The DOI matches its Crossref record; 35 of the 35 references it cites were found in a registry or an index.
Co-release of acetylcholine and gamma-aminobutyric acid by a retinal neuron
Open accessAbstract
Rabbit retinas were vitally stained with 4',6-diamidino-2-phenylindole (DAPI), a fluorescent compound that selectively accumulates within the cholinergic amacrine cells. The retinas were then incubated in vitro in the presence of radioactive gamma-aminobutyric acid (GABA) and autoradiographed. The cells that accumulated DAPI were found to accumulate GABA, confirming immunohistochemical evidence that the cholinergic amacrine cells contain GABA. Incubation of retinas in the presence of elevated concentrations of K+ caused them to release acetylcholine and GABA, and autoradiography showed depletion of radioactive GABA from the cholinergic amacrine cells. This indicates that the cholinergic amacrine cells can secrete acetylcholine and GABA. Retinas were double-labeled with [14C]GABA and [3H]acetylcholine, allowing simultaneous measurement of their release. The release of [14C]GABA was found to be independent of extracellular Ca2+. Radioactive GABA synthesized endogenously from [14C]glutamate behaved the same way as radioactive GABA accumulated from the medium. In the same experiments the simultaneously measured release of [3H]acetylcholine was strongly Ca2+-dependent, indicating that the releases of acetylcholine and GABA are controlled by different mechanisms. Synaptic vesicles immunologically isolated from double-labeled retinas contained much [3H]acetylcholine and little or no [14C]GABA. These results suggest that the cholinergic amacrine cells release acetylcholine primarily by vesicle exocytosis and release GABA primarily by means of a carrier.
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Cites
Role of Transmitter Uptake Mechanisms in Synaptic Neurotransmission
Iversen, L. L. (1971) · British Journal of Pharmacology · doi:10.1111/j.1476-5381.1971.tb07066.x · Cited by 776
Buckley, K. M., & Kelly, R. B. (1985) · The Journal of Cell Biology · doi:10.1083/jcb.100.4.1284 · Cited by 713
Jung, M. J., Lippert, B. J., Metcalf, B. W., Böhlen, P., & Schechter, P. J. (1977) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.1977.tb10721.x · Cited by 481
Eckenstein, F. P., & Thoenen, H. (1982) · The EMBO Journal · doi:10.1002/j.1460-2075.1982.tb01175.x · Cited by 442
Kosaka, T., Tauchi, M., & Dahl, J. L. (1988) · Experimental Brain Research · doi:10.1007/bf00247609 · Cited by 417
The shape and arrangement of the cholinergic neurons in the rabbit retina
Tauchi, M., & Masland, R. H. (1984) · Proceedings of the Royal Society B Biological Sciences · doi:10.1098/rspb.1984.0085 · Cited by 385
Self-citationDepolarization Without Calcium Can Release γ-Aminobutyric Acid from a Retinal Neuron
Schwartz, E. A. (1987) · Science · doi:10.1126/science.2443977 · Cited by 345
Autoradiographic identification of acetylcholine in the rabbit retina.
Masland, R. H., & Mills, J. W. (1979) · The Journal of Cell Biology · doi:10.1083/jcb.83.1.159 · Cited by 286
Self-citationCholinergic amacrine cells in the rat retina
Voigt, T. (1986) · Journal of Comparative Neurology · doi:10.1002/cne.902480103 · Cited by 284
Pharmacological analysis of directionally sensitive rabbit retinal ganglion cells
Ariel, M., & Daw, N. W. (1982) · The Journal of Physiology · doi:10.1113/jphysiol.1982.sp014105 · Cited by 282
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Kaufman, D. L., Houser, C. R., & Tobin, A. J. (1991) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.1991.tb08211.x · Cited by 789
Two isoforms of glutamate decarboxylase: why?
