The DOI matches its Crossref record; 42 of the 42 references it cites were found in a registry or an index.
Vesicular Neurotransmitter Transporter Expression in Developing Postnatal Rodent Retina: GABA and Glycine Precede Glutamate
Open accessAbstract
Vesicular transporters regulate the amount and type of neurotransmitter sequestered into synaptic vesicles and, hence, the kind of signal transmitted to postsynaptic neurons. Glutamate is the prominent excitatory neurotransmitter in retina; GABA and glycine are the main inhibitory neurotransmitters. Little is known about the ontogeny of vesicular neurotransmission in retina. We investigated expression of glutamatergic [vesicular glutamate transporter 1 (VGLUT1)] and GABA/glycinergic [vesicular GABA/glycine transporter (VGAT)] vesicular transporters in postnatal retina. VGLUT1 labels glutamatergic synapses. VGLUT1 and synaptic vesicle 2 colocalized to photoreceptor terminals. VGLUT1 colocalized with PKC to rod bipolar terminals and to ON bipolar terminals in metabotropic glutamate receptor 6+/- mice. Developmentally, VGAT expression precedes VGLUT1. In rat and mouse retina, VGAT occurred in the inner retina by postnatal day 1 (P1). In rat retina, VGLUT1 was in the outer retina by P5-P7 and the inner retina by P7. In the mouse retina, VGLUT1 expression was in the outer retina by P3 and the inner retina by P5. Both rat and mouse retina had an adult pattern of VGLUT1 expression by P14. VGLUT1 expression precedes ribbon synapses, which are first observed in the inner retina at P11 (Fisher, 1979) in mouse and P13 (Horsburgh and Sefton, 1987) in rat. The ribbon synapse marker RIBEYE was not detected in inner retina of P5 or P7 rat. Spontaneous EPSCs in mouse ganglion cells were recorded as early as P7. Together, these findings indicate that vesicular GABA and glycine transmission precedes vesicular glutamate transmission in developing rodent retina. Furthermore, vesicular glutamate transmission likely occurs before ribbon synapse formation in the inner retina.
Overview
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
The cited source says what the claim attributes to it.
In the citing paper
“We examined changes in endogenous vesicular glutamate transporter 1 (VGLUT-1), a presynaptic protein expressed at bipolar ribbon synapses [37], and postsynaptic density protein 95 (PSD95) in the inner plexiform layer, where RGC dendrites are located.”
From AMPK hyperactivation promotes dendrite retraction, synaptic loss, and neuronal dysfunction in glaucoma (2021) · cites this paper as [37]
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Citations
Cites
The Expression of Vesicular Glutamate Transporters Defines Two Classes of Excitatory Synapse
Fremeau, R. T., Troyer, M. D., Pahner, I., Nygaard, G. O., Tran, C. H., Reimer, R. J., Bellocchio, E. E., Fortin, D. L., Storm‐Mathisen, J., & Edwards, R. H. (2001) · Neuron · doi:10.1016/s0896-6273(01)00344-0 · Cited by 1,266
Self-citationIdentification and characterization of the vesicular GABA transporter
McIntire, S. L., Reimer, R. J., Schuske, K., Edwards, R. H., & Jørgensen, E. M. (1997) · Nature · doi:10.1038/39908 · Cited by 886
