ライフサイエンスコーパス: disc membrane

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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 tin-1 essentially as well as P-Rh* in native disc membranes.

4 hiometry, as previously determined in native disc membranes.

5 affect rhodopsin's activity or transport to disc membranes.

6 n packing were examined in rod outer segment disc membranes.

7 aptured by opsins in continually synthesized disc membranes.

8 tin-1 and phosphorylated rhodopsin in native disc membranes.

9 cross the cytoplasmic gap between plasma and disc membranes.

10 ed wild-type and Gtgamma-deficient mouse rod disc membranes.

11 hly constrained spaces between outer segment disc membranes.

12 ment filled with hundreds of tightly packed "disc" membranes.

13 of labeling abnormal discs and a measure of disc membrane addition.

14 abeled ROS is consistent with fusion between disc membranes and the surrounding plasma membrane.

15 corporation into newly forming outer segment disc membranes and their degradation.

16 iesterase, it is a peripheral protein of the disc membranes, but it binds membranes much more tightly

17 RGS9.Gbeta5 is anchored to photoreceptor disc membranes by the transmembrane protein, R9AP.

18 The influence of calcium and disc membrane cholesterol content on fusion between ROS

19 re investigated by increasing and decreasing disc membrane cholesterol content using well established

20 also contribute to molecular replacement of disc membrane DHA-phospholipids, particularly phosphatid

21 on electron microscopy of negatively stained disc membranes from Rho+/- mice indicated a typical morp

22 eres with the morphogenesis of outer segment disc membrane in photoreceptors.

23 ilibrates phospholipids across photoreceptor disc membranes in mammalian retina, a process required f

24 n of dissociated G-protein subunits from the disc membranes into the cytoplasm, and a relatively high

25 The diffusion of EGFP-PDE6C on disc membranes investigated with fluorescence recovery a

26 High expression levels of Rho in the disc membranes of rod outer segments and the propensity

27 localization was examined in the plasma and disc membranes of ROS.

28 hotoreceptor cilium formed normally, and the disc membranes of the nascent outer segment remained nor

29 opsin from the inner segments to the nascent disc membranes of the outer segments.

30 No elaboration of disc membrane or outer segment formation was observed at

31 arily conserved domains of the photoreceptor disc membrane protein peripherin/rds by analysis of the

32 Power spectra calculated from disc membrane regions on such electron micrographs displ

33 Atomic force microscopy of WT and Rho+/- disc membranes revealed, in both cases, Rho organized in

34 sociation of RGS9-Gbeta5L with photoreceptor disc membranes serves not only as a means of targeting i

35 ilium containing approximately 1,000 stacked disc membranes that are densely packed with visual pigme

36 s within internal membrane structures called disc membranes that are found in the rod outer segments

37 he localization of ABCR to rod outer segment disc membranes, these data suggest that retinoids, and m

38 meta III formation in Gtgamma-deficient rod disc membranes were identical with those observed in wil

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