Analysis of an even-skipped rescue transgene reveals both composite and discrete neuronal and early blastoderm enhancers, and multi-stripe positioning by gap gene repressor gradients.
about
Consequences of eukaryotic enhancer architecture for gene expression dynamics, development, and fitnessTranscription factors bind thousands of active and inactive regions in the Drosophila blastodermFunctional evolution of a cis-regulatory moduleExploiting transcription factor binding site clustering to identify cis-regulatory modules involved in pattern formation in the Drosophila genomeComputational identification of developmental enhancers: conservation and function of transcription factor binding-site clusters in Drosophila melanogaster and Drosophila pseudoobscuraAssessing the impact of comparative genomic sequence data on the functional annotation of the Drosophila genomeTranscriptional control in the segmentation gene network of DrosophilaAn Sp1/KLF binding site is important for the activity of a Polycomb group response element from the Drosophila engrailed gene.Predicting Ancestral Segmentation Phenotypes from Drosophila to Anopheles Using In Silico EvolutionBig genomes facilitate the comparative identification of regulatory elementseven skipped is required to produce a trans-acting signal for larval neuroblast proliferation that can be mimicked by ecdysoneLocal action of long-range repressors in the Drosophila embryoNELF potentiates gene transcription in the Drosophila embryoTranscriptional integration of competence modulated by mutual repression generates cell-type specificity within the cardiogenic mesodermAnalysis of pattern precision shows that Drosophila segmentation develops substantial independence from gradients of maternal gene productsMicrotubules are organized independently of the centrosome in Drosophila neurons.A resource for manipulating gene expression and analyzing cis-regulatory modules in the Drosophila CNS.Interleukin-10 haplotypes in Celiac Disease in the Spanish population.Sepsid even-skipped enhancers are functionally conserved in Drosophila despite lack of sequence conservation.Nonparametric identification of regulatory interactions from spatial and temporal gene expression dataNon-autonomous modulation of heart rhythm, contractility and morphology in adult fruit flies.Atlas-builder software and the eNeuro atlas: resources for developmental biology and neuroscience.The role of binding site cluster strength in Bicoid-dependent patterning in Drosophila.Non-additive interactions involving two distinct elements mediate sloppy-paired regulation by pair-rule transcription factors.Polycomb group response elements in Drosophila and vertebratesMultiple modular promoter elements drive graded brinker expression in response to the Dpp morphogen gradient.Rearrangements of 2.5 kilobases of noncoding DNA from the Drosophila even-skipped locus define predictive rules of genomic cis-regulatory logicA complex array of DNA-binding proteins required for pairing-sensitive silencing by a polycomb group response element from the Drosophila engrailed gene.Cis-regulatory complexity within a large non-coding region in the Drosophila genomeHomotypic regulatory clusters in Drosophila.A gene expression atlas of a bicoid-depleted Drosophila embryo reveals early canalization of cell fate.Extraction of functional binding sites from unique regulatory regions: the Drosophila early developmental enhancers.Shadow enhancers enable Hunchback bifunctionality in the Drosophila embryoThe Drosophila eve insulator Homie promotes eve expression and protects the adjacent gene from repression by polycomb spreading.Chip interacts with diverse homeodomain proteins and potentiates bicoid activity in vivoQuantitative modeling of a gene's expression from its intergenic sequence.Multiple enhancers ensure precision of gap gene-expression patterns in the Drosophila embryo.Combinatorial activation and concentration-dependent repression of the Drosophila even skipped stripe 3+7 enhancer.The role of chromatin accessibility in directing the widespread, overlapping patterns of Drosophila transcription factor binding.Functional interaction between the Drosophila knirps short range transcriptional repressor and RPD3 histone deacetylase.