Self-citationTakamori, S., Rhee, J. S., Rosenmund, C., & Jahn, R. (2000) · Nature · doi:10.1038/35025070 · Cited by 862
Uptake of Glutamate into Synaptic Vesicles by an Inorganic Phosphate Transporter
Bellocchio, E. E., Reimer, R. J., Fremeau, R. T., & Edwards, R. H. (2000) · Science · doi:10.1126/science.289.5481.957 · Cited by 795
Self-citationBuckley, K. M., & Kelly, R. B. (1985) · The Journal of Cell Biology · doi:10.1083/jcb.100.4.1284 · Cited by 713
Chaudhry, F. A., Reimer, R. J., Bellocchio, E. E., Danbolt, N. C., Osen, K. K., Edwards, R. H., & Storm‐Mathisen, J. (1998) · Journal of Neuroscience · doi:10.1523/jneurosci.18-23-09733.1998 · Cited by 640
Self-citationRIBEYE, a Component of Synaptic Ribbons
Schmitz, F., Königstorfer, A., & Südhof, T. C. (2000) · Neuron · doi:10.1016/s0896-6273(00)00159-8 · Cited by 581
Dynamics of synaptic vesicle fusion and membrane retrieval in synaptic terminals
von Gersdorff, H., & Mathews, G. (1994) · Nature · doi:10.1038/367735a0 · Cited by 457
Rod bipolar cells in the mammalian retina show protein kinase C‐like immunoreactivity
Greferath, U., Grünert, U., & Wässle, H. (1990) · The Journal of Comparative Neurology · doi:10.1002/cne.903010308 · Cited by 420
Lee, R., Sawin, E. R., Chalfie, M., Horvitz, H. R., & Avery, L. (1999) · Journal of Neuroscience · doi:10.1523/jneurosci.19-01-00159.1999 · Cited by 351
Cited by
Sorted by citations
Functional architecture of the retina: Development and disease
Hoon, M., Okawa, H., Santina, L. D., & Wong, R. (2014) · Progress in Retinal and Eye Research · doi:10.1016/j.preteyeres.2014.06.003 · Cited by 628
Sensorineural Deafness and Seizures in Mice Lacking Vesicular Glutamate Transporter 3
Seal, R. P., Akil, O., Yi, E., Weber, C. M., Grant, L. M., Yoo, J. W., Clause, A. R., Kandler, K., Noebels, J. L., Glowatzki, E., et al. (2008) · Neuron · doi:10.1016/j.neuron.2007.11.032 · Cited by 414
Self-citationTypes of bipolar cells in the mouse retina
Ghosh, K. K., Bujan, S., Haverkamp, S., Feigenspan, A., & Wässle, H. (2003) · The Journal of Comparative Neurology · doi:10.1002/cne.10985 · Cited by 378
Visual Stimulation Is Required for Refinement of ON and OFF Pathways in Postnatal Retina
Tian, N., & Copenhagen, D. R. (2003) · Neuron · doi:10.1016/s0896-6273(03)00389-1 · Cited by 304
Self-citationLateral interactions in the outer retina
Thoreson, W. B., & Mangel, S. C. (2012) · Progress in Retinal and Eye Research · doi:10.1016/j.preteyeres.2012.04.003 · Cited by 253
Wang, X., Zhao, L., Zhang, J., Fariss, R. N., Ma, W., Kretschmer, F., Wang, M., Qian, H., Badea, T. C., Diamond, J. S., et al. (2016) · Journal of Neuroscience · doi:10.1523/jneurosci.3575-15.2016 · Cited by 249
Synaptic transmission at retinal ribbon synapses
Heidelberger, R., Thoreson, W. B., & Witkovsky, P. (2005) · Progress in Retinal and Eye Research · doi:10.1016/j.preteyeres.2005.04.002 · Cited by 239
Ellis, E. M., Gauvain, G., Sivyer, B., & Murphy, G. J. (2016) · Journal of Neurophysiology · doi:10.1152/jn.00227.2016 · Cited by 216
Functional and structural modifications during retinal degeneration in the rd10 mouse
Barhoum, R., Martı́nez, G., Corrochano, S., Germaín, F., Fernández‐Sánchez, L., de la Rosa, E. J., de la Villa, P., & Cuenca, N. (2008) · Neuroscience · doi:10.1016/j.neuroscience.2008.06.042 · Cited by 193
