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1 s recapitulate the phenotypes of Enhancer of bithorax, a positive regulator of the Bithorax-Complex p
2 age T7 RNA polymerase were inserted into the bithorax (bx) regulatory region of the endogenous Ultrab
4 purpose we have investigated the Drosophila bithorax complex (BX-C) because genetic studies suggest
5 iption is prevented when Hox proteins of the Bithorax Complex (BX-C) bind to cis-regulatory elements
6 ch influences were first detected within the bithorax complex (BX-C) by E.B. Lewis, who coined the te
7 on of mobile element Delta 88 at +200 on the bithorax complex (BX-C) DNA map, 5' of all Abdominal-B (
9 correct spatial expression of two Drosophila bithorax complex (BX-C) genes, abdominal-A (abdA) and Ab
15 mplex (ANT-C) and the IAB5 enhancer from the Bithorax complex (BX-C) preferentially activate TATA-con
16 t bithoraxoid (bxd) ncRNAs of the Drosophila bithorax complex (BX-C) prevent silencing of Ultrabithor
21 to initiate the activation of the Drosophila bithorax complex and define the domains of activity for
22 ax protein (TRX) binding elements within the bithorax complex and have found that within the bxd/pbx
24 -range enhancer-promoter interactions in the bithorax complex are regulated by a tethering element 5'
25 which is required for the functioning of the Bithorax complex boundary Fab-7, interacts specifically
30 from the Abdominal-B locus of the Drosophila bithorax complex facilitates the activity of a distantly
31 b-7 cis-regulatory domains in the Drosophila Bithorax Complex from early embryogenesis through to the
36 A fragment from the middle of the Drosophila bithorax complex insert preferentially into the bithorax
37 The iab-4 noncoding RNA from the Drosophila bithorax complex is the substrate for a microRNA (miRNA)
38 ries of mutations have been recovered in the bithorax complex of D. melanogaster that transform the f
41 horax complex insert preferentially into the bithorax complex or into the adjacent chromosome regions
42 from the Abdominal-B locus of the Drosophila Bithorax complex overcomes an insulator, and facilitates
43 from the Abdominal-B locus of the Drosophila bithorax complex overcomes the enhancer-blocking activit
44 contrast, control test sites outside of the bithorax complex permitted Gal4, T7RNAP, and FLP activit
45 n this study, the chromatin structure of the bithorax complex was probed with three separate assays f
48 One additional protein- coding gene in the bithorax complex, Glut3, a sugar-transporter homolog, ca
49 olycomb response element from the Drosophila bithorax complex, is able to mediate physical interactio
50 a domain boundary within the context of the bithorax complex, making Fab-7 one of the first boundary
56 ts other than evaluating their effect on the Bithorax-Complex (BXC) Abdominal B (Abd-B) mutant tuh-3.
57 al and, by genetic analysis, we identify the bithorax-complex genes and the ecdysone hormone as criti
58 cer of bithorax, a positive regulator of the Bithorax-Complex previously localized to the same geneti
60 s of high EGFR signalling activity depend on bithorax gene function and that they account for the mai
61 and temporal expression of the Antennapedia-bithorax homeotic genes determining the fruit fly's body
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