| scholarly article | Q13442814 |
| P356 | DOI | 10.1038/323777A0 |
| P698 | PubMed publication ID | 3022153 |
| P2093 | author name string | Schaufele F | |
| Birnstiel ML | |||
| Gilmartin GM | |||
| Bannwarth W | |||
| P2860 | cites work | Processing of yeast mitochondrial RNA: involvement of intramolecular hybrids in splicing of cob intron 4 RNA by mutation and reversion | Q70373239 |
| Accumulation of the early histone messenger RNAs during the development of Strongylocentrotus purpuratus | Q70541235 | ||
| The RNA lariat: a new ring to the splicing of mRNA precursors | Q70887114 | ||
| Biochemical complementation with RNA in the Xenopus oocyte: A small rna is required for the generation of 3′ histone mRNA termini | Q72714199 | ||
| 32 Oligonucleotide-directed mutagenesis of DNA fragments cloned into M13 vectors | Q72795456 | ||
| The 5′ terminus of the RNA moiety of U1 small nuclear ribonucleoprotein particles is required for the splicing of messenger RNA precursors | Q72821863 | ||
| Analysis of a sea urchin gene cluster coding for the small nuclear U7 RNA, a rare RNA species implicated in the 3' editing of histone precursor mRNAs | Q24630124 | ||
| The RNA moiety of ribonuclease P is the catalytic subunit of the enzyme | Q28262778 | ||
| Are snRNPs involved in splicing? | Q28281898 | ||
| Accurate cleavage and polyadenylation of exogenous RNA substrate | Q28646786 | ||
| Transcription termination and 3' processing: the end is in site! | Q29618288 | ||
| A compensatory base change in U1 snRNA suppresses a 5' splice site mutation | Q29618292 | ||
| The generality of self-splicing RNA: relationship to nuclear mRNA splicing | Q30457101 | ||
| Role of conserved sequence elements 9L and 2 in self-splicing of the Tetrahymena ribosomal RNA precursor | Q30457134 | ||
| RNA splicing: Three themes with variations | Q30463513 | ||
| Compilation analysis of histones and histone genes | Q36144809 | ||
| 3' editing of mRNAs: sequence requirements and involvement of a 60-nucleotide RNA in maturation of histone mRNA precursors. | Q36249030 | ||
| A mechanism for RNA splicing | Q36362761 | ||
| Nucleotide sequences of H1 histone genes from Xenopus laevis. A recently diverged pair of H1 genes and an unusual H1 pseudogene | Q36634548 | ||
| On the origin of RNA splicing and introns | Q38151500 | ||
| The organization and expression of histone gene families | Q40262119 | ||
| Integration of eukaryotic genes for 5S RNA and histone proteins into a phage lambda receptor | Q40578385 | ||
| Multiple factors including the small nuclear ribonucleoproteins U1 and U2 are necessary for pre-mRNA splicing in vitro. | Q54443873 | ||
| Changing the identity of a transfer RNA. | Q54780307 | ||
| Reconstitution of RNAase P activity using inactive subunits from E. coli and HeLa cells. | Q54784958 | ||
| Splice-site selection by a self-splicing RNA of Tetrahymena | Q59089994 | ||
| Site-specific polyadenylation in a cell-free reaction | Q64380699 | ||
| Splicing of messenger RNA precursors is inhibited by antisera to small nuclear ribonucleoprotein | Q64380857 | ||
| Expression of sea urchin histone genes in the oocyte of Xenopus laevis | Q66994232 | ||
| U2 as well as U1 small nuclear ribonucleoproteins are involved in premessenger RNA splicing | Q70104555 | ||
| Introduction of cloned DNA into sea urchin egg cytoplasm: replication and persistence during embryogenesis | Q70118296 | ||
| Persistence and integration of cloned DNA in postembryonic sea urchins | Q70118299 | ||
| The terminal RNA stem-loop structure and 80 bp of spacer DNA are required for the formation of 3′ termini of sea urchin H2A mRNA | Q70179284 | ||
| P433 | issue | 6091 | |
| P407 | language of work or name | English | Q1860 |
