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1 Mcp mediates its regulatory function in the bithorax complex.
2 ility that other such genes occur within the Bithorax complex.
3 Abdominal-B homeotic genes at the Drosophila bithorax complex.
4 ogaster, including the homeotic genes of the bithorax complex.
5 he white gene and help activate genes of the bithorax complex.
6 gment identity genes of the Antennapedia and Bithorax complexes.
7 to initiate the activation of the Drosophila bithorax complex and define the domains of activity for
8 ax protein (TRX) binding elements within the bithorax complex and have found that within the bxd/pbx
9 msa is nested in the HOX gene cluster of the Bithorax complex and is known to contain a micro-RNA wit
10 The Abdominal-B (Abd-B) gene belongs to the bithorax complex and its expression is controlled by fou
12 -range enhancer-promoter interactions in the bithorax complex are regulated by a tethering element 5'
13 which is required for the functioning of the Bithorax complex boundary Fab-7, interacts specifically
14 purpose we have investigated the Drosophila bithorax complex (BX-C) because genetic studies suggest
15 iption is prevented when Hox proteins of the Bithorax Complex (BX-C) bind to cis-regulatory elements
16 ch influences were first detected within the bithorax complex (BX-C) by E.B. Lewis, who coined the te
18 on of mobile element Delta 88 at +200 on the bithorax complex (BX-C) DNA map, 5' of all Abdominal-B (
20 we report that the blocking activity of the Bithorax complex (BX-C) Fub-1 boundary is segmentally re
21 correct spatial expression of two Drosophila bithorax complex (BX-C) genes, abdominal-A (abdA) and Ab
25 the unexpected observation that deletion of Bithorax complex (BX-C) miRNAs converts virgin female fl
28 mplex (ANT-C) and the IAB5 enhancer from the Bithorax complex (BX-C) preferentially activate TATA-con
29 t bithoraxoid (bxd) ncRNAs of the Drosophila bithorax complex (BX-C) prevent silencing of Ultrabithor
34 ts other than evaluating their effect on the Bithorax-Complex (BXC) Abdominal B (Abd-B) mutant tuh-3.
39 from the Abdominal-B locus of the Drosophila bithorax complex facilitates the activity of a distantly
40 b-7 cis-regulatory domains in the Drosophila Bithorax Complex from early embryogenesis through to the
43 al and, by genetic analysis, we identify the bithorax-complex genes and the ecdysone hormone as criti
44 One additional protein- coding gene in the bithorax complex, Glut3, a sugar-transporter homolog, ca
47 A fragment from the middle of the Drosophila bithorax complex insert preferentially into the bithorax
48 f segment-specific regulatory domains in the Bithorax complex is conferred by boundary elements and a
49 The iab-4 noncoding RNA from the Drosophila bithorax complex is the substrate for a microRNA (miRNA)
50 olycomb response element from the Drosophila bithorax complex, is able to mediate physical interactio
51 a domain boundary within the context of the bithorax complex, making Fab-7 one of the first boundary
52 ries of mutations have been recovered in the bithorax complex of D. melanogaster that transform the f
55 horax complex insert preferentially into the bithorax complex or into the adjacent chromosome regions
56 from the Abdominal-B locus of the Drosophila Bithorax complex overcomes an insulator, and facilitates
57 from the Abdominal-B locus of the Drosophila bithorax complex overcomes the enhancer-blocking activit
58 contrast, control test sites outside of the bithorax complex permitted Gal4, T7RNAP, and FLP activit
59 cer of bithorax, a positive regulator of the Bithorax-Complex previously localized to the same geneti
60 n this study, the chromatin structure of the bithorax complex was probed with three separate assays f