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 he artery and breaks tissue tolerance in the perivascular space.
2 productively infected MNLs into a potential perivascular space.
3 ased number of Gaucher cells in the cerebral perivascular space.
4 ron-laden macrophages, predominately seen in perivascular space.
5 blue around the nerves in the hepatic hilar perivascular space.
6 was found in myeloid populations and in the perivascular space.
7 lls can engraft in the cerebral vascular and perivascular space.
8 allowing substances in the CSF to enter the perivascular space.
9 lexity of regulation of hematopoiesis in the perivascular space.
10 s play an important role in the integrity of perivascular space.
11 al stromal cells (MSCs) are important in the perivascular space.
12 l TSP-1 upregulation in the interstitial and perivascular space.
13 nels and elevate [K(+)](o) in the restricted perivascular space.
14 humoral immunity targeting an antigen in the perivascular space.
15 e immune responses from mucosal surfaces and perivascular spaces.
16 lymphocytes in both the brain parenchyma and perivascular spaces.
17 sular foci at MR imaging are due to enlarged perivascular spaces.
18 of CD68+ macrophages in the interstitial and perivascular spaces.
19 o) type, and they phagocytosed fibrinogen in perivascular spaces.
20 on of white matter tracts and penetration of perivascular spaces.
21 laying a role in enlargement of white matter perivascular spaces.
22 sing microglia in fetal brain parenchyma and perivascular spaces.
23 phatic assessment with detection of enlarged perivascular spaces.
24 spaces in concentric shells surrounding the perivascular spaces.
25 11195 binding (P < 0.001) in the vicinity of perivascular spaces.
26 matrix and reduces NP confinement within the perivascular spaces.
27 t, Tregs were restricted to the meninges and perivascular spaces.
28 ter confinement of CD4(+) lymphocytes to CNS perivascular spaces.
29 9 expression was confined to the vasculature/perivascular spaces.
30 in deposition was found in blood vessels and perivascular spaces.
31 most infiltrating cells remain localized to perivascular spaces.
32 oid space and infiltrated the Virchow-Robin (perivascular) space.
33 erivascular macrophages (PVM) located in the perivascular space, a major site of brain Abeta collecti
34 eased burden of frontal cortical MRI-visible perivascular spaces, a putative neuroimaging marker of g
35 diffusion-tensor imaging analysis along the perivascular space (ALPS) index, is involved in developm
36 Rac in the Nestin(+) cells would perturb the perivascular space, altering HSC localization and hemato
37 ecruitment prolonged T cell retention in the perivascular space, although no difference in overall CN
38 endfeet syncytium abutting subarachnoid and perivascular spaces, although direct evidence remains in
40 ity that allowed angiotensin II to enter the perivascular space and activate angiotensin type 1 recep
41 ich are immune cells that are present in the perivascular space and are a major peripheral source of
43 ancer cells were specifically located in the perivascular space and closely associated with blood ves
44 CD40(-/-) mice, T cells were retained in the perivascular space and did not migrate into the parenchy
45 essing mononuclear cells into and out of the perivascular space and leading to progression of disease
46 ouble-negative CD3(+)CD4(-)CD8(-) T cells in perivascular space and reduced vascular oxidative stress
47 rebral ischemia, CD8+ T cells infiltrate the perivascular space and secrete interleukin-16 (IL-16), a
49 roid plexus in early inflammation and in the perivascular space and SIV encephalitis (SIVE) lesions l
51 fluid changes are correlated with changes to perivascular space and spaceflight associated neuro-ocul
52 s not required for monocyte migration to the perivascular space and that vascular remodeling followin
53 entitially released drug is cleared from the perivascular space and those by which drug enters the bl
55 t the bottlenose dolphin possesses prominent perivascular spaces and aquaporin-4 astroglial water cha
56 There was no association between markers of perivascular spaces and blood biomarkers of systemic inf
57 We investigated the relationship between perivascular spaces and both CNS and peripheral inflamma
58 acytic inflammation, with a predilection for perivascular spaces and collagenous tissues, was observe
59 vasoconstriction, which in turn enlarged the perivascular spaces and doubled glymphatic inflow speeds
60 the morphological and functional aspects of perivascular spaces and how those spaces can be visualiz
61 r matrix proteins, obstructing CSF access to perivascular spaces and impairing CNS perfusion and clea
63 arenchyma towards the outer surfaces and the perivascular spaces and is formed by a subset of astrocy
65 lation of mature thymocytes within medullary perivascular spaces and reduced numbers of recent thymic
66 odies exhibited size-dependent access to the perivascular spaces and tunica media basement membranes
67 he deposited drug diffuses directly from the perivascular space, and little arrives from the endovasc
71 cal superficial siderosis, centrum semiovale perivascular spaces, and white matter hyperintensities.
72 cal superficial siderosis, centrum semiovale perivascular spaces, and white matter hyperintensities.
