| scholarly article | Q13442814 |
| P2093 | author name string | T Shenk | |
| J L Manley | |||
| J Wilusz | |||
| Y Takagaki | |||
| P2860 | cites work | 3' non-coding region sequences in eukaryotic messenger RNA | Q27860858 |
| 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 | ||
| Peptide mapping by limited proteolysis in sodium dodecyl sulfate and analysis by gel electrophoresis | Q29547747 | ||
| 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 | ||
| Complex transcriptional units: diversity in gene expression by alternative RNA processing | Q34048629 | ||
| Functional analysis of point mutations in the AAUAAA motif of the SV40 late polyadenylation signal | Q35228128 | ||
| Two proteins crosslinked to RNA containing the adenovirus L3 poly(A) site require the AAUAAA sequence for binding | Q35989261 | ||
| Components required for in vitro cleavage and polyadenylation of eukaryotic mRNA. | Q36009672 | ||
| The consensus sequence YGTGTTYY located downstream from the AATAAA signal is required for efficient formation of mRNA 3' termini | Q36136653 | ||
| Multiple forms of poly(A) polymerases purified from HeLa cells function in specific mRNA 3'-end formation | Q36761870 | ||
| Sequences downstream of AAUAAA signals affect pre-mRNA cleavage and polyadenylation in vitro both directly and indirectly | Q36764593 | ||
| Sedimentation analysis of polyadenylation-specific complexes | Q36780246 | ||
| Assembly of a polyadenylation-specific 25S ribonucleoprotein complex in vitro | Q36788795 | ||
| The C proteins of heterogeneous nuclear ribonucleoprotein complexes interact with RNA sequences downstream of polyadenylation cleavage sites | Q36847550 | ||
| Identification of sequences in the herpes simplex virus thymidine kinase gene required for efficient processing and polyadenylation | Q36892344 | ||
| Identification of a sequence element on the 3' side of AAUAAA which is necessary for simian virus 40 late mRNA 3'-end processing. | Q36894844 | ||
| Identification of a complex associated with processing and polyadenylation in vitro of herpes simplex virus type 1 thymidine kinase precursor RNA | Q36921323 | ||
| Sequences on the 3' side of hexanucleotide AAUAAA affect efficiency of cleavage at the polyadenylation site. | Q36946265 | ||
| Definition of essential sequences and functional equivalence of elements downstream of the adenovirus E2A and the early simian virus 40 polyadenylation sites | Q36951086 | ||
| 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 | ||
| Polyadenylation of mRNA precursors | Q39467361 | ||
| snRNP mediators of 3' end processing: functional fossils? | Q39473317 | ||
| Poly(A) polymerase purified from HeLa cell nuclear extract is required for both cleavage and polyadenylation of pre-mRNA in vitro | Q40644140 | ||
| Specific pre-cleavage and post-cleavage complexes involved in the formation of SV40 late mRNA 3' termini in vitro | Q41360882 | ||
| A 64 kd nuclear protein binds to RNA segments that include the AAUAAA polyadenylation motif | Q41862487 | ||
| Four factors are required for 3'-end cleavage of pre-mRNAs | Q43727383 | ||
| The sequence 5'-AAUAAA-3'forms parts of the recognition site for polyadenylation of late SV40 mRNAs | Q48410195 | ||
| 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 | ||
| 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 | ||
| Requirement of a downstream sequence for generation of a poly(A) addition site | Q64380598 | ||
| 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 | ||
| Mutations downstream of the polyadenylation site of a Xenopus beta-globin mRNA affect the position but not the efficiency of 3' processing | Q69882952 | ||
| Accurate and specific polyadenylation of mRNA precursors in a soluble whole-cell lysate | Q72555182 | ||
| Role of the Conserved AAUAAA Sequence: Four AAUAAA Point Mutants Prevent Messenger RNA 3′ End Formation | Q72749074 | ||
| P433 | issue | 3 | |
| P407 | language of work or name | English | Q1860 |
| P304 | page(s) | 1244-8 | |
| P577 | publication date | 1990-03-01 | |
| P1433 | published in | Molecular and Cellular Biology | Q3319478 |
| P1476 | title | A multicomponent complex is required for the AAUAAA-dependent cross-linking of a 64-kilodalton protein to polyadenylation substrates | |
| P478 | volume | 10 |
| Q33960046 | A history of poly A sequences: from formation to factors to function |
| Q45002161 | A simple procedure for isolation of eukaryotic mRNA polyadenylation factors |
| Q36774538 | A uridylate tract mediates efficient heterogeneous nuclear ribonucleoprotein C protein-RNA cross-linking and functionally substitutes for the downstream element of the polyadenylation signal |
| Q41864496 | Alternative poly(A) site utilization during adenovirus infection coincides with a decrease in the activity of a poly(A) site processing factor |
| Q34365145 | An uncapped RNA suggests a model for Caenorhabditis elegans polycistronic pre-mRNA processing |
| Q24564750 | Assembly of a processive messenger RNA polyadenylation complex |
| Q39724192 | Auxiliary downstream elements are required for efficient polyadenylation of mammalian pre-mRNAs |
| Q24607835 | Characterization of cleavage and polyadenylation specificity factor and cloning of its 100-kilodalton subunit |
| Q36554283 | Characterization of the Polyomavirus Late Polyadenylation Signal |
