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1  vivo microdialysis procedure in the mPOA of Japanese quail.
2 g active (YF), and old senescent female (OF) Japanese quail.
3  was derived from precardiac mesoderm of the Japanese quail.
4 rived estrogens on sexual motivation in male Japanese quail.
5  a female but not sexual performance in male Japanese quail.
6 eCDF was more potent than TCDD at activating Japanese quail (13- to 26-fold) and common tern (23- to
7 Coturnix japonica; Val324_Ala380), and three Japanese quail AHR1 mutants.
8   In this study, the amino acid sequences of Japanese quail and northern bobwhite myoglobin were dedu
9  in all genes and species, but especially in Japanese quail and pearl guinea fowl and in internal pro
10 al transplants between two bird species, the Japanese quail and the domestic chicken, to demonstrate
11 S. commercial industries are small), namely, Japanese quail, bobwhite quail, pearl guinea fowl, chuka
12  in substantial amounts in the retina of the Japanese quail Coturnix japonica.
13  of transgenic birds, including a transgenic Japanese quail (Coturnix coturnix japonica) line showing
14 d from a methylcholanthrene-induced tumor in Japanese quail (Coturnix coturnix japonica).
15 g of chickens (Gallus gallus domesticus) and Japanese quail (Coturnix coturnix japonica).
16 sed to examine whether imitative learning in Japanese quail (Coturnix japonica) depends on the motiva
17                                              Japanese quail (Coturnix japonica) observers exposed to
18 The conditioned responses of male and female Japanese quail (Coturnix japonica) were compared in a Pa
19                                         Male Japanese quail (Coturnix japonica) were trained individu
20 to the production of male sexual behavior in Japanese quail (Coturnix japonica), a species that exhib
21 estigate carotenoid content in the retina of Japanese quail (Coturnix japonica), for comparison with
22 ant (Phasianus colchicus; Ile324_Ala380) and Japanese quail (Coturnix japonica; Val324_Ala380), and t
23 ubstrate selection in a ground-nesting bird (Japanese quail, Coturnix japonica).
24  opioid receptor densities in regions of the Japanese quail, Coturnix japonica, brain that regulates
25 ibodies with the native antigen HEL and with Japanese quail egg white lysozyme (JQL), a naturally occ
26 y dimorphic medial preoptic nucleus (POM) in Japanese quail has for many years been the focus of inte
27                                     When the Japanese quail is held in constant darkness, retinal res
28 ulated pre- and/or post-natal stress in both Japanese quail mothers and offspring and examined the co
29                                              Japanese quail myoglobin was isolated from quail cardiac
30          Intranasal inoculation of chickens, Japanese quail, pigeons, Pekin ducks, Mallard ducks, Mus
31 ts), copulatory mounting (male mice and male Japanese quail), reproductive clasping (pre-copulatory m
32 ng sensitivity and rod-cone dominance in the Japanese quail retina.
33 modulates the functional organization of the Japanese quail retina.
34 d locomotor time series of visually isolated Japanese quails sampled every 0.5 s during 6.5 days (>10
35 gical verification was based on two lines of Japanese quail selected for 6-week weight; one line was
36        When compared with chicken myoglobin, Japanese quail showed 98% sequence identity, and norther

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