| scholarly article | Q13442814 |
| P2093 | author name string | Keller W | |
| Christofori G | |||
| P2860 | cites work | Separation of multiple components of HeLa cell nuclear extracts required for pre-messenger RNA splicing. | Q54395405 |
| Poly(A) site cleavage in a HeLa nuclear extract is dependent on downstream sequences. | Q55060176 | ||
| Alpha-thalassaemia caused by a polyadenylation signal mutation. | Q55062701 | ||
| Inhibition of RNA cleavage but not polyadenylation by a point mutation in mRNA 3′ consensus sequence AAUAAA | Q58451156 | ||
| A sequence downstream of AAUAAA is required for rabbit β-globin mRNA 3′-end formation | Q59058833 | ||
| 3' cleavage and polyadenylation of mRNA precursors in vitro requires a poly(A) polymerase, a cleavage factor, and a snRNP | Q64379456 | ||
| Multiple factors are required for specific RNA cleavage at a poly(A) addition site | Q64379503 | ||
| Electrophoretic separation of polyadenylation-specific complexes | Q64379710 | ||
| A small nuclear ribonucleoprotein associates with the AAUAAA polyadenylation signal in vitro | Q64380127 | ||
| Stepwise assembly of a pre-mRNA splicing complex requires U-snRNPs and specific intron sequences | Q64380337 | ||
| Requirement of a downstream sequence for generation of a poly(A) addition site | Q64380598 | ||
| Site-specific polyadenylation in a cell-free reaction | Q64380699 | ||
| Splicing of in vitro synthesized messenger RNA precursors in HeLa cell extracts | Q64380855 | ||
| Multiple factors are required for poly(A) addition to a mRNA 3' end | Q68413214 | ||
| Separation and characterization of a poly(A) polymerase and a cleavage/specificity factor required for pre-mRNA polyadenylation | Q69820089 | ||
| A functionally redundant downstream sequence in SV40 late pre-mRNA is required for mRNA 3'-end formation and for assembly of a precleavage complex in vitro | Q69823612 | ||
| Role of the Conserved AAUAAA Sequence: Four AAUAAA Point Mutants Prevent Messenger RNA 3′ End Formation | Q72749074 | ||
| The 5′ terminus of the RNA moiety of U1 small nuclear ribonucleoprotein particles is required for the splicing of messenger RNA precursors | Q72821863 | ||
| Specific contacts between mammalian U7 snRNA and histone precursor RNA are indispensable for the in vitro 3' RNA processing reaction | Q24564263 | ||
| Structural and functional characterization of mouse U7 small nuclear RNA active in 3' processing of histone pre-mRNA | Q24632127 | ||
| A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding | Q25938984 | ||
| Accurate transcription initiation by RNA polymerase II in a soluble extract from isolated mammalian nuclei | Q27860728 | ||
| 3' non-coding region sequences in eukaryotic messenger RNA | Q27860858 | ||
| Efficientin vitrosynthesis of biologically active RNA and RNA hybridization probes from plasmids containing a bacteriophage SP6 promoter | Q27861016 | ||
| Identification of the human U7 snRNP as one of several factors involved in the 3' end maturation of histone premessenger RNA's | Q28280579 | ||
| U1, U2, and U4/U6 small nuclear ribonucleoproteins are required for in vitro splicing but not polyadenylation | Q28302647 | ||
| Accurate cleavage and polyadenylation of exogenous RNA substrate | Q28646786 | ||
| Transcription termination and 3' processing: the end is in site! | Q29618288 | ||
| Cleavage and polyadenylation of messenger RNA precursors in vitro occurs within large and specific 3' processing complexes. | Q33930140 | ||
| The conserved CAAGAAAGA spacer sequence is an essential element for the formation of 3' termini of the sea urchin H3 histone mRNA by RNA processing | Q33930981 | ||
| Fractionation of HeLa cell nuclear extracts reveals minor small nuclear ribonucleoprotein particles | Q34370740 | ||
| Simple, efficientin vitrosynthesis of capped RNA useful for direct expression of cloned eukaryoti genes | Q35716200 | ||
| Two proteins crosslinked to RNA containing the adenovirus L3 poly(A) site require the AAUAAA sequence for binding | Q35989261 | ||
| The consensus sequence YGTGTTYY located downstream from the AATAAA signal is required for efficient formation of mRNA 3' termini | Q36136653 | ||
| Sedimentation analysis of polyadenylation-specific complexes | Q36780246 | ||
| Mutations in poly(A) site downstream elements affect in vitro cleavage activity | Q36787633 | ||
| Assembly of a polyadenylation-specific 25S ribonucleoprotein complex in vitro | Q36788795 | ||
| Requirements for accurate and efficient mRNA 3' end cleavage and polyadenylation of a simian virus 40 early pre-RNA in vitro | Q36834250 | ||
