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1 ds between the Bogota and U.S. subspecies of Drosophila pseudoobscura.
2 g empirical estimates of these parameters in Drosophila pseudoobscura.
3 approximately 1.5 million shotgun reads from Drosophila pseudoobscura.
4 irect genetic evidence for such an allele in Drosophila pseudoobscura.
5 ion between the Bogota and USA subspecies of Drosophila pseudoobscura.
6 sm was analyzed for the second chromosome of Drosophila pseudoobscura.
7 s and deaths for populations of genotypes in Drosophila pseudoobscura.
8 ion between the Bogota and USA subspecies of Drosophila pseudoobscura.
9 rryae in the Mojave Desert of California and Drosophila pseudoobscura across the western United State
10 males protects populations of the fruit fly Drosophila pseudoobscura against extinction caused by a
11 Drosophila melanogaster, the version 2 draft Drosophila pseudoobscura, an assembly of the Assemblatho
13 t is underexpressed in adult male hybrids of Drosophila pseudoobscura and D. persimilis relative to p
16 22 genes between two species of Drosophila, Drosophila pseudoobscura and D. subobscura, in codons th
17 ed and sequenced the PLC-gamma homologs from Drosophila pseudoobscura and D. virilis and compared the
18 sterility and female species preferences in Drosophila pseudoobscura and Drosophila persimilis, two
19 ticular, we isolated a dos homolog from both Drosophila pseudoobscura and Drosophila virilis and comp
20 for all Cys(2)His(2) zinc finger proteins in Drosophila pseudoobscura and identified associations wit
22 d the genome of a second Drosophila species, Drosophila pseudoobscura, and compared this to the genom
23 er Drosophila species, Drosophila yakuba and Drosophila pseudoobscura, and the mosquito Anopheles gam
25 to study variation in natural populations of Drosophila pseudoobscura, at a set of loci that had been
26 ion initiated with two allopatric strains of Drosophila pseudoobscura, BogER from Colombia and AH162
27 ssayed recombination across a 40Kb region of Drosophila pseudoobscura chromosome 2, with one 20kb int
28 ree recently diverged species of Drosophila: Drosophila pseudoobscura, D. persimilis, and D. pseudoob
29 onserved between Drosophila melanogaster and Drosophila pseudoobscura, despite extensive divergence o
31 nts of fitness of three experimental sets of Drosophila pseudoobscura females: monogamous females all
32 ing Drosophila miranda BAC sequences and the Drosophila pseudoobscura genome sequence, we aligned cod
33 dynamics of recently duplicated genes in the Drosophila pseudoobscura genome to understand the factor
40 ila melanogaster and esterase 5B (Est-5B) of Drosophila pseudoobscura show very little similarity.
41 PRDM9-like proteins across taxa, we use the Drosophila pseudoobscura species group in an attempt to
43 h and Adh-related genes was sequenced in 139 Drosophila pseudoobscura strains collected from 13 popul
44 esterase 5, and Heat-shock protein 83, in 40 Drosophila pseudoobscura strains collected from two popu
45 elective effects of PTC mutations within the Drosophila pseudoobscura subclade using 18 resequenced g
46 tudy to examine simultaneously in outbred WT Drosophila pseudoobscura the lifetime costs and benefits
47 licly available genomes of another fruit fly Drosophila pseudoobscura, the malaria mosquito Anopheles
49 nversions in two experimental populations of Drosophila pseudoobscura was subdivided into the effects
50 ionary conserved between D. melanogaster and Drosophila pseudoobscura, we found that many key develop
51 egions conserved between D. melanogaster and Drosophila pseudoobscura, we tag 5.3 kb of noncoding DNA
53 ding to previously sequenced Est-5B genes in Drosophila pseudoobscura were determined to compare patt
54 lassic speciation experiment, populations of Drosophila pseudoobscura were subjected to divergent die
55 compared gene orders on three chromosomes of Drosophila pseudoobscura with its close relative, D. mir
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