戻る
「早戻しボタン」を押すと検索画面に戻ります。 [閉じる]

コーパス検索結果 (１語後でソート)

通し番号をクリックするとPubMedの該当ページを表示します
1  1.0mM was delivered through each cup on the dura mater.
2 in response to electrical stimulation of the dura mater.
3  not observe any lymphatic vessels in spinal dura mater.
4 ssion and delayed inflammation within rodent dura mater.
5 nd the consequences of its inhibition within dura mater.
6 ere observed outside the vasculature was the dura mater.
7 lbumin from postcapillary venules within the dura mater.
8 hatic Lyve-1+ cells in both brain and spinal dura mater.
9  pain-sensitive meningeal tissues, including dura mater.
10 safe distance between the needle tip and the dura mater.
11 ivation in the sagittal sinus regions of the dura mater.
12  that protect fenestrated vasculature in the dura mater.
13  venous sinuses, and among the layers of the dura mater.
14 ctive tissue between suboccipital muscle and dura mater.
15 rectly enter the subarachnoid space from the dura mater.
16 d microvascular endothelial cells from human dura mater.
17 e atlanto-axial interspace and attach to the dura mater.
18 order between the central nervous system and dura mater.
19 ce, and then attaches to the cervical spinal dura mater.
20 nhibited plasma protein extravasation within dura mater after electrical trigeminal ganglion stimulat
21                         Sclera, pericardium, dura mater and cornea are available as a patch graft.
22 lls in the most external connective tissues (dura mater and epineurium) versus electron-lucent cells
23 ome contusion injuries do not compromise the dura mater and in such cases implantation of preformed s
24 ating intracranial tissues, for example, the dura mater and large vessels, as well as their downstrea
25 ast cells in the interparietal region of the dura mater and the levels of mast cell activation in the
26 subarachnoid space and then travel along the dura mater and/or cranial nerves.
27 eases in 3-NT expression in both the TGs and dura mater, and attenuated TG neuronal hyperexcitability
28 eral prefrontal cortex, other brain regions, dura mater, and dural fibroblasts of a single neurotypic
29       Our study demonstrates that postmortem dura mater, and to a lesser extent, scalp, are viable so
30 ding the central retinal vessels, and in the dura mater, arachnoid, and pia mater of the meningeal sh
31 t surround the central nervous system (CNS)- dura mater, arachnoid, and piamater - possess unique fea
32 dies that the intracranial blood vessels and dura mater are important pain-producing structures since
33                 The large venous sinuses and dura mater are pain-sensitive and are innervated primari
34        They drain the epidural space and the dura mater around the spinal cord and associate with leu
35                     These data implicate the dura mater as a primary location of action for CGRP in m
36  involve neurogenic inflammation (NI) of the dura mater associated with the sensation of throbbing pa
37 e detected induction of interleukin 1beta in dura mater at 2 and 6 h and increased interleukin 6 in d
38  [inducible NOS (iNOS)] mRNA upregulation in dura mater beginning at 2 h and an increase in the corre
39 body selectively depleted macrophages in the dura mater but not in the leptomeninges, without affecti
40 BMS cells, calvarial-derived osteoblasts and dura mater cells to heal critical-size mouse calvarial d
41  parenchyma, pia-enriched subdural meninges, dura mater, choroid plexus and cerebrospinal fluid.
42 vanced Maillard reaction was investigated in dura mater collagen and lens proteins from dogs that wer
43 C severely impairs cell proliferation in the dura mater, consequently resulting in calvaria agenesis.
44      The maximum force was different for the dura mater (Crosado 25 +/- 13 N vs. fresh 21 +/- 20 N; m
45 almed and 35 embalmed specimens) and cranial dura mater (DM, 60 unembalmed cadavers, and 25 embalmed
46   The F12W sections showed evidence that the dura mater dominated by fibroblasts, attached to the pos
47 o the soft neurotechnology called electronic dura mater, e-dura.
48                                 We show that dura mater-engrafted islets integrate with host vascular
49 immunological perspective and posit that the dura mater evolved an elaborate innate and adaptive immu
50 fects of ELA on sucrose preference behavior, dura mater expression of inflammatory markers and mast c
51 or in males or females, but it increases the dura mater expression of the genes coding for mast cell
52  nerves or plexuses, which are surrounded by dura mater extending from the dura mater surrounding the
53 s of contaminated growth hormone extracts or dura mater grafts derived from cadavers.