73 rtical infarcts, microinfarcts, microbleeds, perivascular spacing, and white matter attenuation is co
76 Our findings demonstrate that white matter perivascular spaces are associated with increased 11C-PK
77 The mechanisms underlying enlargement of perivascular spaces are not fully understood, but both i
79 caused by a leak of blood and fluid into the perivascular space around the artery, as in several pati
80 hed to VE-cadherin(+) cells, implicating the perivascular space as a near-homogenous location of LT-H
82 the endothelium; (iii) it is detected in the perivascular spaces at early time points (by 1 min) and
84 with the flow in the thin annular gap of the perivascular space between an impermeable artery and the
86 ensity - WMH, microbleeds, lacunes, enlarged perivascular spaces, brain atrophy) as seen on structura
89 m-dependent activation of the T cells in the perivascular space, but not within the vascular lumen.
90 orrhages where plasma fibrinogen leaked into perivascular spaces, but it did not affect the distribut
91 associated with increasing age and enlarged perivascular spaces, but these did not explain the lacun
93 hite matter hyperintensities (WMH), enlarged perivascular spaces, cerebral microbleeds and lacunes.
94 al (thymic epithelial space) and peripheral (perivascular space) components that functions well into
95 ild inflammatory exudates, in endomysial and perivascular spaces, consisted of lymphocytes, histiocyt
98 highly dendritic cells localized within the perivascular space, dermal-epidermal junction, and retic
99 infarcts, microinfarcts, arteriolosclerosis, perivascular space dilation and myelin loss-predicted co
100 orrhage, fibrinoid necrosis, microaneurysms, perivascular space dilation, perivascular haemosiderin l
101 white matter, tissue in closest proximity to perivascular spaces displayed greater 11C-PK11195 bindin
102 d to characterize how drug released into the perivascular space enters the arterial wall and how it i
104 able, 3D neural network for grading enlarged perivascular spaces (EPVS) severity at the level of the
105 (PVWM) and deep white matter (DWM), enlarged perivascular spaces (ePVS), lacunar strokes, and cerebra
106 hite matter hyperintensities (WMH), enlarged perivascular spaces (EPVS), microbleeds and lacunes.
109 ject-based morphologic estimates of enlarged perivascular spaces (ePVSs) in clinical-field-strength (
110 thereby drains the brain's interstitial and perivascular spaces, facilitates outward signaling beyon
111 enlargement and eccentric thickening of the perivascular space (fibrillar collagen type I deposition
113 mas are highly invasive tumours that use the perivascular space for invasion and co-opt existing vess
116 advances have facilitated in vivo studies of perivascular space function in intact rodent models duri
117 remain, but what is now clear is that normal perivascular space function is important for maintaining
118 have pleomorphic lymphoid infiltrates in the perivascular spaces, had significantly increased numbers
119 lthough T cells could reach the meninges and perivascular space in the absence of TNFR1, recruitment
120 te matter characteristic (ie, severe visible perivascular spaces in centrum semiovale or white matter
122 eability in the local vicinity of individual perivascular spaces in concentric shells surrounding the
123 ive review is to summarize the literature on perivascular spaces in human neuroinflammation and assoc
126 grade), whereas the severity of MRI-visible perivascular spaces in the basal ganglia was associated
127 justed analyses, the severity of MRI-visible perivascular spaces in the centrum semi-ovale was indepe
129 's disease, we hypothesized that MRI-visible perivascular spaces in the centrum semi-ovale would be a
130 nocytes into the choroid plexus stromata and perivascular spaces in the cerebra of rhesus macaques ac
131 iods when fluid and solutes are driven along perivascular spaces in the reverse direction to the flow
132 ng scale and by measurement of the volume of perivascular spaces in the white matter and the basal ga
133 e attachment of solutes to the lining of the perivascular space, in order to produce a valve-like eff
135 en cerebrospinal fluid (CSF) influx from the perivascular spaces into the interstitial fluid space ra
136 though almost all the drug released into the perivascular space is cleared through the extravascular
137 n through the endothelial cell wall into the perivascular space is well characterized; however, mecha
139 Cerebrospinal fluid (CSF) drains along the perivascular space, known as the glymphatic system, to t
141 uding white matter hyperintensities, dilated perivascular spaces, lacunar infarcts, microbleeds, and
142 on structural MRI, visual scores and volume; perivascular spaces; lacunes and microbleeds), and vascu
144 CSF mobility in humans, down to the level of perivascular spaces located around penetrating vessels,
146 e more than a century of intense research on perivascular spaces, many open questions remain about th
147 t the anatomical distribution of MRI-visible perivascular spaces may reflect the underlying cerebral
148 cts, lacunes, white matter hyperintensities, perivascular spaces, microbleeds, and brain atrophy.
149 ess and sleep, and MRI in humans has enabled perivascular space morphology to be related to cognitive
150 ted by vascular dynamics, the maintenance of perivascular spaces, neural activity during sleep, and l
153 inent lymphocyte population infiltrating the perivascular space of choroidal neovascularization (CNV)
155 and inflammatory cells that appeared in the perivascular space of intramural coronary arteries and a
157 quantify human brain CSF dynamics along the perivascular space of major arteries and their branches.
