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1  and of the anesthetic used (isofluorance or alpha-chloralose).
2 transection (SCT) in cats anaesthetized with alpha-chloralose.
3 e hindlimb muscle of cats anaesthetized with alpha-chloralose.
4 vated in an animal that is anesthetized with alpha-chloralose.
5 flurane, desflurane, sevoflurane, halothane, alpha-chloralose, 2,2,2-trichloroethanol [TCE], and chlo
6                     Cats were anaesthetized (alpha-chloralose 60 mg/kg, intraperitoneally), and prepa
7 (MCA), and anesthesia was either switched to alpha-chloralose (60 mg/kg bolus, 30 mg/kg/h; n=10) or w
8  superior sagittal sinus was isolated in the alpha-chloralose (60 mg/kg i.p. and 20 mg/kg i.v. inject
9                 Cats were anaesthetized with alpha-chloralose (60 mg/kg, intraperitoneally), paralyse
10                 Cats were anaesthetised with alpha-chloralose (60 mg/kg, ip; supplements 20 mg/kg iv)
11 of control and vigabatrin-treated rats under alpha-chloralose/70% nitrous oxide anesthesia, with tota
12                 Dogs were anaesthetized with alpha-chloralose, a cardiopulmonary bypass was establish
13 ments were conducted in 11 female cats under alpha-chloralose anaesthesia when the bladder was infuse
14 ses during cortical spreading depression and alpha-chloralose anaesthesia.
15                Studies were conducted in the alpha-chloralose anaesthetised cat to examine bulk carot
16  of KCl in agar upon the cortical surface of alpha-chloralose anaesthetised cats.
17                                           In alpha-chloralose anaesthetised female Sprague-Dawley rat
18 t, sulpiride, at 2 Tesla in the brain of the alpha-chloralose anaesthetised rat.
19              Experiments were carried out in alpha-chloralose anaesthetized cats to determine if thes
20 x recorded under isovolumetric conditions in alpha-chloralose anaesthetized cats.
21 A and baroreflex control of LSNA and RSNA in alpha-chloralose anaesthetized female rats, but only dur
22                                           In alpha-chloralose anaesthetized, artificially ventilated
23        These experiments were carried out on alpha-chloralose-anaesthetized, artificially ventilated
24                Experiments were performed in alpha-chloralose-anaesthetized, paralysed and artificial
25          Mongrel cats were anesthetized with alpha-chloralose and heart rate, arterial pressure, and
26     Thirty-three cats were anesthetized with alpha-chloralose and the esophagus was stimulated by slo
27                                           In alpha-chloralose and urethane anesthetized rats, microin
28  the day of shock, the animals were sedated (alpha-chloralose) and 50 mL/kg of arterial blood was rem
29            Adult cats were anesthetized with alpha-chloralose, and in each case, the experimental int
30               Animals were anesthetized with alpha-chloralose, and received one of four stimulus prot
31 el with electrical forepaw stimulation under alpha-chloralose anesthesia using laser Doppler (LD) mea
32                                        After alpha-chloralose anesthesia, blood gases and vital signs
33 d studies of focal ischemia in the rat under alpha-chloralose anesthesia.
34 being activated and remain functional during alpha-chloralose-anesthesia.
35     Closed cranial windows were implanted in alpha-chloralose anesthetized piglets 4 days following c
36 l ensemble during forepaw stimulation in the alpha-chloralose anesthetized rat.
37             In six decerebrated and in eight alpha-chloralose anesthetized, paralyzed and mechanicall
38 ms of carbachol-induced muscle atonia in the alpha-chloralose-anesthetized animal.
39  and total infarct volumes are larger in the alpha-chloralose-anesthetized animals, while the functio
40 ents (PIFTs) is also significantly longer in alpha-chloralose-anesthetized animals.
41 tion of non-convulsive seizures (NCS) in the alpha-chloralose-anesthetized animals.
42 aneously at 16 recording sites in area A2 of alpha-chloralose-anesthetized cats.
43                                       In the alpha-chloralose-anesthetized preparation, stimulation o
44 ic components were investigated at 11.7 T in alpha-chloralose-anesthetized rats and combined with ele
45                                           In alpha-chloralose-anesthetized rats, changes in the blood
46 ng-state fMRI measurements were conducted in alpha-chloralose-anesthetized rats.
47 to somatosensory stimulation was measured in alpha-chloralose-anesthetized rats.
48                                         Nine alpha-chloralose-anesthetized, splenectomized dogs were
49 ied out in animals under anesthesia, usually alpha-chloralose because of its lesser effects on cardio
50 re inhibited by TTX and anaesthetics such as alpha-chloralose but not by the intracellular applicatio
51  was determined in the rat anesthetized with alpha-chloralose by independent and concurrent (17)O NMR
52                                Halothane and alpha-chloralose established baseline states of high and
53                                         With alpha-chloralose, forepaw stimulation induced strong and
54 3, whereas the larger carbon tetraiodide and alpha-chloralose inhibit.
55       Accordingly, in cats anesthetized with alpha-chloralose, intracellular records were obtained fr
56                        This study shows that alpha-chloralose is a safe anesthetic for ischemia studi
57                                              alpha-Chloralose is widely used as an anesthetic in stud
58  in the primary somatosensory cortex (SI) in alpha-chloralose/Nembutal, or halothane (in N2O/O2) anes
59 neurons exhibited visceral inputs than under alpha-chloralose/Nembutal.
60 in conscious rats and rats anesthetized with alpha-chloralose the effects of vibrissal stimulation on
61          Open-chest swine, anesthetized with alpha-chloralose, underwent 10 mins of nonperfused VF fo
62                    In rats anesthetized with alpha-chloralose, we measured SEPs by signal-averaging f

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