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1 1.0mM was delivered through each cup on the dura mater.
2 in response to electrical stimulation of the dura mater.
3 ssion and delayed inflammation within rodent dura mater.
4 nd the consequences of its inhibition within dura mater.
5 ere observed outside the vasculature was the dura mater.
6 lbumin from postcapillary venules within the dura mater.
7 nhibited plasma protein extravasation within dura mater after electrical trigeminal ganglion stimulat
9 lls in the most external connective tissues (dura mater and epineurium) versus electron-lucent cells
10 ating intracranial tissues, for example, the dura mater and large vessels, as well as their downstrea
12 ding the central retinal vessels, and in the dura mater, arachnoid, and pia mater of the meningeal sh
13 dies that the intracranial blood vessels and dura mater are important pain-producing structures since
15 involve neurogenic inflammation (NI) of the dura mater associated with the sensation of throbbing pa
16 e detected induction of interleukin 1beta in dura mater at 2 and 6 h and increased interleukin 6 in d
17 [inducible NOS (iNOS)] mRNA upregulation in dura mater beginning at 2 h and an increase in the corre
18 BMS cells, calvarial-derived osteoblasts and dura mater cells to heal critical-size mouse calvarial d
19 vanced Maillard reaction was investigated in dura mater collagen and lens proteins from dogs that wer
20 C severely impairs cell proliferation in the dura mater, consequently resulting in calvaria agenesis.
21 nerves or plexuses, which are surrounded by dura mater extending from the dura mater surrounding the
22 ation, and plasma protein leakage within the dura mater in part by a neurokinin-1-receptor mechanism.
24 tion of nociceptive afferent C-fibres of the dura mater leads to a sensitization of second-order neur
30 hat TGFbeta signaling within the CNC-derived dura mater provides essential inductive instruction for
31 cultures generated from 146 scalp and/or 53 dura mater samples from 146 postmortem human brain donor
32 presents extracerebral tissue (scalp, skull, dura mater, subarachnoid space, etc.) and the bottom lay
33 ediscoveries of lymphatic vessels within the dura mater surrounding the brain, made possible by moder
35 al implants with the shape and elasticity of dura mater, the protective membrane of the brain and spi
36 riggers NI and mast cell activation in mouse dura mater through the activation of NK-1 receptors.
37 or control solution were applied to the rat dura mater to elicit a presumed state of cephalic pain.
38 ceptive signals transmitted from the cranial dura mater to the brain, is uniquely exacerbated by expo
40 Trigeminal afferents of the supratentorial dura mater were activated by mustard oil (MO) and the re
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