Cholinergic and GABAergic Inputs Drive Patterned Spontaneous Motoneuron Activity before Target Contact
暂无分享,去创建一个
[1] L. Landmesser,et al. The development of hindlimb motor activity studied in the isolated spinal cord of the chick embryo , 1987, The Journal of neuroscience : the official journal of the Society for Neuroscience.
[2] M. Stryker,et al. Prenatal tetrodotoxin infusion blocks segregation of retinogeniculate afferents. , 1988, Science.
[3] G. Thiriet,et al. Distribution of cholinergic neurons in the chick spinal cord during embryonic development. Comparison of ChAT immunocytochemistry with AChE histochemistry , 1992, International Journal of Developmental Neuroscience.
[4] N. Kudo,et al. N-Methyl-d,l-aspartate-induced locomotor activity in a spinal cord-indlimb muscles preparation of the newborn rat studied in vitro , 1987, Neuroscience Letters.
[5] Viktor Hamburger,et al. A series of normal stages in the development of the chick embryo , 1992, Journal of morphology.
[6] V. Hamburger,et al. Observations and experiments on spontaneous rhythmical behavior in the chick embryo. , 1963, Developmental biology.
[7] P. Stein,et al. Coordinated motor output in the hindlimb of the 7-day chick embryo. , 1975, Proceedings of the National Academy of Sciences of the United States of America.
[8] A. Bekoff. Ontogeny of leg motor output in the chick embryo: A neural analysis , 1976, Brain Research.
[9] C. Shatz,et al. Developmental mechanisms that generate precise patterns of neuronal connectivity , 1993, Cell.
[10] J. Elliott,et al. The role of inactivation in the effects of n‐alkanols on the sodium current of cultured rat sensory neurones. , 1989, The Journal of physiology.
[11] D. Berg,et al. Neuronal acetylcholine receptors that bind alpha-bungarotoxin mediate neurite retraction in a calcium-dependent manner , 1994, The Journal of neuroscience : the official journal of the Society for Neuroscience.
[12] J. Sanes,et al. Developmentally Regulated Spontaneous Activity in the Embryonic Chick Retina , 1998, The Journal of Neuroscience.
[13] L. Landmesser,et al. Regulation and activity-dependence of N-cadherin, NCAM isoforms, and polysialic acid on chick myotubes during development , 1993, The Journal of cell biology.
[14] R. Lester,et al. Influence of Subunit Composition on Desensitization of Neuronal Acetylcholine Receptors at Low Concentrations of Nicotine , 1997, The Journal of Neuroscience.
[15] K. Walton,et al. Postnatal changes in motoneurone electrotonic coupling studied in the in vitro rat lumbar spinal cord. , 1991, The Journal of physiology.
[16] J. Patrick,et al. Pharmacology of neuronal nicotinic acetylcholine receptor subtypes. , 1997, Advances in pharmacology.
[17] R. Oppenheim,et al. Synaptogenesis in the chick embryo spinal cord. , 1972, Nature: New biology.
[18] R. Wong,et al. Neuronal coupling in the developing mammalian retina , 1994, The Journal of neuroscience : the official journal of the Society for Neuroscience.
[19] W. F. Hughes,et al. On the synaptogenic sequence in the chick retina , 1974, The Anatomical record.
[20] Anna A Penn,et al. Thalamic Relay of Spontaneous Retinal Activity Prior to Vision , 1996, Neuron.
[21] L. Landmesser,et al. Polysialic acid regulates growth cone behavior during sorting of motor axons in the plexus region , 1994, Neuron.
[22] Michael J. O'Donovan,et al. Developmental expression of glycine immunoreactivity and its colocalization with gaba in the embryonic chick lumbosacral spinal cord , 1995, The Journal of comparative neurology.
[23] M. Nolan,et al. Electrotonic coupling between rat sympathetic preganglionic neurones in vitro. , 1996, The Journal of physiology.
[24] R. Traub,et al. Electrical coupling underlies high-frequency oscillations in the hippocampus in vitro , 1998, Nature.
[25] D. Hubel,et al. The period of susceptibility to the physiological effects of unilateral eye closure in kittens , 1970, The Journal of physiology.
[26] T. Jessell,et al. Motor Neuron–Derived Retinoid Signaling Specifies the Subtype Identity of Spinal Motor Neurons , 1998, Cell.
