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1 u]-PTSM showed lower perfusion than [(14)Cu]-iodoantipyrine.
2 ke and subsequent bolus injection of [(14)C]-iodoantipyrine.
3 C]2-deoxyglucose (2-DG) and LCBF with [(14)C]iodoantipyrine 48 h after MCAo.
4 ) was measured autoradiographically with 14C-iodoantipyrine after 1 h of recirculation.
5  measured by the tissue distribution of [14C]iodoantipyrine and autoradiography.
6 )F-FEtOH uptake corresponded well with (14)C-iodoantipyrine and reflected the tumor perfusion-modifyi
7            Cerebral regional blood flow (14C-iodoantipyrine) and O2 consumption (cryomicrospectrophot
8                 CBF was measured using [14C]-iodoantipyrine autoradiography at 4 h.
9  and 60 min occlusion using quantitative 14C-iodoantipyrine autoradiography.
10 ebral blood flow (CBF) was determined by 14C-iodoantipyrine autoradiography.
11 f glucose (lCMRglu) were measured using [14C]iodoantipyrine (IAP) and [14C]2-deoxyglucose (2-DG) auto
12 that of the classic perfusion tracer [(14)C]-iodoantipyrine in a rat model during treadmill walking.
13   Cerebral blood flow was measured with [14C]iodoantipyrine in anesthetized rats.
14 ow < 40 ml/100g/min) was determined with 14C-iodoantipyrine in five coronal brain sections.
15                                         [14C]iodoantipyrine is the most prevalent tracer for the auto
16  rCBF measured autoradiographically with 14C iodoantipyrine (Kety method) in the mid-line thalamus (b
17 rtex with 10(-2) M NMDA, the blood flow (14C-iodoantipyrine method) increased from 98 +/- 11 ml/min/1
18 edated, nontethered animal using the ((14))C-iodoantipyrine method, in which the tracer was administe
19  found between the [(64)Cu]-PTSM and [(14)C]-iodoantipyrine patterns of cerebral activation in cortic
20  uptake was directly compared with the (14)C-iodoantipyrine perfusion reporter, and the perfusion-mod
21 d by laser Doppler flowmetry or by the (14)C-iodoantipyrine technique with quantitative autoradiograp
22 with the quantitative autoradiographic (14)C-Iodoantipyrine technique, in conscious animals, 4 days,
23                     Six weeks later, [(14)C]-iodoantipyrine was injected intravenously during treadmi
24 que, the bulk diffusion coefficient for [14C]iodoantipyrine was measured in brain tissue (2.1 x 10(-6
25 X-1(-/-) mice, resting CBF assessed by (14)C-iodoantipyrine was reduced (-13% to -20%) in cerebral co

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