Soghomonian, J., & Martin, D. L. (1998) · Trends in Pharmacological Sciences · doi:10.1016/s0165-6147(98)01270-x · Cited by 643
Direction selectivity in the retina: symmetry and asymmetry in structure and function
Vaney, D. I., Sivyer, B., & Taylor, W. R. (2012) · Nature reviews. Neuroscience · doi:10.1038/nrn3165 · Cited by 330
Ion channel expression by white matter glia: The O-2A glial progenitor cell
Barres, B. A., Koroshetz, W. J., Swartz, K. J., Chun, L. L. Y., & Corey, D. P. (1990) · Neuron · doi:10.1016/0896-6273(90)90109-s · Cited by 306
Role of ACh-GABA cotransmission in detecting image motion and motion direction
Lee, S., Kim, K., & Zhou, Z. J. (2010) · Neuron · doi:10.1016/j.neuron.2010.11.031 · Cited by 241
Inhibitory synapses in the developing auditory system are glutamatergic
Gillespie, D. C., Kim, G., & Kandler, K. (2005) · Nature Neuroscience · doi:10.1038/nn1397 · Cited by 222
Dual-transmitter neurons: functional implications of co-release and co-transmission
Vaaga, C. E., Borisovska, M., & Westbrook, G. L. (2014) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2014.04.010 · Cited by 221
Inhibitory Interneurons in the Retina: Types, Circuitry, and Function
Diamond, J. S. (2017) · Annual Review of Vision Science · doi:10.1146/annurev-vision-102016-061345 · Cited by 211
Calcium-independent release of amino acid neurotransmitters: Fact or artifact?
Bernáth, S. (1992) · Progress in Neurobiology · doi:10.1016/0301-0082(92)90035-d · Cited by 175
Zheng, J., Lee, S., & Zhou, Z. (2004) · Neuron · doi:10.1016/j.neuron.2004.11.015 · Cited by 155
Basal forebrain cholinergic signalling: development, connectivity and roles in cognition
Ananth, M. R., Rajebhosale, P., Kim, R., Talmage, D. A., & Role, L. W. (2023) · Nature Reviews Neuroscience · doi:10.1038/s41583-023-00677-x · Cited by 148
Yang, G., & Masland, R. H. (1992) · Science · doi:10.1126/science.1470920 · Cited by 146
Self-citationBeaulieu, C., & Somogyi, P. (1991) · The Journal of Comparative Neurology · doi:10.1002/cne.903040412 · Cited by 125
Control of GABA release at single mossy fiber-CA3 connections in the developing hippocampus
Safiulina (2010) · Frontiers in Synaptic Neuroscience · doi:10.3389/neuro.19.001.2010 · Cited by 123
Synaptic circuitry of the retina and olfactory bulb
DeVries, S. H., & Baylor, D. A. (1993) · Cell · doi:10.1016/s0092-8674(05)80033-9 · Cited by 113
Haverkamp, S., & Wässle, H. (2004) · Journal of Comparative Neurology · doi:10.1002/cne.10962 · Cited by 110
New directions in retinal research
Taylor, W. R., & Vaney, D. I. (2003) · Trends in Neurosciences · doi:10.1016/s0166-2236(03)00167-x · Cited by 107
The role of starburst amacrine cells in visual signal processing
Taylor, W. R., & Smith, R. G. (2012) · Visual Neuroscience · doi:10.1017/s0952523811000393 · Cited by 102
Cotransmission of acetylcholine and GABA
Granger, A. J., Mulder, N., Saunders, A. B., & Sabatini, B. L. (2015) · Neuropharmacology · doi:10.1016/j.neuropharm.2015.07.031 · Cited by 101
Koulen, P., Malitschek, B., Kuhn, R. R., Wässle, H., & Brandstätter, J. H. (1996) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.1996.tb00739.x · Cited by 101
