scholarly article | Q13442814 |
P50 | author | Nicholas Jarvis Proudfoot | Q21166845 |
Eduardo Eyras | Q30503190 | ||
Javier Caceres | Q43165847 | ||
Mireya Plass | Q56501770 | ||
Sara Macias | Q61117481 | ||
P2093 | author name string | Natalia Gromak | |
Martin Dienstbier | |||
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Human senataxin resolves RNA/DNA hybrids formed at transcriptional pause sites to promote Xrn2-dependent termination | Q24307617 | ||
The Microprocessor complex mediates the genesis of microRNAs | Q24312976 | ||
The FHA domain proteins DAWDLE in Arabidopsis and SNIP1 in humans act in small RNA biogenesis | Q24314338 | ||
Human 5' --> 3' exonuclease Xrn2 promotes transcription termination at co-transcriptional cleavage sites | Q24317135 | ||
Ars2 links the nuclear cap-binding complex to RNA interference and cell proliferation | Q24317359 | ||
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RNA exosome depletion reveals transcription upstream of active human promoters | Q24321777 | ||
SNIP1 is a candidate modifier of the transcriptional activity of c-Myc on E box-dependent target genes | Q24323701 | ||
Recognition and cleavage of primary microRNA precursors by the nuclear processing enzyme Drosha | Q24557506 | ||
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The human DiGeorge syndrome critical region gene 8 and Its D. melanogaster homolog are required for miRNA biogenesis | Q28297566 | ||
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Ars2 regulates both miRNA- and siRNA- dependent silencing and suppresses RNA virus infection in Drosophila | Q33486941 | ||
Diverse endonucleolytic cleavage sites in the mammalian transcriptome depend upon microRNAs, Drosha, and additional nucleases | Q34038435 | ||
Canonical and alternate functions of the microRNA biogenesis machinery. | Q34102263 | ||
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Primary microRNA transcripts are processed co-transcriptionally. | Q34931030 | ||
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DGCR8 HITS-CLIP reveals novel functions for the Microprocessor | Q36233919 | ||
Microprocessor, Setx, Xrn2, and Rrp6 co-operate to induce premature termination of transcription by RNAPII. | Q36679818 | ||
The splicing factor SC35 has an active role in transcriptional elongation | Q36952048 | ||
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Posttranscriptional crossregulation between Drosha and DGCR8. | Q37188339 | ||
The DEAD box RNA helicases p68 (Ddx5) and p72 (Ddx17): novel transcriptional co-regulators. | Q37217745 | ||
Two cap-binding proteins CBP20 and CBP80 are involved in processing primary MicroRNAs | Q37292978 | ||
Coupled RNA processing and transcription of intergenic primary microRNAs | Q37374749 | ||
Transcription regulation through promoter-proximal pausing of RNA polymerase II. | Q39442921 | ||
The 3'-end of the human beta-actin gene enhances activity of the beta-actin expression vector system: construction of improved vectors | Q41057998 | ||
Chromatin structure is implicated in "late" elongation checkpoints on the U2 snRNA and beta-actin genes | Q42068307 | ||
Chromatin-associated RNA interference components contribute to transcriptional regulation in Drosophila | Q42721062 | ||
Post-transcriptional control of DGCR8 expression by the Microprocessor | Q43123531 | ||
Autoregulation of polypyrimidine tract binding protein by alternative splicing leading to nonsense-mediated decay | Q44734157 | ||
Evolutionary trends of GC/AT distribution patterns in promoters | Q48058356 | ||
Tissue-specific histone modification and transcription factor binding in alpha globin gene expression. | Q53026451 | ||
The multifunctional RNA-binding protein hnRNP A1 is required for processing of miR-18a | Q64462273 | ||
P433 | issue | 6 | |
P304 | page(s) | 1499-1510 | |
P577 | publication date | 2013-12-19 | |
P1433 | published in | Cell Reports | Q5058165 |
P1476 | title | Drosha regulates gene expression independently of RNA cleavage function | |
P478 | volume | 5 |
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