Distribution of mRNA for the calmodulin-sensitive adenylate cyclase in rat brain: Expression in areas associated with learning and memory
暂无分享,去创建一个
[1] Randall R. Reed,et al. Identification of a specialized adenylyl cyclase that may mediate odorant detection. , 1990, Science.
[2] M. Olianas,et al. Ca2+‐Independent Stimulation of Adenylate Cyclase Activity by Muscarinic Receptors in Rat Olfactory Bulb , 1990, Journal of neurochemistry.
[3] L. Haberly,et al. NMDA-dependent induction of long-term potentiation in afferent and association fiber systems of piriform cortex in vitro , 1990, Brain Research.
[4] T. Bonner,et al. Structure of a cannabinoid receptor and functional expression of the cloned cDNA , 1990, Nature.
[5] Y. Ben-Ari,et al. Brief seizure episodes induce long-term potentiation and mossy fibre sprouting in the hippocampus , 1990, Trends in Neurosciences.
[6] D. Cooper,et al. Differential expression of low molecular weight form of Gs-α in neostriatum and cerebellum: correlation with expression of calmodulin-independent adenylyl cyclase , 1990, Brain Research.
[7] R. Nicoll,et al. Comparison of two forms of long-term potentiation in single hippocampal neurons. , 1990, Science.
[8] M. Tota,et al. Reconstitution of muscarinic receptor-mediated inhibition of adenylyl cyclase. , 1990, Molecular pharmacology.
[9] M. Feany. Rescue of the learning defect in dunce, a Drosophila learning mutant, by an allele of rutabaga, a second learning mutant. , 1990, Proceedings of the National Academy of Sciences of the United States of America.
[10] A. Mørk,et al. 5-Hydroxytryptamine receptor agonists influence calcium-stimulated adenylate cyclase activity in the cerebral cortex and hippocampus of the rat. , 1990, European journal of pharmacology.
[11] E R Kandel,et al. Ca2+/calmodulin sensitivity may be common to all forms of neural adenylate cyclase. , 1989, Proceedings of the National Academy of Sciences of the United States of America.
[12] M. Miller,et al. Distribution of neurotensin/neuromedin N mRNA in rat forebrain: unexpected abundance in hippocampus and subiculum. , 1989, Proceedings of the National Academy of Sciences of the United States of America.
[13] G. McKnight,et al. Distinct patterns of cAMP-dependent protein kinase gene expression in mouse brain , 1989, Neuron.
[14] C. Slaughter,et al. Adenylyl cyclase amino acid sequence: possible channel- or transporter-like structure. , 1989, Science.
[15] E. Kandel,et al. Is contiguity detection in classical conditioning a system or a cellular property? Learning in Aplysia suggests a possible molecular site , 1988, Trends in Neurosciences.
[16] M. Gnegy,et al. Differential Regulation by Calmodulin of Basal, GTP‐, and Dopamine‐Stimulated Adenylate Cyclase Activities in Bovine Striatum , 1988, Journal of neurochemistry.
[17] L. Iversen,et al. Differences between high-affinity forskolin binding sites in dopamine-rich and other regions of rat brain. , 1988, Proceedings of the National Academy of Sciences of the United States of America.
[18] D. T. Jones,et al. G protein mRNA mapped in rat brain by in situ hybridization. , 1988, Proceedings of the National Academy of Sciences of the United States of America.
[19] D. Johnston,et al. Noradrenergic enhancement of long-term potentiation at mossy fiber synapses in the hippocampus. , 1988, Journal of neurophysiology.
[20] T. Teyler,et al. A critical period for long-term potentiation in the developing rat visual cortex , 1988, Brain Research.
[21] W. Singer,et al. Long-term potentiation and NMDA receptors in rat visual cortex , 1987, Nature.
[22] S. Shenolikar,et al. Evidence that forskolin binds to the glucose transporter of human erythrocytes. , 1987, The Journal of biological chemistry.
[23] M. Brann,et al. Localization of mRNAs encoding the α‐subunits of signal‐transducing G‐proteins within rat brain and among peripheral tissues , 1987, FEBS letters.
[24] James H. Schwartz,et al. A molecular mechanism for long-term sensitization in Aplysia , 1987, Nature.
[25] A. Levitzki. Regulation of hormone-sensitive adenylate cyclase , 1987 .
[26] D. Storm,et al. Direct interaction between the catalytic subunit of the calmodulin-sensitive adenylate cyclase from bovine brain with 125I-labeled wheat germ agglutinin and 125I-labeled calmodulin. , 1987, Biochemistry.
[27] Carl W. Cotman,et al. Anatomical organization of excitatory amino acid receptors and their pathways , 1987, Trends in Neurosciences.
[28] W. A. Toscano,et al. Calmodulin-mediated adenylate cyclase from mammalian sperm. , 1987, The Journal of biological chemistry.
[29] D. Storm,et al. Immunological distinction between calmodulin-sensitive and calmodulin-insensitive adenylate cyclases. , 1987, The Journal of biological chemistry.
[30] M. Shanahan,et al. [3H]forskolin. Direct photoaffinity labeling of the erythrocyte D-glucose transporter. , 1987, The Journal of biological chemistry.
