ライフサイエンスコーパス: sensory ending

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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 ensory organs are often composed of neuronal sensory endings accommodated in a lumen formed by enshea

8 ly complete loss of hair follicle-associated sensory endings among Brn3a(-/-) neurons.

9 nits, and had P2X3 immunoreactivity in their sensory endings and cell bodies.

10 These receptors localize to sensory endings and confer responses to ethologically re

11 ry organs, disrupt contacts between neuronal sensory endings and cuticular structures.

12 vil-hPLAP mice, sensory axons, the exquisite sensory endings, as well as the fine central axonal coll

13 ort segments of the afferent axons and their sensory endings beneath each inner hair cell.

14 In some areas, sensory ending density was lower than expected based upo

15 d spike initiation functions in these unique sensory endings distinguishes them from the axonal nodes

16 lopment of peripheral target innervation and sensory ending formation is an ordered process with spec

17 ate that some trigeminal ganglion cells with sensory endings in the nasal epithelium also have branch

18 ng of mechanically activated ion channels at sensory endings in the skin.

19 ses production of the neuropeptide CGRP from sensory endings innervating the pancreatic islets, subse

20 e (trk) receptors can form the same types of sensory endings (Merkel endings) in the same target (Mer

21 n contrast, glial sheath cells harboring the sensory endings of C. elegans' major chemosensory neuron

22 AP staining in these mice demonstrated that sensory endings of muscle spindles and Golgi tendon orga

23 ctive cation channel Piezo2 was expressed in sensory endings of proprioceptors innervating muscle spi

24 Whirlin localizes to the peripheral sensory endings of pSNs and facilitates pSN afferent fir

25 etic neurons and the development of selected sensory endings of the skin.

26 ible in the cell bodies, central relays, and sensory endings of these neurons, revealing the full ext

27 agglutinin-horseradish peroxidase (to label sensory endings) or 1% cholera toxin subunit B-horseradi

28 Thus, in the lanceolate sensory ending SLV recycling is itself regulated, at lea

29 ata and processes, morphology of specialized sensory endings, synaptic partners and expression profil

30 number and enhanced innervation of specific sensory ending types.

31 Subsequently the ramifications of the sensory ending were reconstructed histologically, and th

32 In nonhairy plantar skin, Meissner corpuscle sensory endings were larger, and the number of Merkel ce

33 prisingly, the outer spiral fibers and their sensory endings were well labeled beneath the outer hair

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