scholarly article | Q13442814 |
P356 | DOI | 10.1128/MCB.8.11.4829 |
P8608 | Fatcat ID | release_tavzwphqo5ffrijte2ykyul54u |
P932 | PMC publication ID | 365576 |
P698 | PubMed publication ID | 2463466 |
P5875 | ResearchGate publication ID | 20691601 |
P2093 | author name string | C N Cole | |
R M Denome | |||
P2860 | cites work | Detection of specific sequences among DNA fragments separated by gel electrophoresis | Q25939003 |
3' non-coding region sequences in eukaryotic messenger RNA | Q27860858 | ||
Accurate cleavage and polyadenylation of exogenous RNA substrate | Q28646786 | ||
Selective extraction of polyoma DNA from infected mouse cell cultures | Q29547500 | ||
Sizing and mapping of early adenovirus mRNAs by gel electrophoresis of S1 endonuclease-digested hybrids | Q29618273 | ||
Synthesis of two mRNAs by utilization of alternate polyadenylation sites: expression of SV40-mouse immunoglobulin mu chain gene recombinants in Cos monkey cells | Q33939424 | ||
Complex transcriptional units: diversity in gene expression by alternative RNA processing | Q34048629 | ||
Synthesis of secreted and membrane-bound immunoglobulin mu heavy chains is directed by mRNAs that differ at their 3' ends | Q34056363 | ||
Calcium-dependent bacteriophage DNA infection | Q34223120 | ||
Nucleotide sequence of the rightward operator of phage lambda | Q35074385 | ||
Expression of simian virus 40-rat preproinsulin recombinants in monkey kidney cells: use of preproinsulin RNA processing signals | Q35301051 | ||
Sequence signals which may be required for efficient formation of mRNA 3' termini | Q36098195 | ||
The consensus sequence YGTGTTYY located downstream from the AATAAA signal is required for efficient formation of mRNA 3' termini | Q36136653 | ||
Duplication of functional polyadenylation signals in polyomavirus DNA does not alter efficiency of polyadenylation or transcription termination | Q36863412 | ||
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 | ||
Fine-structure analysis of the processing and polyadenylation region of the herpes simplex virus type 1 thymidine kinase gene by using linker scanning, internal deletion, and insertion mutations | Q36902305 | ||
A novel RNA in which the 5' end is generated by cleavage at the poly(A) site of immunoglobulin heavy-chain secreted mRNA | Q36902826 | ||
Simian virus 40-rabbit beta-globin recombinants lacking late mRNA splice sites express cytoplasmic RNAs with altered structures | Q36921417 | ||
Independent 5' and 3'-end determination of multiple dihydrofolate reductase transcripts | Q36922937 | ||
Analysis in Cos-1 Cells of Processing and Polyadenylation Signals by Using Derivatives of the Herpes Simplex Virus Type 1 Thymidine Kinase Gene | Q36936614 | ||
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 | ||
Effect of adenovirus on metabolism of specific host mRNAs: transport control and specific translational discrimination | Q36981533 | ||
Regulated production of mu m and mu s mRNA requires linkage of the poly(A) addition sites and is dependent on the length of the mu s-mu m intron | Q37408665 | ||
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 | ||
SV40 recombinants carrying a functional RNA splice junction and polyadenylation site from the chromosomal mouse βmaj globin gene | Q40251553 | ||
High efficiency polyoma DNA transfection of chloroquine treated cells | Q40490478 | ||
SV40 gene expression is modulated by the cooperative binding of T antigen to DNA | Q43915434 | ||
Transcription maps of polyoma virus-specific RNA: analysis by two-dimensional nuclease S1 gel mapping. | Q44693409 | ||
Nucleotide sequence surrounding multiple polyadenylation sites in the mouse dihydrofolate reductase gene | Q48404695 | ||
The sequence 5'-AAUAAA-3'forms parts of the recognition site for polyadenylation of late SV40 mRNAs | Q48410195 | ||
Mode of regulation of immunoglobulin mu- and delta-chain expression varies during B-lymphocyte maturation. | Q52276349 | ||
Poly(A) site cleavage in a HeLa nuclear extract is dependent on downstream sequences. | Q55060176 | ||
A sequence downstream of AAUAAA is required for rabbit β-globin mRNA 3′-end formation | Q59058833 | ||
Regulation of adenovirus-2 gene expression at the level of transcriptional termination and RNA processing | Q59098268 | ||
Site-specific polyadenylation in a cell-free reaction | Q64380699 | ||
Production of RNA for secreted immunoglobulin μ chains does not require transcriptional termination 5′ to the μM exons | Q72687818 | ||
Rapid purification of plasmid DNA by a single centrifugation in a two-step cesium chloride-ethidium bromide gradient | Q72724514 | ||