[27] L. Role,et al. Functional contribution of the α7 subunit to multiple subtypes of nicotinic receptors in embryonic chick sympathetic neurones , 1998, The Journal of physiology.
[28] M. Szente,et al. Activation patterns of embryonic chick hind‐limb muscles following blockade of activity and motoneurone cell death. , 1986, The Journal of physiology.
[29] R. O'brien,et al. Observations on the elimination of polyneuronal innervation in developing mammalian skeletal muscle. , 1978, The Journal of physiology.
[30] R. Provine,et al. Neural correlates of embryonic motility in the chick. , 1972, Brain research.
[31] S. Pfaff,et al. LIM Homeodomain Factors Lhx3 and Lhx4 Assign Subtype Identities for Motor Neurons , 1998, Cell.
[32] K. Clark,et al. The maternal and fetal physiologic effects of nicotine. , 1996, Seminars in perinatology.
[33] L. Role,et al. Physiological diversity of nicotinic acetylcholine receptors expressed by vertebrate neurons. , 1995, Annual review of physiology.
[34] N. Spitzer,et al. Regulation of intracellular Cl- levels by Na(+)-dependent Cl- cotransport distinguishes depolarizing from hyperpolarizing GABAA receptor-mediated responses in spinal neurons , 1996, The Journal of neuroscience : the official journal of the Society for Neuroscience.
[35] L. McMahon,et al. Nicotinic receptor activation facilitates gabaergic neurotransmission in the avian lateral spiriform nucleus , 1994, Neuroscience.
[36] Motor patterns for two distinct rhythmic behaviors evoked by excitatory amino acid agonists in the Xenopus embryo spinal cord. , 1996, Journal of neurophysiology.
[37] M. Rathouz,et al. Acetylcholine Differentially Affects Intracellular Calcium via Nicotinic and Muscarinic Receptors on the Same Population of Neurons (*) , 1995, The Journal of Biological Chemistry.
[38] C. Shatz,et al. Blockade of action potential activity alters initial arborization of thalamic axons within cortical layer 4. , 1995, Proceedings of the National Academy of Sciences of the United States of America.
[39] J. Changeux,et al. Role of Ca2+ Ions in Nicotinic Facilitation of GABA Release in Mouse Thalamus , 1997, The Journal of Neuroscience.
[40] N. Spitzer,et al. Calcium dependence of differentiation of GABA immunoreactivity in spinal neurons , 1993, The Journal of comparative neurology.
[41] L. Role,et al. Nicotine enhancement of fast excitatory synaptic transmission in CNS by presynaptic receptors. , 1995, Science.
[42] L. Landmesser,et al. A reevaluation of the role of innervation in primary and secondary myogenesis in developing chick muscle. , 1991, Developmental biology.
[43] J. Horton. Disruption of orientation tuning in visual cortex by artificially correlated neuronal activity. , 1997, Survey of ophthalmology.
[44] L. Role,et al. Nicotinic Receptors in the Development and Modulation of CNS Synapses , 1996, Neuron.
[45] R. Perrins,et al. Cholinergic contribution to excitation in a spinal locomotor central pattern generator in Xenopus embryos. , 1995, Journal of neurophysiology.
[46] Y. Ben-Ari,et al. GABA: an excitatory transmitter in early postnatal life , 1991, Trends in Neurosciences.
[47] A. Harris. Embryonic growth and innervation of rat skeletal muscles. II. Neural regulation of muscle cholinesterase. , 1981, Philosophical transactions of the Royal Society of London. Series B, Biological sciences.
[48] T. Jessell,et al. Topographic organization of embryonic motor neurons defined by expression of LIM homeobox genes , 1994, Cell.
[49] Michael J. O'Donovan,et al. Motor activity in the isolated spinal cord of the chick embryo: synaptic drive and firing pattern of single motoneurons , 1989, The Journal of neuroscience : the official journal of the Society for Neuroscience.
[50] Michael J. O'Donovan,et al. The effects of excitatory amino acids and their antagonists on the generation of motor activity in the isolated chick spinal cord. , 1987, Brain research.
[51] David J. Anderson,et al. Functionally Related Motor Neuron Pool and Muscle Sensory Afferent Subtypes Defined by Coordinate ETS Gene Expression , 1998, Cell.
[52] J. E. Vaughn,et al. Embryonic development of four different subsets of cholinergic neurons in rat cervical spinal cord , 1990, The Journal of comparative neurology.
