ライフサイエンスコーパス: photoreceptor inner segment

1 d by an L-type Ca2+ conductance (gCa) in the photoreceptor inner segment.

2 ge-gated potassium channels localized to the photoreceptor inner segment.

3 sylated protein which is mislocalized to the photoreceptor inner segment.

4 ve stress and mtDNA damage, primarily in the photoreceptor inner segments.

5 cells, outer and inner plexiform layers, and photoreceptor inner segments.

6 nd the site of increase was localized to the photoreceptor inner segments.

7 d to the outer plexiform layer as well as to photoreceptor inner segments.

8 ITRL was expressed constitutively on RPE and photoreceptor inner segments.

9 constitutively on RPE and in high levels on photoreceptor inner segments.

10 ted, and oxidative stress was noted in their photoreceptor inner segments.

11 re labeled, as are retinal cells, especially photoreceptor inner segments.

12 duced in the superior central retina, within photoreceptor inner segments, 24 hours after light treat

13 s localized to actin filament bundles of the photoreceptor inner segment and calycal processes.

14 maller-sized isoform of Hmgb1 was present in photoreceptor inner segments and bound to a membrane fra

15 In the photoreceptor inner segments and cells expressing enhanc

16 omote the formation of apical cell features: photoreceptor inner segments and cilia in renal and audi

17 11 disruption affects retinoid metabolism in photoreceptor inner segments and delays the kinetics of

18 b2a and crb2b genes at the cell membranes of photoreceptor inner segments and Muller cell apical proc

19 S, and alphaA crystallin localization in the photoreceptor inner segments and outer plexiform layer i

20 X-gal staining was restricted to photoreceptor inner segments and synaptic termini.

21 Here we show that RDH12 localizes to the photoreceptor inner segments and that deletion of this g

22 u hybridization, cGK I mRNA was localized to photoreceptor inner segments and the ganglion cell and i

23 In the retina, MrdgB protein is localized to photoreceptor inner segments and the outer and inner ple

24 emical analysis showed DRAM2 localization to photoreceptor inner segments and to the apical surface o

25 nuclear layer, inner/outer plexiform layers, photoreceptor inner segments, and RPE.

26 nels, PMCAs and mitochondrial Ca2+ stores in photoreceptor inner segments, and suggest a role for CIC

27 th significant amounts in ganglion cells and photoreceptor inner segments as well.

28 t rhodopsin-C185R protein accumulated in the photoreceptor inner segments, cellular bodies, or both.

29 Photoreceptor inner segments contain LGN, which can bind

30 ranslocation of free [3H]DHA from ROS to the photoreceptor inner segment contributed to an additional

31 duction in intrinsic signal amplitude at the photoreceptor inner segment ellipsoid (ISe).

32 Photoreceptor inner segments have a high O(2) demand (QO

33 Photoreceptor inner segments have the highest concentrat

34 tae are located towards the periphery of the photoreceptor inner-segment in rods, whilst they are fou

35 in binding studies revealed a mosaic of cone photoreceptor inner segments indistinguishable from that

36 However, RDH12 function in the photoreceptor inner segments is also key, because loss o

37 ive optics scanning laser ophthalmoscopy and photoreceptor inner segment (IS), outer segment (OS), an

38 homo- and hetero-tetramers with Rom-1 in the photoreceptor inner segment (IS), while higher-order, di

39 nner (IPL) and outer plexiform (OPL) layers, photoreceptor inner segments (IS), and retinal pigment e

40 localizes to the plasma membrane (PM) of rod photoreceptor inner segments (ISs), and causes autosomal

41 eated with pegcetacoplan exhibited a thicker photoreceptor inner segment layer along the 5.16 degrees

42 se mutations cause retention of ABCA4 in the photoreceptor inner segment, likely by impairing correct

43 Photoreceptor inner segment morphology was markedly affe

44 We demonstrate that disruption of photoreceptor inner segment-outer segment (ellipsoid) la

45 those without (P < .001), regardless of the photoreceptor inner segment/outer segment (IS/OS) condit

46 masked observers evaluated the integrity of photoreceptor inner segment/outer segment (IS/OS) juncti

47 The OCT data showed a loss of the photoreceptor inner segment/outer segment (IS/OS) juncti

48 Generalized loss of the photoreceptor inner segment/outer segment junction was s

49 Evaluation of the photoreceptor inner segment/outer segment junction, usin

50 atively normal SD OCT results with preserved photoreceptor inner segment/outer segment junction, wher

51 difference was most apparent for the foveal photoreceptor inner segment (p=0.001).

52 Photoreceptor inner segments produce the highest of thes

53 lium (RPE) layer (mean 47, range 20-76 ppm), photoreceptor inner segments (RIS) ellipsoid zone, outer

54 on and membrane adhesion, in maintaining the photoreceptor inner segment stability and architecture.

55 gh level of constitutive GITRL expression on photoreceptor inner segments suggests that photoreceptor

56 s upregulation is localized primarily in the photoreceptor inner segments, the site of mitochondrial

57 ogs demonstrated GFP immunoreactivity in rod photoreceptor inner segments throughout the retina, indi

58 H12 plays a unique, nonredundant role in the photoreceptor inner segments to regulate the flow of ret

59 hannels are highly expressed in rod and cone photoreceptor inner segments, where they shape the light

60 (+) retinas was mostly restricted to the rod photoreceptor inner segments, whereas GCAP1 immunofluore

61 d proteins were localized exclusively in the photoreceptor inner segments, which are known to be dens

62 outer leaflet of the plasma membrane of the photoreceptor inner segments, which synthesize and secre

63 of opsin, arrestin, and membranes within the photoreceptor inner segment, while the localization of a

64 l improvement was in the segmentation of the photoreceptor inner segment, with Dice coefficient incre