Structurally and functionally unique complexins at retinal ribbon synapses
Reim, K., Wegmeyer, H., Brandstätter, J. H., Xue, M., Rosenmund, C., Dresbach, T., Hofmann, K., & Brose, N. (2005) · The Journal of Cell Biology · doi:10.1083/jcb.200502115 · Cited by 185
Sherry, D. M., Wang, M. M., Bates, J., & Frishman, L. J. (2003) · The Journal of Comparative Neurology · doi:10.1002/cne.10838 · Cited by 181
Neurotransmission selectively regulates synapse formation in parallel circuits in vivo
Kerschensteiner, D., Morgan, J., Parker, E. D., Lewis, R. M., & Wong, R. (2009) · Nature · doi:10.1038/nature08236 · Cited by 175
Dumitrescu, O. N., Pucci, F. G., Wong, K. Y., & Berson, D. M. (2009) · The Journal of Comparative Neurology · doi:10.1002/cne.22158 · Cited by 176
Ben‐Ari, Y., Woodin, M. A., Sernagor, E., Cancedda, L., Vinay, L., Rivera, C., Legendre, P., Luhmann, H. J., Bordey, A., Wenner, P., et al. (2012) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2012.00035 · Cited by 159
Stage‐dependent dynamics and modulation of spontaneous waves in the developing rabbit retina
Syed, M., Lee, S., Zheng, J., & Zhou, Z. (2004) · The Journal of Physiology · doi:10.1113/jphysiol.2004.066597 · Cited by 139
Agostinone, J., Alarcon-Martinez, L., Gamlin, C., Yu, W.-Q., Wong, R. O. L., & Di Polo, A. (2018) · Brain · doi:10.1093/brain/awy142 · Cited by 124
Diversity of glycine receptors in the mouse retina: Localization of the α4 subunit
Heinze, L., Harvey, R. J., Haverkamp, S., & Wässle, H. (2006) · The Journal of Comparative Neurology · doi:10.1002/cne.21201 · Cited by 119
Control of cell proliferation by neurotransmitters in the developing vertebrate retina
Martins, R. A. P., & Pearson, R. A. (2007) · Brain Research · doi:10.1016/j.brainres.2007.04.076 · Cited by 126
An opsin 5–dopamine pathway mediates light-dependent vascular development in the eye
Nguyen, M., Vemaraju, S., Nayak, G., Odaka, Y., Buhr, E. D., Alonzo, N., Tran, U., Batie, M. R., Upton, B. A., Darvas, M., et al. (2019) · Nature Cell Biology · doi:10.1038/s41556-019-0301-x · Cited by 115
Haverkamp, S., & Wässle, H. (2004) · Journal of Comparative Neurology · doi:10.1002/cne.10962 · Cited by 110
The Molecular Architecture of Ribbon Presynaptic Terminals
Zanazzi, G. J., & Matthews, G. (2009) · Molecular Neurobiology · doi:10.1007/s12035-009-8058-z · Cited by 105
Johnson, J., Sherry, D. M., Liu, X., Fremeau, R. T., Seal, R. P., Edwards, R. H., & Copenhagen, D. R. (2004) · The Journal of Comparative Neurology · doi:10.1002/cne.20250 · Cited by 101
Self-citationCell‐specific expression of plasma membrane calcium ATPase isoforms in retinal neurons
Križaj, D., DeMarco, S. J., Johnson, J., Strehler, E. E., & Copenhagen, D. R. (2002) · The Journal of Comparative Neurology · doi:10.1002/cne.10281 · Cited by 93
Self-citationExtracellular space preservation aids the connectomic analysis of neural circuits
Pallotto, M., Watkins, P. V., Fubara, B. N., Singer, J. H., & Briggman, K. L. (2015) · eLife · doi:10.7554/elife.08206 · Cited by 94
Dendritic mitochondria reach stable positions during circuit development