158 find that glioma cells, as they populate the perivascular space of preexisting vessels, displace astr
159 exclusively target the meninges and vascular/perivascular space of the gray and white matter of the b
160 ion or fibrosis in the media, adventitia, or perivascular space of vessels treated with the beta-part
161 ophages in the choroid plexus, meninges, and perivascular spaces of aged AD mice versus WT control mi
162 distribution to deep brain regions along the perivascular spaces of all vessel types, with sdAb acces
163 to inflammatory changes in the meninges and perivascular spaces of both wild-type and complement-def
164 fluid, although convective transport in the perivascular spaces of cerebral blood vessels was also e
167 nto the cisterna magna of mice migrate along perivascular spaces of dural blood vessels and then trav
172 rease influx of cerebrospinal fluid into the perivascular spaces of the brain, to enhance the uptake
174 OR = 0.94, 95% CI = 0.89 to 0.99), and fewer perivascular spaces (OR = 0.95, 95% CI = 0.91 to 0.99).
176 tions to localize infiltrating leukocytes to perivascular spaces, preventing CNS parenchymal infiltra
178 fluorescently labeled albumin tracer in the perivascular space (PVS) along microvessels, primarily t
180 ctive bulk flow of solutes in the CSF in the perivascular space (PVS) is considered one of the import
185 ite matter lesion load, frequency of dilated perivascular spaces (PVS) and abnormalities in cerebral
187 ssel disease (cSVD), solute transport in the perivascular spaces (PVS) and PVS-to-tissue transfer was
190 to analyze the alterations occurring in the perivascular spaces (PVS) in NASA and European Space Age
191 brospinal fluid (CSF) flow along the brain's perivascular spaces (PVS), aiding in the removal of harm
193 infarcts, cerebral microbleeds, and enlarged perivascular spaces (PVS), as well as PET-based biomarke
194 hite matter hyperintensities (WMH), enlarged perivascular spaces (PVS), microbleeds, and infarcts eme
195 spaces around cerebral blood vessels, called perivascular spaces (PVS), through which cerebrospinal f
197 th advancing age, an increased visibility of perivascular spaces (PVSs) on magnetic resonance imaging
198 thway was defined in rodents as a network of perivascular spaces (PVSs) that facilitates organized di
199 tributions of diffusion and advection in the perivascular spaces (PVSs) that surround penetrating cor
200 have evaluated the effects of spaceflight on perivascular spaces (PVSs) within the brain, which are b
201 (PI), white matter lesions (WMLs), enlarged perivascular spaces (PVSs), and lacunar infarcts are com
202 n cerebrospinal fluid (CSF) flow through the perivascular spaces (PVSs, annular channels lining the b
204 Ms in the choroid plexus, leptomeninges, and perivascular spaces required CSF-1, while IL-34 was crit
208 ibe patterns of contrast distribution in the perivascular space, subarachnoid space, and space surrou
209 genesis, the migration of monocytes into the perivascular space surrounding collateral arteries and t
210 have shown evidence of pulsatile CSF flow in perivascular spaces surrounding pial arteries, with a bu
211 et flow of cerebrospinal fluid (CSF) through perivascular spaces surrounding veins and arteries.
212 el consisting of the vascular smooth muscle, perivascular space, synaptic space, and astrocyte glial
213 can, are not abundant in brain except in the perivascular space that is contacted by astrocytes but n
218 ze CXCR4-expressing mononuclear cells to the perivascular space, thereby limiting the parenchymal inf
219 channels, which locally release K+ into the perivascular space to activate SMC Kir channels and caus
221 cell types and structures in and around the perivascular spaces to support normal CNS vascular funct
222 mall deep infarcts, microbleeds, or enlarged perivascular spaces) to severe disability and cognitive
223 ation away from their vitronectin-containing perivascular space toward fibronectin-rich tumor tissue.
224 appeared to be iron-laden macrophages in the perivascular space tracking a network of injured vessels
225 and blood vessels determine the shape of the perivascular space, ultimately controlling the movement
227 -carboxybenzoylsulphonamide (TFL-Zn)] in the perivascular space was significantly decreased in the ne
233 hite matter hyperintensities [WMH], lacunes, perivascular spaces) were assessed on 3T magnetic resona
234 on MRI] microbleeds, siderosis, and enlarged perivascular spaces) were retrospectively assessed while
235 tivation, and T-cell transmigration into the perivascular space, where (ii) blinatumomab induced B-ce
236 e latter, FAP expression was confined to the perivascular space, whereas neoplastic cells additionall
237 distinct CD206+ macrophage population in the perivascular space, which may modulate T cell entry into
238 optic nerve sheath, the neural axon, and the perivascular space, which might represent the critical s
240 cytes were detected only in the vascular and perivascular spaces while albumin and IgG extravasates w
241 d with inflammation of the vascular wall and perivascular space with cells of monocyte/microglia line
242 ubset of white matter vessels have increased perivascular space (with jagged contours) and collagen i
243 have each been shown to drive CSF flow along perivascular spaces, yet it is unknown how such pulsatio
244 method for multimodal autoidentification of perivascular spaces yields individual whole-brain morpho