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1  3'-seq libraries from Drosophila yakuba and Drosophila virilis.
2 sequence of a tim gene from another species, Drosophila virilis.
3  Kruppel, we cloned the Kruppel homolog from Drosophila virilis.
4 omic clones that cover the Cecropin locus in Drosophila virilis.
5  or in the more remote (40-50 million years) Drosophila virilis.
6  nanos 3'UTRs of Drosophila melanogaster and Drosophila virilis.
7 re conserved from Drosophila melanogaster to Drosophila virilis.
8 on, and regulation of tra-2 are conserved in Drosophila virilis, a species diverged from D. melanogas
9 ISPR-Cas9 to force FruM expression in female Drosophila virilis, a species in which males and females
10 cloned and sequenced from two other insects (Drosophila virilis and Aedes aegypti) and three vertebra
11 ning reverse transcriptase (RT), Penelope in Drosophila virilis and Athena in bdelloid rotifers, have
12 molog from both Drosophila pseudoobscura and Drosophila virilis and compared their gene structures an
13 sterility between two species of Drosophila, Drosophila virilis and D. americana.
14 n two closely related species of Drosophila, Drosophila virilis and D. americana.
15 ation within this domain, ZLD orthologs from Drosophila virilis, Anopheles gambiae, and Nasonia vitri
16          To test this hypothesis, we develop Drosophila virilis as a new model for studies of duettin
17      Rescue activity is provided by tko from Drosophila virilis ClvR (tko) results in germline and ma
18 In this work, we report the localization, in Drosophila virilis, D. montana, and D. novamexicana, of
19                    The virilis phylad of the Drosophila virilis group consists of five closely relate
20 ch to investigate this in two species of the Drosophila virilis group.
21                                              Drosophila virilis has recently been shown to have telom
22           An example of hybrid dysgenesis in Drosophila virilis is unique in that multiple, unrelated
23 highly conserved between D. melanogaster and Drosophila virilis, is required to spatially restrict wg
24 f the RING finger domain were conserved in a Drosophila virilis MSL2 homolog.
25 ted EXSs from a phylogenetic comparison with Drosophila virilis nASI.
26 rved between the Drosophila melanogaster and Drosophila virilis NK-4 genes and serve as binding sites
27 onserved between Drosophila melanogaster and Drosophila virilis NK-4 genes.
28     Further, the timing of yar expression in Drosophila virilis parallels that in D. melanogaster, su
29 cid level to the Drosophila melanogaster and Drosophila virilis proteins.
30 ; in particular, certain dysgenic crosses in Drosophila virilis result in mobilization of a TLE desig
31 TART elements in Drosophila melanogaster and Drosophila virilis show species-specific innovations in
32 e examined the retrotransposon Helena in the Drosophila virilis species group (subgenus Drosophila) a
33 LTR retrotransposable element present in the Drosophila virilis species group.
34 evelopmental gene fused was determined in 15 Drosophila virilis strains.
35                       A laboratory strain of Drosophila virilis was genetically transformed with a ho
36       A hybrid dysgenesis syndrome occurs in Drosophila virilis when males from an established labora