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1  PR1/4 ("red/UV cones") versus PR2/3 ("green/blue cones").
2 and green cones, and prefer ultraviolet over blue cones.
3 toreceptor subtype, the S (short wavelength, blue) cones.
4                       Even though salamander blue cones and green rods share the same visual pigment,
5  result in syndromes characterized by excess blue cones and loss of rods: enhanced S-cone syndrome (E
6 sed in human green/red cones but absent from blue cones and mediated ester hydrolysis for photopigmen
7 a are not detectably affected by ablation of blue cones, and are reduced twofold in mutant larval ret
8 d visual function, involving the minority S (blue) cones, and decreased rod and L/M (red/green) cone
9                                              Blue cones are tuned to capture most remaining variance
10 ods and UV cones, RGB cones (red, green, and blue cones) are structurally similar and unite into mirr
11 ereas DC-A may have arisen from an ancestral blue cone, as suggested by expression of the blue cone T
12 he biocytin wide-field bipolar cell is an ON blue cone bipolar cell in the rabbit retina and is homol
13                 The B1 type is proposed as a blue cone bipolar cell.
14 olar type 6 (DB6; marked with anti-CD15) and blue cone bipolar cells (marked with anti-CCK precursor)
15 n the rabbit retina and is homologous to the blue cone bipolar cells that have been previously descri
16 n those that terminate in stratum 5 (DB6 and blue cone bipolar cells).
17 ive cone terminals contact the dendrites of "blue-cone bipolar" cells instead, showing that they are
18 nd OFF midget bipolar cells as well as (ON) "blue-cone bipolar" cells, we examined 118 contiguous con
19 citatory synaptic outputs from the S-ON (or "blue-cone") bipolar cell to the small bistratified cell
20 een rods share the same visual pigment, only blue cones but not green rods are able to dark-adapt in
21 ust sensitivity recovery in bleached red and blue cones but not in red and green rods, suggesting tha
22 on of the chromophore by opsin in red and in blue cones but not in red rods.
23 despite sharing the same pigment, salamander blue cones, but not green rods, recovered their sensitiv
24 ous fashion; in addition, Crb1 delays UV and blue cones' chromatin condensation caused by UV light ir
25 abundant and branch almost twice as often on blue cones compared to UV cones.
26 ast between color and background, and yellow-blue cone-contrast could account for dichromats' pattern
27 dependent patients had significantly reduced blue cone electroretinogram responses compared with matc
28 pressive system based on ancestral green and blue cones for regulating red/rod and ultraviolet circui
29  in transfected cells, which may explain why blue cone function is lost earlier than red/green-cone f
30 e-withdrawn patients have a dysregulation of blue cone function.
31 d not affect the ability of the red cone and blue cone/green rod pigments to activate transducin.
32                             The red cone and blue cone/green rod pigments were unstable to hydroxylam
33 n the activation pathway of the red cone and blue cone/green rod pigments.
34 a rationale for why mammalian red, green and blue cones have comparable sensitivities, unlike their a
35  areas between the IS of the green, red, and blue cones in differentiated zebrafish retina.
36 cones, green cones are absent, the number of blue cones is approximately doubled, and the number of r
37 omatic resolution acuity under conditions of blue cone isolation (an indirect measure of the underlyi
38                    All cone types, including blue cones, made gap junctions with surrounding rod sphe
39                                              Blue cone monochromacy (BCM) is a rare X-linked retinal
40                                              Blue cone monochromacy (BCM) is an X-linked retinal diso
41                                        Human blue cone monochromacy (BCM) is characterized by functio
42  X-linked cone dysfunction disorders such as Blue Cone Monochromacy and X-linked Cone Dystrophy are c
43  been identified in subjects with congenital blue cone monochromacy or color-vision deficiency.
44  missense mutation presented with congenital blue cone monochromacy, with retinal lamination defects
45 lindness (CSNB), LCA, Stargardt disease, and blue cone monochromacy.