Differential expression of synapsins I and II among rat retinal synapses
Mandell, J., Czernik, A. J., Camilli, P. V. D., Greengard, P., & Townes‐Anderson, E. (1992) · Journal of Neuroscience · doi:10.1523/jneurosci.12-05-01736.1992 · Cited by 96
Multi-transmitter neurons in the mammalian central nervous system
Granger, A. J., Wallace, M. L., & Sabatini, B. L. (2017) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2017.04.007 · Cited by 95
Role of theBarhl2homeobox gene in the specification of glycinergic amacrine cells
Mo, Z., Li, S., Yang, X., & Xiang, M. (2004) · Development · doi:10.1242/dev.01071 · Cited by 94
GABAergic Signaling at Mossy Fiber Synapses in Neonatal Rat Hippocampus
Safiulina, V. F., Fattorini, G., Conti, F., & Cherubini, E. (2006) · Journal of Neuroscience · doi:10.1523/jneurosci.4493-05.2006 · Cited by 94
Direction selectivity in a model of the starburst amacrine cell
TUKKER, J. J., Taylor, W. R., & Smith, R. G. (2004) · Visual Neuroscience · doi:10.1017/s0952523804214109 · Cited by 87
Pei, Z., Chen, Q., Koren, D., Giammarinaro, B., Ledesma, H. A., & Wei, W. (2015) · Journal of Neuroscience · doi:10.1523/jneurosci.0933-15.2015 · Cited by 78
Park, S. J. H., Kim, I.-J., Looger, L. L., Demb, J. B., & Borghuis, B. G. (2014) · Journal of Neuroscience · doi:10.1523/jneurosci.5017-13.2014 · Cited by 83
Wang, M. M., Janz, R., Belizaire, R., Frishman, L. J., & Sherry, D. M. (2003) · The Journal of Comparative Neurology · doi:10.1002/cne.10636 · Cited by 82
Receptive Field Properties of Starburst Cholinergic Amacrine Cells in the Rabbit Retina
Taylor, W. R., & Wässle, H. (1995) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.1995.tb00652.x · Cited by 78
GABAA Receptors: Post-Synaptic Co-Localization and Cross-Talk with Other Receptors
Shrivastava, A. N., Triller, A., & Sieghart, W. (2011) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2011.00007 · Cited by 73
Chapter 4 Structural organization of GABAergic circuitry in ectotherm retinas
Marc, R. E. (1992) · Progress in brain research · doi:10.1016/s0079-6123(08)63609-2 · Cited by 70
Assembly and disassembly of a retinal cholinergic network
Ford, K., & Feller, M. B. (2011) · Visual Neuroscience · doi:10.1017/s0952523811000216 · Cited by 74
Stimulus-dependent recruitment of lateral inhibition underlies retinal direction selectivity
Chen, Q., Pei, Z., Koren, D., & Wei, W. (2016) · eLife · doi:10.7554/elife.21053 · Cited by 63
Acetylcholine release from the rabbit retina mediated by NMDA receptors
Linn, D. M., & Massey, S. C. (1991) · Journal of Neuroscience · doi:10.1523/jneurosci.11-01-00123.1991 · Cited by 68
Aoki, C. J., & Kabak, S. (1992) · Visual Neuroscience · doi:10.1017/s0952523800002832 · Cited by 68
Synaptic physiology of direction selectivity in the retina
Zhou, Z., & Lee, S. (2008) · The Journal of Physiology · doi:10.1113/jphysiol.2008.159020 · Cited by 67
Neuromodulation of Transduction and Signal Processing in the End Organs of Taste
Nagai, T., Kim, D. J., Delay, R. J., & Roper, S. D. (1996) · Chemical Senses · doi:10.1093/chemse/21.3.353 · Cited by 67
Dopaminergic and GABAergic retinal cell populations in mammals
