戻る
「早戻しボタン」を押すと検索画面に戻ります。

今後説明を表示しない

[OK]

コーパス検索結果 (1語後でソート)

通し番号をクリックするとPubMedの該当ページを表示します
1  neurons in adult male Astatotilapia burtoni cichlid fish.
2 ed in many species including any Neotropical cichlid fish.
3  both within and among genera of Lake Malawi cichlid fish.
4 hologically similar species of haplochromine cichlid fish.
5 re than 300 endemic species of haplochromine cichlid fish.
6 ically diverging species pair of crater lake cichlid fishes.
7 solated radiations of Nicaraguan crater lake cichlid fishes.
8 es the species-area relationship for African cichlid fishes.
9 anisms of sex determination and evolution in cichlid fishes.
10 ng of single loci and quantitative traits in cichlid fishes.
11 chnique to amplify RNA from two tissues of a cichlid fish and compared expression levels of unamplifi
12 vidence that the modified pharyngeal jaws of cichlid fishes and several marine fish lineages, a class
13 utterflies, Darwin's finches, sunflowers and cichlid fishes, and the implications of introgression fo
14 d that the conclusions reached regarding the cichlid fishes apply also to other examples of adaptive
15                                              Cichlid fishes are famous for large, diverse and replica
16           We evaluate these hypotheses using cichlid fish as model animals, and although differences
17                                  The African cichlid fish Astatotilapia burtoni has become an importa
18                                          The cichlid fish Astatotilapia burtoni is ideal for studying
19                                  The African cichlid fish Astatotilapia burtoni presents an attractiv
20 linergic neurons in the brain of the African cichlid fish Astatotilapia burtoni using in situ hybridi
21 ricular surfaces in the brain of the African cichlid fish Astatotilapia burtoni.
22                              A gravid female cichlid fish (Astatotilapia burtoni) chose between two s
23                                In an African cichlid fish, Astatotilapia burtoni, fertile females sel
24 localized two known GnRH receptor types in a cichlid fish, Astatotilapia burtoni, in which GnRH1 is s
25 y reared juveniles of cooperatively breeding cichlid fish by varying the social environment and simul
26 on of early-stage adaptive divergence of two cichlid fish ecomorphs in a small (700 meters in diamete
27           Five neighbouring populations of a cichlid fish from Lake Malawi differ in male courtship c
28 e brain development in ecologically distinct cichlid fishes from Lake Malawi and demonstrate that bra
29          Here, using rock- and sand-dwelling cichlid fishes from Lake Malawi, we demonstrate that dif
30 uption of the habitat of a colony of African cichlid fish, Haplochromis burtoni (Gunther) caused male
31      We have shown previously in the African cichlid fish, Haplochromis burtoni, that changes in soci
32                                      African cichlid fishes have repeatedly evolved highly specialize
33        The spectacular adaptive radiation of cichlid fish in Lake Tanganyika encompasses extensive mo
34 results imply that the rate of speciation of cichlid fish in this tropical lake has been extremely ra
35 ke Malawi, Africa, there are >200 species of cichlid fish in which the males form leks and spend seve
36  unrecognized role in the mass extinction of cichlid fishes in Lake Victoria after Nile perch invasio
37 by highly diverse groups such as wrasses and cichlid fishes, is hypothesized to increase foraging cap
38 e Magadi tilapia, Alcolapia grahami, a small cichlid fish of Lake Magadi, Kenya lives in one of the m
39 under sexually antagonistic selection in the cichlid fish of Lake Malawi, East Africa.
40                            The haplochromine cichlid fish of the East African Great Lakes represent s
41                                Haplochromine cichlid fishes of Africa's Lake Victoria region encompas
42                                          The cichlid fishes of Lake Malawi are famously diverse.
43                        On the example of the cichlid fishes of Lake Victoria, we demonstrate how the
44 d one each in salamanders (Desmognathus) and cichlid fishes (Pseudotropheus).
45 ion over a similar time period to the recent cichlid fish radiations, which are an order of magnitude
46                                 East African cichlid fishes represent one of the most striking exampl
47        Our targeted genome modification in a cichlid fish shows that dissection of gene function can
48 rofound influence on the Lake Malawi endemic cichlid fish species flock; the geographically extensive
49 dently for the lake's extraordinary array of cichlid fish species, suggesting a direct link between e
50 ly distinct ecomorphs of the Lake Tanganyika cichlid fish Telmatochromis temporalis.
51 e Malawi contains a flock of >500 species of cichlid fish that have evolved from a common ancestor wi
52 cologically diverse radiation of Neotropical cichlid fishes that spans North, Central and South Ameri
53 nization on visual acuity in closely related cichlid fishes (the Ectodini clade).
54  exploit the dental diversity of Lake Malawi cichlid fishes to ask how vertebrates generally replace
55               In previous studies of African cichlid fishes, we found evidence for positive selection
56                     Using genetic mapping in cichlid fishes, we identified shared loci controlling a
57 rds, whereas social signals regulate GnRH in cichlid fishes, with crucial consequences for reproducti

WebLSDに未収録の専門用語(用法)は "新規対訳" から投稿できます。