Faits, M. C., Zhang, C., Soto, F., & Kerschensteiner, D. (2016) · eLife · doi:10.7554/elife.11583 · Cited by 91
Neuroligin 2 Controls the Maturation of GABAergic Synapses and Information Processing in the Retina
Hoon, M., Bauer, G., Fritschy, J., Moser, T., Falkenburger, B. H., & Varoqueaux, F. (2009) · Journal of Neuroscience · doi:10.1523/jneurosci.0534-09.2009 · Cited by 93
Sherry, D. M., Mitchell, R., Standifer, K. M., & du Plessis, B. (2006) · BMC Neuroscience · doi:10.1186/1471-2202-7-54 · Cited by 86
Developmental patterning of glutamatergic synapses onto retinal ganglion cells
Morgan, J., Schubert, T., & Wong, R. (2008) · Neural Development · doi:10.1186/1749-8104-3-8 · Cited by 85
Purinergic signaling involved in Müller cell function in the mammalian retina
Wurm, A., Pannicke, T., Iandiev, I., Francke, M., Hollborn, M., Wiedemann, P., Reichenbach, A., Osborne, N. N., & Bringmann, A. (2011) · Progress in Retinal and Eye Research · doi:10.1016/j.preteyeres.2011.06.001 · Cited by 80
Bayley, P. R., & Morgans, C. W. (2006) · The Journal of Comparative Neurology · doi:10.1002/cne.21188 · Cited by 79
Calcium Channel-Dependent Molecular Maturation of Photoreceptor Synapses
Zabouri, N., & Haverkamp, S. (2013) · PLoS ONE · doi:10.1371/journal.pone.0063853 · Cited by 79
Diversity of glycine receptors in the mouse retina: Localization of the α2 subunit
Haverkamp, S., Müller, U., Zeilhofer, H. U., Harvey, R. J., & Wässle, H. (2004) · The Journal of Comparative Neurology · doi:10.1002/cne.20267 · Cited by 77
Soto, F., Watkins, K. L., Johnson, R. E., Schottler, F., & Kerschensteiner, D. (2013) · Journal of Neuroscience · doi:10.1523/jneurosci.1521-13.2013 · Cited by 76
Puthussery, T., Gayet‐Primo, J., & Taylor, W. R. (2009) · The Journal of Comparative Neurology · doi:10.1002/cne.22234 · Cited by 73
DNA methylation reader MECP2: cell type- and differentiation stage-specific protein distribution
Song, C., Feodorova, Y. N., Guy, J., Peichl, L., Jost, K. L., Kimurâ, H., Cardoso, M. C., Bird, A. P., Leonhardt, H., Joffe, B. I., et al. (2014) · Epigenetics & Chromatin · doi:10.1186/1756-8935-7-17 · Cited by 75
Assembly and disassembly of a retinal cholinergic network
Ford, K., & Feller, M. B. (2011) · Visual Neuroscience · doi:10.1017/s0952523811000216 · Cited by 74
Evidence for the involvement of purinergic P2X7receptors in outer retinal processing
Puthussery, T., Yee, P., Vingrys, A. J., & Fletcher, E. L. (2006) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2006.04895.x · Cited by 68
Contribution of voltage‐gated sodium channels to the b‐wave of the mammalian flash electroretinogram
Mojumder, D. K., Sherry, D. M., & Frishman, L. J. (2008) · The Journal of Physiology · doi:10.1113/jphysiol.2008.150755 · Cited by 68
Belforte, N., Agostinone, J., Alarcon-Martinez, L., Villafranca-Baughman, D., Dotigny, F., Cueva Vargas, J. L., & Di Polo, A. (2021) · Molecular Neurodegeneration · doi:10.1186/s13024-021-00466-z · Cited by 67
“We examined changes in endogenous vesicular glutamate transporter 1 (VGLUT-1), a presynaptic protein expressed at bipolar ribbon synapses [37], and postsynaptic density protein 95 (PSD95) in the inner plexiform layer, where RGC dendrites are located.”
