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1 onselective connections with neighboring red/green cones.
2 tely from a coarse-grained mosaic of red and green cones.
3 rbonic anhydrase histochemistry to label red-green cones.
4 s and ectopic synapses are made with red and green cones.
5 in inputs drawn nonselectively from red and green cones and (ii) tissue mosaicism due to X chromosom
7 of macaque monkeys, that neighboring red and green cones are homologously and heterologously coupled
8 s, our results show that signals in blue and green cones are processed separately in the photorecepto
10 ones were retained in higher number than red/green cones for the first 3 months of the degeneration.
14 S, blue) and middle wavelength-sensitive (M, green) cones is sampled by approximately ten bipolar cel
16 tions indicate that coupling between red and green cones may cause a modest decrease in human color d
19 ructural modeling suggesting that Pro-205 in green cone opsin could prevent entry and binding of 11-c
20 inct, this would indicate that this rod-like green cone opsin gene, although absent in mammals, is co
21 phylogenetic clade with the rod and rod-like green cone opsin genes from other vertebrate species.
23 ly, deletion of 16 N-terminal amino acids in green cone opsin partially restored the binding of 11-ci
24 nes before they are reactive for blue or red/green cone opsin suggests an important role for TULP1 in
25 d antibodies against blue cone opsin and red-green cone opsin to identify the individual cone types.
26 However, this substitution did not enable green cone opsin to regenerate with 11-cis-6mr-retinal.
28 way determines the regeneration of mammalian green cone opsin with chromophore analogues such as 11-c
29 action spectra conformed to the spectrum of green cone opsin, with a main sensitivity peak at 510 nm
32 W, red) and medium-wavelength-sensitive (MW, green) cone opsin genes that segregated with disease.
34 pared the regenerative properties of rod and green cone opsins with 11-cis-6mr-retinal and demonstrat
35 chromatic ground-squirrel retina, that green-green cone pairs are routinely coupled with an average c
36 nal conductance between green-green and blue-green cone pairs in slices from the dichromatic ground-s
38 urrent recordings were obtained from red and green cone photoreceptors in isolated retina from macaqu
41 o4D2, which recognizes chicken rhodopsin and green cone pigment, and by reverse transcription-polymer
42 =NH stretching frequencies of rhodopsin, the green cone pigment, and the red cone pigment in H2O (D2O
49 timulate specifically the differentiation of green cones, without the previously suggested effects on
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