| scholarly article | Q13442814 |
| P819 | ADS bibcode | 2015NatCo...6.6104K |
| P6179 | Dimensions Publication ID | 1043466023 |
| P356 | DOI | 10.1038/NCOMMS7104 |
| P932 | PMC publication ID | 4299874 |
| P698 | PubMed publication ID | 25598145 |
| P5875 | ResearchGate publication ID | 271139887 |
| P50 | author | Peter Baumann | Q7172713 |
| P2093 | author name string | Rachel M Helston | |
| Ram Kannan | |||
| Richard O Dannebaum | |||
| P2860 | cites work | Comparative functional genomics of the fission yeasts | Q22065619 |
| The telomere syndromes | Q24632444 | ||
| Secondary structure of vertebrate telomerase RNA | Q28138961 | ||
| Pot1, the putative telomere end-binding protein in fission yeast and humans | Q28188476 | ||
| U1 snRNP protects pre-mRNAs from premature cleavage and polyadenylation | Q29032058 | ||
| Telomerase catalytic subunit homologs from fission yeast and human | Q29615387 | ||
| Mechanism for cryptic splice site activation during pre-mRNA splicing | Q33746053 | ||
| Spliceosome discards intermediates via the DEAH box ATPase Prp43p | Q33933327 | ||
| Identification and characterization of the Schizosaccharomyces pombe TER1 telomerase RNA. | Q34586455 | ||
| Repositioning of the reaction intermediate within the catalytic center of the spliceosome. | Q52568800 | ||
| Evidence for an essential non-Watson–Crick interaction between the first and last nucleotides of a nuclear pre-mRNA intron | Q59064262 | ||
| 5' cleavage site in eukaryotic pre-mRNA splicing is determined by the overall 5' splice region, not by the conserved 5' GU | Q69336145 | ||
| Both catalytic steps of nuclear pre-mRNA splicing are reversible | Q81534595 | ||
| Identification of telomerase RNAs from filamentous fungi reveals conservation with vertebrates and yeasts | Q34650480 | ||
| Budding yeast telomerase RNA transcription termination is dictated by the Nrd1/Nab3 non-coding RNA termination pathway. | Q36061897 | ||
| Biogenesis of telomerase ribonucleoproteins | Q36246606 | ||
| Intronic sequence elements impede exon ligation and trigger a discard pathway that yields functional telomerase RNA in fission yeast | Q36732545 | ||
| Replication of telomeres and the regulation of telomerase | Q36783452 | ||
| A flexible template boundary element in the RNA subunit of fission yeast telomerase | Q36855843 | ||
| Identification of purple sea urchin telomerase RNA using a next-generation sequencing based approach | Q36932894 | ||
| Exon ligation is proofread by the DExD/H-box ATPase Prp22p | Q37059609 | ||
| "Nought may endure but mutability": spliceosome dynamics and the regulation of splicing | Q37197189 | ||
| Telomeres and telomerase in cancer | Q37627017 | ||
| Yeast Nrd1, Nab3, and Sen1 transcriptome-wide binding maps suggest multiple roles in post-transcriptional RNA processing | Q38782355 | ||
| TER1, the RNA subunit of fission yeast telomerase | Q39752449 | ||
| Human telomerase and Cajal body ribonucleoproteins share a unique specificity of Sm protein association | Q40315687 | ||
| Mutations in conserved intron sequences affect multiple steps in the yeast splicing pathway, particularly assembly of the spliceosome. | Q41899857 | ||
| Telomerase RNA biogenesis involves sequential binding by Sm and Lsm complexes | Q41967731 | ||
| Human telomerase RNA and box H/ACA scaRNAs share a common Cajal body-specific localization signal. | Q42057695 | ||
| Identification and comparative analysis of telomerase RNAs from Candida species reveal conservation of functional elements | Q42147960 | ||
| A phylogenetically based secondary structure for the yeast telomerase RNA. | Q43520446 | ||
| 5' splice site selection in yeast: genetic alterations in base-pairing with U1 reveal additional requirements | Q44055786 | ||
| Opposing classes of prp8 alleles modulate the transition between the catalytic steps of pre-mRNA splicing | Q45828510 | ||
| Suppression of multiple substrate mutations by spliceosomal prp8 alleles suggests functional correlations with ribosomal ambiguity mutants | Q47654036 | ||
| Spliceosomal cleavage generates the 3' end of telomerase RNA. | Q50336096 | ||
| P275 | copyright license | Creative Commons Attribution 4.0 International | Q20007257 |
| P6216 | copyright status | copyrighted | Q50423863 |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | spliceosome | Q915868 |
| P304 | page(s) | 6104 | |
| P577 | publication date | 2015-01-19 | |
| P1433 | published in | Nature Communications | Q573880 |
| P1476 | title | Diverse mechanisms for spliceosome-mediated 3' end processing of telomerase RNA. | |
| P478 | volume | 6 |
| Q36912474 | A Fleeting Glimpse Inside microRNA, Epigenetics, and Micropeptidomics |
| Q91956493 | Early splicing functions of fission yeast Prp16 and its unexpected requirement for gene Silencing is governed by intronic features |
| Q37194197 | Evolutionary perspectives of telomerase RNA structure and function. |
| Q90133931 | Identification of telomerase RNAs in species of the Yarrowia clade provides insights into the co-evolution of telomerase, telomeric repeats and telomere-binding proteins |
| Q61797636 | Integrator is a key component of human telomerase RNA biogenesis |
| Q49538825 | LARP7-like protein Pof8 regulates telomerase assembly and poly(A)+TERRA expression in fission yeast |
| Q47184251 | New perspectives on telomerase RNA structure and function |
| 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 |
| Q56267127 | TERribly Difficult: Searching for Telomerase RNAs in Saccharomycetes |
| Q39111969 | Telomerase Mechanism of Telomere Synthesis |
| Q90316146 | Termination of pre-mRNA splicing requires that the ATPase and RNA unwindase Prp43p acts on the catalytic snRNA U6 |
| Q28585522 | The functional requirement of two structural domains within telomerase RNA emerged early in eukaryotes |
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