Nguyen‐Legros, J., Versaux‐Botteri, C., & Savy, C. (1997) · Microscopy Research and Technique · doi:10.1002/(sici)1097-0029(19970101)36:1 · Cited by 65
Baldridge, W. H. (1996) · Journal of Neuroscience · doi:10.1523/jneurosci.16-16-05060.1996 · Cited by 65
Tetrodotoxin‐resistant voltage‐gated sodium channels Nav1.8 and Nav1.9 are expressed in the retina
O’Brien, B. J., Caldwell, J. H., Ehring, G. R., O’Brien, K. M. B., Luo, S., & Levinson, S. R. (2008) · The Journal of Comparative Neurology · doi:10.1002/cne.21701 · Cited by 64
Tkatch, T., Baranauskas, G., & Surmeier, D. J. (1998) · Neuroreport · doi:10.1097/00001756-199806220-00004 · Cited by 63
Neurotransmitter receptors of starburst amacrine cells in rabbit retinal slices
Zhou, Z., & Fain, G. (1995) · Journal of Neuroscience · doi:10.1523/jneurosci.15-07-05334.1995 · Cited by 61
Co-stratification of GABAA receptors with the directionally selective circuitry of the rat retina
Brandstätter, J. H., Greferath, U., Euler, T., & Wässle, H. (1995) · Visual Neuroscience · doi:10.1017/s0952523800008026 · Cited by 60
Synaptic and circuit functions of multitransmitter neurons in the mammalian brain
Wallace, M. L., & Sabatini, B. L. (2023) · Neuron · doi:10.1016/j.neuron.2023.06.003 · Cited by 59
Receptor targets of amacrine cells
Zhang, C., & McCall, M. A. (2012) · Visual Neuroscience · doi:10.1017/s0952523812000028 · Cited by 59
Synaptic input to the on–off directionally selective ganglion cell in the rabbit retina
Dacheux, R. F., Chimento, M. F., & Amthor, F. R. (2003) · The Journal of Comparative Neurology · doi:10.1002/cne.10521 · Cited by 57
Cross-compartmental Modulation of Dendritic Signals for Retinal Direction Selectivity
Koren, D., Grove, J. C. R., & Wei, W. (2017) · Neuron · doi:10.1016/j.neuron.2017.07.020 · Cited by 49
Hendrickson, A. E., Tillakaratne, N. J. K., Mehra, R. D., Esclapez, M., Erickson, A., Vician, L. J., & Tobin, A. J. (1994) · The Journal of Comparative Neurology · doi:10.1002/cne.903430407 · Cited by 52
The DAPI-3 amacrine cells of the rabbit retina
Wright, L. L., Macqueen, C. L., Elston, G. N., Young, H. M., Pow, D. V., & Vaney, D. I. (1997) · Visual Neuroscience · doi:10.1017/s0952523800012141 · Cited by 51
Dudás, B., Mihály, A., & Merchenthaler, I. (2000) · The Journal of comparative neurology · doi:10.1002/1096-9861(20001127)427:4 · Cited by 57
The development of GABA immunoreactivity in the retina of the zebrafish (brachydanio rerio)
Sandell, J. H., Martin, S. C., & Heinrich, G. (1994) · The Journal of Comparative Neurology · doi:10.1002/cne.903450409 · Cited by 50
Schimchowitsch, S., Vuillez, P., Tappaz, M., Klein, M. J., & Stoeckel, M. E. (1991) · Experimental Brain Research · doi:10.1007/bf00229836 · Cited by 50
Poznański, R. R. (1992) · Bulletin of Mathematical Biology · doi:10.1007/bf02460658 · Cited by 49
OFF‐cholinergic‐pathway‐selective localization of P2X2 purinoceptors in the mouse retina
Kaneda, M., Ishii, K., Morishima, Y., Akagi, T., Yamazaki, Y., Nakanishi, S., & Hashikawa, T. (2004) · The Journal of Comparative Neurology · doi:10.1002/cne.20208 · Cited by 49
Kisv�rday, Z. F., Cowey, A., Stoerig, P., & Somogyi, P. (1991) · Experimental Brain Research · doi:10.1007/bf00228951 · Cited by 49