54         The outer layer of the meninges, the dura mater, has recently been described to contain both
55 AD mice, there is impaired CSF efflux to the dura mater, impaired CSF flow along bridging veins, and
56 ation, and plasma protein leakage within the dura mater in part by a neurokinin-1-receptor mechanism.
57                                          The dura mater is a vascularized membrane surrounding the br
58 n between the central nervous system and the dura mater is crucial for waste clearance and immune sur
59                                          The dura mater is rich in tissue-resident macrophages origin
60     Rather, IL-17 produced by T cells in the dura mater is the mediator released in the cerebrospinal
61           The most exterior CNS barrier, the dura mater, is unique because it resembles a peripheral
62 tion of nociceptive afferent C-fibres of the dura mater leads to a sensitization of second-order neur
63 t pull of this muscle on the cervical spinal dura mater may affect the circulation of the cerebrospin
64 cantly increased 99Tc-G extravasation in the dura mater of C57BL mice.
65 ndothelial Lyve-1+ cells are also present in dura mater of meninges.
66  are widely present in the leptomeninges and dura mater of meninges.
67 f mast cells, SP and its receptor (NK-1R) in dura mater of mice in response to acute stress.
68 n 2015 of lymphatic vessels localized to the dura mater of mice, there has been a growing interest in
69 d adjacent to the blood vessels in the brain dura mater of rats.
70  By transplanting pancreatic islets onto the dura mater of the mouse brain, we establish a microscopy
71 finding of a lymphatic vessel network in the dura mater of the mouse brain.
72 ultimodal neural implants, termed electronic dura mater or e-dura, to fulfill this need.
73            We eliminate postulated roles for dura mater or skull base changes in craniosynostosis.
74 ons (ABVI) and periosteal appositions of the dura mater (PADM).
75 tonin gene-related peptide (CGRP) to the rat dura mater produces cutaneous periorbital hypersensitivi
76 hat TGFbeta signaling within the CNC-derived dura mater provides essential inductive instruction for
77  cultures generated from 146 scalp and/or 53 dura mater samples from 146 postmortem human brain donor
78 presents extracerebral tissue (scalp, skull, dura mater, subarachnoid space, etc.) and the bottom lay
79 ssociated macrophages (BAMs) residing in the dura mater, subdural meninges and choroid plexus consist
80 causes headache via MrgprB2 of mast cells in dura mater, suggesting that MrgprB2 is a potential targe
81 embranes-the pia mater, arachnoid mater, and dura mater-surround the CNS, encompassing the cerebrospi
82 ediscoveries of lymphatic vessels within the dura mater surrounding the brain, made possible by moder
83  surrounded by dura mater extending from the dura mater surrounding the spinal cord.
84 lymphoid structure around vasculature in the dura mater that can sample antigens and rapidly support
85 al implants with the shape and elasticity of dura mater, the protective membrane of the brain and spi
86 riggers NI and mast cell activation in mouse dura mater through the activation of NK-1 receptors.
87 e structures were observed blending into the dura mater through the gap.
88                                          The dura mater thus offers long-term optical access to funct
89 d by corticotropin-releasing factor (CRF) in dura mater to drive nociception.
90  or control solution were applied to the rat dura mater to elicit a presumed state of cephalic pain.
91 ceptive signals transmitted from the cranial dura mater to the brain, is uniquely exacerbated by expo
92 ste products travel along the laminae of the dura mater toward the jugular fossa, lamina cribrosa, an
93 d, and a chondrogenic-like population in the dura mater underlying the suture.
94  cell degranulation by alcohol withdrawal in dura mater was dependent on the presence of MrgprB2.
95                               Involvement of dura mater was noted in another.
96 cting the suboccipital muscles to the spinal dura mater was originally discovered in humans.
97   Trigeminal afferents of the supratentorial dura mater were activated by mustard oil (MO) and the re
98 cells located in the transverse sinus of the dura mater, where the meningeal lymphatics run along, an
99  in the dorsal and caudobasal regions of the dura mater, where they ensure waste product elimination
100                               The electronic dura mater, which we call e-dura, embeds interconnects,