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1 d by an L-type Ca2+ conductance (gCa) in the photoreceptor inner segment.
2 ve stress and mtDNA damage, primarily in the photoreceptor inner segments.
3 cells, outer and inner plexiform layers, and photoreceptor inner segments.
4 nd the site of increase was localized to the photoreceptor inner segments.
5 ted, and oxidative stress was noted in their photoreceptor inner segments.
6 d to the outer plexiform layer as well as to photoreceptor inner segments.
7 ITRL was expressed constitutively on RPE and photoreceptor inner segments.
8 constitutively on RPE and in high levels on photoreceptor inner segments.
9 re labeled, as are retinal cells, especially photoreceptor inner segments.
10 duced in the superior central retina, within photoreceptor inner segments, 24 hours after light treat
12 maller-sized isoform of Hmgb1 was present in photoreceptor inner segments and bound to a membrane fra
14 omote the formation of apical cell features: photoreceptor inner segments and cilia in renal and audi
15 11 disruption affects retinoid metabolism in photoreceptor inner segments and delays the kinetics of
16 b2a and crb2b genes at the cell membranes of photoreceptor inner segments and Muller cell apical proc
17 S, and alphaA crystallin localization in the photoreceptor inner segments and outer plexiform layer i
19 Here we show that RDH12 localizes to the photoreceptor inner segments and that deletion of this g
20 u hybridization, cGK I mRNA was localized to photoreceptor inner segments and the ganglion cell and i
21 In the retina, MrdgB protein is localized to photoreceptor inner segments and the outer and inner ple
22 emical analysis showed DRAM2 localization to photoreceptor inner segments and to the apical surface o
24 nels, PMCAs and mitochondrial Ca2+ stores in photoreceptor inner segments, and suggest a role for CIC
26 t rhodopsin-C185R protein accumulated in the photoreceptor inner segments, cellular bodies, or both.
28 ranslocation of free [3H]DHA from ROS to the photoreceptor inner segment contributed to an additional
31 in binding studies revealed a mosaic of cone photoreceptor inner segments indistinguishable from that
33 homo- and hetero-tetramers with Rom-1 in the photoreceptor inner segment (IS), while higher-order, di
34 nner (IPL) and outer plexiform (OPL) layers, photoreceptor inner segments (IS), and retinal pigment e
35 se mutations cause retention of ABCA4 in the photoreceptor inner segment, likely by impairing correct
38 those without (P < .001), regardless of the photoreceptor inner segment/outer segment (IS/OS) condit
40 masked observers evaluated the integrity of photoreceptor inner segment/outer segment (IS/OS) juncti
43 atively normal SD OCT results with preserved photoreceptor inner segment/outer segment junction, wher
46 on and membrane adhesion, in maintaining the photoreceptor inner segment stability and architecture.
47 gh level of constitutive GITRL expression on photoreceptor inner segments suggests that photoreceptor
48 s upregulation is localized primarily in the photoreceptor inner segments, the site of mitochondrial
49 ogs demonstrated GFP immunoreactivity in rod photoreceptor inner segments throughout the retina, indi
50 H12 plays a unique, nonredundant role in the photoreceptor inner segments to regulate the flow of ret
51 d proteins were localized exclusively in the photoreceptor inner segments, which are known to be dens
52 outer leaflet of the plasma membrane of the photoreceptor inner segments, which synthesize and secre
53 of opsin, arrestin, and membranes within the photoreceptor inner segment, while the localization of a
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