N‐acetylaspartylglutamate immunoreactivity in neurons of the monkey's visual pathway
Tieman, S. B., Neale, J. H., & Tieman, D. G. (1991) · The Journal of Comparative Neurology · doi:10.1002/cne.903130105 · Cited by 46
Chapter 7 GABAergic circuits in the mammalian retina
Freed, M. A. (1992) · Progress in brain research · doi:10.1016/s0079-6123(08)63611-0 · Cited by 45
Agarwala, S., & Kalil, R. E. (1998) · The Journal of Comparative Neurology · doi:10.1002/(sici)1096-9861(19980309)392:2 · Cited by 59
Brombas, A., de Croft, S., Cooper, E. J., & Williams, S. R. (2017) · Nature Communications · doi:10.1038/ncomms15683 · Cited by 42
Glutamate in Life and Death of Retinal Amacrine Cells*
Duarte, C. B., Ferreira, I. L., Santos, P. F., Carvalho, A. L., Agostinho, P. M., & Carvalho, A. P. (1998) · General Pharmacology The Vascular System · doi:10.1016/s0306-3623(97)00360-1 · Cited by 42
Hofmann, H., & Möckel, V. (1991) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.1991.tb02010.x · Cited by 41
Transient nuclear localization of fyn kinase during development in zebrafish
Rongish, B. J., & Kinsey, W. H. (2000) · The Anatomical Record · doi:10.1002/1097-0185(20001001)260:2 · Cited by 19
Transmitter release: prepackaging and random mechanism or dynamic and deterministic process
Kriebel, M. E., Vautrin, J., & Holsapple, J. W. (1990) · Brain Research Reviews · doi:10.1016/0165-0173(90)90017-i · Cited by 40
Contemporary approaches to neural circuit manipulation and mapping: focus on reward and addiction
Saunders, B. T., Richard, J. M., & Janak, P. H. (2015) · Philosophical Transactions of the Royal Society B Biological Sciences · doi:10.1098/rstb.2014.0210 · Cited by 40
Spontaneous Oscillatory Activity of Starburst Amacrine Cells in the Mouse Retina
Petit-Jacques, J., Völgyi, B., Rudy, B., & Bloomfield, S. A. (2005) · Journal of Neurophysiology · doi:10.1152/jn.00279.2005 · Cited by 38
Duarte, C. B., Ferreira, I. L., Santos, P. F., Oliveira, C. R., & Carvalho, A. P. (1993) · Brain Research · doi:10.1016/0006-8993(93)91784-p · Cited by 37
Ugarte, M., & Osborne, N. N. (1998) · General Pharmacology The Vascular System · doi:10.1016/s0306-3623(97)00358-3 · Cited by 36
Retinal direction selectivity in the absence of asymmetric starburst amacrine cell responses
Hanson, L., Sethuramanujam, S., deRosenroll, G., Jain, V., & Awatramani, G. B. (2019) · eLife · doi:10.7554/elife.42392 · Cited by 34
Spiking and nonspiking models of starburst amacrine cells in the rabbit retina
Velte, T. J., & Miller, R. F. (1997) · Visual Neuroscience · doi:10.1017/s0952523800011780 · Cited by 35
do Nascimento, J. L. M., Ventura, A. L. M., & Paes‐de‐Carvalho, R. (1998) · Brain Research · doi:10.1016/s0006-8993(98)00417-x · Cited by 35
Tonon, M., Bosler, O., Stoeckel, M. E., Pelletier, G., Tappaz, M., & Vaudry, H. (1992) · The Journal of Comparative Neurology · doi:10.1002/cne.903190409 · Cited by 35
Sperk, G., Wieselthaler, A., Pirker, S., Tasan, R. O., Strasser, S. S., Drexel, M., Pifl, C., Marschalek, J., Ortler, M., Trinka, E., et al. (2011) · Hippocampus · doi:10.1002/hipo.20923 · Cited by 34
