ライフサイエンスコーパス: efferent fiber

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1 leus accumbens are important targets of RAIC efferent fibers.

2 elin on local collaterals and some myelin on efferent fibers.

3 fugal modulation of individual olivocochlear efferent fibers.

4 number and soma size was quantified for the efferent fibers.

5 ian degeneration is restricted to myelinated efferent fibers.

6 However, electrical stimulation of OC efferent fibers activates presynaptic GABA(B(1a,2)) rece

7 ortion product otoacoustic emissions) during efferent fiber activation, demonstrating the key role al

8 Efferent fibers also were observed to regenerate.

9 The rapid time course of efferent fiber and SGN loss in the chinchilla may make i

10 To study the time course of efferent fiber and SGN loss, chinchillas were injected w

11 results indicate that activation of the STN efferent fibers and resultant changes in the temporal fi

12 tric oxide as a possible transmitter used by efferent fibers and to localize these NADPH-diaphorase-p

13 Efferent fibers and varicosities were visualized in the

14 vide such information, we labeled developing efferent fibers at a constant location within the gerbil

15 These bundles seem to be largely composed of efferent fibers, because in material in which pyramidal

16 osomatic) as well as apposed to afferent and efferent fibers below IHCs prior to P5.

17 nd regeneration was assessed in afferent and efferent fibers by bulk labeling the peripheral axons of

18 the body to neural signals and then through efferent fibers conveys this information to several cent

19 We compared the efferent fiber distributions anterogradely traced from t

20 Efferent fibers do not form an intraganglionic spiral bu

21 ner hair cells are transiently innervated by efferent fibers, even before sensory function begins.

22 Although a few olivocochlear efferent fibers formed such branches, counts indicated t

23 rons or the absence of Schwann cells affects efferent fiber growth to the organ of Corti.

24 Here we show that dopaminergic efferent fibers innervate the acousticolateralis epithel

25 ults suggest that degeneration in myelinated efferent fibers is sufficient to induce spontaneous acti

26 Estimates of efferent fiber loss and density changes were made after

27 nsen's supporting cells was not derived from efferent fibers of the olivocochlear bundle, but its ori

28 es synaptically linked autonomic ganglia and efferent fibers of the vagus and splanchnic nerves to in

29 alcitonin gene-related peptide (CGRP) in the efferent fibers of virtually every hair cell organ studi

30 olinergic synapses are made by olivocochlear efferent fibers on the outer hair cells that express alp

31 acterized, little is known about the fate of efferent fibers or spiral ganglion neurons (SGNs) in thi

32 ed by descending, predominately cholinergic, efferent fibers originating in the CNS.

33 he nucleus tractus solitarius (NTS), and the efferent fibers originating in the dorsal motor nucleus

34 Both inferior and superior efferent fibers richly innervated the basal two thirds o

35 e used to label axons and nerve terminals of efferent fibers that innervate the chick basilar papilla

36 ese results strongly suggest that all of the efferent fibers that innervate the chick BP are choliner

37 transmission in the dentate gyrus and in its efferent fibers, the mossy fiber pathway.

38 ry gustatory center in the medulla and sends efferent fibers to several nuclei in the inferior lobe o

39 The cholinergic efferent fibers to the outer hair cells (OHCs) of the ma

40 shedding requires that input from circadian efferent fibers to the retina precedes the light trigger

41 versus 15-30 days for SGNs, and the loss of efferent fibers was essentially complete within 1 month,

42 s close to the turtle posterior crista while efferent fibers were electrically stimulated.

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