BackgroundJohnson, J., Fremeau, R. T., Duncan, J. L., Renterı́a, R. C., Yang, H., Hua, Z., Liu, X., LaVail, M. M., Edwards, R. H., & Copenhagen, D. R. (2007) · Journal of Neuroscience · doi:10.1523/jneurosci.0815-07.2007 · Cited by 65
Self-citationDistribution of vesicular glutamate transporters in rat and human retina
Gong, J., Jellali, A., Mutterer, J., Sahel, J., Rendón, Á., & Picaud, S. A. (2006) · Brain Research · doi:10.1016/j.brainres.2006.01.111 · Cited by 64
Spontaneous Network Activity and Synaptic Development
Kerschensteiner, D. (2013) · The Neuroscientist · doi:10.1177/1073858413510044 · Cited by 67
Munc13-Independent Vesicle Priming at Mouse Photoreceptor Ribbon Synapses
Cooper, B. H., Hemmerlein, M., Ammermüller, J., Imig, C., Reim, K., Lipstein, N., Kalla, S., Kawabe, H., Brose, N., Brandstätter, J. H., et al. (2012) · Journal of Neuroscience · doi:10.1523/jneurosci.4240-11.2012 · Cited by 63
Koch, S. M., Cruz, C. G. D., Hnasko, T. S., Edwards, R. H., Huberman, A. D., & Ullian, E. M. (2011) · Neuron · doi:10.1016/j.neuron.2011.05.045 · Cited by 60
Self-citationHirano, A. A., Brandstätter, J. H., & Brecha, N. C. (2005) · The Journal of Comparative Neurology · doi:10.1002/cne.20577 · Cited by 57
Wang, C., Blankenship, A. G., Anishchenko, A., Elstrott, J., Fikhman, M., Nakanishi, S., & Feller, M. B. (2007) · Journal of Neuroscience · doi:10.1523/jneurosci.1293-07.2007 · Cited by 58
Downie, L. E., Vessey, K. A., Miller, A., Ward, M. M., Pianta, M. J., Vingrys, A. J., Wilkinson‐Berka, J. L., & Fletcher, E. L. (2009) · Neuroscience · doi:10.1016/j.neuroscience.2009.02.084 · Cited by 55
Plasmalemmal and vesicular γ‐aminobutyric acid transporter expression in the developing mouse retina
Guo, C., Stella, S., Hirano, A. A., & Brecha, N. C. (2008) · The Journal of Comparative Neurology · doi:10.1002/cne.21846 · Cited by 54
Expression of the vesicular glutamate transporter vGluT2 in a subset of cones of the mouse retina
Wässle, H., Regus‐Leidig, H., & Haverkamp, S. (2006) · The Journal of Comparative Neurology · doi:10.1002/cne.20942 · Cited by 54
Immunocytochemical localization of three vesicular glutamate transporters in the cat retina
Fyk‐Kolodziej, B. E., Dzhagaryan, A., Qin, P., & Pourcho, R. G. (2004) · The Journal of Comparative Neurology · doi:10.1002/cne.20199 · Cited by 54
Singh, R. K., Occelli, L. M., Binette, F., Petersen‐Jones, S. M., & Nasonkin, I. O. (2019) · Stem Cells and Development · doi:10.1089/scd.2019.0090 · Cited by 52
Fyk‐Kolodziej, B. E., & Pourcho, R. G. (2007) · The Journal of Comparative Neurology · doi:10.1002/cne.21287 · Cited by 51
Intersecting circuits generate precisely patterned retinal waves
Akrouh, A., & Kerschensteiner, D. (2013) · Neuron · doi:10.1016/j.neuron.2013.05.012 · Cited by 50
Grados, M. A., Huselid, R., & Duque, L. (2018) · Brain Sciences · doi:10.3390/brainsci8070129 · Cited by 49
Liang, X., Zhou, H. J., Ding, Y., Li, J., Yang, C., Luo, Y., Li, S., Sun, G., Liao, X., & Wang, M. (2012) · Investigative Ophthalmology & Visual Science · doi:10.1167/iovs.11-9315 · Cited by 48
Retinal degeneration in two lines of transgenic S334ter rats
Martı́nez, G., Seiler, M. J., Aramant, R. B., Fernández‐Sánchez, L., Pinilla, I., & Cuenca, N. (2010) · Experimental Eye Research · doi:10.1016/j.exer.2010.12.001 · Cited by 48
Neuronal expression of P2X3 purinoceptors in the rat retina
