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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
8                         Sclera, pericardium, dura mater and cornea are available as a patch graft.
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
11       Our study demonstrates that postmortem dura mater, and to a lesser extent, scalp, are viable so
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
14                 The large venous sinuses and dura mater are pain-sensitive and are innervated primari
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.
23                                          The dura mater is a vascularized membrane surrounding the br
24 tion of nociceptive afferent C-fibres of the dura mater leads to a sensitization of second-order neur
25 cantly increased 99Tc-G extravasation in the dura mater of C57BL mice.
26 f mast cells, SP and its receptor (NK-1R) in dura mater of mice in response to acute stress.
27 finding of a lymphatic vessel network in the dura mater of the mouse brain.
28 ultimodal neural implants, termed electronic dura mater or e-dura, to fulfill this need.
29            We eliminate postulated roles for dura mater or skull base changes in craniosynostosis.
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
34  surrounded by dura mater extending from the dura mater surrounding the spinal cord.
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
39                               Involvement of dura mater was noted in another.
40   Trigeminal afferents of the supratentorial dura mater were activated by mustard oil (MO) and the re
41                               The electronic dura mater, which we call e-dura, embeds interconnects,

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