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1 he fractional shift of the charge across the disk membrane.
2 ation of 11-cis-retinal complexes across the disk membrane.
3  directly coupled as it is in the native rod disk membrane.
4 cteristic of classical Meta II in the native disk membrane.
5  encounter frequency between proteins on the disk membrane.
6 chain packing in the rod outer segment (ROS) disk membrane.
7 e PM renewal is coordinated with that of the disk membranes.
8 ted to be the sole species present in native disk membranes.
9 from the lumen to the cytoplasmic leaflet of disk membranes.
10 f two compartments: plasma membrane (PM) and disk membranes.
11 cribed monomer, in retinal rod outer segment disk membranes.
12 der found in native bovine rod outer segment disk membranes.
13 psin, may indeed exist as a homodimer in rod disk membranes.
14 336 of peripherin/rds localized uniformly to disk membranes.
15 P phosphodiesterase (PDE6) at the surface of disk membranes.
16 cesses inhibited the ingestion of additional disk membranes.
17  oxidative damage of DHA-PC in photoreceptor disk membranes.
18 activated, unphosphorylated rhodopsin in ROS disk membranes.
19 x in the rims of photoreceptor outer segment disk membranes.
20 niformly distributed and freely diffusing on disk membranes.
21 nsion, the area expansion coefficient of the disk membrane also increases as thermally induced fluctu
22 een shown to directly mediate fusion between disk membranes and opposing membranes to maintain the hi
23                                      For rod disk membranes and recombinant membranes containing rhod
24 died and cones have lost their outer-segment disk membranes and synaptic pedicles.
25 g a photoconversion technique, we found that disk membranes are assembled at the base of cone-shaped
26                                          The disk membranes are continually renewed, but how new disk
27                            Rod outer segment disk membranes are densely packed with rhodopsin.
28                                              Disk membranes are separated from the surrounding plasma
29 the T(m) of rhodopsin and of opsin in native disk membranes, as well as in cross-linked disk membrane
30 helium (RPE), offsetting the addition of new disk membrane at the base of the OS.
31 data of nascent and mature rod photoreceptor disk membranes at unprecedented z-axis depth and resolut
32 imply from partial solubilization of the ROS disk membranes because detergent-treated low buoyant den
33 r rhodopsin bleaching moved laterally in the disk membrane bilayer with an apparent diffusion coeffic
34 recoverin facilitates its binding to retinal disk membranes by a mechanism known as the Ca(2+)-myrist
35 ilitates the binding of recoverin to retinal disk membranes by a mechanism known as the Ca2+-myristoy
36 allow rhodopsin to be examined in the native disk membranes by a number of methods.
37 ely involved in the removal of outer segment disk membranes by the RPE.
38  but not all, of this complex is tethered to disk membranes by the transmembrane protein R9AP.
39  in phototransduction that take place on the disk membrane, by restricting the lateral movement of, a
40 -Dendra2 was also trafficked from old to new disk membranes, consistent with the hypothesis that retr
41                                          Rod disk membranes containing different average receptor pho
42 gests that the local density of rhodopsin in disk membranes could be much higher than the average den
43  highest temperature was detected for native disk membranes: di22:6-PC < 16:0,22:6-PC < di16:0,18:1-P
44              PP-5 was able to inhibit R18-PM disk membrane fusion and promoted ANTS/DPX contents mixi
45 is unlikely mediated by diffusion, since the disk membranes have a closed configuration, as evidenced
46  Ca(2+) is high, and to be released from the disk membrane in light when Ca(2+) is low, accelerating
47 umulation of 11-cis-retinal in photoreceptor disk membranes in excess of what is required for visual
48 quired for the normal processing of ingested disk membranes in the RPE, primarily in the basal transp
49 e disk membranes, as well as in cross-linked disk membranes in which rhodopsin dimers are known to be
50 ated channel in the PM, while preventing the disk membrane incorporation.
51 gestion of photoreceptor outer segment (POS) disk membranes, is a major role of the retinal pigment e
52 e PM domains, which are the proposed site of disk membrane maturation.
53 which are known to disrupt F-actin-dependent disk membrane morphogenesis, prevented the entrance of n
54 aments, both of which play critical roles in disk membrane morphogenesis.
55 embrane components contributes to the larger disk membrane observed toward the base of the cone-shape
56  the G protein-coupled receptor rhodopsin on disk membranes of living rod photoreceptors from transge
57                             Rhodopsin in the disk membranes of rod outer segments serves as the dim-l
58 gether with its specific localization to the disk membranes of the rod cell, has also enabled direct
59 vestigate the effect of partial bleaching of disk membranes on the T(m) of rhodopsin and of opsin in
60   To visualize the dynamic reorganization of disk membranes, opsin and peripherin/rds were fused to a
61 18-labeled ROS plasma membrane (R18-PM) with disk membranes or peripherin/rds-enriched large unilamme
62  to the membrane evaginations believed to be disk membrane precursors.
63   We discuss how pathological alterations of disk membrane properties by mutant proteins may lead to
64 otein constituting >90% of rod outer segment disk membrane protein.
65 not affect the localization of outer segment disk membrane proteins, such as rhodopsin, Peripherin-rd
66  from homogenates of rod outer segment (ROS) disk membranes purified free of the surrounding plasma m
67 e dual wavelength absorbance response of rod disk membrane (RDM) suspensions to a series of small ble
68                   In the bleached bovine rod disk membranes (RDM), opsin and membrane lipids were dom
69                   We conclude that in native disk membranes, rhodopsin behaves predominantly as a mon
70 iliary PM, and coordinates the formations of disk membrane rim region and OS PM.
71 n processes associated with the formation of disk membranes, specialized organelles of photoreceptor
72 role in the morphogenesis and maintenance of disk membrane structure, with peripherin/rds gene mutati
73 in the maintenance of photoreceptor rod cell disk membrane structure.
74  high-curvature rim domains of outer segment disk membranes suggests that it may act to shape these s
75  notion of raft or microdomain structures in disk membranes suggests that the local density of rhodop
76  proposed that it arises from cone opsin and disk membrane swelling triggered by isomerization and ra
77 RK in a ternary complex on rod outer segment disk membranes, thereby blocking RK interaction with rho
78 odopsin in detergent-solubilized retinal rod disk membranes, using 1-5 pmol of digest per sample.
79 inal domain of RGS9-1, and anchors it to the disk membrane via a C-terminal transmembrane helix.
80 ral solutes on acyl chain packing in the ROS disk membrane was assessed via measurements of the fluor
81                         A portion of the ROS disk membrane was found to be resistant to Triton X-100
82 trast, the T(m) of cross-linked rhodopsin in disk membranes was dependent on the extent of bleaching.
83                  Moreover, the outer segment disk membranes were greatly overgrown and misoriented, i
84                   Moreover, fewer packets of disk membranes were ingested in vivo, possibly because r
85 contribution to rhodopsin kinetic stability, disk membranes were systematically disrupted by octyl-be
86 e fascia adherens region of the intercalated disk membrane, while N-RAP extends approximately 100 nm
87 e polyunsaturated nature of phospholipids in disk membranes, with rhodopsin/lipid ratios ranging from