| P1104 | number of pages | 5 | |
| P304 | page(s) | 777-781 | |
| P577 | publication date | 1986-10-01 | |
| P1433 | published in | Nature | Q180445 |
| P1476 | title | Compensatory mutations suggest that base-pairing with a small nuclear RNA is required to form the 3' end of H3 messenger RNA | |
| P478 | volume | 323 |
| Q24631601 | 2'-O-methyl, 2'-O-ethyl oligoribonucleotides and phosphorothioate oligodeoxyribonucleotides as inhibitors of the in vitro U7 snRNP-dependent mRNA processing event |
| Q68421101 | 3 processing of histone RNA precursors |
| Q34324943 | 3' end processing of Drosophila melanogaster histone pre-mRNAs: requirement for phosphorylated Drosophila stem-loop binding protein and coevolution of the histone pre-mRNA processing system |
| Q24605803 | 3' end processing of mouse histone pre-mRNA: evidence for additional base-pairing between U7 snRNA and pre-mRNA |
| Q34361520 | A 5'-3' exonuclease activity involved in forming the 3' products of histone pre-mRNA processing in vitro |
| Q24302708 | A human histone H2B.1 variant gene, located on chromosome 1, utilizes alternative 3' end processing |
| Q24672946 | A novel zinc finger protein is associated with U7 snRNP and interacts with the stem-loop binding protein in the histone pre-mRNP to stimulate 3'-end processing |
| Q28596144 | A subset of replication-dependent histone mRNAs are expressed as polyadenylated RNAs in terminally differentiated tissues |
| Q24623991 | A synthetic histone pre-mRNA-U7 small nuclear RNA chimera undergoingciscleavage in the cytoplasm ofXenopusoocytes |
| Q92282657 | ALYREF links 3'-end processing to nuclear export of non-polyadenylated mRNAs |
| Q61807594 | Abrogation of Stem Loop Binding Protein (Slbp) function leads to a failure of cells to transition from proliferation to differentiation, retinal coloboma and midline axon guidance deficits |
| Q28145207 | Assembly of U7 small nuclear ribonucleoprotein particle and histone RNA 3' processing in Xenopus egg extracts |
| Q24624098 | Assembly, nuclear import and function of U7 snRNPs studied by microinjection of synthetic U7 RNA into Xenopus oocytes |
| Q40789290 | Base pairing between U3 and the pre-ribosomal RNA is required for 18S rRNA synthesis. |
| Q24555701 | Biochemical demonstration of complex formation of histone pre-mRNA with U7 small nuclear ribonucleoprotein and hairpin binding factors |
| Q36839834 | Both conserved signals on mammalian histone pre-mRNAs associate with small nuclear ribonucleoproteins during 3' end formation in vitro |
| Q28263105 | Cell cycle-dependent regulation of histone precursor mRNA processing by modulation of U7 snRNA accessibility |
| Q38346758 | Characterization of the calf thymus hairpin-binding factor involved in histone pre-mRNA 3' end processing. |
| Q24681285 | Cloning and characterization of the Drosophila U7 small nuclear RNA |
| Q33997693 | Compilation of DNA sequences of Escherichia coli (update 1990) |
| Q91833236 | Composition and processing activity of a semi-recombinant holo U7 snRNP |
| Q24612755 | Conserved terminal hairpin sequences of histone mRNA precursors are not involved in duplex formation with the U7 RNA but act as a target site for a distinct processing factor |
| Q24337535 | Conserved zinc fingers mediate multiple functions of ZFP100, a U7snRNP associated protein |
| Q47110577 | Coordinating cell cycle-regulated histone gene expression through assembly and function of the Histone Locus Body |
| Q39756702 | Cotranscriptional processing of Drosophila histone mRNAs. |
| Q29618484 | Depletion of U14 small nuclear RNA (snR128) disrupts production of 18S rRNA in Saccharomyces cerevisiae |
| Q38319470 | Differences and similarities between Drosophila and mammalian 3' end processing of histone pre-mRNAs |