Puthussery, T., & Fletcher, E. L. (2007) · Neuroscience · doi:10.1016/j.neuroscience.2007.01.055 · Cited by 47
Hirano, A. A., Liu, X., Boulter, J., Grove, J. C. R., Müller, L. P. D. S., Barnes, S., & Brecha, N. C. (2016) · eNeuro · doi:10.1523/eneuro.0148-15.2016 · Cited by 46
Guo, C., Hirano, A. A., Stella, S., Bitzer, M., & Brecha, N. C. (2009) · The Journal of Comparative Neurology · doi:10.1002/cne.22294 · Cited by 45
Linden, R., Martins, R. A. P., & Silveira, M. S. (2004) · Progress in Retinal and Eye Research · doi:10.1016/j.preteyeres.2004.10.001 · Cited by 45
Ribic, A., Liu, X., Crair, M. C., & Biederer, T. (2013) · The Journal of Comparative Neurology · doi:10.1002/cne.23452 · Cited by 45
Brandstätter, J. H., Dick, O., & Boeckers, T. M. (2004) · The Journal of Comparative Neurology · doi:10.1002/cne.20194 · Cited by 43
Development of Presynaptic Inhibition Onto Retinal Bipolar Cell Axon Terminals Is Subclass-Specific
Schubert, T., Kerschensteiner, D., Eggers, E. D., Misgeld, T., Kerschensteiner, M., Lichtman, J. W., Lukasiewicz, P. D., & Wong, R. (2008) · Journal of Neurophysiology · doi:10.1152/jn.90202.2008 · Cited by 43
Soto, F., Bleckert, A., Lewis, R. M., Kang, Y., Kerschensteiner, D., Craig, A. M., & Wong, R. (2011) · Neural Development · doi:10.1186/1749-8104-6-31 · Cited by 43
Localization of glycine receptor alpha subunits on bipolar and amacrine cells in primate retina
Jusuf, P. R., Haverkamp, S., & Grünert, U. (2005) · The Journal of Comparative Neurology · doi:10.1002/cne.20555 · Cited by 42
Bleckert, A., Parker, E. D., Kang, Y., Pancaroglu, R., Soto, F., Lewis, R. M., Craig, A. M., & Wong, R. (2013) · PLoS ONE · doi:10.1371/journal.pone.0069612 · Cited by 41
Expression and function of P2Y receptors on Müller cells of the postnatal rat retina
Wurm, A., Erdmann, I., Bringmann, A., Reichenbach, A., & Pannicke, T. (2009) · Glia · doi:10.1002/glia.20883 · Cited by 40
P2X2receptors on ganglion and amacrine cells in cone pathways of the rat retina
Puthussery, T., & Fletcher, E. L. (2006) · The Journal of Comparative Neurology · doi:10.1002/cne.20889 · Cited by 40
Distribution of group‐III metabotropic glutamate receptors in the retina
Quraishi, S., Gayet, J., Morgans, C. W., & Duvoisin, R. M. (2007) · The Journal of Comparative Neurology · doi:10.1002/cne.21274 · Cited by 40
Sun, C., Speer, C. M., Wang, G.-Y., Chapman, B., & Chalupa, L. M. (2008) · Journal of Neurophysiology · doi:10.1152/jn.90303.2008 · Cited by 40
Distribution of soluble guanylyl cyclase in rat retina
Ding, J., & Weinberg, R. J. (2006) · The Journal of Comparative Neurology · doi:10.1002/cne.21206 · Cited by 40
Adenosine triphosphate‐induced photoreceptor death and retinal remodeling in rats
Vessey, K. A., Greferath, U., Aplin, F. P., Jobling, A. I., Phipps, J. A., Ho, T., de Iongh, R. U., & Fletcher, E. L. (2014) · The Journal of Comparative Neurology · doi:10.1002/cne.23558 · Cited by 39
Stella, S., Li, S., Sabatini, A., Vila, A., & Brecha, N. C. (2008) · Brain Research · doi:10.1016/j.brainres.2008.03.038 · Cited by 38
Localization and possible function of P2Y4 receptors in the rodent retina
Ward, M. M., Puthussery, T., & Fletcher, E. L. (2008) · Neuroscience · doi:10.1016/j.neuroscience.2008.06.035 · Cited by 37
The specification of glycinergic neurons and the role of glycinergic transmission in development
Chalphin, A. V. (2010) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2010.00011 · Cited by 37
