Q42125754 | 3'-processing of yeast tRNATrp precedes 5'-processing. |
Q40315347 | A complex pathway for 3' processing of the yeast U3 snoRNA. |
Q91504201 | A novel 5'-hydroxyl dinucleotide hydrolase activity for the DXO/Rai1 family of enzymes |
Q40409484 | A novel tertiary interaction in M1 RNA, the catalytic subunit of Escherichia coli RNase P |
Q36060838 | Affinity resins containing enzymatically resistant mRNA cap analogs--a new tool for the analysis of cap-binding proteins |
Q36676485 | Apoptotic signals induce specific degradation of ribosomal RNA in yeast |
Q64073611 | Arabidopsis DXO1 links RNA turnover and chloroplast function independently of its enzymatic activity |
Q64246894 | Arabidopsis DXO1 links RNA turnover and chloroplast function independently of its enzymatic activity |
Q36963318 | Arabidopsis thaliana LSM proteins function in mRNA splicing and degradation. |
Q34020217 | Arabidopsis thaliana XRN2 is required for primary cleavage in the pre-ribosomal RNA. |
Q81938678 | Bisphosphonate mRNA cap analog attached to Sepharose for affinity chromatography of decapping enzymes |
Q47558111 | Defective XRN3-mediated transcription termination in Arabidopsis impacts expression of protein-coding genes |
Q40689793 | Distinct 18S rRNA precursors are targets of the exosome complex, the exoribonuclease RRP6L2 and the terminal nucleotidyltransferase TRL in Arabidopsis thaliana |
Q24657729 | Efficient termination of transcription by RNA polymerase I requires the 5' exonuclease Rat1 in yeast |
Q36956974 | Functional analysis of the uL11 protein impact on translational machinery |
Q24529845 | Functions of the exosome in rRNA, snoRNA and snRNA synthesis |
Q42238512 | Increased levels of RNA oxidation enhance the reversion frequency in aging pro-apoptotic yeast mutants |
Q28215280 | Lsm Proteins are required for normal processing and stability of ribosomal RNAs |
Q39695481 | Lsm proteins are required for normal processing of pre-tRNAs and their efficient association with La-homologous protein Lhp1p |
Q27938447 | Microarray detection of novel nuclear RNA substrates for the exosome. |
Q92875175 | Non-canonical translation initiation in yeast generates a cryptic pool of mitochondrial proteins |
Q54943541 | Nuclear fate of yeast snoRNA is determined by co-transcriptional Rnt1 cleavage. |
Q40177492 | Nuclear pre-mRNA decapping and 5' degradation in yeast require the Lsm2-8p complex. |
Q42263113 | Phosphorylation of the N- and C-terminal UPF1 domains plays a critical role in plant nonsense-mediated mRNA decay. |
Q34344228 | Plant nonsense-mediated mRNA decay is controlled by different autoregulatory circuits and can be induced by an EJC-like complex. |
Q27937994 | Polyadenylation linked to transcription termination directs the processing of snoRNA precursors in yeast |
Q39454500 | Precursors to the U3 small nucleolar RNA lack small nucleolar RNP proteins but are stabilized by La binding. |
Q44042962 | Processing of 3'-extended read-through transcripts by the exosome can generate functional mRNAs. |
Q90327700 | RNA Helicases from the DEA(D/H)-Box Family Contribute to Plant NMD Efficiency |
Q89409711 | Rat1 and Xrn2: The Diverse Functions of the Nuclear Rat1/Xrn2 Exonuclease |
Q34370199 | RiboSys, a high-resolution, quantitative approach to measure the in vivo kinetics of pre-mRNA splicing and 3'-end processing in Saccharomyces cerevisiae. |
Q90621274 | Small Nucleolar RNAs Tell a Different Tale |
Q24791779 | Substrate discrimination in RNase P RNA-mediated cleavage: importance of the structural environment of the RNase P cleavage site |
Q93040786 | Synergistic defects in pre-rRNA processing from mutations in the U3-specific protein Rrp9 and U3 snoRNA |
Q41982240 | The P15-loop of Escherichia coli RNase P RNA is an autonomous divalent metal ion binding domain. |
Q55260276 | mRNA Decapping and 5'-3' Decay Contribute to the Regulation of ABA Signaling in Arabidopsis thaliana. |
Q27935208 | tRNA 3' processing in yeast involves tRNase Z, Rex1, and Rrp6. |