Co-release of acetylcholine and gamma-aminobutyric acid by a retinal neuron

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 · see citing works

Identification of a transmembrane glycoprotein specific for secretory vesicles of neural and endocrine cells.

Buckley, K. M., & Kelly, R. B. (1985) · The Journal of Cell Biology · doi:10.1083/jcb.100.4.1284 · Cited by 713 · see citing works

γ‐VINYL GABA (4‐amino‐hex‐5‐enoic acid), A NEW SELECTIVE IRREVERSIBLE INHIBITOR OF GABA‐T: EFFECTS ON BRAIN GABA METABOLISM IN MICE1

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 · see citing works

Production of specific antisera and monoclonal antibodies to choline acetyltransferase: characterization and use for identification of cholinergic neurons.

Eckenstein, F. P., & Thoenen, H. (1982) · The EMBO Journal · doi:10.1002/j.1460-2075.1982.tb01175.x · Cited by 442 · see citing works

Cholinergic neurons containing GABA-like and/or glutamic acid decarboxylase-like immunoreactivities in various brain regions of the rat

Kosaka, T., Tauchi, M., & Dahl, J. L. (1988) · Experimental Brain Research · doi:10.1007/bf00247609 · Cited by 417 · see citing works

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 · see citing works

Depolarization Without Calcium Can Release γ-Aminobutyric Acid from a Retinal Neuron

Schwartz, E. A. (1987) · Science · doi:10.1126/science.2443977 · Cited by 345 · see citing works

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 · see citing works

Cholinergic amacrine cells in the rat retina

Voigt, T. (1986) · Journal of Comparative Neurology · doi:10.1002/cne.902480103 · Cited by 284 · see citing works

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 · see citing works

Responses to acetylcholine of ganglion cells in an isolated mammalian retina

Masland, R. H., & Ames, A. (1976) · Journal of Neurophysiology · doi:10.1152/jn.1976.39.6.1220 · Cited by 256 · see citing works

Calcium‐independent release of GABA from isolated horizontal cells of the toad retina.

Schwartz, E. A. (1982) · The Journal of Physiology · doi:10.1113/jphysiol.1982.sp014069 · Cited by 228 · see citing works

Cholinergic amacrine cells of the rabbit retina contain glutamate decarboxylase and gamma-aminobutyrate immunoreactivity

Brecha, N., Johnson, D., Peichl, L., & Wässle, H. (1988) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.85.16.6187 · Cited by 225 · see citing works

GABA-like immunoreactivity in cholinergic amacrine cells of the rabbit retina

Vaney, D. I., & Young, H. M. (1988) · Brain Research · doi:10.1016/0006-8993(88)91366-2 · Cited by 211 · see citing works

The functions of acetylcholine in the rabbit retina

Masland, R. H., Mills, J. W., & Cassidy, C. (1984) · Proceedings of the Royal Society of London. Series B. Biological Sciences · doi:10.1098/rspb.1984.0086 · Cited by 200 · see citing works

Screening for neurotransmitters: A rapid radiochemical procedure

Hildebrand, J. G., Barker, D. L. A., Herbert, E., & Kravitz, E. A. (1971) · Journal of Neurobiology · doi:10.1002/neu.480020305 · Cited by 197 · see citing works

‘Coronate’ amacrine cells in the rabbit retina have the ‘starburst’ dendritic morphology

Di, V. (1984) · Proceedings of the Royal Society B Biological Sciences · doi:10.1098/rspb.1984.0016 · Cited by 193 · see citing works

Acetylcholine-synthesizing amacrine cells: identification and selective staining by using radioautography and fluorescent markers

Masland, R. H., Mills, J. W., & Hayden, S. (1984) · Proceedings of the Royal Society B Biological Sciences · doi:10.1098/rspb.1984.0084 · Cited by 190 · see citing works

Endocrine secretory granules and neuronal synaptic vesicles have three integral membrane proteins in common.

Lowe, A. W., Madeddu, L., & Kelly, R. B. (1988) · The Journal of Cell Biology · doi:10.1083/jcb.106.1.51 · Cited by 185 · see citing works

Novel inhibitors of gamma-aminobutyric acid (GABA) uptake: anticonvulsant actions in rats and mice.

