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1 rived estrogens on sexual motivation in male Japanese quail.
2  a female but not sexual performance in male Japanese quail.
3  vivo microdialysis procedure in the mPOA of Japanese quail.
4 g active (YF), and old senescent female (OF) Japanese quail.
5  was derived from precardiac mesoderm of the Japanese quail.
6  of the most relevant minor poultry species, Japanese quail.
7 eCDF was more potent than TCDD at activating Japanese quail (13- to 26-fold) and common tern (23- to
8 Coturnix japonica; Val324_Ala380), and three Japanese quail AHR1 mutants.
9   In this study, the amino acid sequences of Japanese quail and northern bobwhite myoglobin were dedu
10  in all genes and species, but especially in Japanese quail and pearl guinea fowl and in internal pro
11 o characterize a molecular seasonal clock in Japanese quail and second, to identify the key transcrip
12 al transplants between two bird species, the Japanese quail and the domestic chicken, to demonstrate
13 S. commercial industries are small), namely, Japanese quail, bobwhite quail, pearl guinea fowl, chuka
14  in substantial amounts in the retina of the Japanese quail Coturnix japonica.
15 bient temperature influences the response of Japanese quail (Coturnix coturnix japonica) chicks to en
16                                          The Japanese quail (Coturnix coturnix japonica) is an attrac
17  of transgenic birds, including a transgenic Japanese quail (Coturnix coturnix japonica) line showing
18 d from a methylcholanthrene-induced tumor in Japanese quail (Coturnix coturnix japonica).
19 g of chickens (Gallus gallus domesticus) and Japanese quail (Coturnix coturnix japonica).
20 rioallantoic membrane (CAM) assays utilizing Japanese quail (Coturnix japonica) are a cost-effective
21 sed to examine whether imitative learning in Japanese quail (Coturnix japonica) depends on the motiva
22 vision models, we compared the camouflage of Japanese quail (Coturnix japonica) eggs among females wh
23                                              Japanese quail (Coturnix japonica) observers exposed to
24                 A first generation (G(1)) of Japanese quail (Coturnix japonica) were bred from a 2 x
25 The conditioned responses of male and female Japanese quail (Coturnix japonica) were compared in a Pa
26                                         Male Japanese quail (Coturnix japonica) were trained individu
27 to the production of male sexual behavior in Japanese quail (Coturnix japonica), a species that exhib
28 ed and unrelated individuals of domesticated Japanese quail (Coturnix japonica), and monitored the pe
29 estigate carotenoid content in the retina of Japanese quail (Coturnix japonica), for comparison with
30  collected in the Norwegian coast in growing Japanese quail (Coturnix japonica).
31 ant (Phasianus colchicus; Ile324_Ala380) and Japanese quail (Coturnix japonica; Val324_Ala380), and t
32                                  Here, using Japanese quails (Coturnix japonica) as our model, we sho
33 ubstrate selection in a ground-nesting bird (Japanese quail, Coturnix japonica).
34  opioid receptor densities in regions of the Japanese quail, Coturnix japonica, brain that regulates
35 ibodies with the native antigen HEL and with Japanese quail egg white lysozyme (JQL), a naturally occ
36 dvantage of a domesticated bird species, the Japanese quail, for which parental behaviour towards chi
37 y dimorphic medial preoptic nucleus (POM) in Japanese quail has for many years been the focus of inte
38                                     When the Japanese quail is held in constant darkness, retinal res
39 aluated n = 55 RNA-seq profiles derived from Japanese quail liver tissue following exposure to chlorp
40 ulated pre- and/or post-natal stress in both Japanese quail mothers and offspring and examined the co
41                                              Japanese quail myoglobin was isolated from quail cardiac
42          Intranasal inoculation of chickens, Japanese quail, pigeons, Pekin ducks, Mallard ducks, Mus
43 ts), copulatory mounting (male mice and male Japanese quail), reproductive clasping (pre-copulatory m
44  body weight (BW) (~3 and 9% of IMI LD50 for Japanese quail, respectively) for 1 or 10 days.
45 ng sensitivity and rod-cone dominance in the Japanese quail retina.
46 modulates the functional organization of the Japanese quail retina.
47 d locomotor time series of visually isolated Japanese quails sampled every 0.5 s during 6.5 days (>10
48 gical verification was based on two lines of Japanese quail selected for 6-week weight; one line was
49        When compared with chicken myoglobin, Japanese quail showed 98% sequence identity, and norther
50                                   Adult male Japanese quail were orally dosed with wheat seeds coated
51 ol can modulate the immune response of adult Japanese quail when simultaneously exposed to an inoculu