ライフサイエンスコーパス: sensory function

1 Adaptation is a hallmark of sensory function.

2 he above processes in addition to a specific sensory function.

3 word recognition to compensate for decreased sensory function.

4 two identical odor maps would contribute to sensory function.

5 ssed as noise and thought to play no role in sensory function.

6 nsive lesions, fully regenerates to maintain sensory function.

7 nization and provide systems for analysis of sensory function.

8 xamine how morphological form contributes to sensory function.

9 alized environment that enables and sustains sensory function.

10 ach cortical layer serves a distinct role in sensory function.

11 tis elegans aristaless orthologue, in amphid sensory function.

12 nucleotide ATP has long been associated with sensory function.

13 in newborns can cause deficits in motor and sensory function.

14 ation led to near-normal recovery of thermal sensory function.

15 rative failure leads to a persistent loss of sensory function.

16 strabismic patients with variable binocular sensory function.

17 his sensory accessory membrane in vestibular sensory function.

18 regeneration and poor recovery of motor and sensory function.

19 hages, neuronal apoptosis, and impairment of sensory function.

20 regeneration and poor recovery of motor and sensory function.

21 circuitry, yet least understood in terms of sensory function.

22 nchops birds [8] and were likely involved in sensory function.

23 st 10 segments below the injury to influence sensory function.

24 the whisker to barrel map and for efficient sensory function.

25 ptic dynamics in the mouse barrel cortex and sensory function.

26 cterized by progressive loss of motor and/or sensory function.

27 sily damaged, resulting in loss of motor and sensory function.

28 s characterized by impaired distal motor and sensory function.

29 regenerate auditory hair cells that restore sensory function.

30 to our knowledge, a new perspective on their sensory functions.

31 otile organelles implicated in signaling and sensory functions.

32 xpression of transcripts related to specific sensory functions.

33 epithelia suggest that primary cilia possess sensory functions.

34 ed organelles that have diverse motility and sensory functions.

35 immune responses while protecting olfactory sensory functions.

36 ant changes in vocalization, locomotion, and sensory functions.

37 tic lineages and have essential motility and sensory functions.

38 variety of affective, cognitive, motor, and sensory functions.

39 e normal with respect to other cognitive and sensory functions.

40 tive cells and mediate important defense and sensory functions.

41 ry movement might tune and calibrate ciliary sensory functions.

42 conferred benefits apply to a wide range of sensory functions.

43 y distinct components, which serve different sensory functions.

44 nd consequently compromise the corresponding sensory functions.

45 lla are ancient organelles with motility and sensory functions.

46 cidate further roles of primary cilia beyond sensory functions.

47 tes, both nonmotile and motile cilia possess sensory functions.

48 ptivity; most of these mutations also impair sensory functioning.

49 during development and precede the onset of sensory functions [4, 5].

50 amined whether physical exercise can improve sensory function after experimental SCI by promoting neu

51 NgR may be a potential therapy for restoring sensory function after injuries to sensory roots.

52 Recovery of motor and sensory function after peripheral nerve injury is subopt

53 represent a promising therapy for restoring sensory function after spinal cord injury.

54 s one of the approaches to restore motor and sensory functions after an injury to the peripheral nerv

55 l growth and new insights on the recovery of sensory functions after root injury and repair.

56 Despite adequate motor and sensory functions, all failed to develop language (or lo

57 bnormal layout of cortical areas may disrupt sensory function and behavior.

58 e important for maintaining better binocular sensory function and better interocular alignment at lat

59 es in monkeys for defining hidden aspects of sensory function and for investigating the neuronal proc

60 L1-deficient mice had reduced sensory function and loss of unmyelinated axons, while s

61 They contribute to sensory function and nociception in the peripheral nervo

62 of ligating and cutting one tibial nerve on sensory function and on density of innervation in hind p

63 illuminate the logic supporting an important sensory function and provides a conceptually new algorit

64 has important implications for understanding sensory function and signaling mediated by carotenoid pi

65 Here we describe the effects of eliminating sensory function and structure on the development of the

66 ith the polar clusters being associated with sensory function and the mobile complexes with maintenan

67 connection between the pattern of effects on sensory function and the nerve fiber types that appear t

68 CD73 to be a novel regulator of carotid body sensory function and therefore suggest that this enzyme

69 tudies show that ocean acidification impairs sensory functions and alters the behavior of teleost fis

70 the disruption of cdh23 abolishes the ear's sensory functions and identified a candidate lesion in l

71 leading to progressive decline of motor and sensory functions and permanent disability.

72 tivity in a subset of around 30 neurons with sensory functions and the uv1 cells of the vulva in herm

73 ms have been implicated in axonal targeting, sensory function, and cell survival.

