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1 tail and grafted into the site of a complete spinal cord transection.
2 gliogenesis and neurogenesis occurred after spinal cord transection.
3 ed Wnt signaling in bone-derived cells after spinal cord transection.
4 on of novel gait patterns following complete spinal cord transection.
5 in rats after a complete midthoracic (T8-T9) spinal cord transection.
6 us laevis tadpoles functionally recover from spinal cord transection.
7 rks that generate sympathetic activity after spinal cord transection.
8 d increases in Na(v)1.9 expression following spinal cord transection.
9 f these neurons regenerate their axons after spinal cord transection.
10 ied RS neurons, regenerate their axons after spinal cord transection.
11 d by 65 % by alpha1-adrenoceptor blockade or spinal cord transection.
12 scenario of a 2-yr old with a high cervical spinal-cord transection.
13 s not appear to be affected significantly by spinal cord transections.
14 elated activity are activated selectively by spinal cord transections.
16 interruption of ascending spinal barrage by spinal cord transection above the level of the injury.
18 n of back-labeled lamprey spinal axons after spinal cord transection and detected mRNA in axon tips b
19 d loading conditions changes with time after spinal cord transection and is unaltered by small amount
20 systems are up-regulated following complete spinal cord transection and that step training results i
21 promoted axon regeneration across a complete spinal cord transection and that this regeneration alter
22 rtial midcervical or complete upper thoracic spinal cord transections and examined whether combinator
23 alpha mRNA was induced within 2 hr after rat spinal cord transection, and its upregulation was suppre
24 ls in bladder afferent neurons changes after spinal cord transection, and these changes may contribut
25 the behavioural and physiological effects of spinal cord transection are reflected in adaptations in
31 ately 3 months after a complete mid-thoracic spinal cord transection at P5 in non-trained and in step
32 trained 6 min/day) spinal rats (mid-thoracic spinal cord transection at post-natal day 5) at differen
37 ental synaptic transmission was prevented by spinal cord transection at the thoracic level on postnat
40 fied reticulospinal neurons by 5 weeks after spinal cord transection, but was reexpressed at 10 weeks
41 s postsympathectomy were increased following spinal cord transection (C2) and suppressed by the alpha
45 ng can be reacquired after complete thoracic spinal cord transection in adult cats with appropriate,
49 double-labeling study suggest that following spinal cord transection in larval lamprey, axonal regene
52 LAR-targeting peptides in mice with thoracic spinal cord transection injuries induce significant axon
54 of the vsx1 promoter, that after a complete spinal cord transection, large numbers of V2 interneuron
60 inical dose of lithium to rats with thoracic spinal cord transection or contusion injuries induce sig
61 profen via minipumps to rats with a thoracic spinal cord transection or contusion injury result in su
64 act spinal cord, animals that had a complete spinal cord transection (SCT) and animals with SCT who e
65 y PN stimulation before and up to 16 h after spinal cord transection (SCT) in cats anaesthetized with
69 llowed to survive for 12 or more weeks after spinal cord transection, several identified reticulospin
78 ginning at 14 d after a complete midthoracic spinal cord transection, the mice were trained daily (10
80 t 10% BL; and, eight weeks or 16 weeks after spinal cord transection, TRDA was applied to the spinal
81 dlimb locomotion in adult rats with complete spinal cord transection, we hypothesized that more 5-HT-
82 uire the ability to stand and step following spinal cord transection with repetitive exposure to stan
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