[53] L. C. Katz,et al. Coordination of Neuronal Activity in Developing Visual Cortex by Gap Junction-Mediated Biochemical Communication , 1998, The Journal of Neuroscience.
[54] L. Landmesser,et al. The development of motor projection patterns in the chick hind limb. , 1978, The Journal of physiology.
[55] J. Jansen,et al. The innervation of skeletal muscles in chickens curarized during early development , 1983, Journal of neurocytology.
[56] P. M. Lundquist,et al. Organic Glasses: A New Class of Photorefractive Materials , 1996, Science.
[57] L. Maffei,et al. Spontaneous impulse activity of rat retinal ganglion cells in prenatal life. , 1988, Science.
[58] A. Roberts,et al. Cholinergic and electrical motoneuron-to-motoneuron synapses contribute to on-cycle excitation during swimming in Xenopus embryos. , 1995, Journal of neurophysiology.
[59] M. Stryker,et al. The Role of Activity in the Development of Long-Range Horizontal Connections in Area 17 of the Ferret , 1996, The Journal of Neuroscience.
[60] Jian-Zhong Guo,et al. Glutamate and GABA Release Are Enhanced by Different Subtypes of Presynaptic Nicotinic Receptors in the Lateral Geniculate Nucleus , 1998, The Journal of Neuroscience.
[61] R. Oppenheim,et al. Motility in the chick embryo in the absence of sensory input , 1966 .
[62] R. Douglas Fields,et al. Action Potential-Dependent Regulation of Gene Expression: Temporal Specificity in Ca2+, cAMP-Responsive Element Binding Proteins, and Mitogen-Activated Protein Kinase Signaling , 1997, The Journal of Neuroscience.
[63] L. C. Katz,et al. Fast Synaptic Signaling by Nicotinic Acetylcholine and Serotonin 5-HT3 Receptors in Developing Visual Cortex , 1997, The Journal of Neuroscience.
[64] A. Kriegstein,et al. Excitatory GABA Responses in Embryonic and Neonatal Cortical Slices Demonstrated by Gramicidin Perforated-Patch Recordings and Calcium Imaging , 1996, The Journal of Neuroscience.
[65] F. Werblin,et al. Requirement for Cholinergic Synaptic Transmission in the Propagation of Spontaneous Retinal Waves , 1996, Science.
[66] Michael J. O'Donovan,et al. Blockade and Recovery of Spontaneous Rhythmic Activity after Application of Neurotransmitter Antagonists to Spinal Networks of the Chick Embryo , 1998, The Journal of Neuroscience.
[67] Michael J. O'Donovan,et al. Regionalization and intersegmental coordination of rhythm-generating networks in the spinal cord of the chick embryo , 1993, The Journal of neuroscience : the official journal of the Society for Neuroscience.
[68] Michael J. O'Donovan,et al. Pharmacological characterization of the rhythmic synaptic drive onto lumbosacral motoneurons in the chick embryo spinal cord , 1995, The Journal of neuroscience : the official journal of the Society for Neuroscience.
[69] LM Dahm,et al. The regulation of synaptogenesis during normal development and following activity blockade , 1991, The Journal of neuroscience : the official journal of the Society for Neuroscience.
[70] D. Baylor,et al. Synchronous bursts of action potentials in ganglion cells of the developing mammalian retina. , 1991, Science.
[71] C. Shatz,et al. Competition in retinogeniculate patterning driven by spontaneous activity. , 1998, Science.
[72] V. Hamburger,et al. An autoradiographic study of the formation of the lateral motor column in the chick embryo , 1977, Brain Research.
[73] C. Shatz,et al. Synaptic Activity and the Construction of Cortical Circuits , 1996, Science.
[74] I. McLennan. Differentiation of muscle fiber types in the chicken hindlimb. , 1983, Developmental biology.
[75] Michael J. O'Donovan,et al. Activation patterns of embryonic chick hind limb muscles recorded in ovo and in an isolated spinal cord preparation. , 1984, The Journal of physiology.
[76] P. Mobbs,et al. Spontaneous Ca2+ transients and their transmission in the developing chick retina , 1998, Current Biology.
[77] G. Vrbóva,et al. Neuromuscular contacts in the developing rat soleus depend on muscle activity. , 1991, Brain research. Developmental brain research.