74 level of consciousness, cranial nerve, motor-sensory function, and simple behavioral tests (best = 10

75 tubule (MT)-based organelles with motile and sensory functions, and ciliary defects have been linked

76 s involved in autonomic, somatic, motor, and sensory functions, and in control of vigilance.

77 TRPP complex ciliary localization and sensory function are evolutionarily conserved.

78 As the molecular bases of colonic motor and sensory function are identified, new disease entities ar

79 Current detailed descriptions of anatomy and sensory function are limited to nematodes that recent mo

80 sensory cortical area is damaged, its basic sensory functions are 'taken over' by the corresponding

81 we must therefore understand how the skin's sensory functions are divided among signalling molecules

82 easing evidence suggests that both motor and sensory functions are regulated by rhythmic processes re

83 Here, we show that distinct sensory functions arise from different combinations of O

84 atus--on chemoreceptor expression highlights sensory function as a key source of plasticity in neural

85 n substantial and often irreversible loss of sensory functions as a result of the limited regenerativ

86 ects is quite heterogeneous affecting visual sensory function at the levels of the ciliary body, reti

87 s showed significant subclinical deficits in sensory function before any therapy compared with health

88 y innervated by efferent fibers, even before sensory function begins.

89 ults in complete loss of voluntary motor and sensory function below the site of injury.

90 tein-coupled receptors which serve important sensory functions beyond their role as odorant detectors

91 ese organs are believed to be adapted to the sensory functions, but had not been probed directly.

92 cerebellar degeneration on primary auditory sensory function by means of a pitch discrimination task

93 ly from mechanical ventilation and preserved sensory function by multiple regression analysis.

94 Here, we show that sensory functions can be restored in the adult mouse if

95 Through both motility and sensory functions, cilia play critical roles in developm

96 les in mice led to improved ciliogenesis and sensory functions compared with those of either mutant a

97 Index finger sensory function correlated with MEP size during precisi

98 Sensory function declined more rapidly than autonomic fu

99 Sensory functions declined significantly after therapy (

100 avulsion results in permanent impairment of sensory functions due to disconnection between the perip

101 individuals is reorganized to a compensatory sensory function during development.

102 a and allodynia, that compensate for loss of sensory function during injury and help protect against

103 gives rise to a merging of cognitive and/or sensory functions (e.g. in grapheme-colour synaesthesia,

104 designed to assess complementary aspects of sensory functions, emotional reactivity, and cognitive o

105 ed controls, with respect to basic motor and sensory function, feeding behavior, reproduction, mood,

106 AWC-specific chemotaxis assays reveal novel sensory functions for kinesin II in these wing cilia.

107 e provide an overview of top down control of sensory functions from the PAG, including selective cont

108 e neural structures that support post-stroke sensory function have not been described.

109 s important than mental health (loneliness), sensory function (hearing), mobility, and bone fractures

110 taste organs are dynamic in cell biology and sensory function, homeostasis requires tight regulation

111 produced by these medications affect visual sensory function; however, some produce disturbances of

112 ions in sudomotor, vasomotor, pilomotor, and sensory function in capsaicin-treated subjects (p < 0.01

113 ight determination in mammalian development, sensory function in ciliated neurons, and opsin transpor

114 The C1 nerve may have an important sensory function in headache disorders that have orbital

115 l motion asymmetries and anomalous binocular sensory function in infantile esotropia (ET) has led to

116 We found that we could rescue sensory function in neurons expressing mutant dSpt1 by c

117 otonin, gastrointestinal symptoms, and motor-sensory function in patients with FC or IBS-C compared w

118 ERP) markers of impaired auditory and visual sensory function in schizophrenia.

119 e terminals, which are postulated to serve a sensory function in the enteric plexuses.

120 n activities of daily living and worse motor-sensory function in the following year.

121 Results indicated that preservation of sensory function in the T11-L2 dermatomes is associated

122 sts was performed weekly to assess motor and sensory functions in all 3 groups for 12 weeks.

123 d involved in a wide range of regulatory and sensory functions in all domains of life.

124 derived appendage required for a variety of sensory functions including olfaction and audition.

125 und Phr1 expression in cells with a possible sensory function, including peripheral retinal ganglion

126 By contrast, this sensory function is apparently shared by one or more oth

127 Sensory function is mediated by interactions between ext

128 Whether gastrointestinal motor and sensory function is primary cause or secondary effect of

129 It seems that sound sensory function is provided to the denervated skin of t

130 static environment where the requirement for sensory functions is expected to be relaxed.

