ライフサイエンスコーパス: spinal cord transection

1 tail and grafted into the site of a complete spinal cord transection.

2 gliogenesis and neurogenesis occurred after spinal cord transection.

3 h and at distinct time points after complete spinal cord transection.

4 ed Wnt signaling in bone-derived cells after spinal cord transection.

5 on of novel gait patterns following complete spinal cord transection.

6 y, fully determined by P5, is revealed after spinal cord transection.

7 in rats after a complete midthoracic (T8-T9) spinal cord transection.

8 with complete hind limb paralysis due to T8 spinal cord transection.

9 us laevis tadpoles functionally recover from spinal cord transection.

10 rks that generate sympathetic activity after spinal cord transection.

11 d increases in Na(v)1.9 expression following spinal cord transection.

12 f these neurons regenerate their axons after spinal cord transection.

13 ied RS neurons, regenerate their axons after spinal cord transection.

14 d by 65 % by alpha1-adrenoceptor blockade or spinal cord transection.

15 scenario of a 2-yr old with a high cervical spinal-cord transection.

16 s not appear to be affected significantly by spinal cord transections.

17 elated activity are activated selectively by spinal cord transections.

18 In the present study, spinal cord transection above the known level of entry o

19 interruption of ascending spinal barrage by spinal cord transection above the level of the injury.

20 At eight weeks and 16 weeks after spinal cord transection, an average of 49% and 68%, resp

21 n of back-labeled lamprey spinal axons after spinal cord transection and detected mRNA in axon tips b

22 d loading conditions changes with time after spinal cord transection and is unaltered by small amount

23 systems are up-regulated following complete spinal cord transection and that step training results i

24 promoted axon regeneration across a complete spinal cord transection and that this regeneration alter

25 rtial midcervical or complete upper thoracic spinal cord transections and examined whether combinator

26 alpha mRNA was induced within 2 hr after rat spinal cord transection, and its upregulation was suppre

27 ls in bladder afferent neurons changes after spinal cord transection, and these changes may contribut

28 the behavioural and physiological effects of spinal cord transection are reflected in adaptations in

29 ty, axon crossing, and tissue bridging after spinal cord transection, associated with disrupted indic

30 Rats (n = 48) received spinal cord transection at 5 days of age, and 4 weeks la

31 regeneration in the adult rat after complete spinal cord transection at a midthoracic level.

32 We confirmed that a complete spinal cord transection at approximately T12 increases g

33 nal segment of anesthetized rats after acute spinal cord transection at C(2).

34 creased Voc-T and PD after sham procedure or spinal cord transection at either level.

35 7 and 1.0 m/s before and after recovery from spinal cord transection at low thoracic level.

36 ately 3 months after a complete mid-thoracic spinal cord transection at P5 in non-trained and in step

37 trained 6 min/day) spinal rats (mid-thoracic spinal cord transection at post-natal day 5) at differen

38 Renshaw cells (RCs) is disrupted by thoracic spinal cord transection at postnatal day 5 (P5TX).

39 Sprague Dawley rats received a spinal cord transection at T12 and were assigned to SCI-

40 Male Sprague-Dawley rats underwent complete spinal cord transection at T8.

41 pmol), and completely abolished by cervical spinal cord transection at the C6 level.

42 ental synaptic transmission was prevented by spinal cord transection at the thoracic level on postnat

43 In ovariectomized rats, after spinal cord transection at thoracic 7 (T7X), lumbar 5 (L

44 After spinal cord transection, axons regenerate both in larval

45 fied reticulospinal neurons by 5 weeks after spinal cord transection, but was reexpressed at 10 weeks

46 s postsympathectomy were increased following spinal cord transection (C2) and suppressed by the alpha

47 Because spinal cord transection eliminates all descending inputs

48 Acute mid-thoracic spinal cord transection eliminates hindlimb air-stepping

49 Groups of animals which received a spinal cord transection followed by either an exercise r

50 ng can be reacquired after complete thoracic spinal cord transection in adult cats with appropriate,

51 promotes axon regeneration across a complete spinal cord transection in adult rats.

52 plants acutely after a complete low-thoracic spinal cord transection in adult rats.

53 After spinal cord transection in lampreys, axons of the large,

54 double-labeling study suggest that following spinal cord transection in larval lamprey, axonal regene

55 monitor of spinal neurons responding to high spinal cord transection in the rat.

56 Spinal cord transection induced neurons to express FLI i

57 LAR-targeting peptides in mice with thoracic spinal cord transection injuries induce significant axon

58 After spinal cord transection, lampreys recover functionally a

59 of the vsx1 promoter, that after a complete spinal cord transection, large numbers of V2 interneuron

60 xons across and beyond an extensive thoracic spinal cord transection lesion in adult rats.

61 rotein (GFP) were transplanted into a dorsal spinal cord transection lesion of SD rats.

62 cells/progenitors (RN-NSCs) into a complete spinal cord transection lesion site in adult female rats

63 In response to thoracic spinal cord transection lesions, ephrin-B2 and EphB2 pro

64 We used a complete spinal cord transection model and olfactory ensheathing

65 Following cervical spinal cord transection, NaCN and also dinitrophenol (DN

66 inical dose of lithium to rats with thoracic spinal cord transection or contusion injuries induce sig

67 profen via minipumps to rats with a thoracic spinal cord transection or contusion injury result in su

68 ue and restore motor function after complete spinal cord transection owing to a complex cellular resp

69 Spinal cord transection prevents development of secondar

70 Development of a rat complete spinal cord transection/SC bridge model allowed the demo

71 act spinal cord, animals that had a complete spinal cord transection (SCT) and animals with SCT who e

72 y PN stimulation before and up to 16 h after spinal cord transection (SCT) in cats anaesthetized with

73 motor function recovery 14 to 28 days after spinal cord transection (SCT) in rats.

74 After spinal cord transection (SCT), we found no evidence of s

75 Fourteen days after spinal cord transection Sema4 mRNA expression was absent

76 llowed to survive for 12 or more weeks after spinal cord transection, several identified reticulospin

77 n survive and orient longitudinally across a spinal cord transection site and form myelin.

78 ation of fetal neural stem cells (NSCs) into spinal cord transection sites.

79 GDNF into complete and partial mid-thoracic spinal cord transection sites.

80 Seven weeks after complete T3 spinal cord transection (T3-SCI, n = 15) or sham injury

81 ition reflex pathways 6 weeks after complete spinal cord transection (T8).

82 Adult rats received a complete spinal cord transection (T9), and epidural stimulation (

83 After spinal cord transection, TH1(+) immunoreactivity is comp

84 After spinal cord transection, the generation of stepping depe

85 ginning at 14 d after a complete midthoracic spinal cord transection, the mice were trained daily (10

86 Following spinal cord transections, the numbers of descending proj

87 t 10% BL; and, eight weeks or 16 weeks after spinal cord transection, TRDA was applied to the spinal

88 dlimb locomotion in adult rats with complete spinal cord transection, we hypothesized that more 5-HT-

89 uire the ability to stand and step following spinal cord transection with repetitive exposure to stan