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 lly similar protein modules involved in blue-light sensing.

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

4 paradigm in sensory biology and evolution of light sensing.

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

6 siological processes not directly related to light sensing.

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

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

9 a five-carbon linker (25) showed the highest light-sensing ability after irradiation with visible lig

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

11 evice demonstrates promising sensitivity for light sensing and captures across a broad spectral range

12 Photoreceptors are important for light sensing and downstream gene regulation.

13 in the relative coupling forces between the light sensing and non-sensing populations.

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

15 mperature utilizes diverse components of the light sensing and signal transduction network to trigger

16 Several putative light sensing and signaling proteins were associated wit

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

18 For light sensing and signaling, phytochromes need to associ

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

20 3 isoforms upsilon and mu display defects in light sensing and/or response.

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

22 try, as well as for possible applications in lighting, sensing, and catalysis.

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

24 for the design of metal NCs with high PL for lighting, sensing, and optoelectronic applications.

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

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

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

28 Red light-sensing bacteriophytochromes are attractive target

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

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

31 Light sensing by Arabidopsis thaliana phots is predomina

32 Light sensing by photoreceptors controls phototropism, c

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

34 Light sensing by the phototropins is mediated by a repea

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

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

37 ely active or inactive mutants, showing that light sensing can be decoupled from activation of kinase

38 eved that mammals do not have an extraocular light sensing capacity, recent evidence suggests otherwi

39 Rod and cone photoreceptors are light-sensing cells in the human retina.

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

41 ylcobalamin (or coenzyme B(12)) can act as a light-sensing chromophore heralded a new field of B(12)-

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

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

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

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

46 is a tetraspanin protein concentrated in the light-sensing cilium (called the outer segment) of the v

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

48 raspanin protein abundantly expressed in the light-sensing cilium, the outer segment, of the vertebra

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

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

51 oscopy of the Cry-Tim complex, we show how a light-sensing cryptochrome recognizes its target.

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

53 ols is an allosteric control of proteins via light-sensing domain (LOV2), which allows direct and rob

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

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

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

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

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

59 iconductor photodiode and photomultiplier as light sensing elements.

60 A light-sensing focal plane array (FPA) used in imagers is

61 most animals also use opsins for extraocular light sensing for seasonal behavior and camouflage.

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

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

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

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

66 technology that can be applied to broadband light sensing, highly sensitive fluorescence imaging, ul

67 l changes upon activation of a minimal, blue-light-sensing histidine kinase from Erythrobacter litora

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

69 (OPN5) are both known to mediate extraocular light sensing in mice.

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

71 Light sensing is one of the most important capabilities

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

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

74 Phototropins combine two blue-light-sensing Light-Oxygen-Voltage (LOV) domains (LOV1 a

75 icipate in multiple processes connected with light sensing, light absorption, and pigment binding wit

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

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

78 Cyanobacterial light sensing may have been facilitated by regulators pr

79 r a previously unrecognized cell-autonomous, light-sensing mechanism in brown adipocytes via Opn3-GPC

80 To control endogenous molecules, OTs combine light-sensing modules from natural photoreceptors with s

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

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

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

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

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

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

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

88 The light-sensing organelle of the vertebrate rod photorecep

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

90 Diverse light-sensing organs (i.e., eyes) have evolved across an

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

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

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

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

95 odules including temperature and ultraviolet light sensing particles, pH sensing sheets, oil sensing

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

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

98 Here we describe a light-sensing pathway in which POA neurons that express

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

100 We show that both circadian and light-sensing pathways define the temporal window in whi

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

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

103 Many retinal diseases involve the loss of light-sensing photoreceptor cells (rods and cones) over

104 Phytochromes are red/far-red light sensing photoreceptors employing linear tetrapyrro

105 res a complex interaction of cells, spanning light sensing photoreceptors to neurons that transfer th

106 , where it serves the metabolic needs of the light-sensing photoreceptors in the retina.

107 iological life, with most mammals possessing light-sensing photoreceptors in various organs.

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

109 ngth control in combination with blue and UV light-sensing photoreceptors.

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

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

112 signalling pathway downstream of the far-red light-sensing phytochrome, phyA, that depends on the hig

113 Red and far-red light-sensing phytochromes are widespread in nature, occ

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

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

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

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

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

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

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

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

122 Photoreceptors are a class of light-sensing proteins with critical biological function

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

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

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

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

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

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

129 copy (STORM) to define subdomains within the light-sensing rod sensory cilium of mouse retinas and re

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

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

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

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

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

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

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

137 Blue light sensing using flavin (BLUF) domains constitute a f

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

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

140 ently in several lineages, whereas redox and light sensing via flavin adenine dinucleotide and flavin