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1 ed in many species including any Neotropical cichlid fish.
2  neurons in adult male Astatotilapia burtoni 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 endrobatid frogs, and Xenotilapia species of cichlid fishes.
7 ically diverging species pair of crater lake cichlid fishes.
8 solated radiations of Nicaraguan crater lake cichlid fishes.
9 es the species-area relationship for African cichlid fishes.
10 anisms of sex determination and evolution in cichlid fishes.
11 al role for these nORFs in speciation of the cichlid fishes.
12 ng of single loci and quantitative traits in cichlid fishes.
13 oidance of paternal care among haplochromine cichlid fishes.
14 lding, a recently-evolved social behavior in cichlid fishes.
15 tionary radiations, as inferred from work in cichlid fish [9], white-eye birds [10], new world lupins
16 dark polymorphism that is eponymous of Midas cichlid fish (Amphilophus spp.) adaptive radiations in N
17 ithin a young species complex of neotropical cichlid fishes (Amphilophus spp.), we analysed genomic d
18 chnique to amplify RNA from two tissues of a cichlid fish and compared expression levels of unamplifi
19 tial methylome divergence in closely-related cichlid fishes and represents a resource to study the ro
20 vidence that the modified pharyngeal jaws of cichlid fishes and several marine fish lineages, a class
21 utterflies, Darwin's finches, sunflowers and cichlid fishes, and the implications of introgression fo
22 d that the conclusions reached regarding the cichlid fishes apply also to other examples of adaptive
23                                              Cichlid fishes are famous for large, diverse and replica
24           We evaluate these hypotheses using cichlid fish as model animals, and although differences
25 during the ontogeny of the direct-developing cichlid fish Astatotilapia burtoni Distinct transcriptio
26                                  The African cichlid fish Astatotilapia burtoni has become an importa
27                                  The African cichlid fish Astatotilapia burtoni is a powerful model s
28                                  The African cichlid fish Astatotilapia burtoni is an ideal study spe
29                                          The cichlid fish Astatotilapia burtoni is ideal for studying
30                                  The African cichlid fish Astatotilapia burtoni presents an attractiv
31 linergic neurons in the brain of the African cichlid fish Astatotilapia burtoni using in situ hybridi
32 on between dominance and influence using the cichlid fish Astatotilapia burtoni, comparing the influe
33 r examining the AVT system in female African cichlid fish Astatotilapia burtoni, including immunohist
34 ntified two tac3 genes in the social African cichlid fish Astatotilapia burtoni, only one of which pr
35 ricular surfaces in the brain of the African cichlid fish Astatotilapia burtoni.
36                              A gravid female cichlid fish (Astatotilapia burtoni) chose between two s
37                                          The cichlid fish, Astatotilapia burtoni, can switch between
38                                In an African cichlid fish, Astatotilapia burtoni, fertile females sel
39 localized two known GnRH receptor types in a cichlid fish, Astatotilapia burtoni, in which GnRH1 is s
40 e used females of the mouth brooding African cichlid fish, Astatotilapia burtoni, to test for reprodu
41 y reared juveniles of cooperatively breeding cichlid fish by varying the social environment and simul
42 assive evolutionary radiation of Lake Malawi cichlid fishes displaying extensive phenotypic diversity
43 on of early-stage adaptive divergence of two cichlid fish ecomorphs in a small (700 meters in diamete
44 ase is Perissodus microlepis, a scale-eating cichlid fish endemic to Lake Tanganyika.
