ライフサイエンスコーパス: internodal

1 ectin-like (Necl) proteins Necl-1 and -4 are internodal adhesion molecules that are critical for myel

2 In the CNS, Cx29 antibodies labeled the internodal and juxtaparanodal regions of small myelin sh

3 ndrocytes requires the coordinated action of internodal and paranodal CAMs.

4 4.1G contributes to the organization of the internodal axolemma by targeting and/or maintaining glia

5 n an isolated internode, indicating that the internodal axolemma can actively extrude Na+.

6 pha1, alpha3, and beta1 were detected in the internodal axolemma of myelinated fibers in both control

7 ical importance of differentiating nodal and internodal axolemma, very little is known about the proc

8 le nutrients and metabolites to and from the internodal axon and constitutes a pathway through which

9 ess of antibodies and toxic molecules to the internodal axon in paraneoplastic syndromes and demyelin

10 In mammalian myelinated nerves, the internodal axon that is normally concealed by the myelin

11 s was significantly larger in juxtaparanodal/internodal axoplasm than in nodal/paranodal axoplasm.

12 ondria are located within juxtaparanodal and internodal axoplasm.

13 ntly reduced in nodal axoplasm compared with internodal axoplasm.

14 very close vicinity of electrically excited internodal C. corallina cells.

15 In contrast, GA3 and FC promoted internodal cell wall synthesis (initiated between 1 and

16 c moduli, and turgor pressures of sequential internodal cells of intact Chara corallina plants by dir

17 tion of Ca2+ in cytoplasm of Chara corallina internodal cells plays important role in electrical exci

18 he atrial septum with possible injury to the internodal conducting pathways may be the genesis of the

19 monstrates a functional relationship between internodal distance and conduction speed.

20 Reducing the TANG-TANG internodal distance increases the 2D bandwidth dispersio

21 re significant on the scale of the network's internodal distance of approximately 60-80 nm.

22 Internodal distance remained significantly shorter in re

23 h, surface area, volume, fiber diameter, and internodal distance were quantified for afferent fibers

24 e points but provide accurate information on internodal distances and points of origin for ancestral

25 Internodal distances have been proposed to affect the ve

26 li that conduction speeds should increase as internodal distances lengthen until a "flat maximum" is

27 predicted on theoretical grounds, decreased internodal distances strikingly decrease conduction velo

28 atic nerves displayed dramatically shortened internodal distances.

29 ith gibberellin, both of which promote rapid internodal elongation, induced accumulation of Os-EXP4 m

30 These results demonstrate juxtaparanodal/internodal enrichment of stationary mitochondria and neu

31 ns are present at high levels in the growing internodal epidermis, which has thick cell walls and act

32 echanism, we revealed enhanced abundance and internodal expression of axonal membrane proteins normal

33 anterman incisures, and increased amounts of internodal fast VGKCs.

34 was occasionally observed in ganglionic and internodal fibers.

35 ic neurons, as well as in numerous myenteric internodal fibers; immunoreactivity was rarely observed

36 Here we show that internodal growth in wild-type nerves is precisely match

37 ociated with a significant increase (33%) of internodal length (0.95-1.3 mm) in axons of the tibial n

38 Uniformly shortened internodal length in Charcot-Marie-Tooth disease type 1A

39 s plastic in the adult but that increases in internodal length of myelinated adult nerve axons do not

40 Nevertheless, the influence of internodal length on conduction speed has limited experi

41 nces of axon diameter, myelin thickness, and internodal length on the velocity of conduction of perip

42 Internodal length was uniformly shortened in patients wi

43 ress, whereas decreased myelin thickness and internodal length were detected only in the medial prefr

44 nset of myelination, thinner myelin, shorter internodal length, and smaller axonal caliber in adultho

45 The presence of myelin, the internodal length, and the thickness of the myelin sheat

46 156 (miR156) show a bushy phenotype, reduced internodal length, delayed flowering time, and enhanced

47 Despite the substantial increase in internodal length, no significant change was detected in

48 ties are no longer sensitive to increases in internodal length.

49 strong dependence of conduction velocity on internodal length.

50 suggests a potential developmental defect of internodal lengthening.

51 Nevertheless, they do not have the short internodal lengths and associated reduced nerve conducti

52 Internodal lengths defined by Schwann cells in hindlimb

53 posal that remyelination is occurring, short internodal lengths of myelin have been found in the nerv

54 , there must be an increase in the number of internodal lengths of myelin with age, as would occur if

55 ads to the formation of some new and shorter internodal lengths of myelin.

56 ction velocity and support the view that the internodal lengths of nerves reach a plateau beyond whic

57 uction velocity brought about by the shorter internodal lengths of remyelinated nerve fibers in the f

58 Consistent with thinner axonal diameters and internodal lengths, conduction velocities in mutant quad

59 tered at the juxtaparanodal region and at an internodal line located along the mesaxon and below the

60 zation of these channels along the mesaxonal internodal line still persists in the absence of each on

61 ersed along the axolemma, demonstrating that internodal localization of Kv1 channels requires either

62 The internodal maize pulvinus responds to gravistimulation w

63 Age-related disruption in the integrity of internodal myelin sheaths is well described and includes

64 lin basic protein and morphologically normal internodal myelin sheaths.

65 In each heart, the interatrial and internodal pathways were similarly involved, and in the

66 revealed amyloid-beta aggregation within the internodal periaxonal space and paranodal/juxtaparanodal

67 ere we show that the precise localization of internodal proteins depends on the expression of the cyt

68 within a highly specialized region, the stem internodal pulvinus.

69 of Ranvier, the paranode, and the myelinated internodal region.

70 The internodal regions of individual teased fibers distal to

71 ions but was diffusely distributed along the internodal regions.

72 ross zones that extended into both nodal and internodal regions; a few days later they were undetecta

73 ansverse bands of cytoplasm or trabeculae in internodal Schwann cells and suggested that they had a n

74 t in the longitudinal bands of Cajal permits internodal Schwann cells to lengthen in response to axon

75 Potato internodal segments (INS) treated with the auxin 2,4-dic

76 atic nerve (SN) showed increased nonuniform, internodal segments suggesting demyelination, and remyel

77 east two major determinants: the preterminal internodal shortening and axonal slow K channels.

78 These internodal sites create core regulatory circuits essenti

79 eadily impaled in myenteric ganglia close to internodal strands and in microganglia.

80 nes at the corners of large ganglia close to internodal strands and in microganglia.

81 Electrical train stimulation of internodal strands did not evoke activity in the ENS of

82 s commonly, nerve endings were identified in internodal strands, blood vessels, submucosal ganglia, a

83 quasiparticle scattering along the a axis is internodal, then a nonchiral B(3)(u) state is the most c

84 ned to the pulvinus and were not detected in internodal tissue, highlighting the importance of the pu

85 af-sheath pulvinus and gibberellin-sensitive internodal tissue.

86 nd conduction system including two nodes and internodal tracts.

87 s IAA and gravistimulus caused a decrease in internodal uptake.