戻る
「早戻しボタン」を押すと検索画面に戻ります。

今後説明を表示しない

[OK]

コーパス検索結果 (1語後でソート)

通し番号をクリックするとPubMedの該当ページを表示します
1 on channels mediate the response to light in retinal rods.
2 sion of CaBP5, for example, is restricted to retinal rod and cone bipolar cells.
3                                              Retinal rod and cone cells are not required for photoent
4                                              Retinal rod and cone cGMP phosphodiesterases (PDE6 famil
5                                              Retinal rod and cone phosphodiesterases are oligomeric e
6                                              Retinal rod and cone photoreceptors arguably represent t
7 is transduced into electrical signals by the retinal rod and cone photoreceptors in vertebrates.
8                                       In the retinal rod and cone photoreceptors, light photoactivate
9 isorder characterized by the degeneration of retinal rod and cone photoreceptors.
10 s may explain functional differences between retinal rod and cone photoreceptors.
11                                              Retinal rod and cone pigments consist of an apoprotein,
12         Light isomerizes 11-cis-retinal in a retinal rod and produces an active form of rhodopsin (Rh
13                         To determine whether retinal rods and cones are required for this response, t
14 lyl cyclase when free Ca2+ concentrations in retinal rods and cones fall after illumination and inhib
15                 The transduction of light by retinal rods and cones is effected by homologous G-prote
16                                              Retinal rods and cones share a phototransduction pathway
17                                              Retinal rods and cones were evaluated in wild-type (WT),
18 t mouse (Crx(-/-) ) with degeneration of the retinal rods and cones, but a preserved non-image formin
19   By generating the second messenger cGMP in retinal rods and cones, ROS-GC plays a central role in v
20                                              Retinal rods and cones, which are the front-end light de
21  tested a passive vesicle diffusion model of retinal rod bipolar cell ribbon synapses.
22 +)-dependent delayed asynchronous release in retinal rod bipolar cell synapses, that its function can
23                                     However, retinal rod bipolar cells (RBCs) generally do not produc
24              Axon terminals of glutamatergic retinal rod bipolar cells (RBCs) receive GABAA and GABAC
25 s to study the synaptic transmission between retinal rod bipolar cells and AII amacrine cells.
26 a(2+) channel and transmitter release in rat retinal rod bipolar cells depends on the G(alpha) subuni
27                                           In retinal rods, Ca(2+) exerts negative feedback control on
28               The single photon responses of retinal rod cells are remarkably reproducible, allowing
29            Quenching of phototransduction in retinal rod cells involves phosphorylation of photoactiv
30  that this normal pattern is reversed in the retinal rod cells of mice.
31 er protein (ABCR) plays an important role in retinal rod cells presumably transporting retinal.
32           In rhodopsin, the photoreceptor of retinal rod cells, we substituted histidine residues for
33 ys an important role in the outer segment of retinal rod cells, where it functions as a transporter o
34 ch protein is recoverin, a calcium sensor in retinal rod cells, which controls the lifetime of photoe
35 ducin (Gt) to transmit the light signal into retinal rod cells.
36  regulates rhodopsin kinase (RK) activity in retinal rod cells.
37 n superfamily, serves as a calcium sensor in retinal rod cells.
38 d superfamily, serves as a calcium sensor in retinal rod cells.
39              Dim-light vision is mediated by retinal rod cells.
40 gulation of the phototransduction cascade in retinal rod cells.
41                                              Retinal rod cGMP phosphodiesterase (PDE6 family) is the
42 ic nucleotide-binding domain from the bovine retinal rod CNG channel alpha subunit (Bralpha) to the D
43                            Expression of the retinal rod cng channel, however, can be detected only i
44                                    As native retinal rod CNG channels comprise CNGA1 and CNGB1 subuni
45 cGMP (6) are well tolerated by olfactory and retinal rod CNG channels.
46                                 By contrast, retinal rod, cone, and bipolar cells appear to use homom
47                                              Retinal rod cyclic nucleotide-gated channels are compose
48  the activation of homomeric and heteromeric retinal rod cyclic nucleotide-gated channels with the fo
49 0 pmol of rhodopsin in detergent-solubilized retinal rod disk membranes, using 1-5 pmol of digest per
50 ation channel mediating phototransduction in retinal rods has recently been shown to be inhibited by
51 a and is enriched in biochemical extracts of retinal rod inner segments.
52                         Phototransduction in retinal rods involves a G protein-coupled signaling casc
53        We recorded photocurrent responses of retinal rods isolated from cane toads Bufo marinus and c
54                                           In retinal rods, light-induced isomerization of 11-cis-reti
55                                          The retinal rod Na(+)/Ca(2+),K(+) exchanger (RodX) is a poly
56             Rhodopsin, the light receptor of retinal rod neurons, is produced in large amounts of hom
57 S11 as the key GAPs in the mGluR6 pathway of retinal rod ON bipolar cells that set the sensitivity an
58 ct of n-3 FA deficiency on GPCR signaling in retinal rod outer segment (ROS) membranes isolated from
59 oliposomes consisting of asolectin or native retinal rod outer segment disk lipids using n-octyl beta
60 rast to the previously described monomer, in retinal rod outer segment disk membranes.
61          The C-terminus of the intracellular retinal rod outer segment disk protein peripherin-2 bind
62                                              Retinal rod outer segments (ROS) contained approximately
63 ic acid (DHA), the major fatty acid found in retinal rod outer segments (ROS).
64                                              Retinal rod outer segments and the cerebellar granular l
65  the regulation of cGMP phosphodiesterase in retinal rod outer segments.
66                               We studied the retinal rod pathway of Carollia perspicillata and Glosso
67 ting a failure of signal transmission in the retinal rod pathway.
68 leted the Phlp1 gene in mouse (Mus musculus) retinal rod photoreceptor cells and measured the effects
69                                              Retinal rod photoreceptor cells have double membrane dis
70 e of Pd in regulating G-protein signaling in retinal rod photoreceptor cells, we have measured the ab
71 r alterations in ABCR, a gene that encodes a retinal rod photoreceptor protein and is defective in St
72 e individual subcellular compartments of the retinal rod photoreceptor.
73 e adult, PPEF-2 is expressed specifically in retinal rod photoreceptors and the pineal.
74                                              Retinal rod photoreceptors are depolarized in darkness t
75                             Specification of retinal rod photoreceptors is determined by several diff
76         Efficient single-photon detection by retinal rod photoreceptors requires timely and reproduci
77                              Furthermore, in retinal rod photoreceptors the low cytoplasmic concentra
78        This high amplification system allows retinal rod photoreceptors to detect single photons of l
79                                           In retinal rod photoreceptors, a long-lived photoisomerized
80 e central effector of visual transduction in retinal rod photoreceptors, cGMP phosphodiesterase (PDE6
81 n coupled receptor, most abundant protein in retinal rod photoreceptors, is glycosylated at asparagin
82 oated vesicles to selected membrane sites in retinal rod photoreceptors.
83  biological relevance of Mef2c expression in retinal rod photoreceptors.
84         Termination of the light response of retinal rods requires GTP hydrolysis by the G-protein tr
85                                              Retinal rods signal the activation of a single receptor
86 ng the single photon responses of vertebrate retinal rods so remarkably reproducible.
87                                In vertebrate retinal rods, the light stimulus is transmitted from rho
88  cyclic nucleotides first were discovered in retinal rods where they generate the cell's response to
89 es were compared in wild-type and transgenic retinal rods with and without guanylate cyclase activati

WebLSDに未収録の専門用語(用法)は "新規対訳" から投稿できます。