[31] R. Davis,et al. Molecular analysis of cDNA clones and the corresponding genomic coding sequences of the Drosophila dunce+ gene, the structural gene for cAMP phosphodiesterase. , 1986, Proceedings of the National Academy of Sciences of the United States of America.
[32] E. Kandel,et al. Facilitatory transmitters and cAMP can modulate accommodation as well as transmitter release in Aplysia sensory neurons: Evidence for parallel processing in a single cell. , 1986, Proceedings of the National Academy of Sciences of the United States of America.
[33] S. Snyder,et al. Mapping second messenger systems in the brain: differential localizations of adenylate cyclase and protein kinase C. , 1986, Proceedings of the National Academy of Sciences of the United States of America.
[34] A. Gilman,et al. Reconstitution of catecholamine-stimulated adenylate cyclase activity using three purified proteins. , 1985, The Journal of biological chemistry.
[35] M S Livingstone,et al. Genetic dissection of Drosophila adenylate cyclase. , 1985, Proceedings of the National Academy of Sciences of the United States of America.
[36] J. Sarvey,et al. Depletion of norepinephrine, but not serotonin, reduces long-term potentiation in the dentate gyrus of rat hippocampal slices , 1985, The Journal of neuroscience : the official journal of the Society for Neuroscience.
[37] Y. Dudai,et al. Multiple Defects in the Activity of Adenylate Cyclase from the Drosophila Memory Mutant Rutabaga , 1985, Journal of neurochemistry.
[38] W. Heideman,et al. Purification of the calmodulin-sensitive adenylate cyclase from bovine cerebral cortex. , 1985, Biochemistry.
[39] F. F. Weight,et al. Perforant pathway-evoked long-term potentiation of CA1 neurons in the hippocampal slice preparation , 1985, Brain Research.
[40] T. Dawson,et al. Localization of [3H]forskolin binding sites in the rat brain using quantitative autoradiography. , 1984, European journal of pharmacology.
[41] Y. Dudai,et al. Adenylate cyclase in the Drosophila memory mutant rutabaga displays an altered Ca2+ sensitivity , 1984, Neuroscience Letters.
[42] M. Livingstone,et al. Loss of calcium/calmodulin responsiveness in adenylate cyclase of rutabaga, a Drosophila learning mutant , 1984, Cell.
[43] G. Brooker,et al. Distinct mechanisms of forskolin-stimulated cyclic AMP accumulation and forskolin-potentiated hormone responses in C6-2B cells. , 1984, Molecular pharmacology.
[44] M. Piascik,et al. Calmodulin stimulation and calcium regulation of smooth muscle adenylate cyclase activity. , 1983, The Journal of biological chemistry.
[45] R. Racine,et al. Long-term potentiation phenomena in the rat limbic forebrain , 1983, Brain Research.
[46] E. Kandel,et al. A cellular mechanism of classical conditioning in Aplysia: activity-dependent amplification of presynaptic facilitation. , 1983, Science.
[47] J. Byrne,et al. Associative conditioning of single sensory neurons suggests a cellular mechanism for learning. , 1983, Science.
[48] E. Kandel,et al. Molecular biology of learning: modulation of transmitter release. , 1982, Science.
[49] K. Toyama,et al. Long-term potentiation investigated in a slice preparation of striate cortex of young kittens , 1981, Neuroscience Letters.
[50] J. Daly,et al. Activation of adenylate cyclase by the diterpene forskolin does not require the guanine nucleotide regulatory protein. , 1981, The Journal of biological chemistry.
[51] P. Greengard,et al. Protein phosphorylation in the brain , 1980, Nature.
[52] W. Levy,et al. Functional effects of lesion-induced plasticity: Long term potentiation in normal and lesion-induced temporodentate connections , 1979, Brain Research.
[53] W. Malaisse,et al. Calmodulin activation of adenylate cyclase in pancreatic islets. , 1979, Science.
[54] J. Maeda,et al. Long-term potentiation of synaptic transmission in kitten visual cortex. , 1988, Journal of neurophysiology.
[55] T. Pfeuffer,et al. Two different adenylyl cyclases in brain distinguished by monoclonal antibodies. , 1988, European journal of biochemistry.
[56] Y. Dudai. Neurogenetic dissection of learning and short-term memory in Drosophila. , 1988, Annual review of neuroscience.
[57] D. Storm,et al. Reconstitution of calmodulin-sensitive adenylate cyclase from bovine brain with phospholipids, calmodulin, and beta-adrenergic receptors. , 1987, Methods in enzymology.
[58] P. Greengard,et al. Protein kinases in the brain. , 1985, Annual review of biochemistry.
[59] D. Green,et al. Direct evidence for the role of the coupling proteins in forskolin activation of adenylate cyclase. , 1982, Journal of cyclic nucleotide research.
[60] A. Gilman,et al. Biochemical properties of hormone-sensitive adenylate cyclase. , 1980, Annual review of biochemistry.
[61] E. Krebs,et al. Phosphorylation-dephosphorylation of enzymes. , 1979, Annual review of biochemistry.
[62] Avdonin Pv,et al. [Participation of Ca2+ activator in regulating the activity of cardiac adenylate cyclase by calcium ions]. , 1978 .
[63] D. J. Wolff,et al. Identification of a calcium-binding protein as a calcium-dependent regulator of brain adenylate cyclase. , 1975, Proceedings of the National Academy of Sciences of the United States of America.