Yunger, L. M., Fowler, P. J., Zarevics, P., & SETLER, P. E. (1984) · Journal of Pharmacology and Experimental Therapeutics · doi:10.1016/s0022-3565(25)21468-9 · Cited by 181 · see citing works

Carrier-mediated release of GABA from retinal horizontal cells

Yazulla, S., & Kleinschmidt, J. (1983) · Brain Research · doi:10.1016/0006-8993(83)91201-5 · Cited by 176 · see citing works

Glial and neuronal uptake of GABA, glutamic acid, glutamine and glutathione in the rabbit retina

Ehinger, B. (1977) · Experimental Eye Research · doi:10.1016/0014-4835(77)90089-6 · Cited by 135 · see citing works

THE METABOLISM OF γ‐AMINOBUTYRIC ACID (GABA) IN THE LOBSTER NERVOUS SYSTEM–UPTAKE OF GABA IN NERVE‐MUSCLE PREPARATIONS1

Iversen, L. L., & Kravitz, E. A. (1968) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.1968.tb08960.x · Cited by 106 · see citing works

A tonic gamma-aminobutyric acid-mediated inhibition of cholinergic amacrine cells in rabbit retina

Massey, S., & Redburn, D. (1982) · Journal of Neuroscience · doi:10.1523/jneurosci.02-11-01633.1982 · Cited by 92 · see citing works

Autoradiographic identification of the cells accumulating3H γ-aminobutyric acid in mammalian retinae: A species comparison

Marshall, J. A., & Voaden, M. J. (1975) · Vision Research · doi:10.1016/0042-6989(75)90102-9 · Cited by 82 · see citing works

Reconstitution and purification of the sodium- and chloride-coupled gamma-aminobutyric acid transporter from rat brain.

Radian, R., & Kanner, B. I. (1985) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(17)39110-x · Cited by 77 · see citing works

Number and distribution of putative cholinergic neurons in the cat retina

Schmidt, M., Wässle, H., & Humphrey, M. F. (1985) · Neuroscience Letters · doi:10.1016/0304-3940(85)90137-5 · Cited by 77 · see citing works

Starburst amacrine cells: morphological constancy and systematic variation in the anisotropic field of rabbit retinal neurons

Famiglietti, E. V. (1985) · Journal of Neuroscience · doi:10.1523/jneurosci.05-02-00562.1985 · Cited by 76 · see citing works

Efflux and exchange of γ-aminobutyric acid and nipecotic acid catalysed by synaptic plasma membrane vesicles isolated from immature rat brain

Kanner, B. I., Bendahan, A., & Radian, R. (1983) · Biochimica et Biophysica Acta (BBA) - Biomembranes · doi:10.1016/0005-2736(83)90397-8 · Cited by 42 · see citing works

Dopaminergic regulation of GABA release from the intact goldfish retina

O'Brien, D. R., & Dowling, J. E. (1985) · Brain Research · doi:10.1016/0006-8993(85)91218-1 · Cited by 40 · see citing works

Retinal Gaba neuron labelling with [3H]isoguvacine in different species

Agardh, E., & Ehinger, B. (1983) · Experimental Eye Research · doi:10.1016/0014-4835(83)90007-6 · Cited by 30 · see citing works

PHOTIC RELEASE OF RADIOACTIVITY FROM RABBIT RETINA PRELOADED WITH [3H]GABA

Bauer, B. (1978) · Acta Ophthalmologica · doi:10.1111/j.1755-3768.1978.tb01353.x · Cited by 28 · see citing works

The resting release of acetylcholine by a retinal neuron

Masland, R. H., & Cassidy, C. (1987) · Proceedings of the Royal Society B Biological Sciences · doi:10.1098/rspb.1987.0071 · Cited by 18 · see citing works

Effects of the ?-aminobutyrate transaminase inhibitors gabaculine and ?-vinyl GABA on ?-aminobutyric acid release from slices of rat cerebral cortex

BEDWANI, J. R., & Mehta, A. (1987) · Neurochemical Research · doi:10.1007/bf00971363 · Cited by 5 · see citing works

The release of (3H)‐GABA from the rabbit retina

Agardh, E., & Bauer, B. (1984) · Acta Physiologica Scandinavica · doi:10.1111/j.1748-1716.1984.tb07485.x · Cited by 4 · see citing works