Antagonistic Center-Surround Mechanisms for Direction Selectivity in the Retina
Ankri, L., Tsur, E. E., Maimon, S. R., Kaushansky, N., & Rivlin‐Etzion, M. (2020) · Cell Reports · doi:10.1016/j.celrep.2020.107608 · Cited by 30
Maggesissi, R. S., Gardino, P. F., Guimarães‐Souza, E. M., Paes‐de‐Carvalho, R., da Silva, R. B., & Calaza, K. D. C. (2009) · Vision Research · doi:10.1016/j.visres.2009.08.004 · Cited by 33
Transporter mediated GABA release in the retina: Role of excitatory amino acids and dopamine
Calaza, K. D. C., Gardino, P. F., & Mello, F. G. D. (2006) · Neurochemistry International · doi:10.1016/j.neuint.2006.07.003 · Cited by 32
Connections of the basal forebrain of the weakly electric fish, Eigenmannia virescens
Wong, C. J. H. (1997) · The Journal of Comparative Neurology · doi:10.1002/(sici)1096-9861(19971208)389:1 · Cited by 56
Choline Acetyltransferase in the Rat Cochlear Nuclei: Immunolocalization with a Monoclonal Antibody
Vetter, D. E., Cozzari, C., Hartman, B. K., & Mugnaini, E. (1993) · Springer eBooks · doi:10.1007/978-1-4615-2932-3_22 · Cited by 32
All indoleamine‐accumulating cells in the rabbit retina contain GABA
Massey, S. C., Mills, S. L., & Marc, R. E. (1992) · The Journal of Comparative Neurology · doi:10.1002/cne.903220213 · Cited by 32
Two distinct types of ON directionally selective ganglion cells in the rabbit retina
Hoshi, H., Tian, L., Massey, S. C., & Mills, S. L. (2011) · The Journal of Comparative Neurology · doi:10.1002/cne.22678 · Cited by 30
GABA‐like immunoreactive cells containing nicotinic acetylcholine receptors in the chick retina
Hamassaki‐Britto, D. E., Brzozowska‐Prechtl, A., Karten, H. J., Lindstrom, J. M., & Keyser, K. T. (1991) · The Journal of Comparative Neurology · doi:10.1002/cne.903130213 · Cited by 31
Differential acetylcholine and GABA release from cultured chick retina cells
Santos, P. F., Carvalho, A. L., Carvalho, A. P., & Duarte, C. B. (1998) · European Journal of Neuroscience · doi:10.1046/j.1460-9568.1998.00281.x · Cited by 28
Lee, H. Y., & Brecha, N. C. (2010) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2010.07181.x · Cited by 27
AMPA receptors mediate acetylcholine release from starburst amacrine cells in the rabbit retina
Firth, S. I., Li, W., Massey, S. C., & MARSHAK, D. W. (2003) · The Journal of Comparative Neurology · doi:10.1002/cne.10880 · Cited by 27
Inhibitory input to the direction-selective ganglion cell is saturated at low contrast
Lipin, M. Y., Taylor, W. R., & Smith, R. G. (2015) · Journal of Neurophysiology · doi:10.1152/jn.00413.2015 · Cited by 24
Brandon, C. J., & Criswell, M. H. (1995) · Visual Neuroscience · doi:10.1017/s0952523800006714 · Cited by 25
Subsets of retinal neurons and glia express P2Y1 receptors
Ward, M. M., & Fletcher, E. L. (2009) · Neuroscience · doi:10.1016/j.neuroscience.2009.02.022 · Cited by 24
Calcium dependent release of acetylcholine and γ-aminobutyric acid from the rabbit retina
Neal, M. J., Cunningham, J. M., Hutson, P. H., & Semark, J. E. (1992) · Neurochemistry International · doi:10.1016/0197-0186(92)90124-a · Cited by 23
GABA inhibits ACh release from the rabbit retina: A direct effect or feedback to bipolar cells?
