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1 at intercellular junctions of arachnoid and pia mater cells that form the leptomeninges and border t
2 s into the SAS bordered by the arachnoid and pia mater during health and neuroinflammation, and detec
3 ture and function of the dura, arachnoid and pia mater in the context of conventional views, recent p
5 ssels, and in the dura mater, arachnoid, and pia mater of the meningeal sheath surrounding the optic
8 at affect arteries and veins in the dura and pia, we determined the extent to which CGRP contributes
10 ected in the cerebral cortex, pia mater, and pia-ensheathed leptomeningeal vessels in two GBCA-expose
12 l blood vessels and later within neurons and pia arachnoid (> or =3 hours), particularly within pirif
13 moniae iron uptake ABC transporters, piu and pia, resulted in a strain with impaired growth in two ty
14 treptonigrin of the individual pit, piu, and pia mutant strains and comparison of the growth in iron-
15 e astrocytes interact with blood vessels and pia, we suggest that such contact represents an early st
16 ates comprise three layers (dura, arachnoid, pia mater), representing an important barrier surroundin
18 that are not observed in young animals, but pia is unexpectedly hypertrophied in a mouse model of Al
19 tention was detected in the cerebral cortex, pia mater, and pia-ensheathed leptomeningeal vessels in
20 of overmigrated neurons into the developing pia-arachnoid, scattering its mesenchymal cells througho
21 t in basal laminae of the retina, epidermis, pia, cardiac and striated muscle, kidney, blood vessels,
22 recorded cell was estimated by distance from pia to the layer VI/white matter boundary, and verified
23 in layer VI when vertical cuts extended from pia mater through layers IV or V, but were no longer syn
30 ubarachnoid space (enclosed by the meningeal pia and arachnoid layers), and the outmost meningeal dur
34 ing density was high in the olfactory nerve, pia mater, and aspects of the ventricular ependyma and w
35 that interlaminar processes contact neurons, pia, and capillaries, suggesting a potential role for IL
36 iable and that the structure and function of pia suggests a previously unrecognized role in regulatin
41 issue-resident leukocytes in CNS parenchyma, pia-enriched subdural meninges, dura mater, choroid plex
42 echanical stimulation of adult human and rat pia-arachnoid cell cultures (loaded with calcium indicat
43 pes were observed in layer I: Cajal Retzius, pia surface, vertical axon, and horizontal axon cells.
46 ingle and double mutant strains suggest that pia is the dominant iron transporter during in vitro and
48 landmarks, i.e., the barrels in Layer 4, the pia and white matter surfaces and the blood vessel patte
51 that lie as far as 600 micrometers below the pia mater of primary somatosensory cortex in rat; this d
53 pressing neurons that lie 700 um beneath the pia, calcium dynamics of layer 5b projection neurons and
54 2(-/-) cell lines were implanted between the pia and arachnoid meninges as well as in the sciatic ner
55 n mast cells (or their precursors) enter the pia and access the thalamus by traveling along the ablum
56 then along blood vessels extending from the pia into the telencephalon on posthatch day 4-5, and in
57 he number of cells and microvessels from the pia to the white matter, show a significant correlation
60 intense mGluR1 alpha immunoreactivity in the pia mater and blood vessels in the subarachnoid space an
61 t, in newborn mice, Ink4c is detected in the pia mater and in an adjacent layer of rapidly dividing c
64 ymphatic marker staining was detected in the pia mater, in the arachnoid, in venous sinuses, and amon
68 disturbances that coincide with holes in the pia, and the caudomedial tectum exhibits prominent folds
69 uptake mechanisms, GABA transporters in the pia-arachnoid may help to regulate the amount of GABA av
73 ar implications of the LC insertion into the pia mater are not well understood and should be investig
75 he peripapillary scleral flange and into the pia, and computed the total area of insertion and fracti
77 that abnormalities in a region involving the pia mater and subpial cord occur early in the course of
78 he meninges, a triple layer of membranes-the pia mater, arachnoid mater, and dura mater-surround the
80 tolysin gene) and piaB (permease gene of the pia ABC transporter) are currently used as the gold-stan
81 lted in widespread infection of cells of the pia and arachnoid mater of the leptomeninges over large
84 orresponding to the expected location of the pia mater and subpial region-and in spinal cord white an
86 m to anatomically distinct cell types of the pia, inner arachnoid, outer arachnoid barrier, and dural
87 gration defects leading to disruption of the pia-arachnoid, ectopia of fibroblasts in the cortex, and
92 ortical parenchyma may be transmitted to the pia-arachnoid and might then serve in the induction of n
93 and 3 was almost entirely restricted to the pia-arachnoid, whereas mGATs 1 and 4 were present only i
94 spinal cord, from the ependymal layer to the pia-glial limitans, and from oligodendrocytes surroundin
97 lls in the more internal connective tissues (pia-arachnoid and endoneurium-perineurium) was also foun