| scholarly article | Q13442814 |
| P50 | author | Peter Baumann | Q7172713 |
| P2093 | author name string | J Andrew Berglund | |
| Jonathan P Staley | |||
| Ram Kannan | |||
| Rodger B Voelker | |||
| Sean Hartnett | |||
| P2860 | cites work | Genome-wide association between branch point properties and alternative splicing | Q21092523 |
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| Integrator, a multiprotein mediator of small nuclear RNA processing, associates with the C-terminal repeat of RNA polymerase II | Q24338780 | ||
| Evidence that U5 snRNP recognizes the 3' splice site for catalytic step II in mammals | Q24532589 | ||
| An upstream AG determines whether a downstream AG is selected during catalytic step II of splicing | Q24551016 | ||
| Human branch point consensus sequence is yUnAy | Q24646378 | ||
| Promoter-driven splicing regulation in fission yeast | Q59097207 | ||
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| Formation of the 3' end of U1 snRNA requires compatible snRNA promoter elements | Q69638046 | ||
| pDblet, a stable autonomously replicating shuttle vector for Schizosaccharomyces pombe | Q71817989 | ||
| Mutations in the SF1-U2AF59-U2AF23 complex cause exon skipping in Schizosaccharomyces pombe | Q79386282 | ||
| Effect of mutations at the lariat branch acceptor site on beta-globin pre-mRNA splicing in vitro | Q93551289 | ||
| The spliceosome: design principles of a dynamic RNP machine | Q28131809 | ||
| Distinct binding specificities and functions of higher eukaryotic polypyrimidine tract-binding proteins | Q29618943 | ||
| Protection of telomeres by the Ku protein in fission yeast | Q30306228 | ||
| UACUAAC is the preferred branch site for mammalian mRNA splicing | Q33850531 | ||
| Yeast pre-messenger RNA splicing efficiency depends on critical spacing requirements between the branch point and 3' splice site | Q33879810 | ||
| Spliceosome discards intermediates via the DEAH box ATPase Prp43p | Q33933327 | ||
| Semiquantitative proteomic analysis of the human spliceosome via a novel two-dimensional gel electrophoresis method | Q34181884 | ||
| Genome-wide bioinformatic and molecular analysis of introns in Saccharomyces cerevisiae | Q34361753 | ||
| DEAH-box ATPase Prp16 has dual roles in remodeling of the spliceosome in catalytic steps | Q34415414 | ||
| Rules of engagement: co-transcriptional recruitment of pre-mRNA processing factors | Q34419716 | ||
| Identification and characterization of the Schizosaccharomyces pombe TER1 telomerase RNA. | Q34586455 | ||
| Functional analysis of the polypyrimidine tract in pre-mRNA splicing | Q34625830 | ||
| Both the polypyrimidine tract and the 3' splice site function prior to the first step of splicing in fission yeast | Q34644631 | ||
| A brief review of molecular information theory. | Q35563841 | ||
| Global analysis of mRNA decay intermediates in Saccharomyces cerevisiae | Q36122681 | ||
| Eukaryotic Lsm proteins: lessons from bacteria | Q36331209 | ||
| Exon ligation is proofread by the DExD/H-box ATPase Prp22p | Q37059609 | ||
| RNA splicing and intron turnover are greatly diminished by a mutant yeast branch point | Q37394068 | ||
| Telomerase: an RNP enzyme synthesizes DNA. | Q37775786 | ||
| Staying on message: ensuring fidelity in pre-mRNA splicing | Q38008056 | ||
| Pre-spliceosome formation in S.pombe requires a stable complex of SF1-U2AF(59)-U2AF(23) | Q39659121 | ||
| TER1, the RNA subunit of fission yeast telomerase | Q39752449 | ||
| Insights into branch nucleophile positioning and activation from an orthogonal pre-mRNA splicing system in yeast | Q39978710 | ||
| Fission yeast gene structure and recognition | Q40399675 | ||
| The second catalytic step of pre-mRNA splicing | Q40939314 | ||
