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1 e of the preterminal branches of the primary sensory ending.
2 te first, followed by formation of cutaneous sensory endings.
3 t and includes a wide variety of large fiber sensory endings.
4 e of a putative thermoreceptor(s) in the AFD sensory endings.
5 receptor to maintain the excitability of the sensory endings.
6 aling plays a major role in the formation of sensory endings.
7 ncreased DLK-1 accumulation in the defective sensory endings.
8 d bradykinin B2 receptors on muscle afferent sensory endings.
9 ensory organs are often composed of neuronal sensory endings accommodated in a lumen formed by enshea
10 ly complete loss of hair follicle-associated sensory endings among Brn3a(-/-) neurons.
11 nits, and had P2X3 immunoreactivity in their sensory endings and cell bodies.
12                  These receptors localize to sensory endings and confer responses to ethologically re
13 ry organs, disrupt contacts between neuronal sensory endings and cuticular structures.
14                             Finally, spindle sensory endings and function are impaired in aged mice,
15  neurons with distinct innervation patterns, sensory endings, and function.
16 vil-hPLAP mice, sensory axons, the exquisite sensory endings, as well as the fine central axonal coll
17 ort segments of the afferent axons and their sensory endings beneath each inner hair cell.
18                             Spindle afferent sensory endings contain glutamate-filled synaptic-like v
19                               In some areas, sensory ending density was lower than expected based upo
20 d spike initiation functions in these unique sensory endings distinguishes them from the axonal nodes
21 lopment of peripheral target innervation and sensory ending formation is an ordered process with spec
22 al afferents is clear, the identity of their sensory endings has remained unknown.
23 tes sprouting and sensitivity of nociceptive sensory endings in mouse colon.
24 ecise organization of signaling molecules at sensory endings in regulating response dynamics.
25 ate that some trigeminal ganglion cells with sensory endings in the nasal epithelium also have branch
26 ng of mechanically activated ion channels at sensory endings in the skin.
27 ses production of the neuropeptide CGRP from sensory endings innervating the pancreatic islets, subse
28 e (trk) receptors can form the same types of sensory endings (Merkel endings) in the same target (Mer
29 ifferential roles of ciliary trafficking and sensory ending morphology in shaping chemosensory respon
30 n contrast, glial sheath cells harboring the sensory endings of C. elegans' major chemosensory neuron
31  AP staining in these mice demonstrated that sensory endings of muscle spindles and Golgi tendon orga
32 ctive cation channel Piezo2 was expressed in sensory endings of proprioceptors innervating muscle spi
33          Whirlin localizes to the peripheral sensory endings of pSNs and facilitates pSN afferent fir
34            Adult C. elegans AMsh glia engulf sensory endings of the AFD thermosensory neuron by repur
35 etic neurons and the development of selected sensory endings of the skin.
36 ible in the cell bodies, central relays, and sensory endings of these neurons, revealing the full ext
37 nsing ion channel subtype 1a (ASIC1a) on the sensory endings of thin fibre muscle afferents during sk
38 ane A(2) and bradykinin B2 receptors) on the sensory endings of thin fibre muscle afferents in the ch
39 epsilon, but not IP(3) receptors, within the sensory endings of thin fibre muscle afferents plays a r
40 his study, we demonstrate that ASIC1a on the sensory endings of thin fibre muscle afferents plays a r
41 pe of acid sensing ion channel (ASIC) on the sensory endings of thin fibre muscle afferents, namely A
42 th skeletal muscle contraction stimulate the sensory endings of thin fibre muscle afferents, which, i
43  agglutinin-horseradish peroxidase (to label sensory endings) or 1% cholera toxin subunit B-horseradi
44                      Thus, in the lanceolate sensory ending SLV recycling is itself regulated, at lea
45 ata and processes, morphology of specialized sensory endings, synaptic partners and expression profil
46  number and enhanced innervation of specific sensory ending types.
47        Subsequently the ramifications of the sensory ending were reconstructed histologically, and th
48 In nonhairy plantar skin, Meissner corpuscle sensory endings were larger, and the number of Merkel ce
49 prisingly, the outer spiral fibers and their sensory endings were well labeled beneath the outer hair