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1 transmitter systems in male Syrian hamsters (Mesocricetus auratus).
2 estosterone self-administration in hamsters (Mesocricetus auratus).
3 on intermale aggression in Syrian hamsters (Mesocricetus auratus).
4 stimuli were studied in the golden hamster (Mesocricetus auratus).
5 he chorda tympani (CT) nerve in the hamster (Mesocricetus auratus).
6 onuclear microinjections in Syrian hamsters (Mesocricetus auratus), a species used extensively in beh
7 stration of S2X259 protects Syrian hamsters (Mesocricetus auratus) against challenge with the prototy
11 nanus, Acomys cahirinus, Acomys russatus and Mesocricetus auratus) and measured faecal glucocorticoid
13 his behavior using pubertal Syrian hamsters (Mesocricetus auratus) as an adolescent-animal model.
14 ures of sexual behavior in 73 male hamsters (Mesocricetus auratus) as they interacted with hormone-pr
16 a acquired from midsagittal Syrian hamster ( Mesocricetus auratus ) brain cryosections, we show how o
17 that MAP virus in the Syrian golden hamster (Mesocricetus auratus) can cause a disease that is clinic
19 of the efferent innervation of the hamster (Mesocricetus auratus) cochlea were done during postnatal
21 ltured neural retinas of the golden hamster (Mesocricetus auratus) exhibited circadian rhythms of mel
24 norvegicus), mouse (Mus musculus), hamster (Mesocricetus auratus), green monkey (Ceropithecus aethio
27 induced tumors in the Syrian Golden hamster (Mesocricetus auratus) have been shown to be excellent re
31 S-CoV-2 neutralizing antibodies in hamsters (Mesocricetus auratus), mice (Mus musculus) and cynomolgu
32 ostnatal day (P)0-P2 golden Syrian hamsters (Mesocricetus auratus) of either sex to study the role of
33 techniques, we exposed male golden hamsters (Mesocricetus auratus) on 3 to 4 trials to genital over-m
34 cts of sexual experience in female hamsters (Mesocricetus auratus) on copulatory interactions with ma
35 ed genetic resources for the Syrian hamster (Mesocricetus auratus) presented a major obstacle to clon
39 ero-anterior hypothalamus (LAH) in hamsters (Mesocricetus auratus); that is, an important neural comp
40 xposed estrous or diestrous female hamsters (Mesocricetus auratus) to saline, conspecific male odors,
41 y-old rats (Rattus norvegicus) and hamsters (Mesocricetus auratus) to thermal stimulation were assess
42 eriment 2, male Turkish and golden hamsters (Mesocricetus auratus) treated the flank-gland odors of 2
44 investigated what cues male golden hamsters (Mesocricetus auratus) use to determine the top and botto
45 ight loss reduced in Syrian golden hamsters (Mesocricetus auratus) vaccinated intranasally with COVI-
46 al vestibular nucleus of the golden hamster (Mesocricetus auratus) was evaluated using cholera toxin
48 tomized pre- and postpubertal male hamsters (Mesocricetus auratus) were treated with 0.00, 0.05, 0.10
49 xtures were investigated in golden hamsters (Mesocricetus auratus) with a conditioned taste aversion
50 Remarkably, infection of the Syrian hamster (Mesocricetus auratus) with L. donovani reproduced the cl