Glycinergic amacrine cells of the rat retina
暂无分享,去创建一个
[1] S. R. Y. Cajal. La rétine des vertébrés , 1892 .
[2] M. Abercrombie. Estimation of nuclear population from microtome sections , 1946, The Anatomical record.
[3] B. Boycott,et al. Organization of the Primate Retina: Light Microscopy , 1969 .
[4] B. Ehinger,et al. Autoradiography of some suspected neurotransmitter substances: GABA glycine, glutamic acid, histamine, dopamine, and L-dopa. , 1971, Brain research.
[5] B. Ehinger,et al. Uptake of the putative neurotransmitter, glycine, into the rabbit retina. , 1972, Investigative ophthalmology.
[6] Helga Kolb,et al. Rod and Cone Pathways in the Inner Plexiform Layer of Cat Retina , 1974, Science.
[7] M. Voaden,et al. An investigation of the cells incorporating (3H)GABA and (3H)glycine in the isolated retina of the rat. , 1974, Experimental eye research.
[8] H. Wässle,et al. The distribution of the alpha type of ganglion cells in the cat's retina , 1975, The Journal of comparative neurology.
[9] V. Perry,et al. Amacrine cells, displaced amacrine cells and interplexiform cells in the retina of the rat , 1980, Proceedings of the Royal Society of London. Series B. Biological Sciences.
[10] R. Pourcho. Uptake of [3H]glycine and [3H]GABA by amacrine cells in the cat retina , 1980, Brain Research.
[11] R. Marc,et al. Glycinergic pathways in the goldfish retina , 1981, The Journal of neuroscience : the official journal of the Society for Neuroscience.
[12] Helga Kolb,et al. Amacrine cells, bipolar cells and ganglion cells of the cat retina: A Golgi study , 1981, Vision Research.
[13] R. Nelson,et al. AII amacrine cells quicken time course of rod signals in the cat retina. , 1982, Journal of neurophysiology.
[14] P. Sterling. Microcircuitry of the cat retina. , 1983, Annual review of neuroscience.
[15] P Sterling,et al. Microcircuitry of bipolar cells in cat retina , 1984, The Journal of neuroscience : the official journal of the Society for Neuroscience.
[16] J. Kleinschmidt,et al. Uptake of 3H‐glycine in the outer plexiform layer of the retina of the toad Bufo marinus , 1984, The Journal of comparative neurology.
[17] J. Hollyfield,et al. Glycinergic neurons in the human retina , 1984, The Journal of comparative neurology.
[18] R. Marc,et al. (3H) glycine‐accumulating neurons of the human retina , 1985, The Journal of comparative neurology.
[19] R. Pourcho,et al. A combined golgi and autoradiographic study of (3H)glycine‐accumulating amacrine cells in the cat retina , 1985, The Journal of comparative neurology.
[20] T. Voigt,et al. Cholinergic amacrine cells in the rat retina , 1986, The Journal of comparative neurology.
[21] P Sterling,et al. Accumulation of (3H)glycine by cone bipolar neurons in the cat retina , 1986, The Journal of comparative neurology.
[22] T. Voigt,et al. Analysis of a glycinergic inhibitory pathway in the cat retina , 1986, The Journal of neuroscience : the official journal of the Society for Neuroscience.
[23] P. Sterling,et al. Microcircuitry of beta ganglion cells in cat retina , 1986, The Journal of neuroscience : the official journal of the Society for Neuroscience.
[24] R. Dacheux,et al. The rod pathway in the rabbit retina: a depolarizing bipolar and amacrine cell , 1986, The Journal of neuroscience : the official journal of the Society for Neuroscience.
[25] R. Pourcho,et al. Visualization of endogenous glycine in cat retina: an immunocytochemical study with Fab fragments , 1987, The Journal of neuroscience : the official journal of the Society for Neuroscience.
[26] S. Massey,et al. Transmitter circuits in the vertebrate retina , 1987, Progress in Neurobiology.
[27] A. Hendrickson,et al. Localization of glycine‐containing neurons in the Macaca monkey retina , 1988, The Journal of comparative neurology.
[28] R. Marc. The role of glycine in the mammalian retina , 1988 .
[29] S. Zackson,et al. A promoter that drives transgene expression in cerebellar Purkinje and retinal bipolar neurons. , 1990, Science.
[30] D. I. Vaney,et al. Chapter 2 The mosaic of amacrine cells in the mammalian retina , 1990 .
[31] Ursula Greferath,et al. Rod bipolar cells in the mammalian retina show protein kinase C‐like immunoreactivity , 1990, The Journal of comparative neurology.
[32] R. Pourcho,et al. Connectivity of glycine immunoreactive amacrine cells in the cat retina , 1991, The Journal of comparative neurology.
