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2 nstrated a significant reduction in the mean endoneurial area in diabetic animals with 5 and 8 mm gap
3 anism for the deinhibition of laminin in the endoneurial basal lamina and may play an important role
4 ave shown that diabetes-induced reduction in endoneurial blood flow (EBF) and impaired endothelium-de
8 s corrected the diabetes-induced decrease in endoneurial blood flow, significantly improved motor and
10 ontrast to the endothelial cells forming the endoneurial blood-nerve barrier and the blood-brain barr
13 n axons and the spread of virus to glial and endoneurial cells of the nerve using EM immunocytochemis
14 xposure to 4 mM DOC, but access of K+ to the endoneurial compartment was more restricted after DOC th
15 cence indicated that Schwann cells and other endoneurial components of rat spinal nerve contain serin
17 early- and late-passage adult primary human endoneurial endothelial cells and laser-capture microdis
18 , which interactively control the privileged endoneurial environment and the pathogenesis of the pain
19 ells produced surface basal lamina; however, endoneurial, epineurial, and meningeal fibroblasts did n
22 iopsies, CSF-1 is predominantly expressed by endoneurial fibroblasts, which are closely associated wi
23 ngoing hypoxia to microvascular dysfunction, endoneurial fibrosis, and increased metabolic requiremen
29 tudy, we observed the presence of persistent endoneurial hypoxia in a mouse model of traumatic periph
31 this calibration curve relating delta DC to endoneurial [K+] it was possible to calculate the change
33 on with a Schwann cell-derived CSPG and that endoneurial laminin may be inhibited by this CSPG as wel
36 n by sodium ions returning to their original endoneurial location, given that the axolemmal Na(+)-K(+
37 ent vessels may greatly increase the risk of endoneurial M. leprae bacteremia, and also enhance the r
38 growth factor receptor (p75) expression, and endoneurial macrophage apolipoprotein E (apo E) synthesi
39 owed a significant increase in the number of endoneurial macrophages (EMPhi) that lie around nerves i
40 elial cells and laser-capture microdissected endoneurial microvessels from four cryopreserved normal
41 ence controls, the proportion of TM-positive endoneurial microvessels was 15-fold lower (0.02 vs. 0.3
43 eductions in MNCV, Na,K-ATPase activity, and endoneurial NBF in flurbiprofen-treated ND and STZ-D rat
44 nerve conduction velocity (MNCV), total and endoneurial nerve blood flow (NBF), Na,K-ATPase activity
45 rve functional changes; that is, decrease in endoneurial nutritive blood flow, motor and sensory nerv
46 but not sciatic-tibial motor NCV, corrected endoneurial nutritive but not composite NBF, increased t
47 e pathway by which sodium ions return to the endoneurial space after they have entered the axon durin
49 AMP levels significantly after incubation of endoneurial tissue with various isozyme-specific inhibit
50 ructions regenerating axons encounter in the endoneurial tubes of old animals give rise to slower reg
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