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1 hia and mtDNA, using a large inbred panel of Drosophila simulans.
2 e chromosomes to modulate gene expression in Drosophila simulans.
3 last 5.4 million years since its split from Drosophila simulans.
4 e since the most recent common ancestor with Drosophila simulans.
5 es of Drosophila melanogaster and 6 lines of Drosophila simulans.
6 in the genetic background of sibling species Drosophila simulans.
7 parent in Drosophila melanogaster but not in Drosophila simulans.
8 hila melanogaster with their divergence from Drosophila simulans.
9 10 times faster than its generalist sibling Drosophila simulans.
10 ulations and four moderately inbred lines of Drosophila simulans.
11 rom several loci across chromosome arm 2R in Drosophila simulans.
12 eference laboratory strain and one strain of Drosophila simulans.
13 of nucleotide polymorphisms and fixations in Drosophila simulans.
14 Drosophila melanogaster and in one strain of Drosophila simulans.
15 mal loci from a North American population of Drosophila simulans.
16 to be absent from close relatives, including Drosophila simulans.
17 individual X chromosomes in a population of Drosophila simulans.
18 of Drosophila mauritiana into the genome of Drosophila simulans.
19 referred and unpreferred silent mutations in Drosophila simulans.
21 n comparisons of Drosophila melanogaster and Drosophila simulans, a divergence of approximately 2.5 m
22 e leading to Drosophila melanogaster than in Drosophila simulans, a finding that agrees with other fe
23 stributed across chromosome arms X and 3R of Drosophila simulans, a sibling species of D. melanogaste
24 well as divergence with its sibling species Drosophila simulans, across 24.2 kb of noncoding DNA ide
26 t to function in the innate immune system of Drosophila simulans and compare these data to those from
28 loci misexpressed in sterile male hybrids of Drosophila simulans and D. mauritiana relative to parent
30 m heads of recently diverged sister species, Drosophila simulans and D. mauritiana, to enable detaile
36 es that affect mating discrimination between Drosophila simulans and D. sechellia, quantitative trait
40 id rescue (Lhr) has functionally diverged in Drosophila simulans and interacts with Hybrid male rescu
41 ence using genomewide polymorphism data from Drosophila simulans and the divergence between D. simula
42 sterility between Drosophila mauritiana and Drosophila simulans and were able to verify such a predi
43 eptopilina boulardi) from its infected host (Drosophila simulans) and subsequently undergo diminishin
44 sophila species, Drosophila melanogaster and Drosophila simulans, and find that pulse song responses
46 omosomes from either Drosophila sechellia or Drosophila simulans are introgressed into a common D. si
47 ales of Drosophila melanogaster and males of Drosophila simulans are mated, the male progeny are invi
48 Hybrids between Drosophila melanogaster and Drosophila simulans are sterile, and phenocopy mutations
50 lecular divergence, the three species of the Drosophila simulans clade are closely related to and ess
51 lower in Drosophila melanogaster than in the Drosophila simulans clade, primarily due to Y-linked ret
54 id genotypes involving three sister species: Drosophila simulans, D. mauritiana, and D. sechellia.
55 is sex-ratio (SR) meiotic drive occurring in Drosophila simulans Driver HP1D2 alleles prevent the seg
56 lex (D. melanogaster, Drosophila mauritiana, Drosophila simulans, Drosophila sechellia, Drosophila ya
57 riation in genome-wide gene expression among Drosophila simulans, Drosophila yakuba and four strains
58 a newly compiled data set of 115 genes from Drosophila simulans, each with each orthologs from D. me
59 hia can cause cytoplasmic incompatibility in Drosophila simulans flies: if an infected male mates wit
60 nucleotide polymorphism in three paralogous Drosophila simulans genes, janusA (janA), janusB (janB),
62 ve compared the complete D. melanogaster and Drosophila simulans genome sequences to estimate mean se
64 mitochondrial genomes of the three distinct Drosophila simulans haplotypes with intron 1 of the alco
65 an extreme example, a domesticated strain of Drosophila simulans harbored both strongly photopositive
66 etween adults of Drosophila melanogaster and Drosophila simulans has uncovered the evolution of genes
68 Drosophila melanogaster carrying mtDNA from Drosophila simulans in a D. melanogaster Oregon-R chromo
69 pressed genes (janusA, janusB, and ocnus) in Drosophila simulans included all three of these features
70 Wolbachia and in Drosophila melanogaster and Drosophila simulans infected with wMelPop and wAu strain
71 loci that control innate food preference in Drosophila simulans into the genomic background of D. se
73 eoporin 160kDa (Nup160) gene of the fruitfly Drosophila simulans is incompatible with one or more fac
75 ranscript at the 5' end of the R2 element in Drosophila simulans is rapid and utilizes an unexpected
81 increased mRNA and protein expression of the Drosophila simulans nonmuscle myosin II gene zipper.
82 the evolutionary dynamics of infection of a Drosophila simulans population by a maternally inherited
84 n was addressed in this study using lines of Drosophila simulans previously shown to have either acti
85 la melanogaster with that of divergence from Drosophila simulans shows that the A/S ratio of divergen
87 y, a unique domain of expression is found in Drosophila simulans that does occur in the closely relat
88 study has revealed a mobile DNA insertion in Drosophila simulans that is associated with an apparent
89 and single lines of Drosophila sechellia and Drosophila simulans, the latter two differing by approxi
91 ces of ESTs from the male accessory gland of Drosophila simulans to their orthologs in its close rela
92 related species, Drosophila melanogaster and Drosophila simulans, under different environmental condi
93 achia popcorn strain from D. melanogaster to Drosophila simulans, we demonstrated that initial high d
94 y rescue between Drosophila melanogaster and Drosophila simulans, we show that this hybridization can
95 m genes in a California population sample of Drosophila simulans were shown to bear several hallmarks
96 sofemale lines obtained from a population of Drosophila simulans were surveyed for recent R2 insertio
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