Robust syntaxin-4 immunoreactivity in mammalian horizontal cell processes
Hirano, A. A., Brandstätter, J. H., VILA, A., & Brecha, N. C. (2007) · Visual Neuroscience · doi:10.1017/s0952523807070198 · Cited by 37
Han, B., Bellemer, A., & Koelle, M. R. (2015) · Genetics · doi:10.1534/genetics.114.173963 · Cited by 37
Atlasz, T., Szabadfi, K., Kiss, P., Babai, N. Z., Kőszegi, Z., Tamás, A., Reglődi, D., & Gabriel, R. (2008) · Journal of Molecular Neuroscience · doi:10.1007/s12031-008-9059-5 · Cited by 36
Dorfman, A. L., Cuenca, N., Pinilla, I., Chemtob, S., & Lachapelle, P. (2010) · Investigative Ophthalmology & Visual Science · doi:10.1167/iovs.10-6197 · Cited by 36
Kerschensteiner, D. (2016) · Frontiers in Neural Circuits · doi:10.3389/fncir.2016.00038 · Cited by 35
Prox1 Is a Marker for AII Amacrine Cells in the Mouse Retina
Müller, L. P. D. S., Azar, S. S., Santos, J. D. L., & Brecha, N. C. (2017) · Frontiers in Neuroanatomy · doi:10.3389/fnana.2017.00039 · Cited by 35
Puthussery, T., Gayet‐Primo, J., Taylor, W. R., & Haverkamp, S. (2011) · The Journal of Comparative Neurology · doi:10.1002/cne.22756 · Cited by 33
Assembly of the outer retina in the absence of GABA synthesis in horizontal cells
Schubert, T., Huckfeldt, R. M., Parker, E. D., Campbell, J. E., & Wong, R. (2010) · Neural Development · doi:10.1186/1749-8104-5-15 · Cited by 33
Inputs Underlying the ON–OFF Light Responses of Type 2 Wide-Field Amacrine Cells in TH::GFP Mice
Knop, G. C., Feigenspan, A., Weiler, R., & Dedek, K. (2011) · Journal of Neuroscience · doi:10.1523/jneurosci.6235-10.2011 · Cited by 32
Subcellular distribution of connexin45 in OFF bipolar cells of the mouse retina
Hilgen, G., von Maltzahn, J., Willecke, K., Weiler, R., & Dedek, K. (2010) · The Journal of Comparative Neurology · doi:10.1002/cne.22526 · Cited by 32
Kozuka, T., Chaya, T., Tamalu, F., Shimada, M., Fujimaki-Aoba, K., Kuwahara, R., Watanabe, S., & Furukawa, T. (2017) · Journal of Neuroscience · doi:10.1523/jneurosci.0824-17.2017 · Cited by 32
Michalski, D., Härtig, W., Krügel, K., Edwards, R. H., Böddener, M., Böhme, L., Pannicke, T., Reichenbach, A., & Grosche, A. (2012) · Neuroscience · doi:10.1016/j.neuroscience.2012.11.046 · Cited by 31
Self-citationImmunolocalization of the P2X4 receptor on neurons and glia in the mammalian retina
Ho, T., Vessey, K. A., & Fletcher, E. L. (2014) · Neuroscience · doi:10.1016/j.neuroscience.2014.06.055 · Cited by 30
Raz-Prag, D., Grimes, W. N., Fariss, R. N., Vijayasarathy, C., Campos, M. M., Bush, R. A., Diamond, J. S., & Sieving, P. A. (2010) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0913472107 · Cited by 29
Casini, G., Monte, M. D., Petrucci, C., Gambellini, G., Grouselle, D., Allen, J. P., Kreienkamp, H., Richter, D., Epelbaum, J., & Bagnoli, P. (2004) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2004.03081.x · Cited by 29
Vesicular Release of GABA by Mammalian Horizontal Cells Mediates Inhibitory Output to Photoreceptors
Hirano, A. A., Vuong, H. E., Kornmann, H. L., Schietroma, C., Stella, S., Barnes, S., & Brecha, N. C. (2020) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2020.600777 · Cited by 29
Lee, H. Y., & Brecha, N. C. (2010) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2010.07181.x · Cited by 27
Early Alteration of Retinal Neurons in Aipl1 −/− Animals
Singh, R. K., Kolandaivelu, S., & Ramamurthy, V. (2014) · Investigative Ophthalmology & Visual Science · doi:10.1167/iovs.13-13728 · Cited by 26
