ライフサイエンスコーパス: red cone

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1 proximately 0.1 %) of the pigment content in red cones.

2 n--about 10% of total opsin--in dark-adapted red cones.

3 required for the maintenance or function of red cones.

4 hromophore did not affect the ability of the red cone and blue cone/green rod pigments to activate tr

5 The red cone and blue cone/green rod pigments were unstable

6 t important in the activation pathway of the red cone and blue cone/green rod pigments.

7 E65 was selectively expressed in human green/red cones but absent from blue cones and mediated ester

8 f photoresponsiveness of bleached salamander red cones but not of bleached salamander red rods.

9 ased opsin expression in individual rods and red cones, but decreased opsin expression in individual

10 tinal is reversible in darkness in amphibian red cones, but essentially irreversible in red rods.

11 s an approximately 2-fold desensitization in red cones, equivalent to that produced by a steady light

12 Implicit times of the red cone ERGs were slightly faster for the Neuroline ski

13 normally bias their connectivity in favor of red cones fail to precisely recapture this synaptic part

14 lectrode recordings from the hypothalamus of red cone knockin mice (Opn1mwR).

15 us laevis genes, Prph2 (also called RDS) and red cone opsin (RCO) using a polymerase chain reaction-b

16 sion resulted in a decrease in rhodopsin and red cone opsin expression levels in Xenopus retinas.

17 y that Rx is co-expressed with rhodopsin and red cone opsin in maturing photoreceptors and demonstrat

18 When rod and red cone opsin probes were combined, the number of label

19 n of rAAV5-hCNGB3 with a long version of the red cone opsin promoter in younger animals led to a stab

20 nt therapy with different forms of the human red cone opsin promoter led to the restoration of cone f

21 monstrate that Rx binds to the rhodopsin and red cone opsin promoters in vivo.

22 r of photoreceptors expressing rod opsin and red cone opsin, and decreased the number of photorecepto

23 ess this deficit using mice expressing human red cone opsin, in which rod-, cone-, and melanopsin-dep

24 eceptor-specific genes such as rhodopsin and red cone opsin.

25 We also show that the degeneration of red cone photoreceptors in the mutants occurs independen

26 stability of the chromophore within the deep red cone pigment binding sites.

27 Interestingly, the red cone pigment containing the retinal analogue remaine

28 f rhodopsin, the green cone pigment, and the red cone pigment in H2O (D2O) are found at 1656 (1623),

29 s question by expressing human or salamander red cone pigment in Xenopus rods, and human rod pigment

30 However, red cone pigment isomerizes spontaneously 10,000 times m

31 ow overcome this problem by expressing human red cone pigment transgenically in mouse rods in order t

32 However, for the red cone pigment, the 9-methyl group of retinal appears

33 corresponding control cultures regarding the red cone pigment, which was expressed in all cases, and

34 nel catfish orthologues of rhodopsin and the red cone pigment-the full complement of retinal opsins i

35 Raman spectra of recombinant human green and red cone pigments have been obtained to examine the mole

36 f seven cone pigments indicate that the deep red cone pigments select 6- s- trans chromophore conform

37 igate theoretically the hypothesis that deep red cone pigments select a 6- s- trans conformation of t

38 flash cone, light-adapted 3.0 Hz flicker and red cone responses were analysed, as well as their respe

39 flash cone, light-adapted 3.0 Hz flicker and red cone responses were up to four times larger when rec

40 d opsin is the only known molecule unique to red cones, these data suggest that a novel gene is requi

41 e of transgenic cone pigment to native human red cones, we obtained a dark rate of approximately 10 f

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