コーパス検索結果 (1語後でソート)
通し番号をクリックするとPubMedの該当ページを表示します
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
8 on of mobile element Delta 88 at +200 on the bithorax complex (BX-C) DNA map, 5' of all Abdominal-B (
10 we report that the blocking activity of the Bithorax complex (BX-C) Fub-1 boundary is segmentally re
11 correct spatial expression of two Drosophila bithorax complex (BX-C) genes, abdominal-A (abdA) and Ab
15 the unexpected observation that deletion of Bithorax complex (BX-C) miRNAs converts virgin female fl
18 mplex (ANT-C) and the IAB5 enhancer from the Bithorax complex (BX-C) preferentially activate TATA-con
19 t bithoraxoid (bxd) ncRNAs of the Drosophila bithorax complex (BX-C) prevent silencing of Ultrabithor
24 to initiate the activation of the Drosophila bithorax complex and define the domains of activity for
25 ax protein (TRX) binding elements within the bithorax complex and have found that within the bxd/pbx
26 msa is nested in the HOX gene cluster of the Bithorax complex and is known to contain a micro-RNA wit
27 The Abdominal-B (Abd-B) gene belongs to the bithorax complex and its expression is controlled by fou
29 -range enhancer-promoter interactions in the bithorax complex are regulated by a tethering element 5'
30 which is required for the functioning of the Bithorax complex boundary Fab-7, interacts specifically
35 from the Abdominal-B locus of the Drosophila bithorax complex facilitates the activity of a distantly
36 b-7 cis-regulatory domains in the Drosophila Bithorax Complex from early embryogenesis through to the
41 A fragment from the middle of the Drosophila bithorax complex insert preferentially into the bithorax
42 f segment-specific regulatory domains in the Bithorax complex is conferred by boundary elements and a
43 The iab-4 noncoding RNA from the Drosophila bithorax complex is the substrate for a microRNA (miRNA)
44 ries of mutations have been recovered in the bithorax complex of D. melanogaster that transform the f
47 horax complex insert preferentially into the bithorax complex or into the adjacent chromosome regions
48 from the Abdominal-B locus of the Drosophila Bithorax complex overcomes an insulator, and facilitates
49 from the Abdominal-B locus of the Drosophila bithorax complex overcomes the enhancer-blocking activit
50 contrast, control test sites outside of the bithorax complex permitted Gal4, T7RNAP, and FLP activit
51 n this study, the chromatin structure of the bithorax complex was probed with three separate assays f
54 One additional protein- coding gene in the bithorax complex, Glut3, a sugar-transporter homolog, ca
55 olycomb response element from the Drosophila bithorax complex, is able to mediate physical interactio
56 a domain boundary within the context of the bithorax complex, making Fab-7 one of the first boundary
62 ts other than evaluating their effect on the Bithorax-Complex (BXC) Abdominal B (Abd-B) mutant tuh-3.
63 al and, by genetic analysis, we identify the bithorax-complex genes and the ecdysone hormone as criti
64 cer of bithorax, a positive regulator of the Bithorax-Complex previously localized to the same geneti
66 ion of Chromatin Architecture dataset of the Bithorax gene cluster in Drosophila and show it outperfo
67 s of high EGFR signalling activity depend on bithorax gene function and that they account for the mai
68 and temporal expression of the Antennapedia-bithorax homeotic genes determining the fruit fly's body
70 animal body axis, as revealed by the classic bithorax phenotype of Drosophila melanogaster, in which