ライフサイエンスコーパス: cerebral cortices

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1 din-1, claudin-5 or ZO-1 expression in ovine cerebral cortices.

2 ding through temporal, parietal, and frontal cerebral cortices.

3 to enable generation of larger, convoluted, cerebral cortices.

4 direct communication between left and right cerebral cortices and so, in this subject, a purely cort

5 anterior cingulate, and posterior cingulate cerebral cortices and the cerebellar cortex of 87 end-of

6 n vitro and in vivo in both mouse developing cerebral cortices and zebra fish embryos.

7 nduction and reaches somatosensory and motor cerebral cortices as REM sleep recurs.

8 Arx knockout mice exhibit thinner cerebral cortices because of decreased neural precursor

9 decreased neuronal death was observed in the cerebral cortices, brain stems, and cerebella of caspase

10 ses of lpa(1)((-/-)) lpa(2)((-/-)) embryonic cerebral cortices did not reveal obvious differences in

11 ly in the amygdala, entorhinal, and auditory cerebral cortices during the first REM sleep episodes af

12 nscriptome analysis of human and mouse fetal cerebral cortices exposed to ethanol in vitro and in viv

13 Here we report that intact cerebral cortices exposed to extracellular LPA ex vivo r

14 Cerebral cortices from fetuses at 60%, 70%, and 90% of g

15 carried out electron microscopic analysis of cerebral cortices from fluoxetine-treated guinea pigs.

16 ositive astrocytes acutely isolated from the cerebral cortices of 4- to 12-day old rats were examined

17 gnificantly increased levels of VDAC1 in the cerebral cortices of 6-, 12- and 24-month-old APP transg

18 properties of Glu receptors (GluRs) from the cerebral cortices of AD and non-AD brains and found that

19 To test this hypothesis, the cerebral cortices of developing and adult POMGnT1 knocko

20 Connexin-32 abundance was higher (P<0.05) in cerebral cortices of fetuses at 60% of gestation (3.0+/-

21 re connexin-32 and connexin-43 expression in cerebral cortices of fetuses at 60%, 80%, and 90% of ges

22 connexin-43 abundance was higher (P<0.05) in cerebral cortices of fetuses at 90% of gestation (0.44+/

23 Focal demyelinating lesions induced in cerebral cortices of IL-11Ralpha(-/-) mice using stereot

24 icant brain volume shrinkage occurred in the cerebral cortices of monkeys drinking >/= 3 g/kg ethanol

25 PO2, and thermocouples were implanted in the cerebral cortices of near-term fetal sheep.

26 rimary astrocyte cultures were prepared from cerebral cortices of one-day-old Sprague-Dawley rats.

27 rimary cultured astrocytes prepared from the cerebral cortices of rat pups.

28 exin-32 and connexin-43 protein abundance in cerebral cortices of sheep during development.

29 f IL6, CD11c, IL1beta, CD40 and CD11b in the cerebral cortices of the Tg2576 mice compared with their

30 upratentorial hypoperfusion of the bilateral cerebral cortices on the left side and severe left tempo

31 tor cells (NPCs) and neurons from developing cerebral cortices, revealing hundreds of differentially

32 ers of quantifiable GAD cells in the rostral cerebral cortices were different between groups, both ip

33 aly with partially collapsed skull; (2) thin cerebral cortices with subcortical calcifications; (3) m

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