Two Forms of the γ‐Aminobutyric Acid Synthetic Enzyme Glutamate Decarboxylase Have Distinct Intraneuronal Distributions and Cofactor Interactions

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 · see citing works

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 · see citing works

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 · see citing works

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 301 · see citing works

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 · see citing works

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 · see citing works

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 · see citing works

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 196 · see citing works

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 · see citing works

A Developmental Switch in the Excitability and Function of the Starburst Network in the Mammalian Retina

Zheng, J., Lee, S., & Zhou, Z. (2004) · Neuron · doi:10.1016/j.neuron.2004.11.015 · Cited by 155 · see citing works

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 · see citing works

Direct Visualization of the Dendritic and Receptive Fields of Directionally Selective Retinal Ganglion Cells

Yang, G., & Masland, R. H. (1992) · Science · doi:10.1126/science.1470920 · Cited by 146 · see citing works

Enrichment of cholinergic synaptic terminals on GABAergic neurons and coexistence of immunoreactive GABA and choline acetyltransferase in the same synaptic terminals in the striate cortex of the cat

Beaulieu, C., & Somogyi, P. (1991) · The Journal of Comparative Neurology · doi:10.1002/cne.903040412 · Cited by 126 · see citing works

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 124 · see citing works

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 · see citing works

Characterization of an amacrine cell type of the mammalian retina immunoreactive for vesicular glutamate transporter 3

Haverkamp, S., & Wässle, H. (2004) · Journal of Comparative Neurology · doi:10.1002/cne.10962 · Cited by 110 · see citing works

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 · see citing works

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 · see citing works

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 98 · see citing works

Group II and Group III Metabotropic Glutamate Receptors in the Rat Retina: Distributions and Developmental Expression Patterns

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 · see citing works

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 · see citing works

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 · see citing works

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 · see citing works

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 93 · see citing works

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 · see citing works

Conditional Knock-Out of Vesicular GABA Transporter Gene from Starburst Amacrine Cells Reveals the Contributions of Multiple Synaptic Mechanisms Underlying Direction Selectivity in the Retina

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 · see citing works

Excitatory Synaptic Inputs to Mouse On-Off Direction-Selective Retinal Ganglion Cells Lack Direction Tuning

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 81 · see citing works

Differential distribution and developmental expression of synaptic vesicle protein 2 isoforms in the mouse retina

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 · see citing works

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 · see citing works

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 71 · see citing works

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 · see citing works

Assembly and disassembly of a retinal cholinergic network

Ford, K., & Feller, M. B. (2011) · Visual Neuroscience · doi:10.1017/s0952523811000216 · Cited by 71 · see citing works

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 · see citing works

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 · see citing works

Cholinergic terminals in the cat visual cortex: Ultrastructural basis for interaction with glutamate-immunoreactive neurons and other cells

Aoki, C. J., & Kabak, S. (1992) · Visual Neuroscience · doi:10.1017/s0952523800002832 · Cited by 68 · see citing works

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 · see citing works

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 · see citing works

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 · see citing works

Optical Recordings of the Effects of Cholinergic Ligands on Neurons in the Ganglion Cell Layer of Mammalian Retina

Baldridge, W. H. (1996) · Journal of Neuroscience · doi:10.1523/jneurosci.16-16-05060.1996 · Cited by 65 · see citing works

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 · see citing works

Basal forebrain neurons adjacent to the globus pallidus co-express GABAergic and cholinergic marker mRNAs

Tkatch, T., Baranauskas, G., & Surmeier, D. J. (1998) · Neuroreport · doi:10.1097/00001756-199806220-00004 · Cited by 63 · see citing works

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 · see citing works

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 · see citing works

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 · see citing works

Receptor targets of amacrine cells

Zhang, C., & McCall, M. A. (2012) · Visual Neuroscience · doi:10.1017/s0952523812000028 · Cited by 59 · see citing works

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 · see citing works

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 · see citing works

Differential localization of two glutamic acid decarboxylases (GAD65 and GAD67) in adult monkey visual cortex

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 · see citing works

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 · see citing works

Choline acetyltransferase-immunoreactive neurons in the developing rat retina

Kim, I., Lee, E.-J., Kim, M.-K., Park, D., & Chun, M. (2000) · The Journal of Comparative Neurology · doi:10.1002/1096-9861(20001127)427:4 · Cited by 50 · see citing works