Linn, D. M., & Massey, S. C. (1992) · Visual Neuroscience · doi:10.1017/s0952523800009263 · Cited by 23
Zucker, C. L., Nilson, J. E., Ehinger, B., & Grzywacz, N. M. (2005) · The Journal of Comparative Neurology · doi:10.1002/cne.20766 · Cited by 21
KIAA0369, doublecortin-like kinase, is expressed during brain development
Burgess, H. A., Martı́nez, S., & Reiner, O. (1999) · Journal of Neuroscience Research · doi:10.1002/(sici)1097-4547(19991115)58:4 · Cited by 79
Santos, P. F., Caramelo, O. L., Carvalho, A. P., & Duarte, C. B. (2000) · Brain Research · doi:10.1016/s0006-8993(99)02155-1 · Cited by 20
Nicotinic acetylcholine receptor expression by directionally selective ganglion cells
Strang, C. E., Renna, J. M., Amthor, F. R., & Keyser, K. T. (2007) · Visual Neuroscience · doi:10.1017/s0952523807070435 · Cited by 20
Müller, B., Butz, E. S., Peichl, L., & Haverkamp, S. (2013) · Journal of Neuroscience · doi:10.1523/jneurosci.2072-12.2013 · Cited by 19
Cholinergic amacrine cells in the rabbit retina accumulate muscimol
Massey, S. C., Blankenship, K., & Mills, S. L. (1991) · Visual Neuroscience · doi:10.1017/s0952523800010506 · Cited by 19
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Reimúndez, A., Fernández‐Peña, C., Ordás, P., Hernández‐Ortego, P., Gallego, R., Morenilla‐Palao, C., Navarro, J., Martín‐Cora, F., Pardo‐Vázquez, J. L., Schwarz, L. A., et al. (2022) · Acta Physiologica · doi:10.1111/apha.13896 · Cited by 18
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Chen, Q., & Wei, W. (2018) · Journal of Neurophysiology · doi:10.1152/jn.00716.2017 · Cited by 16
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Saito, Y., Zhang, Y., & Yanagawa, Y. (2015) · European Journal of Neuroscience · doi:10.1111/ejn.12878 · Cited by 15
Metadata
- Authors
- O'Malley, D. M., & Masland, R. H.
- Affiliations
- Harvard University (US)
- Venue
- Proceedings of the National Academy of Sciences
- Publisher
- National Academy of Sciences
- Published
- 1989-05
- Volume
- 86
- Issue
- 9
- Pages
- 3414-3418
- ISSN
- 0027-8424 (ISSN-L)
- 1091-6490
- PMC
- PMC287143
- OpenAlex
- W2126180763
- Cited by
- 150
- References
- 35
- Citations by year
- 2026: 1 · 2025: 3 · 2024: 9 · 2023: 3 · 2022: 2 · 2021: 3 · 2020: 3 · 2019: 3 · 2018: 3 · 2017: 7 · 2016: 2 · 2015: 5 · 2014: 4 · 2013: 5 · 2012: 3
- FWCI
- 3.30
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- Proceedings of the National Academy of Sciences (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- Funders
- National Institutes of Health (5r01ey005747-10, 5r37ey001075-23)
- National Eye Institute (R37 EY01075, R01-EY05747)
- Topics
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cell Biology › Cellular transport and secretion
- Health Sciences › Medicine › Ophthalmology › Retinal Development and Disorders
- Keywords
- acetylcholine release, gamma-aminobutyric acid release, cholinergic amacrine cells, retinal neurons, CO release, calcium-dependent exocytosis, synaptic vesicles, potassium-evoked release, rabbit retina
- MeSH terms
- Acetylcholine, Animals, Autoradiography, Calcium, Carbon Radioisotopes, Choline, Fluorescent Dyes, gamma-Aminobutyric Acid, Glutamates, Indoles, Magnesium, Neurons, Potassium, Rabbits, Retina, Tritium, Glutamic Acid
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
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