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1 ding through temporal, parietal, and frontal cerebral cortices.
2  to enable generation of larger, convoluted, cerebral cortices.
3 din-1, claudin-5 or ZO-1 expression in ovine cerebral cortices.
4 ttern of ischemic infarct was territorial in cerebral cortices.
5 ons between lissencephalic and gyrencephalic cerebral cortices.
6 s of mammalian species with highly developed cerebral cortices.
7 cation for hypoxic-ischemic brain injury was cerebral cortices (82%) and cerebellum (55%).
8 IPs in vitro, and co-localization in vivo in cerebral cortices after exposure to HI injury.
9 using neuronal populations obtained from rat cerebral cortices and hippocampi of both sexes.
10  direct communication between left and right cerebral cortices and so, in this subject, a purely cort
11  anterior cingulate, and posterior cingulate cerebral cortices and the cerebellar cortex of 87 end-of
12 n vitro and in vivo in both mouse developing cerebral cortices and zebra fish embryos.
13                Our results indicate that all cerebral cortices are approximations of the same archety
14 nduction and reaches somatosensory and motor cerebral cortices as REM sleep recurs.
15            Arx knockout mice exhibit thinner cerebral cortices because of decreased neural precursor
16 decreased neuronal death was observed in the cerebral cortices, brain stems, and cerebella of caspase
17 ses of lpa(1)((-/-)) lpa(2)((-/-)) embryonic cerebral cortices did not reveal obvious differences in
18 ly in the amygdala, entorhinal, and auditory cerebral cortices during the first REM sleep episodes af
19 nscriptome analysis of human and mouse fetal cerebral cortices exposed to ethanol in vitro and in viv
20                   Here we report that intact cerebral cortices exposed to extracellular LPA ex vivo r
21                                              Cerebral cortices from fetuses at 60%, 70%, and 90% of g
22 carried out electron microscopic analysis of cerebral cortices from fluoxetine-treated guinea pigs.
23 ositive astrocytes acutely isolated from the cerebral cortices of 4- to 12-day old rats were examined
24 gnificantly increased levels of VDAC1 in the cerebral cortices of 6-, 12- and 24-month-old APP transg
25 properties of Glu receptors (GluRs) from the cerebral cortices of AD and non-AD brains and found that
26 m young, but not aged, mouse brains into the cerebral cortices of aged stroke mice partially restored
27                 To test this hypothesis, the cerebral cortices of developing and adult POMGnT1 knocko
28 Connexin-32 abundance was higher (P<0.05) in cerebral cortices of fetuses at 60% of gestation (3.0+/-
29 re connexin-32 and connexin-43 expression in cerebral cortices of fetuses at 60%, 80%, and 90% of ges
30 connexin-43 abundance was higher (P<0.05) in cerebral cortices of fetuses at 90% of gestation (0.44+/
31       Focal demyelinating lesions induced in cerebral cortices of IL-11Ralpha(-/-) mice using stereot
32 icant brain volume shrinkage occurred in the cerebral cortices of monkeys drinking >/= 3 g/kg ethanol
33 PO2, and thermocouples were implanted in the cerebral cortices of near-term fetal sheep.
34 lish a joint geometric representation of the cerebral cortices of ninety species of extant Euarchonto
35 rimary astrocyte cultures were prepared from cerebral cortices of one-day-old Sprague-Dawley rats.
36 tes, we acutely purified astrocytes from the cerebral cortices of over 40 humans across various ages,
37 rimary cultured astrocytes prepared from the cerebral cortices of rat pups.
38 exin-32 and connexin-43 protein abundance in cerebral cortices of sheep during development.
39 f IL6, CD11c, IL1beta, CD40 and CD11b in the cerebral cortices of the Tg2576 mice compared with their
40 upratentorial hypoperfusion of the bilateral cerebral cortices on the left side and severe left tempo
41 d 10,309 cells from neonatal and adult mouse cerebral cortices, respectively.
42 tor cells (NPCs) and neurons from developing cerebral cortices, revealing hundreds of differentially
43 ated biodistribution and transduction in the cerebral cortices, striatum, thalamus, midbrain, cerebel
44                             Likewise, in the cerebral cortices, they have mirror-imaged waveforms in
45 ers of quantifiable GAD cells in the rostral cerebral cortices were different between groups, both ip
46 allest shrew in our dataset, have diminutive cerebral cortices, which makes the cerebellum appear rel
47 aly with partially collapsed skull; (2) thin cerebral cortices with subcortical calcifications; (3) m