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1 limiting the spread of HER2(+) LC beyond the leptomeninges.
2 as well as those that restrict its growth to leptomeninges.
3 molecular landscape of the developing human leptomeninges.
4 sfully attempted to eliminate B cells in the leptomeninges.
5 risk of melanoma within the skin, brain, or leptomeninges.
6 llaries of the cerebral cortex and overlying leptomeninges.
7 ection of cortex, white matter and overlying leptomeninges.
8 d to the implant pocket and to adjacent host leptomeninges.
9 n regions, and in white and gray matter, and leptomeninges.
10 four mGATs was present to some degree in the leptomeninges.
11 areas of contrast enhancement involving the leptomeninges.
12 dispersed across the surface of the brain's leptomeninges.
13 ecular properties of cell types within human leptomeninges.
14 r cells to control cancer cell growth in the leptomeninges.
15 unique arachnoid clusters specific to ageing leptomeninges.
17 rogeneity as medulloblastoma metastasizes to leptomeninges and as it evolves in the face of radiation
18 arachnoid and pia mater cells that form the leptomeninges and border the subarachnoid space (SAS) fi
19 tia of small arteries and capillaries of the leptomeninges and cerebral cortex and is a major cause o
20 ulates predominantly in the small vessels of leptomeninges and cerebral cortex, leading to fatal stro
23 lso was detected in the lung, as well as the leptomeninges and choroid plexus of the fetal brain.
25 econd most common finding was involvement of leptomeninges and cranial nerves, which manifested as ab
30 c cells (DCs) accumulated in the dorsal root leptomeninges and led to an increase in kynurenine level
31 She had extensive amyloid deposition in the leptomeninges and liver as well as the involvement of th
32 d a specific predilection for binding to the leptomeninges and meningeal blood vessels in human brain
33 ly more serotype A than B spirochetes in the leptomeninges and more serotype B than A spirochetes in
35 increased Fos immunoreactivity in the basal leptomeninges and several regions implicated in autonomi
36 ers was then compared to cells cultured from leptomeninges and to two other types of endothelial cell
38 ne patient developed a relapse in the spinal leptomeninges and was rendered free of disease with spin
39 ll lymphoma in which the brain, spinal cord, leptomeninges and/or eyes are exclusive sites of disease
41 opment of murine BAMs in the choroid plexus, leptomeninges, and perivascular spaces required CSF-1, w
43 in the brain localized predominantly to the leptomeninges, and those in peripheral tissues localized
44 resident within the parenchyma of the brain, leptomeninges, and vascular beds, as well as through sec
45 Thus, the data demonstrate that cells of the leptomeninges are not inert but are active participants
46 of Neisseria meningitidis with cells of the leptomeninges are pivotal events in the progression of b
49 in multiple tissues, including the cerebral leptomeninges, brainstem, peripheral nerves from both fo
50 Although any malignancy can spread to the leptomeninges, breast cancer, particularly the HER2(+) s
51 ated with the cerebral blood vessels and the leptomeninges by immune stimuli such as intravenous admi
52 ith MB-MAFs enhances the colonization of the leptomeninges by medulloblastoma cells and promotes the
54 or cells, as well as explant cultures of the leptomeninges, cortical slice cultures and brain tumor c
55 formed on mRNA isolated from the human fetal leptomeninges detected expression of the G protein-coupl
56 ly, TTR amyloid deposits were present in the leptomeninges, especially the leptomeningeal vessels, an
57 within the cerebrospinal fluid (CSF)-filled leptomeninges face substantial microenvironmental challe
62 cellular heterogeneity within the developing leptomeninges, identifying distinct subpopulations of fi
63 a melatonin receptor expression in the fetal leptomeninges implies that melatonin may play a role in
64 and thus potential barrier properties of the leptomeninges in controlling access of immune mediators
65 esenting cells (APCs) within the spinal cord leptomeninges in experimental autoimmune encephalomyelit
70 NS relapse in the brain parenchyma, eyes, or leptomeninges is an uncommon but devastating complicatio
71 erature shows that amyloid deposition in the leptomeninges is not uncommon in TTR amyloidoses clinica
72 The structural organization of the dura and leptomeninges is reflected in its magnetic resonance (MR
73 1 (SDF1) (CXCL12), which is expressed by the leptomeninges, is necessary and sufficient to cause marg
74 t fibroblast-like transcriptomes in cerebral leptomeninges; link them to anatomically distinct cell t
76 BCC) metastasis and proliferation within the leptomeninges (LM) are poorly understood, which limits t
79 ve, abnormal capillary venous vessels in the leptomeninges of the brain and choroid, glaucoma, seizur
81 with the exception of the choroid plexus and leptomeninges of the brain, where it is expressed from b
82 cular malformations affecting skin, eyes and leptomeninges of the brain, which can lead to glaucoma,
83 es except adult liver and the choroid plexus/leptomeninges of the central nervous system where IGF-II
89 Metastasis to the cerebrospinal-fluid-filled leptomeninges, or leptomeningeal metastasis, represents
90 ignancy that affects the brain, spinal cord, leptomeninges, or vitreoretinal space, without evidence
91 cells of the pia and arachnoid mater of the leptomeninges over large areas of the cerebral hemispher
92 cortex (P<0.001) and seven times more in the leptomeninges (P = 0.013); among the affected blood vess
95 ion was explored in blood vessels located in leptomeninges (pial vessels) and brain parenchyma (paren
97 the subarachnoid space and indicate that the leptomeninges play an important role in experimental aut
98 ly, severe meningitis with thickening of the leptomeninges, prominent vasculitis, and encephalitis wa
103 nescence, with rare metastatic spread to the leptomeninges, suggesting roles for MYCN in both progres
104 lls spread to cerebrospinal fluid-containing leptomeninges surrounding the brain and spinal cord, a c
105 spread to the cerebrospinal fluid-containing leptomeninges surrounding the brain and spinal cord.
106 tonin binding sites were identified over the leptomeninges surrounding the human fetal brain using qu
107 ormative landmark for in vivo imaging of the leptomeninges that can be used to visualize the borders
108 sclerosis have extensive inflammation in the leptomeninges that is associated with increased subpial
110 cement of the parenchyma (three of 20; 15%), leptomeninges (three of 20; 15%), cranial nerves (two of
111 expression of Igf2 in the choroid plexus and leptomeninges, tissues where the gene is thought not to
114 this futile anti-tumour response within the leptomeninges, we developed syngeneic lung cancer, breas
116 at echoviruses specifically replicate in the leptomeninges, where they induce profound inflammation a
117 tic disease to the central nervous system or leptomeninges who met eligibility criteria for (131)I-om
118 macrophages in the dura mater but not in the leptomeninges, without affecting MLVs or CSF drainage.