ライフサイエンスコーパス: infraorbital

1 e innervates neuromasts of the supraorbital, infraorbital, and otic lines, whereas the anteroventral

2 The left, infraorbital, anterior lateral line nerve of brown ghost

3 able neural interface for stimulation of the infraorbital branch of the trigeminal nerve that enables

4 lidation of a novel neural interface for the infraorbital branch of the trigeminal nerve utilizing a

5 thalamus and cortex of awake rats while the infraorbital branch of the trigeminal nerve was stimulat

6 Several months after cauterization of the infraorbital branch of the trigeminal nerve, the tactile

7 s reviewed for reports of enlargement of the infraorbital canal or nerve.

8 The infraorbital canal was enlarged in 20 of the 28 orbits,

9 cranial outflow pressure Pe, we inflated the infraorbital cuff, which led to the Pd increase and dire

10 was to define the location of the accessory infraorbital foramen (AIOF) with reference to accessible

11 ral walls of the nasal cavity (NCd), and the infraorbital foramina (IOFd).

12 e lateral walls of the nasal cavity, and the infraorbital foramina change consistently with maxillary

13 Here, plasticity induced by unilateral infraorbital (IO) nerve resection in 4-week-old rats was

14 teracted blink-evoking supraorbital (SO) and infraorbital (IO) nerve stimuli in alert rats.

15 n, the effect of neonatal transection of the infraorbital nerve (a major component of the trigeminal

16 model of chronic constriction injury to the infraorbital nerve (CCI-ION) to study whether CCI-ION ca

17 following chronic constriction injury to the infraorbital nerve (CCI-ION).

18 ain after chronic constriction injury of the infraorbital nerve (CCI-Pain) displayed higher spontaneo

19 rent study examined the long-term effects of infraorbital nerve (ION) axoplasmic transport attenuatio

20 ith chronic constriction injury (CCI) to the infraorbital nerve (ION) but had minimal effect in rats

21 adult rats that sustained transection of the infraorbital nerve (ION) on P-0 or P-7 or implantation o

22 Transection of the infraorbital nerve (ION) on the day of birth (P-0) disru

23 The effects of infraorbital nerve (ION) transection on gene expression

24 The effects of infraorbital nerve (ION) transection on gene expression

25 The infraorbital nerve (ION) was transected in different coh

26 ither eliminated by transection of the right infraorbital nerve (IoN), or selectively altered by repe

27 Enlargement of the infraorbital nerve and canal is rare and strongly sugges

28 We injected B-HRP into the infraorbital nerve and sciatic nerve, which are known to

29 natal lesion of the primary afferents in the infraorbital nerve causes the death of one-third of the

30 Here, we created infraorbital nerve chronic constrictive injury (ION-CCI)

31 inal neuropathic pain in male rats following infraorbital nerve chronic constrictive injury (ION-CCI)

32 of acute receptive field changes, following infraorbital nerve cut, may contribute to some types of

33 eld shifts with those that did not, prior to infraorbital nerve cut, there was no difference in mean

34 ty than in the deafferented animal after the infraorbital nerve cut.

35 Infraorbital nerve damage at birth kills neurons and alt

36 One of the major consequences of neonatal infraorbital nerve damage is irreversible morphological

37 Transection of the infraorbital nerve directly affected the expression of p

38 sted odds ratio [aOR] = 9.45; P = 0.016) and infraorbital nerve enlargement (aOR = 12.11; P = 0.008)

39 quent in patients with bilateral disease and infraorbital nerve enlargement, showing the importance o

40 ing from extraocular muscle dysfunction, and infraorbital nerve hypesthesia may occur.

41 Transection of the infraorbital nerve in adult rats results in an array of

42 chronic constriction injury (CCI) of the rat infraorbital nerve in the rostral ventromedial medulla (

43 34 showed reasonable activity in the partial infraorbital nerve ligation, a migraine disease model th

44 from the right laminae I and II and the left infraorbital nerve of every experimental animal.

45 I and II at 1, 4, 17, and 90 days after left infraorbital nerve section.

46 Axon number in the infraorbital nerve was highly predictive of terminal and

47 timuli delivered via a cuff electrode to the infraorbital nerve yielded robust sensory responses in V

48 eral PSN (i.e., the target of the transected infraorbital nerve) than in the contralateral PSN.

49 Here we examined whether injury to the infraorbital nerve, a branch of the trigeminal nerves, l

50 hemi-rostrum) and innervated by a prominent infraorbital nerve, containing about 80,000 axons.

51 Unilateral and bilateral sectioning of the infraorbital nerve, which innervates the whiskers, was t

52 ccessfully block the accessory branch of the infraorbital nerve.

53 ced after chronic constriction injury of the infraorbital nerve.

54 nadvertent iatrogenic injury to a duplicated infraorbital nerve.

55 ed following intraorbital transection of the infraorbital nerve.

56 o non-infraorbital regions after cutting the infraorbital nerve.

57 travel to the facial muscles via the sensory infraorbital nerve.

58 posited at the meningeal (True-Blue, TB) and infraorbital nerves (Fluoro-Gold, FG) showed that at the

59 Using an infraorbital optic nerve crush injury, we show that redu

60 lar isolation of 37 interpolaris cells, with infraorbital receptive fields, was maintained following

61 f the braincase, and the abbreviation of the infraorbital region.

62 1.6% exhibited receptive field shifts to non-infraorbital regions after cutting the infraorbital nerv

63 nscriptomics to probe the effects of partial infraorbital transection of the trigeminal nerve at the