P2860
Q21092422-033F487F-08CF-427D-A01D-37D4F7749E21Q21563555-DB487DB5-307E-4FC4-9C4E-2A1CCE0AE468Q21563626-EC5AAA1F-CEC9-4E5C-9A8C-FD20D53C8704Q24530466-3AABE0E9-5812-4686-BA57-2275B95C070BQ24801531-76286F60-E78A-4E1C-B891-8619A3295D55Q24803725-4F88297B-C2CB-4445-80A9-811517A9C7D0Q24803742-95B18D0D-AB06-4236-90B6-81325D72C89BQ24814416-138E7BF3-D017-4DE6-B47B-47461F773E7EQ27308847-86B5993F-B524-4315-B564-6A5D98F4D134Q27350595-7049CDEA-1331-4923-96E4-1C86D3F1369BQ28363295-77079A89-BCD8-4C0D-A0D3-F2D4B11A7E79Q28364104-DF4F9B97-0B01-4E8E-B9FA-80224409A7F1Q28474810-BDB5FB3A-D658-4801-BBE8-8B0B24A54B8EQ28752574-3A4E167C-8779-410E-812F-05E9A8C12167Q30481329-21DD8C58-3499-48AA-A56E-45882AF781EFQ30504690-62A46408-4C6A-4353-8223-BA95AA229A02Q30529918-C4CE387D-28E7-41B3-B015-839A72845935Q33238289-3772B226-2891-4246-AEC0-B317F379A8E4Q33347127-6798FB08-783A-4E8E-B98B-E947058E17D8Q33649170-71CA18BB-B954-471B-A80C-1C0A4DDF2C10Q33693863-1C5A7762-599C-4FB3-A85A-652757E1BB6CQ33731126-E0BE57E4-2E9B-4CF9-BA63-518FBAB521CFQ33935968-6024B6F0-FE22-4CC9-80E1-DD76FA061666Q34036908-5F0025DB-0267-4288-8FF5-0E3D08073FD9Q34148505-6CEC21F2-9C6D-4FE7-B693-BC40521B0192Q34521640-5C8C31B3-CC31-4CC3-88C3-5FF6BCD92459Q34611185-5B182CED-1541-4304-B79F-D0131BDFDFDEQ34614728-71257671-48B2-43FF-8EE6-E65685550E5FQ34683629-B7E9054E-1A34-4B41-B443-0DDB74B09C9EQ34994285-10BE682E-007D-4C93-9BDD-38CF77FDD4DDQ34999620-95F572BD-65E5-43EF-9B3E-E4DB1B171DE9Q35004175-407B5571-E410-49F3-9938-F056CA333FE9Q35031297-16993A7D-5CF0-4F19-9DAB-ADA076478CDFQ35034322-A48CE6D1-36D2-4B89-AD27-8F23A3C9B292Q35079219-50B558F7-EDE8-4D7B-BE6F-42140A538AEDQ35113491-B109D0E5-DA81-47E2-8438-DA440EA56E2FQ35170843-3A2553E8-0F3A-41D8-82B4-7371AC5EAD1DQ35208727-88CEE6F3-3A03-42F6-985D-3272DA7C8F0CQ35557755-7999A1FF-7C60-43D0-9E37-02E3DE2DBA95Q35645917-5E41ECC8-6686-4C6B-81E8-4EAD74E1C3F9
P2860
Analysis of an even-skipped rescue transgene reveals both composite and discrete neuronal and early blastoderm enhancers, and multi-stripe positioning by gap gene repressor gradients.
description
1999 nî lūn-bûn
@nan
1999年の論文
@ja
1999年論文
@yue
1999年論文
@zh-hant
1999年論文
@zh-hk
1999年論文
@zh-mo
1999年論文
@zh-tw
1999年论文
@wuu
1999年论文
@zh
1999年论文
@zh-cn
name
Analysis of an even-skipped re ...... gap gene repressor gradients.
@en
type
label
Analysis of an even-skipped re ...... gap gene repressor gradients.
@en
prefLabel
Analysis of an even-skipped re ...... gap gene repressor gradients.
@en
P2093
P2860
P1433
P1476
Analysis of an even-skipped re ...... gap gene repressor gradients.
@en
P2093
G L Yusibova
J B Jaynes
Y Emi-Sarker
P2860
P304
P407
P577
1999-06-01T00:00:00Z