Self-coded 3'-extension of run-off transcripts produces aberrant products during in vitro transcription with T7 RNA polymerase.
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Comparative analysis of viral RNA signatures on different RIG-I-like receptorsRecognition of 5' triphosphate by RIG-I helicase requires short blunt double-stranded RNA as contained in panhandle of negative-strand virus.A recombinant hepatitis C virus RNA-dependent RNA polymerase capable of copying the full-length viral RNA.Visualization of tRNA movements on the Escherichia coli 70S ribosome during the elongation cycleCryo-EM reveals an active role for aminoacyl-tRNA in the accommodation processYeast DEAD box protein Mss116p is a transcription elongation factor that modulates the activity of mitochondrial RNA polymerase.Nuclease activity of T7 RNA polymerase and the heterogeneity of transcription elongation complexesComplex of transfer-messenger RNA and elongation factor Tu. Unexpected modes of interaction.Simulating in vitro transcriptional response of zinc homeostasis system in Escherichia coli.Nonreplicative RNA recombination in poliovirusUnpaired 5' ppp-nucleotides, as found in arenavirus double-stranded RNA panhandles, are not recognized by RIG-IExpanded CUG repeat RNAs form hairpins that activate the double-stranded RNA-dependent protein kinase PKRIn vivo deuteration of transfer RNAs: overexpression and large-scale purification of deuterated specific tRNAs.Structural mechanism of sensing long dsRNA via a noncatalytic domain in human oligoadenylate synthetase 3Generating the optimal mRNA for therapy: HPLC purification eliminates immune activation and improves translation of nucleoside-modified, protein-encoding mRNA.Selecting rRNA binding sites for the ribosomal proteins L4 and L6 from randomly fragmented rRNA: application of a method called SERF5'-Triphosphate-short interfering RNA: potent inhibition of influenza A virus infection by gene silencing and RIG-I activation.Features of 80S mammalian ribosome and its subunitsShine-Dalgarno interaction prevents incorporation of noncognate amino acids at the codon following the AUGRapid and simple ribozymic aminoacylation using three conserved nucleotides.mRNA transcript therapy.Codon-anticodon interaction at the P site is a prerequisite for tRNA interaction with the small ribosomal subunit.Interaction of mRNA with the Escherichia coli ribosome: accessibility of phosphorothioate-containing mRNA bound to ribosomes for iodine cleavage.Construction of an in vitro bistable circuit from synthetic transcriptional switches.Original Chemical Series of Pyrimidine Biosynthesis Inhibitors That Boost the Antiviral Interferon Response.Reprogramming of Pancreatic Exocrine Cells AR42J Into Insulin-producing Cells Using mRNAs for Pdx1, Ngn3, and MafA Transcription Factors.GATA-1 DNA binding activity is down-regulated in late S phase in erythroid cells.The thumb subdomain of yeast mitochondrial RNA polymerase is involved in processivity, transcript fidelity and mitochondrial transcription factor binding.Mutational analysis of the donor substrate binding site of the ribosomal peptidyltransferase center.A short fragment of 23S rRNA containing the binding sites for two ribosomal proteins, L24 and L4, is a key element for rRNA folding during early assembly.RNA structural domains in noncoding regions of the foot-and-mouth disease virus genome trigger innate immunity in porcine cells and miceThe ability of a variety of polymerases to synthesize past site-specific cis-syn, trans-syn-II, (6-4), and Dewar photoproducts of thymidylyl-(3'-->5')-thymidine.Poly A tail length analysis of in vitro transcribed mRNA by LC-MS.Protection patterns of tRNAs do not change during ribosomal translocation.Ribonucleolytic activities in the Escherichia coli in vitro translation system and in its separate components.Conserved nucleotides of 23 S rRNA located at the ribosomal peptidyltransferase center.Mutational analysis of two highly conserved UGG sequences of 23 S rRNA from Escherichia coli.An origin of the immunogenicity of in vitro transcribed RNA.A specific, promoter-independent activity of T7 RNA polymerase suggests a general model for DNA/RNA editing in single subunit RNA Polymerases3' end additions by T7 RNA polymerase are RNA self-templated, distributive and diverse in character-RNA-Seq analyses
P2860
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P2860
Self-coded 3'-extension of run-off transcripts produces aberrant products during in vitro transcription with T7 RNA polymerase.
description
1995 nî lūn-bûn
@nan
1995年の論文
@ja
1995年論文
@yue
1995年論文
@zh-hant
1995年論文
@zh-hk
1995年論文
@zh-mo
1995年論文
@zh-tw
1995年论文
@wuu
1995年论文
@zh
1995年论文
@zh-cn
name
Self-coded 3'-extension of run ...... iption with T7 RNA polymerase.
@en
type
label
Self-coded 3'-extension of run ...... iption with T7 RNA polymerase.
@en
prefLabel
Self-coded 3'-extension of run ...... iption with T7 RNA polymerase.
@en
P2093
P2860
P356
P1476
Self-coded 3'-extension of run ...... iption with T7 RNA polymerase.
@en
P2093
Dabrowski M
Nierhaus KH
Triana-Alonso FJ
P2860
P304
P356
10.1074/JBC.270.11.6298
P407
P577
1995-03-01T00:00:00Z