ライフサイエンスコーパス: myelinated nerve

1 he paranode and ultimately the physiology of myelinated nerve.

2 in the spinal cord and peripherally in large myelinated nerves.

3 ly placed, nonmyelinated axon segments along myelinated nerves.

4 l terminals and the juxtaparanodal region of myelinated nerves.

5 response protein 2) transcription factors in myelinated nerves.

6 lial junctions flank the nodes of Ranvier in myelinated nerves.

7 ed to regions before the transition zones of myelinated nerves.

8 Nerve terminal arborizations, arising from myelinated nerves and exhibiting variable morphology, we

9 ades as well as some intraepidermal and free myelinated nerve endings.

10 tor in vivo during development and repair of myelinated nerves explaining the deficiency of myelin ob

11 tional ordering of membrane compounds in the myelinated nerve fiber by means of polarized Raman micro

12 nerve fibers and synthetic gel fibers, a non-myelinated nerve fiber carrying an impulse was treated a

13 sults further demonstrate the important role myelinated nerve fiber degeneration plays in the pathoge

14 ermal nerve fiber density, as well as dermal myelinated nerve fiber density, which persisted througho

15 a+-K+-ATPase, nerve conduction velocity, and myelinated nerve fiber pathology.

16 Contactin is downregulated along the entire myelinated nerve fiber.

17 rcumscribed white matter tract consisting of myelinated nerve fibers and neuroglial cells.

18 There was loss of larger myelinated nerve fibers and profuse regenerative activit

19 Myelinated nerve fibers are designed in an optimal manne

20 Paranodal axoglial junctions in myelinated nerve fibers are essential for efficient acti

21 Paranodal junctions of myelinated nerve fibers are important for saltatory cond

22 erest because the global effects of aging on myelinated nerve fibers are more complex and profound th

23 Action potential conduction in myelinated nerve fibers depends on a polarized axonal me

24 that in aging there is a ubiquitous loss of myelinated nerve fibers from the brain and that fiber lo

25 d the middle-aged monkeys the mean number of myelinated nerve fibers in the anterior commissure is 2.

26 correlated with a reduction in the number of myelinated nerve fibers in the anterior commissure, an i

27 ed the morphology and area number density of myelinated nerve fibers in the cingulate bundle and genu

28 The loss of myelinated nerve fibers is accompanied by a significant

29 However, the number of myelinated nerve fibers is the only variable that correl

30 g results in a 20% decrease in the number of myelinated nerve fibers per unit area, while remaining n

31 which may be related to the vulnerability of myelinated nerve fibers to the normal process of aging.

32 Although the development of myelinated nerve fibers was not impaired, Miz1DeltaPOZ m

33 sequential nodal and axonal injury of intact myelinated nerve fibers, recapitulating pathologic featu

34 ction, it had no effect on measures of large myelinated nerve fibers, specifically sural or sciatic n

35 adhesion molecules, such as MAG, present in myelinated nerve fibers.

36 sent a new method to quantify differences in myelinated nerve fibers.

37 e fornix, but there is a significant loss of myelinated nerve fibers.

38 rs, associated with a dramatic loss of large myelinated nerve fibers.

39 to distinct subcellular domains in mammalian myelinated nerve fibers.

40 14 cutaneous nerve biopsies revealed loss of myelinated nerve fibres (86%), increased regenerative cl

41 phology and molecular architecture of dermal myelinated nerve fibres were examined using immunohistoc

42 in the evaluation of non-myelinated, but not myelinated nerve fibres, in sensory neuropathies.

43 al signal generation and transmission in CNS myelinated nerve fibres.

44 gated sodium channels at nodes of Ranvier in myelinated nerves: here, we investigate its role in AIS

45 o myelinate developing nerve and to maintain myelinated nerve in adulthood.

46 We therefore evaluated myelinated nerves in skin biopsies from normal controls

47 es are propagated at nodes of Ranvier in the myelinated nerves of vertebrates.

48 Myelinated nerves, regardless of their source, have in c

49 Fast, saltatory conduction in myelinated nerves requires the clustering of voltage-gat

50 Rapid nerve conduction in myelinated nerves requires the clustering of voltage-gat

51 n depends on specialized membrane domains in myelinated nerve, the node of Ranvier, the paranode, and

52 In mammalian myelinated nerves, the internodal axon that is normally

53 e alterations in ion channel localization in myelinated nerves; this provides a rationale for the aud

54 etic screens for mutants with disruptions in myelinated nerves, we identified mutations in erbb3 and