[33] H. Kolb,et al. Neurons of the human retina: A Golgi study , 1992, The Journal of comparative neurology.
[34] E. Strettoi,et al. Synaptic connections of the narrow‐field, bistratified rod amacrine cell (AII) in the rabbit retina , 1992, The Journal of comparative neurology.
[35] H. Wässle,et al. Electron microscopic analysis of the rod pathway of the rat retina , 1993, The Journal of comparative neurology.
[36] H. Wässle,et al. Immunocytochemical localization of glycine receptors in the mammalian retina , 1993, The Journal of comparative neurology.
[37] D. Pow,et al. Extremely high titre polyclonal antisera against small neurotransmitter molecules: rapid production, characterisation and use in lightand electron-microscopic immunocytochemistry , 1993, Journal of Neuroscience Methods.
[38] C. Cepko,et al. Targeted ablation of diverse cell classes in the nervous system in vivo , 1993, The Journal of neuroscience : the official journal of the Society for Neuroscience.
[39] J. Röhrenbeck,et al. Immunocytochemical staining of AII‐amacrine cells in the rat retina with antibodies against parvalbumin , 1993, The Journal of comparative neurology.
[40] H. Wassle,et al. Voltage- and transmitter-gated currents of all-amacrine cells in a slice preparation of the rat retina , 1993, The Journal of neuroscience : the official journal of the Society for Neuroscience.
[41] D. Pow,et al. Rapid postmortem changes in the cellular localisation of amino acid transmitters in the retina as assessed by immunocytochemistry , 1994, Brain Research.
[42] D. I. Vaney,et al. Patterns of neuronal coupling in the retina , 1994, Progress in Retinal and Eye Research.
[43] H. Wässle,et al. Glycinergic synapses in the rod pathway of the rat retina: cone bipolar cells express the alpha 1 subunit of the glycine receptor , 1994, The Journal of neuroscience : the official journal of the Society for Neuroscience.
[44] S. Massey,et al. Differential properties of two gap junctional pathways made by AII amacrine cells , 1995, Nature.
[45] J. Storm-Mathisen,et al. Glycine transporters are differentially expressed among CNS cells , 1995, The Journal of neuroscience : the official journal of the Society for Neuroscience.
[46] D. Pow,et al. The immunocytochemical detection of amino-acid neurotransmitters in paraformaldehyde-fixed tissues , 1995, Journal of Neuroscience Methods.
[47] R E Marc,et al. Pattern recognition of amino acid signatures in retinal neurons , 1995, The Journal of neuroscience : the official journal of the Society for Neuroscience.
[48] H. Wässle,et al. Immunocytochemical identification of cone bipolar cells in the rat retina , 1995, The Journal of comparative neurology.
[49] Heinz Wässle,et al. The rod pathway of the macaque monkey retina: Identification of AII‐amacrine cells with antibodies against calretinin , 1995, The Journal of comparative neurology.
[50] M. Kalloniatis,et al. Neurochemical architecture of the normal and degenerating rat retina , 1996, The Journal of comparative neurology.
[51] H. Wässle,et al. Glutamate Responses of Bipolar Cells in a Slice Preparation of the Rat Retina , 1996, The Journal of Neuroscience.
[52] J. Nathans,et al. Retina-derived POU-domain factor-1: a complex POU-domain gene implicated in the development of retinal ganglion and amacrine cells , 1996, Journal of Neuroscience.
[53] H. Wässle,et al. Glycine receptors in the rod pathway of the macaque monkey retina , 1996, Visual Neuroscience.
[54] H. Kolb,et al. Hyperpolarizing, small‐field, amacrine cells in cone pathways of cat retina , 1996, The Journal of comparative neurology.
[55] R. Marc,et al. Amino Acid Signatures in the Primate Retina , 1996, The Journal of Neuroscience.
[56] J. Nathans,et al. Molecular biology of retinal ganglion cells. , 1996, Proceedings of the National Academy of Sciences of the United States of America.
[57] C. Cepko,et al. Crx, a Novel otx-like Homeobox Gene, Shows Photoreceptor-Specific Expression and Regulates Photoreceptor Differentiation , 1997, Cell.
[58] M. Meister,et al. The Light Response of Retinal Ganglion Cells Is Truncated by a Displaced Amacrine Circuit , 1997, Neuron.
[59] A. Feigenspan,et al. Control of Dopamine Release in the Retina: a Transgenic Approach to Neural Networks , 1997, Neuron.
[60] P. Gruss,et al. Current views on eye development , 1997, Trends in Neurosciences.
[61] D. Farber,et al. Identification of genes causing photoreceptor degenerations leading to blindness , 1997, Current Opinion in Neurobiology.
[62] C. L. Macqueen,et al. The DAPI-3 amacrine cells of the rabbit retina , 1997, Visual Neuroscience.