Masked excitatory crosstalk between the ON and OFF visual pathways in the mammalian retina
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[1] Béla Völgyi,et al. Light increases the gap junctional coupling of retinal ganglion cells , 2010, The Journal of physiology.
[2] Zhiyin Liang,et al. The ON Pathway Rectifies the OFF Pathway of the Mammalian Retina , 2010, The Journal of Neuroscience.
[3] Frank S Werblin,et al. Six different roles for crossover inhibition in the retina: Correcting the nonlinearities of synaptic transmission , 2010, Visual Neuroscience.
[4] Erika D Eggers,et al. Interneuron circuits tune inhibition in retinal bipolar cells. , 2010, Journal of neurophysiology.
[5] Kwoon Y. Wong,et al. Ectopic retinal ON bipolar cell synapses in the OFF inner plexiform layer: Contacts with dopaminergic amacrine cells and melanopsin ganglion cells , 2009, The Journal of comparative neurology.
[6] B. Völgyi,et al. GABA blockade unmasks an OFF response in ON direction selective ganglion cells in the mammalian retina , 2009, The Journal of physiology.
[7] Alyosha C. Molnar,et al. Crossover inhibition in the retina: circuitry that compensates for nonlinear rectifying synaptic transmission , 2009, Journal of Computational Neuroscience.
[8] S. Massey,et al. ON Inputs to the OFF Layer: Bipolar Cells That Break the Stratification Rules of the Retina , 2009, The Journal of Neuroscience.
[9] B. Völgyi,et al. The diverse functional roles and regulation of neuronal gap junctions in the retina , 2009, Nature Reviews Neuroscience.
[10] B. Völgyi,et al. Tracer coupling patterns of the ganglion cell subtypes in the mouse retina , 2009, The Journal of comparative neurology.
[11] Frank S Werblin,et al. Amacrine-to-amacrine cell inhibition in the rabbit retina. , 2008, Journal of neurophysiology.
[12] J. B. Demb,et al. Disinhibition Combines with Excitation to Extend the Operating Range of the OFF Visual Pathway in Daylight , 2008, The Journal of Neuroscience.
[13] Fred Rieke,et al. Signals and noise in an inhibitory interneuron diverge to control activity in nearby retinal ganglion cells , 2008, Nature Neuroscience.
[14] F. Werblin,et al. Inhibitory feedback shapes bipolar cell responses in the rabbit retina. , 2007, Journal of neurophysiology.
[15] Erika D Eggers,et al. Presynaptic inhibition differentially shapes transmission in distinct circuits in the mouse retina , 2007, The Journal of physiology.
[16] S. Mills,et al. Dopaminergic modulation of tracer coupling in a ganglion-amacrine cell network , 2007, Visual Neuroscience.
[17] Ping Li,et al. Glycine receptor subunit composition alters the action of GABA antagonists , 2007, Visual Neuroscience.
[18] S. Massey,et al. Screening of gap junction antagonists on dye coupling in the rabbit retina , 2007, Visual Neuroscience.
[19] Saskia E. J. de Vries,et al. Retinal Ganglion Cells Can Rapidly Change Polarity from Off to On , 2007, PLoS biology.
[20] Michael P Stryker,et al. Intrinsic ON Responses of the Retinal OFF Pathway Are Suppressed by the ON Pathway , 2006, The Journal of Neuroscience.
[21] S. Mills,et al. A Novel Fluorescent Tracer for Visualizing Coupled Cells in Neural Circuits of Living Tissue , 2006, The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society.
[22] Botond Roska,et al. Parallel processing in retinal ganglion cells: how integration of space-time patterns of excitation and inhibition form the spiking output. , 2006, Journal of neurophysiology.
[23] R. Dacheux,et al. Glycine- and GABA-activated inhibitory currents on axon terminals of rabbit cone bipolar cells , 2005, Visual Neuroscience.
[24] M. McCall,et al. Stimulus size and intensity alter fundamental receptive-field properties of mouse retinal ganglion cells in vivo , 2005, Visual Neuroscience.
[25] M. Slaughter,et al. Effects of GABA receptor antagonists on retinal glycine receptors and on homomeric glycine receptor alpha subunits. , 2005, Journal of neurophysiology.
[26] B. Völgyi,et al. Convergence and Segregation of the Multiple Rod Pathways in Mammalian Retina , 2004, The Journal of Neuroscience.
[27] Heinz Wässle,et al. Parallel processing in the mammalian retina , 2004, Nature Reviews Neuroscience.
[28] Daniel E Feldman,et al. Synaptic basis for developmental plasticity in somatosensory cortex , 2004, Current Opinion in Neurobiology.
[29] H. Wässle,et al. Localization of GABAA receptors in the rabbit retina , 1994, Cell and Tissue Research.
[30] H. K. HAltTLIn. THE RESPONSE OF SINGLE OPTIC NERVE FIBERS OF THE VERTEBRATE EYE TO ILLUMINATION OF THE RETINA , 2004 .