45                                  Lake Malawi cichlid fishes exhibit extensive divergence in form and
46                           Furthermore, while cichlid fishes exhibit extensive parental care, for most
47                                              Cichlids fishes exhibit extensive phenotypic diversifica
48                                          The cichlid fish family provides a notable example of such v
49           Five neighbouring populations of a cichlid fish from Lake Malawi differ in male courtship c
50                     Astatotilapia burtoni, a cichlid fish from the rivers and shoreline around Lake T
51 e brain development in ecologically distinct cichlid fishes from Lake Malawi and demonstrate that bra
52          Here, using rock- and sand-dwelling cichlid fishes from Lake Malawi, we demonstrate that dif
53 uption of the habitat of a colony of African cichlid fish, Haplochromis burtoni (Gunther) caused male
54      We have shown previously in the African cichlid fish, Haplochromis burtoni, that changes in soci
55                                 East African cichlid fishes have diversified in an explosive fashion,
56                                      African cichlid fishes have repeatedly evolved highly specialize
57                              Many species of cichlid fish in Lake Malawi carry a haploid, female-rest
58        The spectacular adaptive radiation of cichlid fish in Lake Tanganyika encompasses extensive mo
59 results imply that the rate of speciation of cichlid fish in this tropical lake has been extremely ra
60 ke Malawi, Africa, there are >200 species of cichlid fish in which the males form leks and spend seve
61 mpatric homoploid hybrid speciation in Midas cichlid fishes in Crater Lake Xiloa, Nicaragua.
62  unrecognized role in the mass extinction of cichlid fishes in Lake Victoria after Nile perch invasio
63  bower construction behaviors in Lake Malawi cichlid fishes, in which males use their mouths to sculp
64 t least 12 of 22 chromosomes in East African cichlid fishes, indicating a high rate of sex chromosome
65  evolution of a courtship behavior in Malawi cichlid fish is associated with rapid, extensive, and sp
66 by highly diverse groups such as wrasses and cichlid fishes, is hypothesized to increase foraging cap
67 D on secondary sexual characteristics in the cichlid fish Metriaclima mbenjii, where one female (W) a
68 transcriptomics and CRISPR gene editing in a cichlid fish model to identify and test the roles of key
69          Here, we show that offspring of the cichlid fish Neolamprologus pulcher developed faster C-s
70 e Magadi tilapia, Alcolapia grahami, a small cichlid fish of Lake Magadi, Kenya lives in one of the m
71 under sexually antagonistic selection in the cichlid fish of Lake Malawi, East Africa.
72                            The haplochromine cichlid fish of the East African Great Lakes represent s
73                                Haplochromine cichlid fishes of Africa's Lake Victoria region encompas
74                                          The cichlid fishes of Lake Malawi are famously diverse.
75 he largest adaptive radiations on Earth, the cichlid fishes of Lake Tanganyika.
76                        On the example of the cichlid fishes of Lake Victoria, we demonstrate how the
77                                          The cichlid fishes of the East African Rift Lakes represent
78 d one each in salamanders (Desmognathus) and cichlid fishes (Pseudotropheus).
79 ying 1375 genomes of the species-rich Malawi cichlid fish radiation, we discovered five large inversi
80 ion over a similar time period to the recent cichlid fish radiations, which are an order of magnitude
81                                 East African cichlid fishes represent one of the most striking exampl
82        Our targeted genome modification in a cichlid fish shows that dissection of gene function can
83 rofound influence on the Lake Malawi endemic cichlid fish species flock; the geographically extensive
84 dently for the lake's extraordinary array of cichlid fish species, suggesting a direct link between e
85 ly distinct ecomorphs of the Lake Tanganyika cichlid fish Telmatochromis temporalis.
86 e Malawi contains a flock of >500 species of cichlid fish that have evolved from a common ancestor wi
87 cologically diverse radiation of Neotropical cichlid fishes that spans North, Central and South Ameri
88 nization on visual acuity in closely related cichlid fishes (the Ectodini clade).
89 oth fossils of Lake Victoria's haplochromine cichlid fish, the most rapid and youngest of the classic
90  exploit the dental diversity of Lake Malawi cichlid fishes to ask how vertebrates generally replace
91 x chromosome evolution in a group of African cichlid fishes (tribe Tropheini) which began to diverge
92               In previous studies of African cichlid fishes, we found evidence for positive selection
93                     Using genetic mapping in cichlid fishes, we identified shared loci controlling a
94 rds, whereas social signals regulate GnRH in cichlid fishes, with crucial consequences for reproducti