ライフサイエンスコーパス: sensory threshold

1 planned motion is unambiguously perceived (a sensory threshold).

2 al heat (p=0.03) and the distension (p=0.02) sensory thresholds.

3 ogical influences are used, they have normal sensory thresholds.

4 Also, stress alters sensory thresholds.

5 /g for 2-MIB, which are both below the human sensory thresholds.

6 changes to the auditory periphery that raise sensory thresholds and alter coding, and is accompanied

7 changes to the auditory periphery that raise sensory thresholds and alter coding, and is accompanied

8 cular mechanisms underlying establishment of sensory thresholds and plasticity of thresholds through

9 he chemosensory apparatus of C. elegans uses sensory thresholds and that a voltage-gated K(+) channel

10 uring each crossover period, primary (rectal sensory thresholds) and secondary (bowel diaries, consti

11 OR expressing cells, did not alter the basal sensory thresholds but abolished the hyperalgesia induce

12 sensory testing demonstrated normal baseline sensory thresholds but an enhanced secondary hyperalgesi

13 a critical source of inhibition to regulate sensory thresholds by gating mechanical inputs in the do

14 At 1 year, 2 of the rectal sensory thresholds (DDV: P = 0.008; MTV: P = 0.008) and

15 Sensory thresholds enable animals to regulate their beha

16 ivity than controls and returned to baseline sensory thresholds faster.

17 melanogaster Although sleep is a state where sensory threshold for arousal is greater, it is known th

18 uces pain and is associated with a 50% lower sensory threshold for pain, a 50% lower threshold for re

19 Despite the importance of sensory thresholds for animal behavior and human health,

20 ere short lived such that by about day 9 the sensory thresholds had reverted to pre-injury baselines

21 e index finger (80 Hz, 1.5 s duration, twice sensory threshold) had no consistent differential effect

22 xtracts at concentration only slightly above sensory threshold levels, had a large and unexpected imp

23 and depression-like behaviors and increased sensory thresholds of SNL rats, but had no effect in sha

24 rats via previously implanted cannulas, and sensory thresholds of the face and hind-paws were charac

25 The importance of urethral sensory threshold on postoperative continence is being e

26 ntly reduced (p < 0.001), and conversely the sensory threshold (p < 0.005) and capacity (p < 0.001) w

27 cations Trial [DCCT] exam), and quantitative sensory threshold (QST).

28 Two weeks after triptan exposure, when sensory thresholds returned to baseline levels, rats sho

29 ve stimulation (SNS) is at or just above the sensory threshold (ST).

30 < .001)-these patients tended to have lower sensory thresholds than patients with FC.

31 s to enter sleep and subsequent increases in sensory threshold; this increased sensory threshold was

32 ased nerve conduction velocity and increased sensory threshold to mechanistic stimulation.

33 effects of acute cystitis on distal colonic sensory thresholds to CRD and the effects of acute colon

34 Sensory thresholds to rectal balloon distension and heat

35 difference), rectal sensorimotor (barostat; sensory thresholds, tone response, compliance), autonomi

36 We demonstrate that Cadherin-16 regulates sensory thresholds via an endocrine organ, the corpuscle

37 sults suggest that TIP39 signaling modulates sensory thresholds via effects on glutamatergic transmis

38 creases in sensory threshold; this increased sensory threshold was not due to sensory adaptation of p

39 This VNS-dependent restoration of sensory thresholds was maintained for several months aft

40 Periorbital and hind paw sensory thresholds were measured to detect cutaneous all

41 et 5.45 mm, air esthesiometer 3.62 mg), mean sensory thresholds were significantly higher in aqueous

42 We conclude that there are elevations in sensory thresholds with age for multimodal somatosensory