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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 halamic projection neurons in the ICC of the Mongolian gerbil.
6 ritis and epithelial (hyper)proliferation 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 pylori-mediated gastric cancer incidence in Mongolian gerbils.
11 153p53, was also found in H. pylori-infected Mongolian gerbils.
12 ify proteins from synaptosomes isolated from Mongolian gerbils.
13 m MSO principal neurons in brain slices from Mongolian gerbils.
14 assessed in a model of ischemic tolerance in Mongolian Gerbils.
15 l model that inspired it-naturally epileptic Mongolian gerbils.
16 as been demonstrated in both albino rats and Mongolian gerbils.
17 and stereotyped vocalization exists in male Mongolian gerbils.
18 train 7.13 rapidly induces gastric cancer in Mongolian gerbils.
19 -nitro-L-arginine (NLA), was investigated in Mongolian gerbils.
20 ocessing, we developed a model of ELS in the Mongolian gerbil, a well-established model for auditory
22 -clamp recordings of binaural neurons in the Mongolian gerbil and pharmacological manipulations to di
23 zed anatomical data of proximal MSO axons in Mongolian gerbils and found that the axon diameter is <1
27 nic FVB/N insulin-gastrin (INS-GAS) mice and Mongolian gerbils as models of H pylori-induced carcinog
28 throughout the dorsal raphe nucleus (DRN) in Mongolian gerbils at selected times during a 12:12 h lig
29 described in a number of species, including Mongolian gerbils, but functional correlates of this opt
30 ient auditory deprivation in male and female Mongolian gerbils caused correlated deficits in behavior
31 l injury of the hippocampus, suggesting that Mongolian gerbils currently available in the US have ano
32 oved the ECM in the auditory cortex of adult Mongolian gerbils during specific phases of cortex-depen
35 ablishing long-term acoustic recordings from Mongolian gerbil families, a core social group that uses
36 We analyzed H. pylori strains isolated from Mongolian gerbils fed either a high-salt diet or a regul
40 ined a new model of human iron overload, the Mongolian gerbil given repeated injections of iron dextr
41 nt bilateral carotid artery occlusion in the Mongolian gerbil is a widely used model of forebrain isc
42 nucleus of the bulbocavernosus (SNB) of the Mongolian gerbil is achieved by two periods of postnatal
43 , spherical bushy cell (SBC) activity in the Mongolian gerbil is rendered sparser and more reliable b
45 n the subcortical auditory structures of the Mongolian gerbil (Meriones unguiculatus), a frequently u
48 cholinergic physiology in MNTB neurons from Mongolian gerbils (Meriones unguiculatus) of both sexes.
49 ons in brainstem slices from male and female Mongolian gerbils (Meriones unguiculatus), we show that
50 athology induced by a Deltafur strain in the Mongolian gerbil model of infection and compared the res
54 d manipulating OFC activity in freely moving Mongolian gerbils of both sexes under two behavioral con
57 ed EPSCs and calcium entry in MSO neurons of Mongolian gerbils of either sex raised in a normal and i
58 nerve fiber recordings were obtained from 41 Mongolian gerbils of either sex, divided between young,
59 eal (i.p.) infections with Brugia pahangi in Mongolian gerbils, or jirds (Meriones unguiculatus), ind
61 in core auditory cortex of trained and awake Mongolian gerbils that are engaged in a tone detection t
62 s required for efficient colonization of the Mongolian gerbil: the mutant strain exhibits a 100-fold
63 uditory ganglion cells within the cochlea of Mongolian gerbils throughout the first 3 weeks of postna
64 sed juxtacellular recordings in anesthetized Mongolian gerbils to assess the effect of acoustically e
65 geniculate nucleus (MGV) of male and female Mongolian gerbils under two different behavioral context
66 e not as extensive as previously observed in Mongolian gerbils using identical techniques, but the re
68 ication, and detailed signal analysis in the Mongolian Gerbil, we demonstrate that inhibition is wide
70 n slices from postnatal day 7 to 24 (P7-P24) Mongolian gerbils, we confirm that activation of GABAB r
76 crobial virulence in gastric carcinogenesis, Mongolian gerbils were maintained on iron-depleted diets
78 ge following cerebral ischaemia/reperfusion, Mongolian gerbils were submitted to 30 min bilateral car
79 red these responses to young and middle-aged Mongolian gerbils, where CND was histologically confirme
80 primary auditory cortical field (AI) in the Mongolian gerbil with subcortical structures of the audi
81 the effects of a high-salt diet, we infected Mongolian gerbils with a wild-type (WT) cagA(+) H. pylor
83 Helicobacter pylori infection was studied in Mongolian gerbils with fresh human isolates that carry o
85 d in the SNB of prepubertally castrated male Mongolian gerbils within 2 days of the start of delayed