46 enital stationary night blindness, albinism, blue cone monochromatism, and achromatopsia.
47 nital stationary night blindness (CSNB), and blue-cone monochromatism (BCM)-in which nystagmus accomp
48 f spectral opponency where red-, green-, and blue-cone "Off" circuits connect to "natively-On" UV-con
49 acted cones whose outer segments stained for blue cone opsin and avoided cones that did not.
50 I to Meta-II transition are more similar for blue cone opsin and green cone opsin.
51 agglutinin, and then used antibodies against blue cone opsin and red-green cone opsin to identify the
52 llowed by regeneration, were hybridized with blue cone opsin cRNA for quantitative analysis of the bl
53 ominantly rods, accompanied by rhodopsin and blue cone opsin mislocalization from 6 to 12 months of a
54  are comparable between bovine rhodopsin and blue cone opsin, the transition kinetics of earlier phot
55  significant effect on the activity of human blue cone opsin.
56 layer are positive for TULP1, recoverin, and blue cone opsin.
57 gly TULP1-reactive and some are positive for blue cone opsin.
58 rhodopsin, human green cone opsin, and human blue cone opsin.
59 n, cyclic nucleotide-gated cation channel-3, blue-cone opsin, and beta-6-PDE) was evaluated by immuno
60 ic nucleotide-gated cation channel-3 [CNG3], blue-cone opsin, and cGMP phosphodiesterase [PDE]); were
61  that may play roles in the rod pathway, the blue cone pathway, and ganglion cell directional selecti
62  opsin cRNA for quantitative analysis of the blue cone pattern.
63 eurons in the short-wavelength cone (S-cone, blue cone) pedicle and to learn more concerning the uniq
64                                 In contrast, blue cone pedicles were smaller with relatively few shor
65                            Additionally, the blue cone photo-intermediate spectra exhibit a high degr
66 xcess of the minority S (short wavelength or blue) cone photoreceptor type, but near absence of funct
67 tions in the outer segments of red/green and blue cone photoreceptors, B-type horizontal cells, sever
68 onal input from short wavelength-sensitive ("blue") cone photoreceptors.
69 y in the outer segments of red-, green-, and blue-cone photoreceptors.
70 entified 12 amino acid residues in the human blue cone pigment that might induce the required green-t
71 of the opsin shift between rhodopsin and the blue cone pigment.
72 ng shifts the spectral maxima of the red and blue cone pigments, but not that of the red rod pigment.
73 ectral shift between the mouse UV and bovine blue cone pigments.
74  Transgene expression regulated by the human blue cone-promoter persisted at least for 20 months.
75 gins of DC-P and DC-A from ancestral red and blue cones, respectively.
76 iolet cones to generate a 5:1 ultraviolet-to-blue cone synapse ratio.
77                                              Blue cone synaptogenesis increases in mutants lacking ul
78   But, if regeneration is delayed or absent, blue-cone synaptogenesis increases and ectopic synapses
79 lodendria are more numerous (1.3 times) than blue cone telodendria.
80 blue cone, as suggested by expression of the blue cone TFs FOXQ2 and SKOR1.
81 ia extends from each cone pedicle (including blue cones) to contact 40-50 nearby rod spherules at sit
82               Connectivity is unaltered when blue cone transmission is suppressed.
83  or green rods (containing the same opsin as blue cones) treated under the same conditions.
84               Pedicles of neighboring UV and blue cones typically converge into contiguous pairs, des
85 sible for the blue-shifted absorption in the blue cone vision pigment.
86 pectra, and transition kinetics of the human blue cone visual pigment have been recorded at room temp
87 the absolute absorption maximum of the human blue cone visual pigment is presented.
88  wild-type mouse ultraviolet (UV) and bovine blue cone visual pigments have absorption maxima of 358
89 reen cones were coupled indiscriminately but blue cones were rarely connected with other cones.
90                                              Blue cones were retained in higher number than red/green
91 , establishing synapses with ultraviolet and blue cones while eliminating red and green cone contacts