ライフサイエンスコーパス: vertebrate photoreceptor

1 ially generate pathogenic effects within the vertebrate photoreceptor.

2 eaches in a manner almost identical to other vertebrate photoreceptors.

3 actions for the formation and maintenance of vertebrate photoreceptors.

4 nonmotile cilia or for sensory cilia such as vertebrate photoreceptors.

5 tivation of the phototransduction cascade in vertebrate photoreceptors.

6 gment extension and IFT protein recycling in vertebrate photoreceptors.

7 all-trans configuration in both rod and cone vertebrate photoreceptors.

8 only recognized phototransduction pathway in vertebrate photoreceptors.

9 entration ([Ca2+]i) in the inner segments of vertebrate photoreceptors.

10 by glutamate, the likely neurotransmitter of vertebrate photoreceptors.

11 in mediates a local function at this site in vertebrate photoreceptors.

12 lerating the GTP hydrolysis of G alpha(t) in vertebrate photoreceptors.

13 TPase accelerating protein for G(alpha t) in vertebrate photoreceptors.

14 otal role in the terminal differentiation of vertebrate photoreceptors.

15 visual perception and the dark adaptation of vertebrate photoreceptors after bright light exposure re

16 nvelope component of the syne gene family in vertebrate photoreceptors also result in the misposition

17 red for rapid recovery of light responses in vertebrate photoreceptors and the only mammalian RGS pro

18 Vertebrate photoreceptors are among the most metabolical

19 The light-detecting outer segments of vertebrate photoreceptors are cilia.

20 Cyclic nucleotide-gated (CNG) channels in vertebrate photoreceptors are crucial for transducing li

21 The cyclic GMP-gated cationic channels of vertebrate photoreceptors are essential for visual photo

22 is currently thought that visual pigments in vertebrate photoreceptors are regenerated exclusively th

23 Vertebrate photoreceptors are thought to adapt to light

24 In the retina of warm-blooded vertebrates, photoreceptors are specified many days befo

25 nsible for regulating visual transduction in vertebrate photoreceptors) are structurally similar but

26 nels shapes the light response properties of vertebrate photoreceptors, but the regulation of rod cou

27 lating the duration of the light response in vertebrate photoreceptors by activating the GTPase activ

28 in the termination of the light response in vertebrate photoreceptors by binding selectively to ligh

29 fied by the cilia-based outer segment of the vertebrate photoreceptor cell and the microvilli-based r

30 The vertebrate photoreceptor cell contains an elaborate cili

31 The outer segment of a vertebrate photoreceptor cell represents the most elabor

32 Vertebrate photoreceptor cells are the basic sensory app

33 Vertebrate photoreceptor cells can signal the absorption

34 inactivation of the G-protein transducin in vertebrate photoreceptor cells during their recovery fro

35 esterase (PDE) is the key effector enzyme of vertebrate photoreceptor cells that regulates the level

36 In vertebrate photoreceptor cells, rapid recovery from ligh

37 In vertebrate photoreceptor cells, transducin mediates sign

38 eric G-protein mediating visual signaling in vertebrate photoreceptor cells.

39 aspects of transport in specialized cilia of vertebrate photoreceptor cells.

40 e effector enzyme, cGMP phosphodiesterase in vertebrate photoreceptor cells.

41 Cyclic AMP regulates melatonin synthesis in vertebrate photoreceptor cells.

42 enzyme in the visual transduction cascade of vertebrate photoreceptor cells.

43 f cGMP on transduction of a visual signal in vertebrate photoreceptor cells.

44 r enzyme that regulates the level of cGMP in vertebrate photoreceptor cells.

45 gnaling and transcription factors that drive vertebrate photoreceptor development and discuss how the

46 we report that functionally active RGS9 from vertebrate photoreceptors exists as a tight complex with

47 de-gated (CNG) channels in outer segments of vertebrate photoreceptors generate electrical signals in

48 in protein, Otx2, is a critical regulator of vertebrate photoreceptor genesis.

49 Vertebrate photoreceptors have a modified cilium compose

50 In vertebrate photoreceptors IFT is required for the early

51 ions corresponding to levels in dark-adapted vertebrate photoreceptors inhibit the ability of GCAPs t

52 Vertebrate photoreceptors initiate vision via a G-protei

53 Light adaptation in vertebrate photoreceptors is commonly attributed to a fe

54 Phototransduction machinery in vertebrate photoreceptors is contained within the membra

55 However, light activation of vertebrate photoreceptors leads to activation of a cGMP-

56 rtant recent advance in the understanding of vertebrate photoreceptor light adaptation has come from

57 In vertebrate photoreceptors, light activates a signaling c

58 Vertebrate photoreceptor neurons have a high demand for

59 traspanin protein family required for normal vertebrate photoreceptor outer segment (OS) architecture

60 ripherin-2/rds is required for biogenesis of vertebrate photoreceptor outer segment organelles.

61 In vertebrate photoreceptor outer segments, numerous reacti

62 In vertebrate photoreceptors, photoexcited rhodopsin intera

63 However, the role of retrograde IFT in vertebrate photoreceptors remains unclear.

64 Darkness serves as a stimulus for vertebrate photoreceptors; they are actively depolarized

65 Calcium enters the outer segment of a vertebrate photoreceptor through a cGMP-gated channel an

66 control the recovery of the photoresponse in vertebrate photoreceptors, through their molecular inter

67 this circuit resembles information flow from vertebrate photoreceptors to 'OFF' bipolar and 'ON' bipo

68 These data indicate that all vertebrate photoreceptors use the evolutionary conserved

69 oreceptor guanylate cyclase (GC) in bleached vertebrate photoreceptors when [Ca2+]free decreases but