| Products of in vitro cleavage and polyadenylation of simian virus 40 late pre-mRNAs | Q36838958 | ||
| RNA sequence containing hexanucleotide AAUAAA directs efficient mRNA polyadenylation in vitro | Q36885633 | ||
| Identification of a sequence element on the 3' side of AAUAAA which is necessary for simian virus 40 late mRNA 3'-end processing. | Q36894844 | ||
| The AAUAAA sequence is required both for cleavage and for polyadenylation of simian virus 40 pre-mRNA in vitro | Q36916774 | ||
| Identification of a complex associated with processing and polyadenylation in vitro of herpes simplex virus type 1 thymidine kinase precursor RNA | Q36921323 | ||
| A sequence downstream of A-A-U-A-A-A is required for formation of simian virus 40 late mRNA 3' termini in frog oocytes | Q37691120 | ||
| The role of small nuclear ribonucleoprotein particles in pre-mRNA splicing | Q39481136 | ||
| In vitro cleavage of the simian virus 40 early polyadenylation site adjacent to a required downstream TG sequence | Q40668071 | ||
| Formation of mRNA 3' termini: stability and dissociation of a complex involving the AAUAAA sequence | Q41330964 | ||
| Analysis of mRNA 3' end formation by modification interference: the only modifications which prevent processing lie in AAUAAA and the poly(A) site | Q41360804 | ||
| Specific pre-cleavage and post-cleavage complexes involved in the formation of SV40 late mRNA 3' termini in vitro | Q41360882 | ||
| Purification of a protein required for the splicing of pre-mRNA and its separation from the lariat debranching enzyme | Q41432590 | ||
| A 64 kd nuclear protein binds to RNA segments that include the AAUAAA polyadenylation motif | Q41862487 | ||
| Analysis of RNA cleavage at the adenovirus-2 L3 polyadenylation site | Q42572169 | ||
| Isolation and partial characterization of the poly(A) polymerases from HeLa cells infected with vaccinia virus | Q44372041 | ||
| The sequence 5'-AAUAAA-3'forms parts of the recognition site for polyadenylation of late SV40 mRNAs | Q48410195 | ||
| P433 | issue | 1 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | HeLa | Q847482 |
| P304 | page(s) | 193-203 | |
| P577 | publication date | 1989-01-01 | |
| P1433 | published in | Molecular and Cellular Biology | Q3319478 |
| P1476 | title | Poly(A) polymerase purified from HeLa cell nuclear extract is required for both cleavage and polyadenylation of pre-mRNA in vitro | |
| P478 | volume | 9 |
| Q45110213 | A dissection of the cauliflower mosaic virus polyadenylation signal |
| Q33960046 | A history of poly A sequences: from formation to factors to function |
| Q28776198 | A multicomponent complex is required for the AAUAAA-dependent cross-linking of a 64-kilodalton protein to polyadenylation substrates |
| Q21146099 | A new yeast poly(A) polymerase complex involved in RNA quality control |
| Q45002161 | A simple procedure for isolation of eukaryotic mRNA polyadenylation factors |
| Q34630891 | Alternative poly(A) site selection in complex transcription units: means to an end? |
| Q41864496 | Alternative poly(A) site utilization during adenovirus infection coincides with a decrease in the activity of a poly(A) site processing factor |
| Q37291806 | An investigation into the role of ATP in the mammalian pre-mRNA 3' cleavage reaction |
| Q35790089 | Ara-ATP impairs 3′-end processing of pre-mRNAs by inhibiting both cleavage and polyadenylation |
| Q24564750 | Assembly of a processive messenger RNA polyadenylation complex |
| Q38322763 | Assembly of the cleavage and polyadenylation apparatus requires about 10 seconds in vivo and is faster for strong than for weak poly(A) sites |
| Q24607835 | Characterization of cleavage and polyadenylation specificity factor and cloning of its 100-kilodalton subunit |
| Q24564625 | Cleavage and polyadenylation factor CPF specifically interacts with the pre-mRNA 3' processing signal AAUAAA |
| Q36559450 | Complex alternative RNA processing generates an unexpected diversity of poly(A) polymerase isoforms |
| Q43566207 | Components involved in 3' processing of precursors to polyadenylated messenger RNA. |
| Q36819714 | Conditional defect in mRNA 3' end processing caused by a mutation in the gene for poly(A) polymerase |
| Q34361064 | Control of poly(A) polymerase level is essential to cytoplasmic polyadenylation and early development in Drosophila |
| Q28751417 | Formation of the 3' end of histone mRNA: getting closer to the end |
| Q40015947 | Identification of an activity in B-cell extracts that selectively impairs the formation of an immunoglobulin mu s poly(A) site processing complex |
