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1 ne transfer to the subventricular zone after intraventricular injection.
2 rotid injection) rhesus monkeys following an intraventricular injection.
3 roduces highly effective analgesia following intraventricular injection.
4 n and neurochemical consequences of a single intraventricular injection.
5 dogenous choroid plexus epithelium following intraventricular injection.
6 ive effects of improgan following once daily intraventricular injections.
7                          We found that after intraventricular injection, a spread of CSF tracers occu
8 ide in the subventricular zone of the brain, intraventricular injection has been used as an administr
9                                              Intraventricular injection of 15d-Delta(12,14)-prostagla
10  2, 4, 8, 12, 24, 48, 78 and 100 weeks after intraventricular injection of 192-saporin, an immunotoxi
11 tensive rats (SHRs) for 40 days, followed by intraventricular injection of 25 ng of Ang II.
12 re, by inhibiting SDF1 signaling in utero by intraventricular injection of a receptor antagonist, we
13 egeneration, which could be prevented by the intraventricular injection of a zinc chelating agent.
14 memory deficits in wild type mice induced by intraventricular injection of Abeta4-42.
15                                      We used intraventricular injection of adeno-associated virus (AA
16                                              Intraventricular injection of an MrgA1 ligand increased
17 y neurons in the mouse neocortex by in utero intraventricular injection of enhanced green fluorescent
18  labelled via their ventricular processes by intraventricular injection of Fast blue in E13 embryos p
19 served in MPTP-lesioned monkeys following an intraventricular injection of glial cell line-derived ne
20                                      Second, intraventricular injection of HA oligosaccharide reduced
21 sistant to the excitotoxic damage induced by intraventricular injection of kainic acid.
22 ic responses of rodents to the peripheral or intraventricular injection of many individual neurotrans
23                                          The intraventricular injection of SB203580, a selective p38
24       Here we show the striking finding that intraventricular injection of the high-affinity Zn2+ che
25 he dentate gyrus, i.e., apoptosis induced by intraventricular injection of the microtubule polymeriza
26            We previously found that although intraventricular injection of the neonatal mouse brain w
27                                              Intraventricular injection of tPA in the absence of isch
28                                              Intraventricular injection of tPA or active PDGF-CC, in
29  to fci, male, Long Evans (LE) rats received intraventricular injections of AO, mismatched AO (MS) or
30      On the test day, rats were administered intraventricular injections of either saline or 200 ng s
31 ctions of 5-bromo-2'-deoxyuridine (BrdU) and intraventricular injections of replication-deficient ret
32                                              Intraventricular injections of Sar Met had no effect on
33 l gastrointestinal tract is not required for intraventricular injections of SENK to suppress sodium a
34 (MPTP)-lesioned rhesus monkeys that received intraventricular injections of vehicle or glial-derived
35                Within 15 to 30 min following intraventricular injection, there is only diffuse, non-s
36 aphic analysis showed that following a bolus intraventricular injection, there was widespread distrib