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1 haracterizes many species of swordtail fish (Xiphophorus).
2 ion within the genetic map of the fish genus Xiphophorus.
3 n the well-established laboratory fish model Xiphophorus.
4                Using swordtail fishes (genus Xiphophorus), an emerging model system, we document over
5 s from hybrid populations of swordtail fish (Xiphophorus) and baboons (Papio) and to inferred Neander
6 ybrids between distinct species of the genus Xiphophorus are often used in varied research investigat
7                            Fish of the genus Xiphophorus are proposed to have evolved with multiple a
8        All 24 acrocentric chromosome sets of Xiphophorus are represented in the assembled linkage map
9           Swordtail fish (Poeciliidae: genus Xiphophorus) are a paradigmatic case of sexual selection
10  (UV) ra-diation (UVR)-induced melanoma in a Xiphophorus backcross hybrid model previously reported t
11 ybrid populations between the swordtail fish Xiphophorus birchmanni and X. cortezi to address this fu
12 ms that act as barriers to gene flow between Xiphophorus birchmanni and Xiphophorus cortezi by combin
13 ved in its maintenance in the swordtail fish Xiphophorus birchmanni.
14 ther in several populations of the swordtail Xiphophorus birchmanni.
15 eported here are the same as the melanoma in Xiphophorus, by assessing mutation of the EGFR gene, Xmr
16 ails to do so, when exogenously expressed in Xiphophorus cells derived from a melanoma.
17 gene flow between Xiphophorus birchmanni and Xiphophorus cortezi by combining genomic sequencing from
18                           Here, we show that Xiphophorus cortezi females from two populations prefer
19                           Previously, select Xiphophorus experimental crosses have been shown to exhi
20 cally melanoma-susceptible specific cross of Xiphophorus fish.
21 n-the "sword"-in males of several species of Xiphophorus fishes.
22                  Further characterization of Xiphophorus FoxO5 will contribute to understanding the m
23                             Expansion of the Xiphophorus gene map by linkage analysis of AP-PCR/RAPD
24                                     Existing Xiphophorus genome assemblies are not at the chromosomal
25 tative phenotypes, fish species of the genus Xiphophorus have contributed to a wide range of research
26 ression properties of a fish CDKN2 gene from Xiphophorus helleri and X. maculatus.
27 me features are also present in a swordtail (Xiphophorus helleri) genomic DXB PCR clone.
28  preferences of female green swordtail fish, Xiphophorus hellerii, for pairs of males differing in bo
29                                         Thus Xiphophorus, in contrast to zebrafish, Danio rerio, and
30 rkers we report can be easily adapted to any Xiphophorus interspecies and some intraspecies crosses,
31 e number of genetic markers available in the Xiphophorus interspecies cross of interest.
32             Melanoma development in the fish Xiphophorus is determined, at least in part, by overexpr
33   CDKN2X was mapped to a region on autosomal Xiphophorus linkage group V (LG V) known to contain the
34          The CDKN2-like polymorphism maps to Xiphophorus linkage group V and exhibits recombination f
35 The gene, which we have named FoxO5, maps to Xiphophorus Linkage Group XV.
36 esulted in the addition of 16 new markers to Xiphophorus linkage groups (LGs) I, II, III, V, IX, X, X
37                        Using a cross between Xiphophorus maculatus and X. andersi, we report a linkag
38 class II B genes from the inbred fish strain Xiphophorus maculatus Jp 163 A.
39 s musculus, Danio rerio, Oryzias latipes and Xiphophorus maculatus.
40 loned an FKHR (FoxO sub-family) homolog from Xiphophorus maculatus.
41 between X. birchmanni and its sister species Xiphophorus malinche.
42                                       In the Xiphophorus melanoma model, a functional oncogene (Xipho
43 horus melanoma model, a functional oncogene (Xiphophorus melanoma receptor kinase Xmrk) has been main
44 easily scored markers by characterization of Xiphophorus microsatellite sequences.
45 melanoma susceptibility in this UV-inducible Xiphophorus model, we genotyped individual animals from
46 diated communication by northern swordtails, Xiphophorus nigrensis, using a custom-built videopolarim
47                       Such observations make Xiphophorus one of the only two vertebrate hybrid incomp
48                We UV-irradiated spotted side Xiphophorus platyfish-swordtail backcross hybrids to ind
49 us melanoma formation in spotted dorsal (Sd) Xiphophorus platyfish-swordtail hybrids has been studied
50                       There are 24 described Xiphophorus species and a greater number of pedigreed st
51        Here we have sequenced CDKN2X in both Xiphophorus species and have characterized its expressio
52 e including annotations for all described 26 Xiphophorus species and three undescribed taxa and resol
53 lar events that led to the divergence of the Xiphophorus species and to progress understanding of gen
54 enome assemblies for three distantly related Xiphophorus species, namely, X. maculatus, X. couchianus
55                                 Melanomas in Xiphophorus spp. fishes (platyfishes and swordtails) hav
56                             Knowledge of the Xiphophorus TP53 sequences will allow assessment of muta
57 sing sworded and swordless sister species of Xiphophorus, we generated a mapping population and show