| Q36189905 | Drosophila Symplekin localizes dynamically to the histone locus body and tricellular junctions |
| Q28776186 | Each of the conserved sequence elements flanking the cleavage site of mammalian histone pre-mRNAs has a distinct role in the 3'-end processing reaction |
| Q34213955 | Ending the message: poly(A) signals then and now |
| Q24540231 | Evolutionary conservation of the U7 small nuclear ribonucleoprotein in Drosophila melanogaster. |
| Q35739332 | FUS/TLS contributes to replication-dependent histone gene expression by interaction with U7 snRNPs and histone-specific transcription factors |
| Q73617933 | Formation of 2',3'-cyclic phosphates at the 3' end of human U6 small nuclear RNA in vitro. Identification of 2',3'-cyclic phosphates at the 3' ends of human signal recognition particle and mitochondrial RNA processing RNAs |
| Q28609911 | Formation of mRNA 3' ends in eukaryotes: mechanism, regulation, and interrelationships with other steps in mRNA synthesis |
| Q28610112 | Formation of the 3' end of histone mRNA |
| Q28751417 | Formation of the 3' end of histone mRNA: getting closer to the end |
| Q34555353 | Four novel U RNAs are encoded by a herpesvirus |
| Q34370740 | Fractionation of HeLa cell nuclear extracts reveals minor small nuclear ribonucleoprotein particles |
| Q24632424 | Functional analysis of the sea urchin U7 small nuclear RNA |
| Q33929711 | Functional characterization of X. laevis U5 snRNA genes |
| Q34361303 | Functional importance of conserved nucleotides at the histone RNA 3' processing site |
| Q37854929 | Functions of U-snRNPs |
| Q39078077 | Guard the guardian: A CRL4 ligase stands watch over histone production |
| Q34377328 | Heat-labile regulatory factor is required for 3' processing of histone precursor mRNAs |
| Q24648855 | Herpesvirus saimiri U RNAs are expressed and assembled into ribonucleoprotein particles in the absence of other viral genes |
| Q36808110 | Heterogeneous nuclear ribonucleoprotein A1 catalyzes RNA.RNA annealing |
| Q48332230 | Histone genes in three sea star species: cluster arrangement, transcriptional polarity, and analyses of the flanking regions of H3 and H4 genes |
| Q40547374 | Homologous genes for mouse 4.5S hybRNA are found in all eukaryotes and their low molecular weight RNA transcripts intermolecularly hybridize with eukaryotic 18S ribosomal RNAs |
| Q34310275 | How to stop: the mysterious links among RNA polymerase II occupancy 3' of genes, mRNA 3' processing and termination |
| Q35851124 | In vitro capping in Trypanosoma cruzi identifies and shows specificity for the spliced leader RNA and U-RNAs |
| Q28302839 | In vivo assembly of functional U7 snRNP requires RNA backbone flexibility within the Sm-binding site |
| Q33851943 | Isolation and structural characterization of cDNA clones encoding the mating pheromone Er-1 secreted by the ciliate Euplotes raikovi |
| Q24651408 | Length suppression in histone messenger RNA 3'-end maturation: processing defects of insertion mutant premessenger RNAs can be compensated by insertions into the U7 small nuclear RNA |
| Q36055301 | Nucleotide sequence determination and secondary structure ofXenopusU3 snRNA |
| Q60522471 | Nucleotide sequence of the histone gene cluster in the coral acropora formosa (cnidaria; scleractinia): Features of histone gene structure and organization are common to diploblastic and triploblastic metazoans |
| Q33315225 | Organization and transient expression of the gene for human U11 snRNA |
| Q70332939 | Polite DNA: functional density and functional compatibility in genomes |
| Q33563787 | Polyadenylated and 3' processed mRNAs are transcribed from the mouse histone H2A.X gene |
