| Q41203548 | AMPA receptor mediated d‐serine release from retinal glial cells |
| Q69900790 | Action and localization of gamma-aminobutyric acid in the cat retina |
| Q70798224 | An intracellular electrophysiological study of the ontogeny of functional synapses in the rabbit retina. II. Amacrine cells |
| Q28582714 | Changes in D-serine levels and localization during postnatal development of the rat vestibular nuclei |
| Q70788891 | Changes of electroretinogram and neurochemical aspects of gabaergic neurons of retina after intraocular injection of kainic acid in rats |
| Q46027349 | Concomitant activation of two types of glutamate receptor mediates excitation of salamander retinal ganglion cells. |
| Q73820017 | Contribution to the kinetics and amplitude of the electroretinogram b-wave by third-order retinal neurons in the rabbit retina |
| Q35836077 | D-Serine as a glial modulator of nerve cells |
| Q81362688 | Dendritic impulse collisions and shifting sites of action potential initiation contract and extend the receptive field of an amacrine cell |
| Q54186907 | Dendritic integration in ganglion cells of the mudpuppy retina. |
| Q70540743 | Differential localization of radioactive gamma-aminobutyric acid and muscimol in isolated and in vivo mouse retina |
| Q70906579 | Effect of aminooxyacetic acid on endogenous GABA release from rat retina |
| Q69393509 | Effects of 2-amino-4-phosphonobutyric acid (APB) and glycine on the oscillatory potentials of the rat electroretinogram |
| Q66981568 | Effects of catecholamines and related compounds on horizontal cells in the fish retina |
| Q67329403 | Effects of picrotoxin and strychnine on rabbit retinal ganglion cells: lateral interactions for cells with more complex receptive fields |
| Q72079406 | Effects of some amino acids (GABA, glycine, taurine) and of their antagonists (picrotoxin, strychnine) on spatial and temporal features of frog retinal ganglion cell responses |
| Q72858586 | Electrophysiological analysis of taurine and glycine action on neurons of the mudpuppy retina. I. Intracellular recording |
| Q72858591 | Electrophysiological analysis of taurine and glycine action on neurons of the mudpuppy retina. II. ERG, PNR and Müller cell recordings |
| Q36409279 | Extracellular K+ activity changes related to electroretinogram components. I. Amphibian (I-type) retinas |
| Q33796392 | GABA-ergic pathways in the goldfish retina |
| Q70148477 | GABAergic amacrine cells in rat retina: immunocytochemical identification and synaptic connectivity |
| Q38346018 | GABAergic neurotransmission and retinal ganglion cell function |
| Q68270984 | Glycine receptor immunoreactivity is localized at amacrine synapses in cat retina |
| Q40101339 | Glycine receptor subunit composition alters the action of GABA antagonists |
| Q42610234 | Glycine transport accounts for the differential role of glycine vs. D-serine at NMDA receptor coagonist sites in the salamander retina |
| Q38584412 | Golgi-impregnated amacrine cells and GABAergic retinal neurons: a comparison of dendritic, immunocytochemical and histochemical stratification in the inner plexiform layer of rat retina |
| Q70581786 | Influence of amacrine cells on receptive field organization of ganglion cells of the generalized vertebrate cone retina: electronic simulation |
| Q36354137 | Interplexiform cell in cat retina: identification by uptake of gamma-[3H]aminobutyric acid and serial reconstruction |
| Q41767611 | Longitudinal changes in photopic OPs occurring with vigabatrin treatment |
| Q41611714 | Morphology of catecholamine-containing amacrine cells in the cat's retina, as seen in retinal whole mounts |
| Q48271226 | Multiple types of spontaneous excitatory synaptic currents in salamander retinal ganglion cells |
| Q52183189 | Oscillatory potentials in the retina: what do they reveal. |
| Q40196597 | Pathways and polarities of synaptic interactions in the inner retina of the mudpuppy: II. Insight revealed by an analysis of latency and threshold |
| Q71019827 | Physiological and morphological identification of amacrine cells in the retina of the larval tiger salamander |
| Q93646459 | Possible role of amacrine cells in the generation of the mammalian ERG b-wave |
| Q46415359 | Properties of stimulus-dependent synchrony in retinal ganglion cells |
| Q70623260 | Strychnine blocks transient but not sustained inhibition in mudpuppy retinal ganglion cells |
| Q44240008 | Suppression by zinc of transient OFF responses of carp amacrine cells to red light is mediated by GABA(A) receptors |
| Q40258142 | Suppression of retinal spike discharge by dipropylacetate (depakene): A possible involvement of GABA |
| Q54495298 | Sustained and transient synaptic inputs to on-off ganglion cells in the mudpuppy retina |
| Q48114761 | The Chemical Specificity of Neurones in the Retina |
| Q48851545 | The Organization of Amacrine Cell Types Which Use Different Transmitters in Chicken Retina |
| Q66981122 | The emergence, localization and maturation of neurotransmitter systems during development of the retina inXenopus laevis. I. ?-aminobutyric acid |
| Q72879488 | The emergence, localization, and maturation of neurotransmitter systems during development of the retina inxenopus laevis: II. Glycine |
| Q42699314 | The glycine transporter GlyT1 controls N-methyl-D-aspartic acid receptor coagonist occupancy in the mouse retina |
| Q70755336 | The release of endogenous amino acids into the vitreous of the intact eye of the albino rat: effect of light, potassium, and ouabain |
| Q70767671 | The uptake and release of [3H]glycine in the goldfish retina |
| Q72924860 | Transmitter-related studies in the isolated, perfused eye of the cat |
| Q72556648 | Transmitters mediating inhibition of ganglion cells in the cat retina: Iontophoretic studies in vivo |
| Q51759524 | Uptake and K+-stimulated release of [14C]glycine from frog retinal synaptosomal fractions. |
| Q72408893 | Uptake of3H-glycine in the outer plexiform layer of the retina of the toadBufo marinus |
| Q70725350 | [3H]taurine-accumulating neurons in the cat retina |
| Q35144299 | d -serine and serine racemase are present in the vertebrate retina and contribute to the physiological activation of NMDA receptors |