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 · see citing works

Systematic presence of GABA-immunoreactivity in the tubero-infundibular and tubero-hypophyseal dopaminergic axonal systems: an ultrastructural immunogold study on several mammals

Schimchowitsch, S., Vuillez, P., Tappaz, M., Klein, M. J., & Stoeckel, M. E. (1991) · Experimental Brain Research · doi:10.1007/bf00229836 · Cited by 50 · see citing works

Modelling the electrotonic structure of starburst amacrine cells in the rabbit retina: A functional interpretation of dendritic morphology

Poznański, R. R. (1992) · Bulletin of Mathematical Biology · doi:10.1007/bf02460658 · Cited by 49 · see citing works

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 · see citing works

Direct and indirect retinal input into degenerated dorsal lateral geniculate nucleus after striate cortical removal in monkey: implications for residual vision

Kisv�rday, Z. F., Cowey, A., Stoerig, P., & Somogyi, P. (1991) · Experimental Brain Research · doi:10.1007/bf00228951 · Cited by 49 · see citing works

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 · see citing works

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 · see citing works

Long-term protection of axotomized neurons in the dorsal lateral geniculate nucleus in the rat following a single administration of basic fibroblast growth factor or ciliary neurotrophic factor

Agarwala, S., & Kalil, R. E. (1998) · The Journal of Comparative Neurology · doi:10.1002/(sici)1096-9861(19980309)392:2 · Cited by 16 · see citing works

Dendro-dendritic cholinergic excitation controls dendritic spike initiation in retinal ganglion cells

Brombas, A., de Croft, S., Cooper, E. J., & Williams, S. R. (2017) · Nature Communications · doi:10.1038/ncomms15683 · Cited by 41 · see citing works

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 · see citing works

Release of γ‐Amino[3H]butyric Acid from Cultured Amacrine‐Like Neurons Mediated by Different Excitatory Amino Acid Receptors

Hofmann, H., & Möckel, V. (1991) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.1991.tb02010.x · Cited by 41 · see citing works

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 · see citing works

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 · see citing works

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 38 · see citing works

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 · see citing works

Glutamate increases the [Ca2+]i but stimulates Ca2+-independent release of [3H]GABA in cultured chick retina cells

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 · see citing works

The Localization of Endogenous Zinc and the in vitro Effect of Exogenous Zinc on the GABA Immunoreactivity and Formation of Reactive Oxygen Species in the Retina*

Ugarte, M., & Osborne, N. N. (1998) · General Pharmacology The Vascular System · doi:10.1016/s0306-3623(97)00358-3 · Cited by 36 · see citing works

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 · see citing works

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 · see citing works

Veratridine- and glutamate-induced release of [3H]-GABA from cultured chick retina cells: possible involvement of a GAT-1-like subtype of GABA transporter

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 · see citing works

Co‐localization of tyrosine hydroxylase, GABA and neuropeptide Y within axon terminals innervating the intermediate lobe of the frog Rana ridibunda

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 · see citing works

Glutamate decarboxylase67 is expressed in hippocampal mossy fibers of temporal lobe epilepsy patients

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 · see citing works

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 · see citing works

Modulation of GABA release by nitric oxide in the chick retina: Different effects of nitric oxide depending on the cell population

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 · see citing works

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 · see citing works

Regional and cellular distribution of serotonin 5-hydroxytryptamine2a receptor mRNA in the nucleus accumbens, olfactory tubercle, and caudate putamen of the rat

Mijnster, M. J., Raimundo, A. G. V., Koskuba, K., Klop, H., Docter, G. J., Groenewegen, H. J., & Voorn, P. (1997) · The Journal of Comparative Neurology · doi:10.1002/(sici)1096-9861(19971208)389:1 · Cited by 59 · see citing works

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 · see citing works

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 · see citing works

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 · see citing works

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 · see citing works

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 · see citing works

Immunocytochemical evidence for SNARE protein‐dependent transmitter release from guinea pig horizontal cells

Lee, H. Y., & Brecha, N. C. (2010) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2010.07181.x · Cited by 27 · see citing works

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 · see citing works

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 · see citing works

Displaced starburst amacrine cells of the rabbit retina contain the 67-kDa isoform, but not the 65-kDa isoform, of glutamate decarboxylase

