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1 ing effects on auditory brainstem neurons of Mongolian gerbil.
2 valuated during vestibular adaptation in the Mongolian gerbil.
3 emia/reperfusion injury was evaluated in the Mongolian gerbil.
4 monstrate social-affiliative learning in the Mongolian gerbil.
5 m MSO principal neurons in brain slices from Mongolian gerbils.
6 train 7.13 rapidly induces gastric cancer in Mongolian gerbils.
7 ynapse in the auditory brainstem of juvenile Mongolian gerbils.
8 n the VNLL and the calyx of Held in juvenile Mongolian gerbils.
9 rrent source density (CSD) analysis in AI of Mongolian gerbils.
10 153p53, was also found in H. pylori-infected Mongolian gerbils.
11 train 7.13 rapidly induces gastric cancer in Mongolian gerbils.
12 ify proteins from synaptosomes isolated from Mongolian gerbils.
13 assessed in a model of ischemic tolerance in Mongolian Gerbils.
14 l model that inspired it-naturally epileptic Mongolian gerbils.
15 as been demonstrated in both albino rats and Mongolian gerbils.
16 and stereotyped vocalization exists in male Mongolian gerbils.
17 -nitro-L-arginine (NLA), was investigated in Mongolian gerbils.
18 ritis and epithelial (hyper)proliferation in Mongolian gerbils.
20 -clamp recordings of binaural neurons in the Mongolian gerbil and pharmacological manipulations to di
21 zed anatomical data of proximal MSO axons in Mongolian gerbils and found that the axon diameter is <1
23 throughout the dorsal raphe nucleus (DRN) in Mongolian gerbils at selected times during a 12:12 h lig
24 described in a number of species, including Mongolian gerbils, but functional correlates of this opt
25 ient auditory deprivation in male and female Mongolian gerbils caused correlated deficits in behavior
26 l injury of the hippocampus, suggesting that Mongolian gerbils currently available in the US have ano
27 oved the ECM in the auditory cortex of adult Mongolian gerbils during specific phases of cortex-depen
30 We analyzed H. pylori strains isolated from Mongolian gerbils fed either a high-salt diet or a regul
34 ined a new model of human iron overload, the Mongolian gerbil given repeated injections of iron dextr
35 nt bilateral carotid artery occlusion in the Mongolian gerbil is a widely used model of forebrain isc
36 nucleus of the bulbocavernosus (SNB) of the Mongolian gerbil is achieved by two periods of postnatal
37 , spherical bushy cell (SBC) activity in the Mongolian gerbil is rendered sparser and more reliable b
39 n the subcortical auditory structures of the Mongolian gerbil (Meriones unguiculatus), a frequently u
42 athology induced by a Deltafur strain in the Mongolian gerbil model of infection and compared the res
45 eal (i.p.) infections with Brugia pahangi in Mongolian gerbils, or jirds (Meriones unguiculatus), ind
47 s required for efficient colonization of the Mongolian gerbil: the mutant strain exhibits a 100-fold
48 uditory ganglion cells within the cochlea of Mongolian gerbils throughout the first 3 weeks of postna
49 sed juxtacellular recordings in anesthetized Mongolian gerbils to assess the effect of acoustically e
50 e not as extensive as previously observed in Mongolian gerbils using identical techniques, but the re
52 ication, and detailed signal analysis in the Mongolian Gerbil, we demonstrate that inhibition is wide
54 n slices from postnatal day 7 to 24 (P7-P24) Mongolian gerbils, we confirm that activation of GABAB r
60 crobial virulence in gastric carcinogenesis, Mongolian gerbils were maintained on iron-depleted diets
62 ge following cerebral ischaemia/reperfusion, Mongolian gerbils were submitted to 30 min bilateral car
63 primary auditory cortical field (AI) in the Mongolian gerbil with subcortical structures of the audi
64 the effects of a high-salt diet, we infected Mongolian gerbils with a wild-type (WT) cagA(+) H. pylor
66 Helicobacter pylori infection was studied in Mongolian gerbils with fresh human isolates that carry o
68 d in the SNB of prepubertally castrated male Mongolian gerbils within 2 days of the start of delayed
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