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

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