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1 cal and immunocytochemical phenotype between protoplasmic and fibrous astrocytes.
2 e heterogeneity of astrocytic states in both protoplasmic and fibrous-like (CD44+) astrocytes.
3                           Significantly, one protoplasmic astrocyte state showed high levels of metal
4 e knowledge of how the complex morphology of protoplasmic astrocytes affects their 3D relationships w
5                                              Protoplasmic astrocytes are critically important to ener
6                                              Protoplasmic astrocytes are increasingly thought to inte
7                              In all mammals, protoplasmic astrocytes are organized into spatially non
8  postnatal months prior to its expression in protoplasmic astrocytes at 41 postconceptional weeks onw
9  Released glutamate acts on receptors on the protoplasmic astrocytes closely apposed to the synapse t
10                                    Mammalian protoplasmic astrocytes develop a dense ramified meshwor
11                       Our findings show that protoplasmic astrocytes establish primarily exclusive te
12 ing was used to directly isolate neurons and protoplasmic astrocytes from the cortex of adult mice.
13  are precursors of oligodendrocytes and some protoplasmic astrocytes in gray matter.
14                          We report here that protoplasmic astrocytes in human neocortex are 2.6-fold
15 iated astrocytes account for the majority of protoplasmic astrocytes in neocortex.
16                                 To this end, protoplasmic astrocytes in the adult rat dentate gyrus w
17 e interactions in detail, groups of adjacent protoplasmic astrocytes in the CA1 stratum radiatum were
18 e rise to a subset of immature, postmitotic, protoplasmic astrocytes in the gray matter of the spinal
19 es throughout the CNS and a subpopulation of protoplasmic astrocytes in the gray matter of the ventra
20 n both gray and white matter and a subset of protoplasmic astrocytes in the gray matter of the ventra
21 as NG2 cells in the embryonic brain generate protoplasmic astrocytes in the gray matter of the ventra
22 g oligodendrocytes and in a subpopulation of protoplasmic astrocytes in the gray matter of ventrolate
23                                        Human protoplasmic astrocytes manifest a threefold larger diam
24 inct contrast to those reported for reactive protoplasmic astrocytes of the gray matter, in which the
25 on of any of the three VGLUTs by gray matter protoplasmic astrocytes of the primary somatosensory cor
26 pared from acutely resected surgical tissue, protoplasmic astrocytes propagate Ca(2+) waves with a sp
27 nule layer, D-serine is found transiently in protoplasmic astrocytes surrounding glomeruli, where it
28          This racemase has been localized to protoplasmic astrocytes that ensheath synapses and modul
29 astrocytes initiates a conversion of normal, protoplasmic astrocytes to astrocytes that display sever
30 fap(+/R236H), resulting in the conversion of protoplasmic astrocytes to cells that have lost their bu
31                                          The protoplasmic astrocytes were either isolated or formed s
32 nctions in balancing the number of dorsal GM protoplasmic astrocytes with dorsal WM fibrous astrocyte
33 intranuclear inclusions were also present in protoplasmic astrocytes, including Bergmann glia in the
34 ration resulted in expression in neurons and protoplasmic astrocytes, respectively.
35 etinal ganglion cell (RGC) somata and axons, protoplasmic astrocytes, vascular endothelial cells, and
36 e telencephalon, D-serine is concentrated in protoplasmic astrocytes, which are abundant in neuropil
37 alized to perivascular end feet in the CD44- protoplasmic astrocytes.
38  was possible to document the development of protoplasmic astrocytes.
39 res that contain both projection neurons and protoplasmic astrocytes.
40 distinct gene expression pattern relative to protoplasmic astrocytes.
41 nal populations, yet abundant in fibrous and protoplasmic astrocytes.
42 cus strongly upregulate Gfap in grey matter (protoplasmic) astrocytes, implying that signalling throu
43 , and solely by phenotypic transformation of protoplasmic astroglia in gray matter.
44                                       Mature protoplasmic astroglia in the mammalian CNS uniquely pos
45  sheath (OS), and within this sheath are the protoplasmic cell cylinder (PC) and periplasmic flagella
46 mbrane sheath, and within this sheath is the protoplasmic cell cylinder and subterminally attached pe
47 a tight-fitting ribbon that wraps around the protoplasmic cell cylinder in a right-handed sense.
48 s) subterminally attached to each end of the protoplasmic cell cylinder, and surrounding the cell is
49  alkaline plasmolysis and separated from the protoplasmic cylinder by sucrose density gradient ultrac
50 rimitia motility that posits rotation of the protoplasmic cylinder within the outer sheath.
51 eta-NADH oxidase activity and the absence of protoplasmic cylinder-associated proteins observed by Co
52 and, in T. pallidum, is tightly bound to the protoplasmic cylinder.
53               The OMV fractions were free of protoplasmic-cylinder material, as judged by immunoblott
54 tions of OMVs were distinct from that of the protoplasmic-cylinder material, which was found in the s
55 ay be useful to distinguish intra- and extra-protoplasmic dimerization.
56 d increase in the density of plasma membrane protoplasmic face intramembrane particles.
57                  The particle density in the protoplasmic face of the oocyte plasma membrane increase
58              The density of particles on the protoplasmic face of the plasma membrane of oocytes expr
59 nits), clusters of particles appeared in the protoplasmic face of the plasma membrane.
60 eze-fracture particle, which appeared in the protoplasmic face only after EAAT3 expression.
61 novel transmembrane particles in the P-face (protoplasmic face) of oocytes injected with TrkA cRNA, b
62                                              Protoplasmic flow carries signals through fungal network
63 vity of brevican occurs predominantly in the protoplasmic islet in the internal granular layer after
64 irst described by Santiago Ramon y Cajal as "protoplasmic kisses that appear to constitute the final
65      It maps given data configuration into a protoplasmic network.
66                                          The protoplasmic networks also show a degree of similarity t
67 ter perhaps representing a shift from CD44- "protoplasmic" to CD44+ "fibrous"-like astrocytes.
68  degrees C, the electrical resistance of the protoplasmic tube increases from approximately 3 MOmega
69 mould spans the sources with networks of its protoplasmic tube.
70 lime mould span two electrodes with a single protoplasmic tube: if the tube is heated to approximatel
71                                  Networks of protoplasmic tubes of organism Physarum polycehpalum are
72 ; proposing that the network connectivity of protoplasmic tubes shows pathway-dependent plasticity.
73 uld computers we explore conductivity of the protoplasmic tubes; proposing that the network connectiv