ライフサイエンスコーパス: light sense

1 yeless fish, excluding a role for nonretinal light senses.

2 siological processes not directly related to light sensing.

3 etinal, flavins, or linear tetrapyrroles for light sensing.

4 -1) and its partner WC-2 are central to blue-light sensing.

5 lly similar protein modules involved in blue-light sensing.

6 a significant role in the modulation of blue light sensing.

7 s of the Acinetobacter genus, was named blue-light-sensing A (blsA).

8 We report 'broadband light-sensing' all-polymer phototransistors with the nan

9 the well-established mechanisms that govern light sensing and photoperiodic flowering control.

10 Several putative light sensing and signaling proteins were associated wit

11 rotein bound chromophore is the basis of the light sensing and signaling responses of many photorecep

12 For light sensing and signaling, phytochromes need to associ

13 h the expansion of gene networks involved in light sensing and signaling.

14 3 isoforms upsilon and mu display defects in light sensing and/or response.

15 ts, as well as bi-functional devices such as light-sensing and light-emitting transistors, are discus

16 ons including energy conversion, solid-state lighting, sensing, and information technology are underg

17 ideal component for various medium-intensity light sensing applications requiring spectrally tailored

18 of BphPs with potentially opposing roles in light sensing are present.

19 First, we identified a light-sensing B12-binding transcriptional regulator and

20 arther through seawater than the red/far-red light sensed by land plant phytochromes.

21 Blue/green light sensing by a well-studied subfamily of CBCRs proce

22 Light sensing by Arabidopsis thaliana phots is predomina

23 Light sensing by photoreceptors controls phototropism, c

24 ed for essential cellular activities and for light sensing by phytochromes.

25 Light sensing by the phototropins is mediated by a repea

26 Background adaptation is known to involve light sensing by the retina and subsequent regulation of

27 results presented in this work suggest that light, sensed by R-LOV-HK, is an important environmental

28 Homologous high-resolution structures of the light-sensing chromophore binding domain (CBD) and the c

29 es this isomer particularly effective as the light-sensing chromophore in all visual pigments.

30 e natural selection of 11-cis-retinal as the light-sensing chromophore in visual pigments.

31 in B12 derivative, adenosylcobalamin, as the light-sensing chromophore to mediate light-dependent gen

32 ism regulating polarized protein delivery in light-sensing cilia, raising the possibility that Numb p

33 r segment (OS) of the rod photoreceptor is a light-sensing cilium containing ~1,000 membrane-bound di

34 These data represent the first known light-sensing circuit in the vertebrate hindbrain.

35 ed a comprehensive proteomic analysis on the light-sensing compartment of photoreceptors called the o

36 The UV-A/blue light sensing cryptochromes and the red/far-red sensing

37 cates that LOV2 functions as the predominant light-sensing domain for phot1.

38 tropins, a group of kinases that contain two light-sensing domains (LOV, light-oxygen-voltage domains

39 Rs, and many family members contain multiple light-sensing domains.

40 ing (p-type) polymer and near infrared (NIR) light-sensing electron-accepting (n-type) polymer.

41 heterojunction (BHJ) layers of visible (VIS) light-sensing electron-donating (p-type) polymer and nea

42 iconductor photodiode and photomultiplier as light sensing elements.

43 Our findings reveal a light-sensing function for mammalian OPN5, until now an

44 ive activity of rhodopsin, distinct from its light-sensing function.

45 evolved in vertebrates to subserve nonvisual light-sensing functions, such as the pupillary reflex an

46 en associated with mutations in rhodopsin, a light-sensing G protein-coupled receptor and phospholipi

47 d for genetic dissection of the mechanism of light sensing in eubacteria.

48 To explore the potential for light sensing in this phototroph, we measured its global

49 Light sensing is one of the most important capabilities

50 We show that directional light sensing is possible because Synechocystis cells ac

51 Phytochromes are a major family of red-light-sensing kinases that control diverse cellular func

52 otoreceptors, preferentially confined to the light-sensing lobe.

