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1 he body (interoception) (e.g., visceral-cold-itch sensations).
2 h is critical for the maintenance of chronic itch sensation.
3 or exploring the mechanism underlying spinal itch sensation.
4 receptor-4 (PAR-4) was recently suggested in itch sensation.
5 nisms underlying the central transmission of itch sensation.
6 s required selectively for histamine-induced itch sensation.
7 to pruritic chemicals and playing a role in itch sensation.
8 erties to initiate and maintain long-lasting itch sensation.
9 nor has any such pathway been identified for itch sensation.
10 ists, playing a fundamental role in pain and itch sensation.
11 y discovered circuits also contribute to the itch sensation.
12 st cells, which leads to vasodilation and an itch sensation.
13 he molecules, cells, and circuits underlying itch sensation.
14 h a focus on the role of Mrgprs in mediating itch sensation.
17 t progress has advanced our understanding of itch sensation and transmission, the neural mechanisms u
19 that hypersensitive subjects had a stronger itch sensation, and that the time to first itch sensatio
23 lation with cowhage induced a more intensive itch sensation compared with stimulation with other subs
24 fiber-dominated itch, (2) the time course of itch sensation differs between subjects with A-fiber- ve
25 t common side effect was a mild tingling and itching sensation during stimulation (100%) and temporar
26 nd unmyelinated fibers, (5) the time of peak itch sensation for subjects with A-fiber-dominated itch
27 myelinated fibers, and (6) the time for peak itch sensation for subjects with C-fiber-dominated itch
28 nown that algogens and cooling could inhibit itch sensation; however, the underlying molecular and ne
30 ggest that broad-band UVB irradiation evokes itch sensation in mice by promoting TRPV1 channel functi
31 molecule that is dedicated to mediating the itch sensation in the dorsal horn of the spinal cord, an
35 strate that PLCbeta3 is required to mediate "itch" sensation in response to histamine acting on the h
39 ovide structural insights into understanding itch sensation, MRGPRX1 activation, and downstream G pro
41 ated G protein-coupled receptors (MRGPRs) in itch sensation promised a search for novel therapeutics
43 rate that GRPR is required for mediating the itch sensation rather than pain, at the spinal level.
46 rst sensation of itch, the strength of their itch sensation, the number of times mosquitoes attempted
47 s of this class of neurons parallel the pure itching sensation this stimulus elicits in humans, and m
48 ave shown a significant role of periostin in itch sensation through direct integrin-mediated stimulat
50 r itch sensation, and that the time to first itch sensation was inversely correlated with wheal diame
51 tone via administration of 5-HT potentiates itch sensation, whereas mice lacking 5-HT or serotonergi
52 es, cells, and circuits known to mediate the itch sensation, which, coupled with advances in understa