戻る
「早戻しボタン」を押すと検索画面に戻ります。 [閉じる]

コーパス検索結果 (１語後でソート)

通し番号をクリックするとPubMedの該当ページを表示します
1 owing peripheral nerve injury, low threshold mechanoreceptive Abeta-fibers sprout from their normal t
2 correlation between functional properties of mechanoreceptive afferent fibers and intrinsic discharge
3 tunity to bridge the gap between first-order mechanoreceptive afferent input codes and their spatial,
4 To examine the contribution of low threshold mechanoreceptive afferent input to the development of al
5 sults support the idea that each of the four mechanoreceptive afferent systems innervating the hand s
6 ht of similar studies of other low-threshold mechanoreceptive afferent terminals in the rat and cat a
7 ntraneural microstimulation (INMS) of single mechanoreceptive afferent units in the median nerve, in
8                   We record the responses of mechanoreceptive afferents and of neurons in areas 3b an
9 raditionally, different classes of cutaneous mechanoreceptive afferents are ascribed different and la
10 tile stimuli conveyed in Abeta low threshold mechanoreceptive afferents become capable of activating
11 n particular, in the elderly, the density of mechanoreceptive afferents decreases with age and the sk
12                      Electrically activating mechanoreceptive afferents inhibits pain.
13                                              Mechanoreceptive afferents innervating the glabrous skin
14                 In contrast, myelinated hair mechanoreceptive afferents proportionally increased thei
15 across one of three populations of cutaneous mechanoreceptive afferents that innervate the fingertips
16 ion with periodic microstimulation of single mechanoreceptive afferents whose receptive fields occupi
17 at stimulus intensities that activated large mechanoreceptive afferents, and grew as additional affer
18 n additional function to vibration-sensitive mechanoreceptive afferents.
19            We show that CTs are unique among mechanoreceptive afferents: they discharged preferential
20 urvival of subpopulations of proprioceptive, mechanoreceptive and nociceptive sensory neurons, where
21 ions for, and possible interactions between, mechanoreceptive and nociceptive signals.
22                                 However, the mechanoreceptive and nociceptive trigeminal ganglion neu
23         Interestingly, Cbln2 is expressed by mechanoreceptive and proprioceptive neurons and in regio
24 tions between low-threshold primary afferent mechanoreceptive axons and dorsal horn cells are invaria
25 ses, selective tracing of proprioceptive and mechanoreceptive axons, and the first simultaneous targe
26  hydroxylase (Th), specific to low-threshold mechanoreceptive C-fibers, which was shown previously to
27 lutionary divergence of these very different mechanoreceptive cell types.
28 he somatosensory system comprises three main mechanoreceptive channels: the slowly adapting channel (
29 tegories included a variety of low threshold mechanoreceptive classes, innocuous thermoreceptive and
30 assively, influence GG EMG activity; and (3) mechanoreceptive control of GG EMG can fully explain all
31  proprioceptive information in tetrapods are mechanoreceptive end organs in skeletal muscle: muscle s
32 ring rates of low-threshold Abeta and D-hair mechanoreceptive fibers were also altered.
33 cting the high innervation density and small mechanoreceptive fields in this area [1, 2].
34 stical model of the excitatory low threshold mechanoreceptive fields of spinocervical, postsynaptic d
35 ent of the trigeminal and cervical cutaneous mechanoreceptive fields was observed in 71% of neurons.
36 eociliary bundles as an essential element of mechanoreceptive function.
37 cture of Eimer's organs is consistent with a mechanoreceptive function.
38 icromechanical properties of the hair cell's mechanoreceptive hair bundle within the apical half of t
39                                          The mechanoreceptive hair bundles of hair cells in the bullf
40 annels that open following the deflection of mechanoreceptive hair bundles that reside on top of thes
41  that impose complex mechanical loads on the mechanoreceptive hair bundles.
42                          The regeneration of mechanoreceptive hair cells occurs throughout life in no
43 ed amplification by an active process in the mechanoreceptive hair cells.
44              Positive C-fibre high threshold mechanoreceptive (HTM) units had receptive fields in der
45 uli as nociceptive (including high-threshold mechanoreceptive (HTM) units), and non-nociceptive (incl
46    Here, we reported the cross-inhibition of mechanoreceptive information in DRG under peripheral inf
47 ts to convey proprioceptive, nociceptive and mechanoreceptive information to the spinal cord.
48 ntation, the pretectum receives electro- and mechanoreceptive inputs in addition to retinal input.
49                             Tapping into the mechanoreceptive interface between the animal and the en
50 and non-nociceptive (including low-threshold mechanoreceptive (LTM) and cooling units).
51 proportion of nociceptive than low threshold mechanoreceptive (LTM) neurons showed Nav1.8-LI, and noc
52 ding nociceptive and cutaneous low-threshold mechanoreceptive (LTM) neurons, 50 had no discernable ri
53 characterized as nociceptive, low- threshold mechanoreceptive (LTM) or unresponsive according to thei
54 mal stimuli, as a nociceptive, low threshold mechanoreceptive (LTM) or unresponsive unit.
55 ies were characterized as: (a) low-threshold mechanoreceptive (LTM) units (5 C-, 10 Adelta- and 57 Aa
56  sensitive (n = 4) nor C-fibre low threshold mechanoreceptive (LTM) units (n = 3) had CGRP-LI.
57  after peripheral injury, some low-threshold mechanoreceptive (LTMR) afferents "sprout" into pain-spe
58                      However, the underlying mechanoreceptive mechanisms are largely unclear.
59 channel, we analyzed Drosophila melanogaster mechanoreceptive mutants for defects in mechanosensory p
60 ype I (RAs) and slowly adapting type I (SAs) mechanoreceptive nerve fibers.
61  sites, genital skin contains small diameter mechanoreceptive nerve fibres that signal pleasant touch
62 e system of the channel catfish is formed by mechanoreceptive neuromasts located within five pairs of
63                    Spike trains from primary mechanoreceptive neurons did not predict choices about i
64 xhibit numerical expansion of large-diameter mechanoreceptive neurons expressing the mechano-gated io
65 l eleven types: three distinct low-threshold mechanoreceptive neurons, two proprioceptive, and six pr
66 s known, however, about the possible role of mechanoreceptive or other somatosensory feedback in the
67  actin-filled stereocilia that serves as the mechanoreceptive organelle of each hair cell in the inne
68                              The hair cell's mechanoreceptive organelle, the hair bundle, is highly s
69  in the hair bundle, the sensory hair cell's mechanoreceptive organelle.
70 ignaling molecules define common features of mechanoreceptive processing across sensory systems.
71 emic episodes that excite chemosensitive and mechanoreceptive receptors in the heart.
72 l activation, probably representing a robust mechanoreceptive reflex.
73 vity is modulated by both chemoreceptive and mechanoreceptive reflexes that help stabilize airway pat
74     To determine the contribution of ongoing mechanoreceptive reflexes to phasic activity of airway d
75                                          The mechanoreceptive sensory hair cells in the inner ear are
76 nish upon damage to the ear's receptors, the mechanoreceptive sensory hair cells.
77 ve shown that non-physiological upper airway mechanoreceptive stimuli (e.g. rapidly imposed pulses of