| Q34762164 | Cleavage site determinants min the mammalian polydenylation signal |
| Q42798304 | Cytoplasmic CstF-77 protein belongs to a masking complex with cytoplasmic polyadenylation element-binding protein in Xenopus oocytes |
| Q33602636 | Delineating the structural blueprint of the pre-mRNA 3'-end processing machinery |
| Q36336778 | ELAV inhibits 3'-end processing to promote neural splicing of ewg pre-mRNA |
| Q28609911 | Formation of mRNA 3' ends in eukaryotes: mechanism, regulation, and interrelationships with other steps in mRNA synthesis |
| Q24314952 | GRSF-1: a poly(A)+ mRNA binding protein which interacts with a conserved G-rich element |
| Q40015947 | Identification of an activity in B-cell extracts that selectively impairs the formation of an immunoglobulin mu s poly(A) site processing complex |
| Q34011581 | Intercistronic region required for polycistronic pre-mRNA processing in Caenorhabditis elegans |
| Q34362676 | Isolation and characterization of polyadenylation complexes assembled in vitro. |
| Q37174524 | Localization of RNAPII and 3' end formation factor CstF subunits on C. elegans genes and operons |
| Q36691462 | Molecular analyses of two poly(A) site-processing factors that determine the recognition and efficiency of cleavage of the pre-mRNA. |
| Q41431707 | Omni-PolyA: a method and tool for accurate recognition of Poly(A) signals in human genomic DNA. |
| Q37012234 | PA-seq for Global Identification of RNA Polyadenylation Sites of Kaposi's Sarcoma-Associated Herpesvirus Transcripts |
| Q50720779 | Phosphorylation of CPEB by Eg2 mediates the recruitment of CPSF into an active cytoplasmic polyadenylation complex. |
| Q41888633 | Polyadenylation proteins CstF-64 and tauCstF-64 exhibit differential binding affinities for RNA polymers. |
| Q40530952 | Potential role of poly(A) polymerase in the assembly of polyadenylation-specific RNP complexes |
| Q24309304 | Purification and characterization of human cleavage factor Im involved in the 3' end processing of messenger RNA precursors |
| Q27932235 | RNA binding analysis of yeast REF2 and its two-hybrid interaction with a new gene product, FIR1. |
| Q24646013 | RNA recognition by the human polyadenylation factor CstF |
| Q40776308 | RNA-protein interactions in mRNA 3'-end formation |
| Q34628809 | Reexamining the polyadenylation signal: were we wrong about AAUAAA? |
| Q33648895 | Regulation of human papillomavirus type 31 polyadenylation during the differentiation-dependent life cycle |
| 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 |
| Q33923193 | Regulation of the subcellular distribution of key cellular RNA-processing factors during permissive human cytomegalovirus infection |
| Q41882662 | Sequence elements upstream of the 3' cleavage site confer substrate strength to the adenovirus L1 and L3 polyadenylation sites |
| Q35857024 | Sequences regulating poly(A) site selection within the adenovirus major late transcription unit influence the interaction of constitutive processing factors with the pre-mRNA. |
| Q40642300 | Sequences regulating temporal poly(A) site switching in the adenovirus major late transcription unit |
| Q24670536 | Specific trans-acting proteins interact with auxiliary RNA polyadenylation elements in the COX-2 3'-UTR |
| Q28245082 | Structural biology of poly(A) site definition |
| Q36667262 | The 64-kilodalton subunit of the CstF polyadenylation factor binds to pre-mRNAs downstream of the cleavage site and influences cleavage site location |
| Q38317290 | The Drosophila homologue of the 64 kDa subunit of cleavage stimulation factor interacts with the 77 kDa subunit encoded by the suppressor of forked gene |
| Q34749544 | The G-rich auxiliary downstream element has distinct sequence and position requirements and mediates efficient 3' end pre-mRNA processing through a trans-acting factor |
| Q28140003 | The gene for a variant form of the polyadenylation protein CstF-64 is on chromosome 19 and is expressed in pachytene spermatocytes in mice |
| Q24301982 | The human 64-kDa polyadenylylation factor contains a ribonucleoprotein-type RNA binding domain and unusual auxiliary motifs |
| Q35690884 | The human papillomavirus type 16 negative regulatory RNA element interacts with three proteins that act at different posttranscriptional levels. |
| Q41491594 | The mechanism of 3' cleavage and polyadenylation of eukaryotic pre-mRNA. |
| Q24307893 | The poly A polymerase Star-PAP controls 3'-end cleavage by promoting CPSF interaction and specificity toward the pre-mRNA |
| Q35186139 | The role of the yeast cleavage and polyadenylation factor subunit Ydh1p/Cft2p in pre-mRNA 3'-end formation |
| Q35207740 | The upstream sequence element of the C2 complement poly(A) signal activates mRNA 3' end formation by two distinct mechanisms. |
| Q37059501 | Transcription termination and polyadenylation in retroviruses |
| Q40789024 | Upstream sequence elements enhance poly(A) site efficiency of the C2 complement gene and are phylogenetically conserved |
| Q24548365 | hnRNP F influences binding of a 64-kilodalton subunit of cleavage stimulation factor to mRNA precursors in mouse B cells |
| Q41569819 | mRNA 3' end processing factors: a phylogenetic comparison |
| Q34366770 | p54nrb is a component of the snRNP-free U1A (SF-A) complex that promotes pre-mRNA cleavage during polyadenylation |
Search more.