Brandon, C. J., & Criswell, M. H. (1995) · Visual Neuroscience · doi:10.1017/s0952523800006714 · Cited by 25 · see citing works

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 · see citing works

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 · see citing works

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 · see citing works

Compartmental localization of γ-aminobutyric acid type B receptors in the cholinergic circuitry of the rabbit retina

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 · see citing works

Enhanced sensitivity to N-methyl-D-aspartate receptor activation in transgenic and knockin mouse models of Huntington's disease

Levine, M. S., Klapstein, G. J., Koppel, A. B., Gruen, E., Cepeda, C., Vargas, M. E., Jokel, E. S., Carpenter, E. M., Zanjani, H., Hurst, R. S., et al. (1999) · Journal of Neuroscience Research · doi:10.1002/(sici)1097-4547(19991115)58:4 · Cited by 351 · see citing works

Adenosine A1 receptors inhibit Ca2+ channels coupled to the release of ACh, but not of GABA, in cultured retina cells

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 · see citing works

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 · see citing works

The Rod Pathway of the Microbat Retina Has Bistratified Rod Bipolar Cells and Tristratified AII Amacrine Cells

Müller, B., Butz, E. S., Peichl, L., & Haverkamp, S. (2013) · Journal of Neuroscience · doi:10.1523/jneurosci.2072-12.2013 · Cited by 19 · see citing works

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 · see citing works

Topical review: Potential mechanisms of atropine for myopia control

Horn, D., Salzano, A. D., Jenewein, E. C., Weise, K. K., Schaeffel, F., Mathis, U., & Khanal, S. (2025) · Optometry and Vision Science · doi:10.1097/opx.0000000000002249 · Cited by 17 · see citing works

Cholinergic excitation complements glutamate in coding visual information in retinal ganglion cells

Sethuramanujam, S., Awatramani, G. B., & Slaughter, M. M. (2018) · The Journal of Physiology · doi:10.1113/jp275073 · Cited by 17 · see citing works

The cold‐sensing ion channel TRPM8 regulates central and peripheral clockwork and the circadian oscillations of body temperature

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 16 · see citing works

Stimulus-dependent engagement of neural mechanisms for reliable motion detection in the mouse retina

Chen, Q., & Wei, W. (2018) · Journal of Neurophysiology · doi:10.1152/jn.00716.2017 · Cited by 15 · see citing works

Bipolar Cell Type-Specific Expression and Conductance of Alpha-7 Nicotinic Acetylcholine Receptors in the Mouse Retina

Hall, L. M., Hellmer, C. B., Koehler, C. C., & Ichinose, T. (2019) · Investigative Ophthalmology & Visual Science · doi:10.1167/iovs.18-25753 · Cited by 16 · see citing works

Electrophysiological and morphological properties of neurons in the prepositus hypoglossi nucleus that express both Ch AT and VGAT in a double‐transgenic rat model

Saito, Y., Zhang, Y., & Yanagawa, Y. (2015) · European Journal of Neuroscience · doi:10.1111/ejn.12878 · Cited by 15 · see citing works

Co-release of acetylcholine and GABA by the starburst amacrine cells

O'Malley, D., Sandell, J. H., & Masland, R. (1992) · Journal of Neuroscience · doi:10.1523/jneurosci.12-04-01394.1992 · Cited by 195 · see citing works

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 · see citing works

Enhanced sensitivity to N-methyl-D-aspartate receptor activation in transgenic and knockin mouse models of Huntington's disease

Levine, M. S., Klapstein, G. J., Koppel, A. B., Gruen, E., Cepeda, C., Vargas, M. E., Jokel, E. S., Carpenter, E. M., Zanjani, H., Hurst, R. S., et al. (1999) · Journal of Neuroscience Research · doi:10.1002/(sici)1097-4547(19991115)58:4 · Cited by 351 · see citing works

A tonic gamma-aminobutyric acid-mediated inhibition of cholinergic amacrine cells in rabbit retina

Massey, S., & Redburn, D. (1982) · Journal of Neuroscience · doi:10.1523/jneurosci.02-11-01633.1982 · Cited by 92 · see citing works

GABA-like immunoreactivity in cholinergic amacrine cells of the rabbit retina

Vaney, D. I., & Young, H. M. (1988) · Brain Research · doi:10.1016/0006-8993(88)91366-2 · Cited by 211 · see citing works