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Referencias:

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• Rodriguez, M.J., Perez-Etchegoyen, C.B., Szczupak, L., Premotor nonspiking neurons regulate coupling among motoneurons that innervate overlapping muscle fiber population (2009) J Comp Physiol A, 195. , 1432-1351
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• Chatzigeorgiou, M., Schafer, W.R., Lateral facilitation between primary mechanosensory neurons controls nose touch perception in C. elegans (2011) Neuron, 70, pp. 299-309
• Rabinowitch, I., Chatzigeorgiou, M., Schafer, W.R., A gap junction circuit enhances processing of coincident mechanosensory inputs (2013) Curr Biol, 23, pp. 963-967
• Farrow, K., Borst, A., Haag, J., Sharing receptive fields with your neighbors: tuning the vertical system cells to wide field motion (2005) J Neurosci, 25, pp. 3985-3993
• Haag, J., Borst, A., Neural mechanism underlying complex receptive field properties of motion-sensitive interneurons (2004) Nat Neurosci, 7, pp. 628-634
• Elyada, Y.M., Haag, J., Borst, A., Different receptive fields in axons and dendrites underlie robust coding in motion-sensitive neurons (2009) Nat Neurosci, 12, pp. 327-332
• Cuntz, H., Haag, J., Forstner, F., Segev, I., Borst, A., Robust coding of flow-field parameters by axo-axonal gap junctions between fly visual interneurons (2007) Proc Natl Acad Sci U S A, 104, pp. 10229-10233
• DeVries, S.H., Qi, X., Smith, R., Makous, W., Sterling, P., Electrical coupling between mammalian cones (2002) Curr Biol, 12, pp. 1900-1907
• Bloomfield, S.A., Volgyi, B., The diverse functional roles and regulation of neuronal gap junctions in the retina (2009) Nat Rev Neurosci, 10, pp. 495-506
• Demb, J.B., Singer, J.H., Functional circuitry of the retina (2015) Ann Rev Vis Sci, 1, pp. 263-289
• Kuo, S.P., Schwartz, G.W., Rieke, F., Nonlinear spatiotemporal integration by electrical and chemical synapses in the retina (2016) Neuron, 90, pp. 320-332. , Retina bipolar cells are connected among themselves through electrical synapses. The authors established that coupling among neighboring bipolar cells enhances their output in response to low-contrast stimulation, generating a supralinear integration of spatiotemporally correlated visual inputs that could be of relevance in encoding motion
• Yaksi, E., Wilson, R.I., Electrical coupling between olfactory glomeruli (2010) Neuron, 67, pp. 1034-1047
• Huang, J., Zhang, W., Qiao, W., Hu, A., Wang, Z., Functional connectivity and selective odor responses of excitatory local interneurons in Drosophila antennal lobe (2010) Neuron, 67, pp. 1021-1033
• Wang, K., Gong, J., Wang, Q., Li, H., Cheng, Q., Liu, Y., Zeng, S., Wang, Z., Parallel pathways convey olfactory information with opposite polarities in Drosophila (2014) Proc Natl Acad Sci U S A, 111, pp. 3164-3169. , This report describes the interactions of GABAergic projection neurons within the antennal lobes in Drosophila using dual-color calcium imaging. These neurons constitute an inhibitory feed forward path in the olfactory system. They receive direct inputs from olfactory receptor neurons, span multiple glomeruli, contacting cholinergic projection neurons with mixed electrical and chemical synapses. These neurons provide additional horizontal processing among different glomeruli and influence animal behavior
• Christie, J.M., Westbrook, G.L., Lateral excitation within the olfactory bulb (2006) J Neurosci, 26, pp. 2269-2277
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• Mulloney, B., Smarandache-Wellmann, C., Neurobiology of the crustacean swimmeret system (2012) Prog Neurobiol, 96, pp. 242-267
• Poppele, R.B.G., Sophisticated spinal contributions to motor control (2003) TINS, 26, pp. 269-276
• Zhen, M., Samuel, A.D., C. elegans locomotion: small circuits, complex functions (2015) Curr Opin Neurobiol, 33, pp. 117-126
• Malyshev, A.Y., Norekian, T.P., Phase-locked coordination between two rhythmically active feeding structures in the mollusk Clione limacina. I. Motor neurons (2002) J Neurophysiol, 87, pp. 2996-3005
• Fan, R.J., Marin Burgin, A., French, K.A., Friesen, W.O., A dye mixture (Neurobiotin and Alexa 488) reveals extensive dye-coupling among neurons in leeches; physiology confirms the connections (2005) J Comp Physiol A, 191, pp. 1157-1171
• Rekling, J.C., Shao, X.M., Feldman, J.L., Electrical coupling and excitatory synaptic transmission between rhythmogenic respiratory neurons in the preBotzinger complex (2000) J Neurosci, 20, p. RC113
• Wenning, A., Norris, B.J., Doloc-Mihu, A., Calabrese, R.L., Variation in motor output and motor performance in a centrally generated motor pattern (2014) J Neurophysiol, 112, pp. 95-109
• Wright, T.M., Jr., Calabrese, R.L., Contribution of motoneuron intrinsic properties to fictive motor pattern generation (2011) J Neurophysiol, 106, pp. 538-553
• Friesen, W.O., Neuronal control of leech swimming movements (1989) Neuronal and Cellular Oscillators, Cellular Clock Series, 2, pp. 269-316. , J.W. Jacklet Marcel Dekker
• Maynard, D.M., Selverston, A.I., Organization of the stomatogastric ganglion of the spiny lobster (1975) J Comp Physiol, 100, pp. 161-182
• Song, J., Ampatzis, K., Bjornfors, E.R., El Manira, A., Motor neurons control locomotor circuit function retrogradely via gap junctions (2016) Nature, 529, pp. 399-402. , This report confirms in zebrafish that motoneurons can participate in motor control networks, as documented in several invertebrate systems. Motoneurons are linked to premotor neurons by electrical synapses and influence the generation of rhythmic activity
• Thompson, S., Watson, W.H., 3rd, Central pattern generator for swimming in Melibe (2005) J Exp Biol, 208, pp. 1347-1361
• Sakurai, A., Newcomb, J.M., Lillvis, J.L., Katz, P.S., Different roles for homologous interneurons in species exhibiting similar rhythmic behaviors (2011) Curr Biol, 21, pp. 1036-1043
• Kawano, T., Po, M.D., Gao, S., Leung, G., Ryu, W.S., Zhen, M., An imbalancing act: gap junctions reduce the backward motor circuit activity to bias C. elegans for forward locomotion (2011) Neuron, 72, pp. 572-586
• Szczupak, L., Recurrent inhibition in motor systems, a comparative analysis (2014) J Physiol Paris, 108, pp. 148-154. , This review summarizes a mechanism of recurrent inhibition uncovered in the leech nervous system and relates it to what has been described in vertebrates. The leech network is centered on a pair of nonspiking neurons that are linked to every excitatory motoneuron in the leech via chemical and electrical synapses. This network achieves two major effects: uncouples motoneurons linked by electrical synapses and controls the general level of motor activity throughout specific motor patterns
• Rodriguez, M.J., Alvarez, R.J., Szczupak, L., Effect of a nonspiking neuron on motor patterns of the leech (2012) J Neurophysiol, 107, pp. 1917-1924

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