[31] S. Bloomfield,et al. Gap Junctional Coupling Underlies the Short-Latency Spike Synchrony of Retinal α Ganglion Cells , 2003, The Journal of Neuroscience.
[32] R. Dacheux,et al. Evidence for glycine, GABAA, and GABAB receptors on rabbit OFF-alpha ganglion cells , 2003, Visual Neuroscience.
[33] J. B. Demb,et al. Different Circuits for ON and OFF Retinal Ganglion Cells Cause Different Contrast Sensitivities , 2003, The Journal of Neuroscience.
[34] L. Arnold,et al. Acute reductions in GABAA receptor binding in layer IV of adult primate somatosensory cortex after peripheral nerve injury , 2002, Brain Research.
[35] Michael B. Calford,et al. Dynamic representational plasticity in sensory cortex , 2002, Neuroscience.
[36] Béla Völgyi,et al. Feedback inhibition in the inner plexiform layer underlies the surround‐mediated responses of AII amacrine cells in the mammalian retina , 2002, The Journal of physiology.
[37] F. Werblin,et al. Vertical interactions across ten parallel, stacked representations in the mammalian retina , 2001, Nature.
[38] S. DeVries,et al. Bipolar Cells Use Kainate and AMPA Receptors to Filter Visual Information into Separate Channels , 2000, Neuron.
[39] S. Bloomfield,et al. A flattened retina-eyecup preparation suitable for electrophysiological studies of neurons visualized with trans-scleral infrared illumination , 2000, Journal of Neuroscience Methods.
[40] Donal G. Sinex,et al. Acute spiral ganglion lesions change the tuning and tonotopic organization of cat inferior colliculus neurons , 2000, Hearing Research.
[41] R. Pourcho,et al. Transmitter‐specific input to OFF‐alpha ganglion cells in the cat retina , 1999, The Anatomical record.
[42] H. Wässle,et al. Glycine and GABA receptors in the mammalian retina , 1998, Vision Research.
[43] M. Nicolelis,et al. Immediate and simultaneous sensory reorganization at cortical and subcortical levels of the somatosensory system. , 1997, Proceedings of the National Academy of Sciences of the United States of America.
[44] S. Bloomfield,et al. Tracer coupling pattern of amacrine and ganglion cells in the rabbit retina , 1997, The Journal of comparative neurology.
[45] N. Vardi,et al. ON cone bipolar cells in rat express the metabotropic receptor mGluR6 , 1997, Visual Neuroscience.
[46] M. Meister,et al. The Light Response of Retinal Ganglion Cells Is Truncated by a Displaced Amacrine Circuit , 1997, Neuron.
[47] R. Dacheux,et al. Alpha ganglion cells of the rabbit retina lose antagonistic surround responses under dark adaptation , 1997, Visual Neuroscience.
[48] D G Pelli,et al. The VideoToolbox software for visual psychophysics: transforming numbers into movies. , 1997, Spatial vision.
[49] D H Brainard,et al. The Psychophysics Toolbox. , 1997, Spatial vision.
[50] A. Burkhalter,et al. Different Balance of Excitation and Inhibition in Forward and Feedback Circuits of Rat Visual Cortex , 1996, The Journal of Neuroscience.
[51] H. Wässle,et al. Immunocytochemical Localization of the GABACReceptor ρ Subunits in the Mammalian Retina , 1996, The Journal of Neuroscience.
[52] S. Dudek,et al. Intracellular blockade of inhibitory synaptic responses in visual cortical layer IV neurons. , 1996, Journal of neurophysiology.
[53] Tomomitsu Miyoshi,et al. Specific deficit of the ON response in visual transmission by targeted disruption of the mGIuR6 gene , 1995, Cell.
[54] Shigetada Nakanishi,et al. Developmentally regulated postsynaptic localization of a metabotropic glutamate receptor in rat rod bipolar cells , 1994, Cell.
[55] G. Thurlow,et al. ON and OFF activity gradients in the lateral geniculate nucleus of the cat: A combined 14C 2-deoxyglucose and D, L-2-amino-4-phosphonobutyric acid study , 1993, Visual Neuroscience.
[56] H. Kolb,et al. Off‐alpha and OFF‐beta ganglion cells in cat retina: II. Neural circuitry as revealed by electron microscopy of HRP stains , 1993, The Journal of comparative neurology.
[57] M. Nicolelis,et al. Induction of immediate spatiotemporal changes in thalamic networks by peripheral block of ascending cutaneous information , 1993, Nature.
[58] T. Wiesel,et al. Receptive field dynamics in adult primary visual cortex , 1992, Nature.
[59] L. Peichl,et al. Alpha ganglion cells in mammalian retinae: Common properties, species differences, and some comments on other ganglion cells , 1991, Visual Neuroscience.
[60] D. I. Vaney,et al. Many diverse types of retinal neurons show tracer coupling when injected with biocytin or Neurobiotin , 1991, Neuroscience Letters.
