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1 s and ectopic synapses are made with red and green cones.
2 onselective connections with neighboring red/green cones.
3 tely from a coarse-grained mosaic of red and green cones.
4 rbonic anhydrase histochemistry to label red-green cones.
5 en alongside equal sign inputs from blue and green cones.
6  in inputs drawn nonselectively from red and green cones and (ii) tissue mosaicism due to X chromosom
7 ss of blue and UV cones, followed by red and green cones and finally the rod cells.
8 orizontal cells (HCs) normally avoid red and green cones, and prefer ultraviolet over blue cones.
9 rmed into hybrid red/ultraviolet (UV) cones, green cones are absent, the number of blue cones is appr
10 of macaque monkeys, that neighboring red and green cones are homologously and heterologously coupled
11 s, our results show that signals in blue and green cones are processed separately in the photorecepto
12 y are dichromats who possess ultraviolet and green cones, but not red cones.
13 let and blue cones while eliminating red and green cone contacts.
14                The reduction in rods and red/green cones correlated with defects in photoreceptor sub
15 We find that the synaptic outputs of red and green cones efficiently rotate the encoding of natural d
16 ones were retained in higher number than red/green cones for the first 3 months of the degeneration.
17 (blue) cones, and decreased rod and L/M (red/green) cone function.
18  blue cone function is lost earlier than red/green-cone function in patients with LCA.
19 ical for the formation of functional red and green cones in the retina.
20 S, blue) and middle wavelength-sensitive (M, green) cones is sampled by approximately ten bipolar cel
21                                     Each red/green cone made nonselective connections with neighborin
22 tions indicate that coupling between red and green cones may cause a modest decrease in human color d
23 ults from the combined activation of red and green cone mechanisms.
24 eate a UV-triggered non-visual response in a green cone monochromat.
25 e structure of active-state, wild-type human green cone opsin (GCO(WT)) stabilized with a mini-G prot
26 ructural modeling suggesting that Pro-205 in green cone opsin could prevent entry and binding of 11-c
27 inct, this would indicate that this rod-like green cone opsin gene, although absent in mammals, is co
28 phylogenetic clade with the rod and rod-like green cone opsin genes from other vertebrate species.
29  expressed at levels approaching that of red/green cone opsin in the macula.
30                                          Red/green cone opsin missense mutations N94K, W177R, P307L,
31 ly, deletion of 16 N-terminal amino acids in green cone opsin partially restored the binding of 11-ci
32 nes before they are reactive for blue or red/green cone opsin suggests an important role for TULP1 in
33 d antibodies against blue cone opsin and red-green cone opsin to identify the individual cone types.
34    However, this substitution did not enable green cone opsin to regenerate with 11-cis-6mr-retinal.
35 ges in the intracellular distribution of red/green cone opsin were observed as early as P80.
36 way determines the regeneration of mammalian green cone opsin with chromophore analogues such as 11-c
37 eaching sequences of bovine rhodopsin, human green cone opsin, and human blue cone opsin.
38 sly observed with bovine rhodopsin and human green cone opsin, on the picosecond to millisecond times
39  action spectra conformed to the spectrum of green cone opsin, with a main sensitivity peak at 510 nm
40 tive for TULP1 and many are reactive for red/green cone opsin.
41 ion are more similar for blue cone opsin and green cone opsin.
42              Only one opsin, of type RH2 (a "green" cone opsin), was expressed in premetamorphic (dev
43 W, red) and medium-wavelength-sensitive (MW, green) cone opsin genes that segregated with disease.
44 sn(2) and Asn(15), whereas human (h) red and green cone opsins (hOPSR and hOPSG, respectively) are N-
45           The genes for the rod and rod-like green cone opsins in two avian species, the budgerigar,
46 pared the regenerative properties of rod and green cone opsins with 11-cis-6mr-retinal and demonstrat
47 sylation is a fundamental feature of red and green cone opsins, which may be relevant to their functi
48 s post-translational modification of red and green cone opsins.
49 chromatic ground-squirrel retina, that green-green cone pairs are routinely coupled with an average c
50 nal conductance between green-green and blue-green cone pairs in slices from the dichromatic ground-s
51 pS, whereas coupling is undetectable in blue-green cone pairs.
52 urrent recordings were obtained from red and green cone photoreceptors in isolated retina from macaqu
53 chromosome to create the present-day red and green cone pigment genes.
54 ion, with concomitant decreases in levels of green cone pigment mRNA.
55 o4D2, which recognizes chicken rhodopsin and green cone pigment, and by reverse transcription-polymer
56 =NH stretching frequencies of rhodopsin, the green cone pigment, and the red cone pigment in H2O (D2O
57 nalogue could regenerate rod pigment but not green cone pigment.
58 significant increases in mRNA levels for the green cone pigment.
59 61W cells expressed SV40 T antigen, blue and green cone pigments, transducin, and cone arrestin.
60 pling blurs the differences between red- and green-cone signals.
61 and the appearance of supernumerary rods and green cones, suggestive of direct transfating.
62 ing degrees of L (long, red)- and M (middle, green)-cone vision, and retinal degeneration.
63 kinetics of the intermediate states of human green-cone visual pigment (mid-wavelength sensitive, or
64                                          Red/green cones were coupled indiscriminately but blue cones
65  including decreased numbers of rods and red/green cones, whereas blue and UV cones were relatively u
66 ture most remaining variance when opposed to green cones, while UV cone present a UV achromatic axis
67 timulate specifically the differentiation of green cones, without the previously suggested effects on