, Trends in Neurosciences.
[11] E. Pugh,et al. The kinetics of inactivation of the rod phototransduction cascade with constant Ca2+i , 1996, The Journal of general physiology.
[12] Y. Koutalos,et al. Characterization of guanylate cyclase activity in single retinal rod outer segments , 1995, The Journal of general physiology.
[13] Y. Koutalos,et al. The cGMP-phosphodiesterase and its contribution to sensitivity regulation in retinal rods , 1995, The Journal of general physiology.
[14] H. Khorana,et al. Mapping light-dependent structural changes in the cytoplasmic loop connecting helices C and D in rhodopsin: a site-directed spin labeling study. , 1995, Biochemistry.
[15] A. Milam,et al. Rhodopsin Phosphorylation and Dephosphorylation in Vivo(*) , 1995, The Journal of Biological Chemistry.
[16] David J. Baylor,et al. Mechanisms of rhodopsin inactivation in vivo as revealed by a COOH-terminal truncation mutant , 1995, Science.
[17] P. Detwiler,et al. The calcium feedback signal in the phototransduction cascade of vertebrate rods , 1994, Neuron.
[18] T Hoshi,et al. Shaker potassium channel gating. III: Evaluation of kinetic models for activation , 1994, The Journal of general physiology.
[19] D. Baylor,et al. Calcium controls light-triggered formation of catalytically active rhodopsin , 1994, Nature.
[20] J. Jin,et al. Modulation of transduction gain in light adaptation of retinal rods , 1994, Visual Neuroscience.
[21] M. Cornwall,et al. Evidence for the prolonged photoactivated lifetime of an analogue visual pigment containing 11 -cis 9-desmethylretinal , 1994, Visual Neuroscience.
[22] P. Detwiler,et al. Visual transduction in dialysed detached rod outer segments from lizard retina. , 1993, The Journal of physiology.
[23] Satoru Kawamura,et al. Rhodopsin phosphorylation as a mechanism of cyclic GMP phosphodiesterase regulation by S-modulin , 1993, Nature.
[24] T. Lamb,et al. Amplification and kinetics of the activation steps in phototransduction. , 1993, Biochimica et biophysica acta.
[25] V. Arshavsky,et al. Regulation of deactivation of photoreceptor G protein by its target enzyme and cGMP , 1992, Nature.
[26] Leon Lagnado,et al. Signal flow in visual transduction , 1992, Neuron.
[27] P. Detwiler,et al. The influence of arrestin (48K protein) and rhodopsin kinase on visual transduction , 1992, Neuron.
[28] W. G. Owen,et al. Temporal filtering in retinal bipolar cells. Elements of an optimal computation? , 1990, Biophysical journal.
[29] L. Lagnado,et al. Extrusion of calcium from rod outer segments is driven by both sodium and potassium gradients , 1989, Nature.
[30] L. Stryer,et al. Highly cooperative feedback control of retinal rod guanylate cyclase by calcium ions , 1988, Nature.
[31] K. Yau,et al. Calcium and light adaptation in retinal rods and cones , 1988, Nature.
[32] T. Lamb,et al. Photoreceptor light adaptation is mediated by cytoplasmic calcium concentration , 1988, Nature.
[33] K. Donner,et al. Low retinal noise in animals with low body temperature allows high visual sensitivity , 1988, Nature.
[34] N. Bennett,et al. Inactivation of photoexcited rhodopsin in retinal rods: the roles of rhodopsin kinase and 48-kDa protein (arrestin). , 1988, Biochemistry.
[35] D. Baylor,et al. Gating kinetics of the cyclic-GMP-activated channel of retinal rods: flash photolysis and voltage-jump studies. , 1988, Proceedings of the National Academy of Sciences of the United States of America.
[36] H R Matthews,et al. Role of calcium in regulating the cyclic GMP cascade of phototransduction in retinal rods. , 1986, Proceedings of the National Academy of Sciences of the United States of America.
[37] D. Baylor,et al. Cyclic GMP-sensitive conductance of retinal rods consists of aqueous pores , 1986, Nature.
[38] K. Yau,et al. Light-suppressible, cyclic GMP-sensitive conductance in the plasma membrane of a truncated rod outer segment , 1985, Nature.
[39] E. Dratz,et al. Phosphorylation at sites near rhodopsin'scarboxyl-terminus regulates light initiated CGMP hydrolysis , 1984, Vision Research.
[40] D. Baylor,et al. The photocurrent, noise and spectral sensitivity of rods of the monkey Macaca fascicularis. , 1984, The Journal of physiology.
[41] J. L. Schnapf. Dependence of the single photon response on longitudinal position of absorption in toad rod outer segments. , 1983, The Journal of physiology.
[42] B. K. Fung. Characterization of transducin from bovine retinal rod outer segments. I. Separation and reconstitution of the subunits. , 1983, The Journal of biological chemistry.
[43] D. Baylor,et al. Two components of electrical dark noise in toad retinal rod outer segments. , 1980, The Journal of physiology.
[44] D. Baylor,et al. The membrane current of single rod outer segments , 1979, Vision Research.
[45] D. Baylor,et al. Responses of retinal rods to single photons. , 1979, The Journal of physiology.
[46] B. Sakitt. Counting every quantum , 1972, The Journal of physiology.
[47] H. Velden,et al. The number of quanta necessary for the perception of light of the human eye. , 1946 .
[48] S. Hecht,et al. ENERGY, QUANTA, AND VISION , 1942, The Journal of general physiology.
[49] K. Yau,et al. Calcium and magnesium fluxes across the plasma membrane of the toad rod outer segment. , 1988, The Journal of physiology.
[50] K. Yau,et al. Guanosine 3',5'‐cyclic monophosphate‐activated conductance studied in a truncated rod outer segment of the toad. , 1988, The Journal of physiology.
[51] H. A. VAN DER VELDEN,et al. The number of quanta necessary for the perception of light of the human eye. , 1946, Ophthalmologica. Journal international d'ophtalmologie. International journal of ophthalmology. Zeitschrift fur Augenheilkunde.