P433 | issue | 11 | |
P407 | language of work or name | English | Q1860 |
P304 | page(s) | 4829-4839 | |
P577 | publication date | 1988-11-01 | |
P1433 | published in | Molecular and Cellular Biology | Q3319478 |
P1476 | title | Patterns of polyadenylation site selection in gene constructs containing multiple polyadenylation signals | |
P478 | volume | 8 |
Q40448813 | A DNA recombination-based approach to eliminate papillomavirus infection. |
Q34855763 | A genetic polymorphism within the third poly(A) signal of the DHFR gene alters the polyadenylation pattern of DHFR transcripts in CHL cells |
Q33960046 | A history of poly A sequences: from formation to factors to function |
Q40453460 | Alterations in the pre-mRNA topology of the bovine growth hormone polyadenylation region decrease poly(A) site efficiency. |
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 |
Q24798039 | Alternative polyadenylation of cyclooxygenase-2. |
Q40452859 | Analysis of polyadenylation site usage of the c-myc oncogene. |
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 |
Q34620261 | B-lineage regulated polyadenylation occurs on weak poly(A) sites regardless of sequence composition at the cleavage and downstream regions |
Q40516921 | Conservation of Bmp2 post-transcriptional regulatory mechanisms |
Q35938476 | Differential utilization of poly (A) signals between DHFR alleles in CHL cells |
Q38334274 | Effect of intron A from human cytomegalovirus (Towne) immediate-early gene on heterologous expression in mammalian cells |
Q41688873 | Efficient CFTR expression from AAV vectors packaged with promoters--the second generation |
Q34213955 | Ending the message: poly(A) signals then and now |
Q34281915 | Fully modified 2' MOE oligonucleotides redirect polyadenylation |
Q41858295 | Genome-wide analysis of poly(A) site selection in Schizosaccharomyces pombe |
Q33584213 | Glucose-inducible expression of rrg1+ in Schizosaccharomyces pombe: post-transcriptional regulation of mRNA stability mediated by the downstream region of the poly(A) site |
Q36655698 | Hierarchy of polyadenylation site usage by bovine papillomavirus in transformed mouse cells. |
Q36727357 | Molecular characterization of the Drosophila melanogaster urate oxidase gene, an ecdysone-repressible gene expressed only in the malpighian tubules |
Q24548945 | Pause sites promote transcriptional termination of mammalian RNA polymerase II |
Q41079693 | Poly(A) site efficiency reflects the stability of complex formation involving the downstream element |
Q34859580 | Polyadenylation and transcription termination in gene constructs containing multiple tandem polyadenylation signals |
Q45849027 | Proximity to the promoter inhibits recognition of cauliflower mosaic virus polyadenylation signal. |
Q64379521 | RNA polymerase II-dependent positional effects on mRNA 3' end processing in the adenovirus major late transcription unit |
Q24534244 | Regulation of gene expression for translation initiation factor eIF-2 alpha: importance of the 3' untranslated region |
Q81363212 | Regulatory role of the 3' untranslated region (3'UTR) of rat 5' deiodinase (D1). effects on messenger RNA translation and stability |
Q40490459 | Role of mRNA transcript stability in modulation of expression of the gene encoding thrombin activable fibrinolysis inhibitor |
Q40021937 | Sequence-mediated regulation of adenovirus gene expression by repression of mRNA accumulation |
Q36795452 | Sequences upstream of AAUAAA influence poly(A) site selection in a complex transcription unit |
Q55092205 | Targeting the Polyadenylation Signal of Pre-mRNA: A New Gene Silencing Approach for Facioscapulohumeral Dystrophy. |
Q73026499 | The 2.1-, 5.4- and 5.7-kb transcripts of the IDS gene are generated by different polyadenylation signals |
Q36796409 | The U3 region is not necessary for 3' end formation of spleen necrosis virus RNA |
Q41491594 | The mechanism of 3' cleavage and polyadenylation of eukaryotic pre-mRNA. |
Q33826903 | The polyadenylation code: a unified model for the regulation of mRNA alternative polyadenylation |
Q39580830 | The role of herpes simplex virus ICP27 in the regulation of UL24 gene expression by differential polyadenylation |
Q28372202 | Transcriptional regulation of the human CYP1B1 gene. Evidence for involvement of an aryl hydrocarbon receptor response element in constitutive expression |
Q74676404 | Upstream elements present in the 3'-untranslated region of collagen genes influence the processing efficiency of overlapping polyadenylation signals |
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