| Q52359095 | Protein composition of catalytically active U7-dependent processing complexes assembled on histone pre-mRNA containing biotin and a photo-cleavable linker. |
| Q24291730 | Purified U7 snRNPs lack the Sm proteins D1 and D2 but contain Lsm10, a new 14 kDa Sm D1-like protein |
| Q34305741 | RNA polymerase II pausing downstream of core histone genes is different from genes producing polyadenylated transcripts |
| Q57077898 | Regulatory structures of gene expression, DNA-replication and DNA-rearrangement in macronuclear genes of Stylonychia lemnae, a hypotrichous ciliate |
| Q74254054 | Restoration of correct splicing of thalassemic beta-globin pre-mRNA by modified U1 snRNAs |
| Q24634140 | Ribozyme, antisense RNA, and antisense DNA inhibition of U7 small nuclear ribonucleoprotein-mediated histone pre-mRNA processing in vitro |
| Q36088349 | Saturation mutagenesis of a +1 programmed frameshift-inducing mRNA sequence derived from a yeast retrotransposon. |
| Q24564263 | Specific contacts between mammalian U7 snRNA and histone precursor RNA are indispensable for the in vitro 3' RNA processing reaction |
| Q24632127 | Structural and functional characterization of mouse U7 small nuclear RNA active in 3' processing of histone pre-mRNA |
| Q24540074 | Structure of the histone mRNA hairpin required for cell cycle regulation of histone gene expression |
| Q24537115 | Symplekin and multiple other polyadenylation factors participate in 3'-end maturation of histone mRNAs |
| Q34546180 | The 3' end formation in small RNAs. |
| Q24655653 | The Drosophila U7 snRNP proteins Lsm10 and Lsm11 are required for histone pre-mRNA processing and play an essential role in development |
| Q24532107 | The gene for histone RNA hairpin binding protein is located on human chromosome 4 and encodes a novel type of RNA binding protein |
| Q36841698 | The highly conserved U small nuclear RNA 3'-end formation signal is quite tolerant to mutation |
| Q34714701 | The inability of the Psammechinus miliaris H3 RNA to be processed in the Xenopus oocyte is associated with sequences distinct from those highly conserved amongst sea urchin histone RNAs |
| Q39481136 | The role of small nuclear ribonucleoprotein particles in pre-mRNA splicing |
| Q24595569 | The site of 3' end formation of histone messenger RNA is a fixed distance from the downstream element recognized by the U7 snRNP |
| Q36841625 | The stem-loop binding protein (SLBP1) is present in coiled bodies of the Xenopus germinal vesicle |
| Q87887544 | Transcription elongation rate affects nascent histone pre-mRNA folding and 3' end processing |
| Q29541446 | Transcription termination by nuclear RNA polymerases |
| Q35989261 | Two proteins crosslinked to RNA containing the adenovirus L3 poly(A) site require the AAUAAA sequence for binding |
| Q24560046 | Two-step affinity purification of U7 small nuclear ribonucleoprotein particles using complementary biotinylated 2'-O-methyl oligoribonucleotides |
| Q24541402 | U7 snRNA mutations in Drosophila block histone pre-mRNA processing and disrupt oogenesis |
| Q51100143 | U7 snRNP is recruited to histone pre-mRNA in a FLASH-dependent manner by two separate regions of the stem-loop binding protein. |
| Q24521637 | U7 snRNP-specific Lsm11 protein: dual binding contacts with the 100 kDa zinc finger processing factor (ZFP100) and a ZFP100-independent function in histone RNA 3' end processing |
| Q34978310 | Variable effects of the conserved RNA hairpin element upon 3' end processing of histone pre-mRNA in vitro. |
| Q24300007 | ZFP100, a component of the active U7 snRNP limiting for histone pre-mRNA processing, is required for entry into S phase |
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