| scholarly article | Q13442814 |
| P2093 | author name string | G R Adami | |
| G G Carmichael | |||
| P2860 | cites work | Genomic sequencing | Q24594942 |
| A new blotting medium for the simple isolation and identification of highly resolved messenger RNA | Q24635270 | ||
| A technique for radiolabeling DNA restriction endonuclease fragments to high specific activity | Q26778490 | ||
| A new technique for the assay of infectivity of human adenovirus 5 DNA | Q27860797 | ||
| Adenovirus VAI RNA is required for efficient translation of viral mRNAs at late times after infection | Q28265093 | ||
| Selective extraction of polyoma DNA from infected mouse cell cultures | Q29547500 | ||
| Possible role of flanking nucleotides in recognition of the AUG initiator codon by eukaryotic ribosomes | Q29618470 | ||
| DNA-mediated transfer of the adenine phosphoribosyltransferase locus into mammalian cells | Q34048204 | ||
| Identification of the SV40 agnogene product: a DNA binding protein | Q34252415 | ||
| Selection of initiation sites by eucaryotic ribosomes: effect of inserting AUG triplets upstream from the coding sequence for preproinsulin | Q35278976 | ||
| Exon mutations that affect the choice of splice sites used in processing the SV40 late transcripts | Q35557966 | ||
| Transcriptional ‘enhancers’ from SV40 and polyoma virus show a cell type preference | Q35726616 | ||
| A small segment of polyoma virus DNA enhances the expression of a cloned β-globin gene over a distance of 1400 base pairs | Q35746409 | ||
| Polyoma virus giant RNAs contain tandem repeats of the nucleotide sequence of the entire viral genome | Q35993639 | ||
| Gaps and duplicated sequences in the leaders of SV40 16S RNA | Q36188285 | ||
| Adenovirus tripartite leader sequence enhances translation of mRNAs late after infection | Q36262361 | ||
| Regulation of Simian Virus 40 Transcription: Sensitive Analysis of the RNA Species Present Early in Infections by Virus or Viral DNA | Q36500705 | ||
| Sequences in the polyomavirus DNA regulatory region involved in viral DNA replication and early gene expression | Q36902040 | ||
| Polyomavirus origin for DNA replication comprises multiple genetic elements | Q36908040 | ||
| Sequences locating the 5' ends of the major simian virus 40 late mRNA forms | Q36909682 | ||
| Polyoma virus early and late mRNAs in productively infected mouse 3T6 cells | Q36925166 | ||
| Mutants deleted in the agnogene of simian virus 40 define a new complementation group | Q36928529 | ||
| Transcription during productive infection with polyoma virus and simian virus 40 | Q40006879 | ||
| Sequence repeats in a polyoma virus DNA region important for gene expression | Q40137631 | ||
| The 5'-terminal leader sequence of late 16 S mRNA from cells infected with simian virus 40 | Q40145981 | ||
| Heterogeneity and 5′-terminal structures of the late RNAs of simian virus 40 | Q40212021 | ||
| Multiple 5′ terminal cap structures in late polyoma virus RNA | Q40237110 | ||
| Comparisons of two early gene functions essential for transformation in polyoma virus and SV-40 | Q40241748 | ||
| The binding of ribosomes to polyoma virus RNA. Possible role of the leader region in initiation site recognition | Q40289762 | ||
| Characterisation of polyoma late mRNA leader sequences by molecular cloning and DNA sequence analysis | Q40482442 | ||
| A region of the polyoma virus genome between the replication origin and late protein coding sequences is required in cis for both early gene expression and viral DNA replication | Q40500615 | ||
| Sequences at the capped 5'-ends of polyoma virus late region mRNAs: an example of extreme terminal heterogeneity | Q40500636 | ||
| Polyomavirus enhancer contains multiple redundant sequence elements that activate both DNA replication and gene expression | Q40665948 | ||
| A new member of the polyomavirus family: the hamster papovavirus. Complete nucleotide sequence and transformation properties. | Q41393337 | ||
| Enchancement of the infectivity of simian virus 40 deoxyribonucleic acid with diethylaminoethyl-dextran. | Q43699011 | ||
| Transcription maps of polyoma virus-specific RNA: analysis by two-dimensional nuclease S1 gel mapping. | Q44693409 | ||
| Late messenger RNA production by viable simian virus 40 mutants with deletions in the leader region | Q45800508 | ||
| Structure of polyoma virus late nuclear RNA. | Q45801191 | ||
| Coding potential and regulatory signals of the polyoma virus genome | Q45803983 | ||
| Non-contiguous segments of the polyoma genome required in cis for DNA replication | Q48402079 | ||
| Two distinct enhancers with different cell specificities coexist in the regulatory region of polyoma. | Q50586207 | ||
| Initiation of translation at internal AUG codons in mammalian cells | Q59085572 | ||
| A minimal intron length but no specific internal sequence is required for splicing the large rabbit beta-globin intron | Q72738345 | ||
| P433 | issue | 2 | |
| P407 | language of work or name | English | Q1860 |
| P304 | page(s) | 417-425 | |
| P577 | publication date | 1986-05-01 | |
| P1433 | published in | Journal of Virology | Q1251128 |
| P1476 | title | Polyomavirus late leader region serves an essential spacer function necessary for viability and late gene expression | |
| P478 | volume | 58 |
| Q41107135 | A rabbit beta-globin polyadenylation signal directs efficient termination of transcription of polyomavirus DNA. |
| Q36293692 | A reiterated leader sequence is present in polyomavirus late transcripts produced by a transformed rat cell line |
| Q36554283 | Characterization of the Polyomavirus Late Polyadenylation Signal |
| Q36916377 | Herpes simplex virus virion stimulatory protein mRNA leader contains sequence elements which increase both virus-induced transcription and mRNA stability. |
| Q36779971 | Leader-to-leader splicing is required for efficient production and accumulation of polyomavirus late mRNAs |
| Q33678489 | Polyomavirus early-late switch is not regulated at the level of transcription initiation and is associated with changes in RNA processing |
| Q36795859 | Polyomavirus late pre-mRNA processing: DNA replication-associated changes in leader exon multiplicity suggest a role for leader-to-leader splicing in the early-late switch |
| Q40106642 | Production of polyomavirus late mRNAs requires sequences near the 5' end of the leader but does not require leader-to-leader splicing |
| Q33897798 | RNA processing in the polyoma virus life cycle |
| Q36801811 | Replication-dependent transactivation of the polyomavirus late promoter |
| Q36738496 | Splice site choice in a complex transcription unit containing multiple inefficient polyadenylation signals |
| Q35766322 | Splice site requirement for the efficient accumulation of polyoma virus late mRNAs |
| Q36629963 | Splice site selection in polyomavirus late pre-mRNA processing. |
| Q36828187 | Splice site skipping in polyomavirus late pre-mRNA processing |
| Q35223801 | Targeted nuclear antisense RNA mimics natural antisense-induced degradation of polyoma virus early RNA. |
| Q40565876 | The length but not the sequence of the polyoma virus late leader exon is important for both late RNA splicing and stability |
| Q34782361 | The sequence and context of the 5' splice site govern the nuclear stability of polyoma virus late RNAs |
| Q36780375 | Translational efficiencies of polyomavirus late mRNA molecules that differ in the sequences of their 5' noncoding late leader exons |
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