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1 1) as efficiently as rhodopsin in the native disc membrane.
2 to its translocation from the cytosol to the disc membrane.
3 ising over 90% of the protein content of the disc membrane.
4  affect rhodopsin's activity or transport to disc membranes.
5 aptured by opsins in continually synthesized disc membranes.
6 tin-1 and phosphorylated rhodopsin in native disc membranes.
7 cross the cytoplasmic gap between plasma and disc membranes.
8 ed wild-type and Gtgamma-deficient mouse rod disc membranes.
9 hly constrained spaces between outer segment disc membranes.
10 ocalized to photoreceptor outer segment (OS) disc membranes.
11 tin-1 essentially as well as P-Rh* in native disc membranes.
12 hiometry, as previously determined in native disc membranes.
13 g PRCD display disoriented and dysmorphic OS disc membranes.
14 n packing were examined in rod outer segment disc membranes.
15 rhodopsin, the major structural component of disc membranes.
16 ment filled with hundreds of tightly packed "disc" membranes.
17 sin incorporation and packaging density into disc membranes, a process which, when dysregulated, like
18  of labeling abnormal discs and a measure of disc membrane addition.
19  of the high rhodopsin density in the native disc membranes and of a bifunctional cross-linker that p
20 abeled ROS is consistent with fusion between disc membranes and the surrounding plasma membrane.
21 corporation into newly forming outer segment disc membranes and their degradation.
22 iesterase, it is a peripheral protein of the disc membranes, but it binds membranes much more tightly
23   Imaging of rod photoreceptor outer-segment disc membranes by atomic force microscopy and cryo-elect
24     RGS9.Gbeta5 is anchored to photoreceptor disc membranes by the transmembrane protein, R9AP.
25                 The influence of calcium and disc membrane cholesterol content on fusion between ROS
26 re investigated by increasing and decreasing disc membrane cholesterol content using well established
27  also contribute to molecular replacement of disc membrane DHA-phospholipids, particularly phosphatid
28 f INPP5E may interrupt axoneme extension and disc membrane elaboration.
29 ransduction proteins, axonemal structure and disc membranes fail to form.
30 l GPCR, embedded in native rod outer segment disc membranes from photoreceptor cells of the retina in
31 on electron microscopy of negatively stained disc membranes from Rho+/- mice indicated a typical morp
32 eres with the morphogenesis of outer segment disc membrane in photoreceptors.
33 ilibrates phospholipids across photoreceptor disc membranes in mammalian retina, a process required f
34 y, atomic force microscopy reveals that many disc membranes in Prcd-KO rod photoreceptor neurons are
35 n of dissociated G-protein subunits from the disc membranes into the cytoplasm, and a relatively high
36               The diffusion of EGFP-PDE6C on disc membranes investigated with fluorescence recovery a
37         High expression levels of Rho in the disc membranes of rod outer segments and the propensity
38  localization was examined in the plasma and disc membranes of ROS.
39 hotoreceptor cilium formed normally, and the disc membranes of the nascent outer segment remained nor
40 opsin from the inner segments to the nascent disc membranes of the outer segments.
41 mall protein residing in the light-sensitive disc membranes of the photoreceptor outer segment.
42                            No elaboration of disc membrane or outer segment formation was observed at
43 arily conserved domains of the photoreceptor disc membrane protein peripherin/rds by analysis of the
44                Power spectra calculated from disc membrane regions on such electron micrographs displ
45 ed cilium filled with hundreds of flattened "disc" membranes responsible for efficient light capture.
46     Atomic force microscopy of WT and Rho+/- disc membranes revealed, in both cases, Rho organized in
47 sociation of RGS9-Gbeta5L with photoreceptor disc membranes serves not only as a means of targeting i
48 , which is composed of a stack of flattened "disc" membranes surrounded by the plasma membrane.
49 ilium containing approximately 1,000 stacked disc membranes that are densely packed with visual pigme
50 s within internal membrane structures called disc membranes that are found in the rod outer segments
51 outer segment contains a stack of flattened "disc" membranes that are surrounded, or "enclosed," by t
52 ed cilium filled with hundreds of flattened 'disc' membranes that provide vast light-absorbing surfac
53 he localization of ABCR to rod outer segment disc membranes, these data suggest that retinoids, and m
54 ors can be released directly from retina rod disc membranes using infrared irradiation in a mass spec
55 rhodopsin, directly from fragments of native disc membranes using mass spectrometry.
56  meta III formation in Gtgamma-deficient rod disc membranes were identical with those observed in wil