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