| Q24534097 | Influenza A virus NS1 protein targets poly(A)-binding protein II of the cellular 3'-end processing machinery |
| Q35036881 | Inhibition of cdk9 during herpes simplex virus 1 infection impedes viral transcription |
| Q24311986 | Inositol 1,4,5-triphosphate receptor-binding protein released with inositol 1,4,5-triphosphate (IRBIT) associates with components of the mRNA 3' processing machinery in a phosphorylation-dependent manner and inhibits polyadenylation |
| Q34362676 | Isolation and characterization of polyadenylation complexes assembled in vitro. |
| Q41083859 | Isolation and expression of cDNA clones encoding mammalian poly(A) polymerase |
| Q36676486 | Mitochondrial poly(A) polymerase is involved in tRNA repair |
| Q24337224 | Multiple forms of poly(A) polymerases in human cells |
| Q36761870 | Multiple forms of poly(A) polymerases purified from HeLa cells function in specific mRNA 3'-end formation |
| Q24337103 | Multiple histone deacetylases and the CREB-binding protein regulate pre-mRNA 3'-end processing |
| Q34622114 | Nucleases of the metallo-beta-lactamase family and their role in DNA and RNA metabolism |
| Q38434984 | Optimizing In Vitro Pre-mRNA 3' Cleavage Efficiency: Reconstitution from Anion-Exchange Separated HeLa Cleavage Factors and from Adherent HeLa Cell Nuclear Extract |
| Q36565604 | PCF11 encodes a third protein component of yeast cleavage and polyadenylation factor I. |
| Q36688304 | Point mutations upstream of the yeast ADH2 poly(A) site significantly reduce the efficiency of 3'-end formation |
| Q38308543 | Poly(A) polymerase contains multiple functional domains |
| Q41079693 | Poly(A) site efficiency reflects the stability of complex formation involving the downstream element |
| Q41806905 | Poly(A) tail length is controlled by the nuclear poly(A)-binding protein regulating the interaction between poly(A) polymerase and the cleavage and polyadenylation specificity factor |
| Q54309389 | Polyadenylation of SV40 late pre-mRNA is dependent on phosphorylation of an essential component associated with the 3' end processing machinery |
| Q36755960 | Polyadenylation of mRNA: minimal substrates and a requirement for the 2' hydroxyl of the U in AAUAAA. |
| Q36713877 | Polyadenylation-specific complexes undergo a transition early in the polymerization of a poly(A) tail |
| Q40530952 | Potential role of poly(A) polymerase in the assembly of polyadenylation-specific RNP complexes |
| Q59097203 | Primary structure and expression of bovine poly(A) polymerase |
| Q41126522 | Purification and characterization of full-length mammalian poly(A) polymerase |
| Q36562192 | RNA structure is a critical determinant of poly(A) site recognition by cleavage and polyadenylation specificity factor |
| Q34430722 | Reconstitution of CPSF active in polyadenylation: recognition of the polyadenylation signal by WDR33. |
| Q36555995 | Regulation of poly(A) site use during mouse B-cell development involves a change in the binding of a general polyadenylation factor in a B-cell stage-specific manner |
| Q40508994 | Regulation of polyadenylation in hepatitis B viruses: stimulation by the upstream activating signal PS1 is orientation-dependent, distance-independent, and additive |
| Q48056546 | Restoration of both structure and function to a defective poly(A) site by in vitro selection |
| Q41882662 | Sequence elements upstream of the 3' cleavage site confer substrate strength to the adenovirus L1 and L3 polyadenylation sites |
| Q36795452 | Sequences upstream of AAUAAA influence poly(A) site selection in a complex transcription unit |
| Q39790864 | Stimulation of poly(A) polymerase through a direct interaction with the nuclear poly(A) binding protein allosterically regulated by RNA. |
| Q40504887 | Termination of transcription in an ‘in vitro’ system is dependent on a polyadenylation sequence |
| Q38336494 | The HTLV-I rex response element mediates a novel form of mRNA polyadenylation |
| Q36065865 | The end of the message: 3'-end processing leading to polyadenylated messenger RNA |
| Q36718455 | The enzyme that adds poly(A) to mRNAs is a classical poly(A) polymerase |
| Q41491594 | The mechanism of 3' cleavage and polyadenylation of eukaryotic pre-mRNA. |
| Q27641148 | X-ray Crystallographic and Steady State Fluorescence Characterization of the Protein Dynamics of Yeast Polyadenylate Polymerase |
| Q41984284 | Xlrbpa, a double-stranded RNA-binding protein associated with ribosomes and heterogeneous nuclear RNPs |
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