53 Phytochromes are light-sensing macromolecules that are part of a two comp

54 Cyanobacterial light sensing may have been facilitated by regulators pr

55 Rhodopsin, the light-sensing molecule in the outer segments of rod phot

56 complex array of potential neurohormones and light-sensing molecules.

57 s), we have identified and characterized the light-sensing mutant elm1 (elongated mesocotyl1).

58 a role for phytochrome C as part of the red light sensing network that modulates phytochrome B signa

59 he otolith, the pigmented sister cell of the light-sensing ocellus.

60 alyzed gene expression patterns in the major light-sensing organ (cotyledons) and in rapidly elongati

61 essing, and occurs in the outer segment, the light-sensing organelle of the photoreceptor cell.

62 The light-sensing organelle of the vertebrate rod photorecep

63 uction signaling proteins into a specialized light-sensing organelle, the rhabdomere, is required for

64 animals living in dark environments without light-sensing organs may not be presumed to be light ins

65 different rhodopsins (RH) are present in the light-sensing organs.

66 ehavior is commonly observed in animals with light-sensing organs.

67 a thin bridge linking the cell body and the light-sensing outer segment.

68 e consistent with the persistence of a novel light sensing pathway in the TKO retina that originates

69 vations indicate that there is an additional light-sensing pathway in fly pacemaker neurons.

70 mportant for proper phasing, whereas the two light-sensing pathways can mediate efficient adjustments

71 hat might modulate core circadian rhythms or light-sensing pathways.

72 ng and molecular inhibition experiments with light-sensing phenotype studies to examine the signaling

73 A striking example is observed in light-sensing photoreceptors, in which the apical sensor

74 The proteins are structurally divided into a light-sensing photosensory module consisting of PAS, GAF

75 The UV-A/blue light sensing phototropins mediate several light respons

76 photoreceptors, among which the red/far-red light-sensing phytochromes have been extensively studied

77 diation with 670 nm light, the inactive, red light sensing Pr form is converted to the active Pfr for

78 e molecular templates for the development of light-sensing probes.

79 the protein and chromophore components of a light-sensing protein interact to create a light cycle,

80 d glycosylation-interfering mutations in the light-sensing protein rhodopsin.

81 n its natural habitat, the majority of known light-sensing proteins are absent from its genome.

82 cadian rhythms in higher organisms relies on light-sensing proteins that communicate to cellular osci

83 ain proteins are an important family of blue light-sensing proteins which control a wide variety of f

84 with formation of a similar species in other light-sensing proteins.

85 Here we show that the green-light sensing receptor rhodopsin 6 (Rh6) acts to exclude

86 Bacteriophytochromes (BphPs) are light-sensing regulatory proteins encoded by photosynthe

87 pleiotropic defects in growth, conidiation, light sensing, responses to stresses and plant infection

88 their terminal differentiation by expressing light-sensing Rhodopsin (Rh) proteins.

89 R8 photoreceptors express one of two light-sensing Rhodopsins, Rh5 or Rh6.

90 hromes perform critical light-harvesting and light-sensing roles in oxygenic photosynthetic organisms

91 a designed chimeric protein that connects a light-sensing signaling domain from a plant member of th

92 and the morphogenesis of the rhabdomere, the light sensing structure of the cell.

93 use cGMP as an internal messenger and their light-sensing structure is also of ciliary origin.

94 sion of a key structural gene in a primitive light-sensing system.

95 BlaC contains a BLUF domain involved in blue-light sensing using FAD and a nucleotidyl cyclase domain

96 photoexcitation of a photosensing BLUF (blue light sensing using FAD) domain protein have been invest

97 his study, we demonstrate that the PixD blue light-sensing using FAD (BLUF) photoreceptor that govern

98 kDa protein that contains an N-terminal blue-light-sensing-using flavin (BLUF) domain and lacks a det