131 f the K(+) channel KVS-1 during aging causes sensory function loss in Caenorhabditis elegans and that

132 ow that brain regions that support motor and sensory function mature earliest, whereas higher-order a

133 cipating in sympathetic, parasympathetic and sensory functions may be functionally different from tho

134 These sensory functions may be profoundly affected by the stat

135 ensory regions, in addition to their primary sensory functions, may be actively involved in perceptua

136 Beyond impaired motor and sensory function, neuropathic pain and loss of bladder c

137 previously reported, transient impairment of sensory function observed following intestinal capsaicin

138 family, myosin VII, plays vital roles in the sensory function of Drosophila and mammals.

139 The sensory function of HOB requires the combined action of

140 ostulate a heme-based redox/dimethyl sulfide sensory function of MA4561 and propose to designate it M

141 factors, altered motility, and/or heightened sensory function of the intestine.

142 re also applicable to study of the motor and sensory function of the other regions of the gastrointes

143 for the proper development, maintenance and sensory function of the piloneural mechanoreceptor.

144 urons, which must be repaired to restore the sensory function of the skin.

145 e at the plasma membrane associated with the sensory function of these cells.

146 hat this release occurs independently of the sensory function of these nerves.

147 To phenotype in rats the sensory function of TRPV1(+) afferents, we rapidly and s

148 daf-19m genetically programs the sensory functions of a subset of ciliated neurons, indep

149 edback, and therefore the putative motor and sensory functions of beta oscillations may reciprocally

150 The sensory functions of cilia reside largely in the membran

151 ssemble normal flagella or in defects in the sensory functions of cilia.

152 First, we assess the specificity of the sensory functions of individual rGC proteins.

153 The motor and sensory functions of muscle are intimately linked, and d

154 Thus, different sensory functions of OCR-2 arise from separable intrinsi

155 Sensory functions of primary cilia rely on ciliary-local

156 Here we elucidate the sensory functions of spinal opioid-related peptides and

157 ata add to the understanding of the multiple sensory functions of the insular cortex and of the corti

158 rthognathic surgery, impairing sensation and sensory function on the face.

159 cular and neural mechanisms underlying these sensory functions remain poorly defined.

160 n of DSBs should generate deficits in distal sensory function remains unclear.

161 es resulting from disorders of the motor and sensory functions represent almost half the patients pre

162 lack rootlets and have dramatically impaired sensory function, resulting in behavior defects associat

163 ventually fully re-extended into muscles and sensory function returned; rather, it resulted from a la

164 Although sensory function seems to be mediated by G proteins, axo

165 is a measure that reflects decline in visual sensory function, slowed visual processing speed, and im

166 corollary, cortical injury strongly impairs sensory function, so we hypothesized that cortical lesio

167 Participants in the binocular sensory function study were a subgroup of 41 children en

168 In the binocular sensory function study, random-dot stereoacuity was abno

169 S, particularly brain tumors, or that impact sensory functioning, such as hearing loss, are associate

170 anosine 3',5'-monophosphate, control several sensory functions, such as phototransduction, chemosensa

171 Although deficits in sensory function suggest that primary sensory cortices a

172 hin regions subserving motor, autonomic, and sensory functions suggests that CNTFR alpha supports man

173 Thermosensation is an essential sensory function that is subserved by a variety of trans

174 mphasizes the importance of daily rhythms in sensory functions that are likely to impact on organism

175 defects in conduction velocity and motor and sensory functions that could be rescued with therapeutic

176 ASICs affect a range of sensory functions that includes perception of gentle tou

177 lity of corresponding laminar differences in sensory function, that is, to examine relationships betw

178 hat, nowadays, we think about vision, somato-sensory function, the spinal cord and the cerebellum.

179 SR1 SNPs associated with individual motor or sensory functions; the associations of SNPs rs2609234, r

180 ncer and cumulative chemotherapeutic dose on sensory function to gain mechanistic insight into the su

181 experimental data with other knowledge about sensory function to obtain a description that optimally

182 be on the engineering of novel couplings of sensory functions to signaling outputs.

183 m adults, including excellent restoration of sensory function (to normal limits in all dermatomes for

184 Sensory function was assessed by measuring thermal and m

185 Recovery of sensory function was assessed by toe pinch, footpad pric

186 Sensory function was restored by 50 days after surgery.

187 olinergic neurotransmission in cognitive and sensory functions, we examined whether alpha4-containing

188 rves, no differences in nerve morphology and sensory function were detected between wild-type and LAR

189 apable of activating the putative hexokinase sensory function were not effective in eliciting the phy

190 their feet while other measures of motor and sensory function were unaffected.

191 ng of cilium and impairment of its motile or sensory function, which was reflected by hearing, vision

192 -synchronization supports the integration of sensory functions, while synchronization in theta/alpha

193 ents of sudomotor, vasomotor, pilomotor, and sensory function with simultaneous assessment of innerva

194 Declines in sensory functioning with aging are evident for many of t

195 IB mice developed progressive impairments in sensory functions, with significantly reduced response t