[61] KM Jacobs,et al. Reshaping the cortical motor map by unmasking latent intracortical connections , 1991, Science.
[62] J. Kaas,et al. Injury-induced reorganization of somatosensory cortex is accompanied by reductions in GABA staining. , 1991, Somatosensory & motor research.
[63] R. Jensen. Involvement of glycinergic neurons in the diminished surround activity of ganglion cells in the dark-adapted rabbit retina , 1991, Visual Neuroscience.
[64] D. Rasmusson,et al. Acute effects of total or partial digit denervation on raccoon somatosensory cortex. , 1990, Somatosensory & motor research.
[65] J. Davidson,et al. Glycyrrhetinic acid derivatives: a novel class of inhibitors of gap-junctional intercellular communication. Structure-activity relationships. , 1988, The Journal of pharmacology and experimental therapeutics.
[66] Michael B. Calford,et al. Immediate and chronic changes in responses of somatosensory cortex in adult flying-fox after digit amputation , 1988, Nature.
[67] J. Donoghue,et al. Rapid reorganization of adult rat motor cortex somatic representation patterns after motor nerve injury. , 1988, Proceedings of the National Academy of Sciences of the United States of America.
[68] B. Boycott,et al. Alpha ganglion cells in mammalian retinae , 1987, Proceedings of the Royal Society of London. Series B. Biological Sciences.
[69] S A Bloomfield,et al. A functional organization of ON and OFF pathways in the rabbit retina , 1986, The Journal of neuroscience : the official journal of the Society for Neuroscience.
[70] Y. Fukuda,et al. Morphological correlates of physiologically identified Y-, X-, and W-cells in cat retina. , 1984, Journal of neurophysiology.
[71] S. Sherman,et al. Structure/function relationships of retinal ganglion cells in the cat , 1984, Brain Research.
[72] J. Horton,et al. Receptive field properties in the cat's lateral geniculate nucleus in the absence of on-center retinal input , 1984, The Journal of neuroscience : the official journal of the Society for Neuroscience.
[73] H. Saito,et al. Morphology of physiologically identified X‐, Y‐, and W‐type retinal ganglion cells of the cat , 1983, The Journal of comparative neurology.
[74] Knapp Ag,et al. Response properties of cells in rabbit's lateral geniculate nucleus during reversible blockade of retinal on-center channel. , 1983 .
[75] D. J. Felleman,et al. Progression of change following median nerve section in the cortical representation of the hand in areas 3b and 1 in adult owl and squirrel monkeys , 1983, Neuroscience.
[76] L. Mistler,et al. Response properties of cells in rabbit's lateral geniculate nucleus during reversible blockade of retinal on-center channel. , 1983, Journal of neurophysiology.
[77] P. H. Schiller. Central connections of the retinal ON and OFF pathways , 1982, Nature.
[78] M. Ariel,et al. Pharmacological analysis of directionally sensitive rabbit retinal ganglion cells , 1982, The Journal of physiology.
[79] A. S. Batuev,et al. Picrotoxin action on the receptive fields of the cat sensorimotor cortex neurons , 1982, Journal of neuroscience research.
[80] B. Boycott,et al. Morphological identification of on- and off-centre brisk transient (Y) cells in the cat retina. , 1981, Proceedings of the Royal Society of London. Series B, Biological sciences.
[81] B. Boycott,et al. Morphology and topography of on- and off-alpha cells in the cat retina , 1981, Proceedings of the Royal Society of London. Series B. Biological Sciences.
[82] M. Slaughter,et al. 2-amino-4-phosphonobutyric acid: a new pharmacological tool for retina research. , 1981, Science.
[83] J. Metzler,et al. Functional changes in cat somatic sensory-motor cortex during short-term reversible epidural blocks , 1979, Brain Research.
[84] H. Kolb,et al. Intracellular staining reveals different levels of stratification for on- and off-center ganglion cells in cat retina. , 1978, Journal of neurophysiology.
[85] A Kaneko,et al. Neuronal architecture of on and off pathways to ganglion cells in carp retina. , 1977, Science.
[86] E. V. Famiglietti,et al. Structural basis for ON-and OFF-center responses in retinal ganglion cells. , 1976, Science.
[87] P. Wall,et al. The immediate shift of afferent drive of dorsal column nucleus cells following deafferentation: A comparison of acute and chronic deafferentation in gracile nucleus and spinal cord , 1976, Experimental Neurology.
[88] H. Wässle,et al. The distribution of the alpha type of ganglion cells in the cat's retina , 1975, The Journal of comparative neurology.
[89] B. Boycott,et al. The morphological types of ganglion cells of the domestic cat's retina , 1974, The Journal of physiology.
[90] J. Dowling,et al. Organization of the retina of the mudpuppy, Necturus maculosus. II. Intracellular recording. , 1969, Journal of neurophysiology.
[91] B. Boycott,et al. Organization of the primate retina: electron microscopy , 1966, Proceedings of the Royal Society of London. Series B. Biological Sciences.