Hirasawa, H., Yamada, M., & Kaneko, A. (2012) · The Journal of Physiological Sciences · doi:10.1007/s12576-012-0220-0 · Cited by 26
Retinal Cell Types are Differentially Affected in Sheep with Scrapie
Smith, J. D., Greenlee, J. J., Hamir, A. N., & Greenlee, M. H. W. (2007) · Journal of Comparative Pathology · doi:10.1016/j.jcpa.2007.09.002 · Cited by 26
Whitaker, C. M., & Cooper, N. G. F. (2009) · Neuroscience · doi:10.1016/j.neuroscience.2009.10.054 · Cited by 26
Kunzevitzky, N. J., Almeida, M. V., & Goldberg, J. L. (2010) · Investigative Ophthalmology & Visual Science · doi:10.1167/iovs.09-4540 · Cited by 27
Pathway-Specific Maturation, Visual Deprivation, and Development of Retinal Pathway
Xu, H., & Tian, N. (2004) · The Neuroscientist · doi:10.1177/1073858404265254 · Cited by 26
Self-citationEAAT1 and d-serine expression are early features of human retinal development
Díaz, C., Macnab, L. T., Williams, S. M., Sullivan, R., & Pow, D. V. (2007) · Experimental Eye Research · doi:10.1016/j.exer.2007.01.008 · Cited by 25
Hajji, S. E., Shiga, Y., Belforte, N., Solorio, Y. C., Tastet, O., D’Onofrio, P. M., Dotigny, F., Prat, A., Arbour, N., Fortune, B. A., et al. (2024) · Science Advances · doi:10.1126/sciadv.adl5722 · Cited by 26
Metadata
- Authors
- Johnson, J., Tian, N., Caywood, M. S., Reimer, R. J., Edwards, R. H., & Copenhagen, D. R.
- Affiliations
- Yale University (US)
- Stanford Medicine (US)
- University of California, San Francisco (US)
- Venue
- The Journal of Neuroscience
- Publisher
- Society for Neuroscience
- Published
- 2003-01-15
- Volume
- 23
- Issue
- 2
- Pages
- 518-529
- ISSN
- 0270-6474 (ISSN-L)
- 1529-2401
- PMC
- PMC6741860
- OpenAlex
- W1545065700
- Cited by
- 197
- References
- 42
- Citations by year
- 2025: 4 · 2024: 5 · 2023: 8 · 2022: 9 · 2021: 11 · 2020: 5 · 2019: 3 · 2018: 7 · 2017: 6 · 2016: 8 · 2015: 5 · 2014: 7 · 2013: 17 · 2012: 13
- FWCI
- 3.47
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Locations
- Journal of Neuroscience (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- Funders
- Research to Prevent Blindness
- That Man May See
- National Institutes of Health
- National Eye Institute (R01EY001869)
- Topics
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
- Health Sciences › Medicine › Ophthalmology › Retinal Development and Disorders
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cell Biology › Cellular transport and secretion
- Keywords
- VGLUT1, vesicular GABA transporter, glutamatergic synapses, GABAergic synapses, photoreceptor terminals, rod bipolar cells, ON bipolar cells, mGluR6, protein kinase C, ribeye, spontaneous EPSCs, retinal ganglion cells
- MeSH terms
- Age Factors, Animals, Carrier Proteins, gamma-Aminobutyric Acid, Glycine, Heterozygote, Membrane Glycoproteins, Membrane Proteins, Mice, Inbred C57BL, Mice, Mutant Strains, Nerve Tissue Proteins, Neurons, Retina, Retinal Ganglion Cells, Presynaptic Terminals, Patch-Clamp Techniques, Glutamic Acid, Excitatory Postsynaptic Potentials, Rats, Long-Evans, Photoreceptor Cells, Vertebrate, Membrane Transport Proteins, Organic Anion Transporters, Vesicular Transport Proteins, GABA Plasma Membrane Transport Proteins, Vesicular Glutamate Transport Protein 1, Mice, Rats, In Vitro Techniques
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 ›
Are you an author, or do you see a problem with this page? Request a review