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3 recombination maps from D. pseudoobscura and D. miranda to explore whether changes in the binding mot
4 oding sequences between D. pseudoobscura and D. miranda, and investigated their patterns of evolution
5 iranda is comparable to conservation between D. miranda and D. melanogaster, which diverged >30 MY ag
7 rates of chromosomal rearrangements between D. miranda and D. pseudoobscura are far higher than thos
8 of chromatin states between male and female D. miranda is comparable to conservation between D. mira
10 advantage of the younger sex chromosomes in D. miranda (XR and the neo-X) to infer how former autoso
13 in D. pseudoobscura, but remains elevated in D. miranda, the species with the younger and larger Y ch
15 Levels of linkage disequilibrium (LD) in D. miranda are comparable to those observed in D. melano
21 e compensation along the neo-X chromosome of D. miranda, the neo-Y chromosome shows surprisingly unif
26 e modifications in male and female larvae of D. miranda (H3K4me1, H3K4me3, H3K36me3, H4K16ac, H3K27me
27 exu1 is conserved in the sibling species of D. miranda, as well as in a more distantly related speci
30 ll-studied sibling species D. pseudoobscura, D. miranda has much less nucleotide sequence variation,
31 phila pseudoobscura with its close relative, D. miranda, and the distant outgroup species, D. melanog
32 o separate recombination maps and 31% of the D. miranda physical genome, and we identified both globa