| Telomerase RNA biogenesis involves sequential binding by Sm and Lsm complexes | Q41967731 | ||
| Identification and comparative analysis of telomerase RNAs from Candida species reveal conservation of functional elements | Q42147960 | ||
| A class of human exons with predicted distant branch points revealed by analysis of AG dinucleotide exclusion zones | Q42148185 | ||
| trans-splicing to spliceosomal U2 snRNA suggests disruption of branch site-U2 pairing during pre-mRNA splicing | Q42381501 | ||
| The role of branchpoint-3' splice site spacing and interaction between intron terminal nucleotides in 3' splice site selection in Saccharomyces cerevisiae | Q42611009 | ||
| Ordered and dynamic assembly of single spliceosomes | Q42726090 | ||
| Competition between the ATPase Prp5 and branch region-U2 snRNA pairing modulates the fidelity of spliceosome assembly | Q43049651 | ||
| A mutational analysis of the polypyrimidine tract of introns. Effects of sequence differences in pyrimidine tracts on splicing. | Q44183759 | ||
| Deciphering 3'ss selection in the yeast genome reveals an RNA thermosensor that mediates alternative splicing | Q44838435 | ||
| A U-rich tract enhances usage of an alternative 3′ splice site in yeast | Q46196387 | ||
| Cytoplasmic degradation of splice-defective pre-mRNAs and intermediates | Q47303263 | ||
| Molecular cloning and characterization of the Schizosaccharomyces pombe his3 gene for use as a selectable marker | Q48086234 | ||
| U2AF homolog required for splicing in vivo | Q48096653 | ||
| Isolation of an active step I spliceosome and composition of its RNP core | Q50336090 | ||
| Spliceosomal cleavage generates the 3' end of telomerase RNA. | Q50336096 | ||
| Repositioning of the reaction intermediate within the catalytic center of the spliceosome. | Q52568800 | ||
| P433 | issue | 6 | |
| P407 | language of work or name | English | Q1860 |
| P304 | page(s) | 627-638 | |
| P577 | publication date | 2013-03-06 | |
| P1433 | published in | Genes & Development | Q1524533 |
| P1476 | title | Intronic sequence elements impede exon ligation and trigger a discard pathway that yields functional telomerase RNA in fission yeast | |
| P478 | volume | 27 |
| Q34988114 | Diverse mechanisms for spliceosome-mediated 3' end processing of telomerase RNA. |
| Q91956493 | Early splicing functions of fission yeast Prp16 and its unexpected requirement for gene Silencing is governed by intronic features |
| Q47201697 | Intron specificity in pre-mRNA splicing |
| Q39001197 | Large-scale analysis of branchpoint usage across species and cell lines |
| Q38123746 | Lives that introns lead after splicing |
| Q47184251 | New perspectives on telomerase RNA structure and function |
| Q35524345 | Non-mRNA 3' end formation: how the other half lives |
| Q39066545 | Peculiarities of Yeasts and Human Telomerase RNAs Processing |
| Q50106845 | Pof8 is a La-related protein and a constitutive component of telomerase in fission yeast |
| Q34987937 | Prevalent and distinct spliceosomal 3'-end processing mechanisms for fungal telomerase RNA. |
| Q92772490 | Rapidly evolving protointrons in Saccharomyces genomes revealed by a hungry spliceosome |
| Q42845283 | Specific features of telomerase RNA from Hansenula polymorpha |
| Q37165431 | Spliceosomal DEAH-Box ATPases Remodel Pre-mRNA to Activate Alternative Splice Sites |
| Q88571202 | Spliceosome Profiling Visualizes Operations of a Dynamic RNP at Nucleotide Resolution |
| Q42650602 | Spliceosome-mediated decay (SMD) regulates expression of nonintronic genes in budding yeast. |
| Q27008926 | Splicing fidelity: DEAD/H-box ATPases as molecular clocks |
| Q90316146 | Termination of pre-mRNA splicing requires that the ATPase and RNA unwindase Prp43p acts on the catalytic snRNA U6 |
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