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1  ribbon-type synaptic terminal, the goldfish retinal bipolar cell.
2 receptors on the axon and dendrites of mouse retinal bipolar cells.
3 on channel expressed by both melanocytes and retinal bipolar cells.
4 lective potentiation on GABA(A) receptors of retinal bipolar cells.
5 ge signals transmitted by ribbon synapses of retinal bipolar cells.
6 common role in regulating gene expression in retinal bipolar cells.
7 ecifically targeted to the dendritic tips of retinal bipolar cells.
8 nits, as well as on the GABA(C) receptors of retinal bipolar cells.
9 gnal transmission between photoreceptors and retinal bipolar cells.
10 -type calcium channel currents in identified retinal bipolar cells.
11  AAV2 gene-therapy vector that targets human retinal bipolar cells.
12 ded pathways, are thought to be initiated in retinal bipolar cells.
13 tudied the representation of motion in mouse retinal bipolar cells and found that some bipolar cells
14                  The intrinsic properties of retinal bipolar cells and synapses contribute to backgro
15 icle movement and release at ribbon sites in retinal bipolar cells, and find that, although ribbon sy
16  pool and the releasable vesicle pool of the retinal bipolar cell are situated at the ribbon-style ac
17                                              Retinal bipolar cells are essential to the transmission
18                                              Retinal bipolar cells are known to form a complex, inter
19                                              Retinal bipolar cells are polarized glutamatergic neuron
20                                              Retinal bipolar cells are slow potential neurons that re
21 e eyes, and the appearance of the IgG in the retinal bipolar cells at the conclusion of the experimen
22                                              Retinal bipolar cells (BCs) are the first neurons along
23 gs from the large axon terminals of goldfish retinal bipolar cells (BCs) have revealed detailed infor
24 hich glutamate release from specific sets of retinal bipolar cells (BCs) is suppressed.
25 mistry (IHC) showed Kir2.1 immunostaining of retinal bipolar cells (BCs) matching the labeling patter
26            Individual transmission-deficient retinal bipolar cells (BCs) reduced synapses with retina
27  GABAergic synapses across axon terminals of retinal bipolar cells (BCs), we uncovered a crucial role
28    Electroretinogram recordings suggest that retinal bipolar cells (BCs), which filter and transmit p
29 s on a heterogeneous class of neurons, mouse retinal bipolar cells (BCs).
30  active in other Otx2-positive cells such as retinal bipolar cells (BPs), retinal pigmented epitheliu
31 t the dendrites and axon terminals of ferret retinal bipolar cells by recording currents evoked by fo
32 ubunit, and a selection of Gbeta subunits in retinal bipolar cells, by using a transgenic mouse strai
33                                              Retinal bipolar cells can be classified by the type of p
34                                              Retinal bipolar cells constitute the first parallel chan
35       Finally, we find that each ribbon in a retinal bipolar cell contains approximately 4000 molecul
36                                              Retinal bipolar cells convey light-evoked potentials fro
37             Synapses of all major classes of retinal bipolar cell encode visual information by using
38 fish, we demonstrate that ribbon synapses of retinal bipolar cells encode contrast through changes in
39  evoked prolonged bouts of exocytosis from a retinal bipolar cell, fixed within seconds, and then stu
40             At the axon terminal of goldfish retinal bipolar cells, GABA(C) receptors have been shown
41                                              Retinal bipolar cells have been assumed to generate pure
42 e dopamine D1 receptor (D1R) is expressed in retinal bipolar cells in a type-dependent manner.
43                Here, we report that OFF-type retinal bipolar cells in mice are an exception to this r
44 xperimentally from glutamatergic synapses of retinal bipolar cells in zebrafish (both sexes) and comp
45                                              Retinal bipolar cells integrate cone signals at dendriti
46           The number of synaptic inputs onto retinal bipolar cells is influenced by transmitter relea
47              However, we now report that, in retinal bipolar cells, low-voltage-activated (LVA) Ca(2+
48                                              Retinal bipolar cells make up a class of at least 11 dis
49 aptation of [Cl(-)](i) to voltage changes in retinal bipolar cells may add a previously unsuspected l
50 py to image synaptic vesicles and ribbons in retinal bipolar cells of goldfish (Carassius auratus) of
51 ndrome whose sera produced immunolabeling of retinal bipolar cells participated in the study.
52 e molecular basis for electrical synapses in retinal bipolar cells, particularly ON cone bipolar cell
53                      GABAergic modulation of retinal bipolar cells plays a crucial role in early visu
54 , physiological, and molecular features with retinal bipolar cells, such as receiving input from phot
55  We monitored quantal glutamate release from retinal bipolar cell terminals (which receive GABA-ergic
56 ed vesicles labeled with styryl dye in mouse retinal bipolar cell terminals whose ribbons had been la
57                                       Unlike retinal bipolar cell terminals, where stimulation trigge
58 known, however, about electrical synapses in retinal bipolar cells than about chemical synapses.
59 ent with the dysfunction at the level of the retinal bipolar cells that is presumed to underlie the M
60          Here, we addressed this question in retinal bipolar cells, the first visual neuron with clas
61                  At the synaptic terminal of retinal bipolar cells, the footprint expands during exoc
62 crement and decrement luminance signals from retinal bipolar cells to cortex.
63         Morphologically distinct subtypes of retinal bipolar cells transmit information along paralle
64                     The presence of AQP-0 in retinal bipolar cells was also demonstrated, whereas it
65                       The synaptic output of retinal bipolar cells was monitored by recording light-e
66 ibbon-type presynaptic terminals of goldfish retinal bipolar cells were coaxed to release a false tra
67                        Synaptic signals from retinal bipolar cells were monitored by measuring EPSCs
68                   The axons and dendrites of retinal bipolar cells, which contact their synaptic part
69 ivo calcium imaging and electrophysiology of retinal bipolar cells, which have been assumed to be pur
70  GABA-elicited membrane current responses of retinal bipolar cells, which have both GABA(A) and GABA(