scholarly article | Q13442814 |
P356 | DOI | 10.1016/0092-8674(92)90619-N |
P698 | PubMed publication ID | 1318785 |
P50 | author | Asit K. Pattnaik | Q67913352 |
Gail W. Wertz | Q111077169 | ||
P2093 | author name string | L. A. Ball | |
A. W. LeGrone | |||
P433 | issue | 6 | |
P407 | language of work or name | English | Q1860 |
P921 | main subject | viral genome replication | Q3933202 |
viral interference | Q70684351 | ||
P304 | page(s) | 1011-1020 | |
P577 | publication date | 1992-06-01 | |
1992-06-12 | |||
P1433 | published in | Cell | Q655814 |
P1476 | title | Infectious defective interfering particles of VSV from transcripts of a cDNA clone | |
P478 | volume | 69 |
Q24529099 | "Rule of six": how does the Sendai virus RNA polymerase keep count? |
Q39577033 | A functional antigenomic promoter for the paramyxovirus simian virus 5 requires proper spacing between an essential internal segment and the 3' terminus. |
Q37155807 | A host-specific function is required for ligation of a wide variety of ribozyme-processed RNAs |
Q39682384 | A novel expression cassette of lyssavirus shows that the distantly related Mokola virus can rescue a defective rabies virus genome |
Q35891812 | A novel type of defective viral genome suggests a unique strategy to establish and maintain persistent lymphocytic choriomeningitis virus infections |
Q40516673 | A reconstituted replication and transcription system for Ebola virus Reston and comparison with Ebola virus Zaire |
Q36177154 | A single amino acid change resulting in loss of fluorescence of eGFP in a viral fusion protein confers fitness and growth advantage to the recombinant vesicular stomatitis virus |
Q39594295 | A single amino acid substitution in the phosphoprotein of respiratory syncytial virus confers thermosensitivity in a reconstituted RNA polymerase system. |
Q36646999 | A small highly basic protein is encoded in overlapping frame within the P gene of vesicular stomatitis virus |
Q40043376 | An RNA polymerase II-driven Ebola virus minigenome system as an advanced tool for antiviral drug screening |
Q35876229 | An amino-terminal domain of the Sendai virus nucleocapsid protein is required for template function in viral RNA synthesis |
Q45331602 | An improved reverse genetics system for Newcastle disease virus genotype VII. |
Q27487781 | Analysis of a structural homology model of the 2'-O-ribose methyltransferase domain within the vesicular stomatitis virus L protein |
Q40563364 | Analysis of the role of predicted RNA secondary structures in Ebola virus replication |
Q40762899 | Antisense catalytic RNAs as therapeutic agents. |
Q40829494 | Arenavirus nucleocapsid protein displays a transcriptional antitermination activity in vivo. |
Q27486193 | Assembly of functional Sindbis virus RNA replication complexes: requirement for coexpression of P123 and P34 |
Q39707380 | Both matrix proteins of Ebola virus contribute to the regulation of viral genome replication and transcription |
Q45784206 | C-terminal phosphorylation of human respiratory syncytial virus P protein occurs mainly at serine residue 232. |
Q39585062 | Characterization and construction of functional cDNA clones of Pariacoto virus, the first Alphanodavirus isolated outside Australasia |
Q26799938 | Cloned Defective Interfering Influenza RNA and a Possible Pan-Specific Treatment of Respiratory Virus Diseases |
Q33653597 | Comparison of the transcription and replication strategies of marburg virus and Ebola virus by using artificial replication systems |
Q37252971 | Construction of a Sonchus Yellow Net Virus minireplicon: a step toward reverse genetic analysis of plant negative-strand RNA viruses. |
Q36653700 | Deletion mapping of a mouse hepatitis virus defective interfering RNA reveals the requirement of an internal and discontiguous sequence for replication. |
Q36634428 | Deletion mapping of the rotavirus metalloprotein NS53 (NSP1): the conserved cysteine-rich region is essential for virus-specific RNA binding |
Q41946566 | Delta ribozyme benefits from a good stability in vitro that becomes outstanding in vivo |
Q90065437 | Development of a minigenome cassette for Lettuce necrotic yellows virus: A first step in rescuing a plant cytorhabdovirus |
Q37727631 | Efficient and Robust Paramyxoviridae Reverse Genetics Systems. |
Q33975389 | Efficient recovery of infectious vesicular stomatitis virus entirely from cDNA clones |
Q39550236 | Enhanced measles virus cDNA rescue and gene expression after heat shock. |
Q42945480 | Evidence that the respiratory syncytial virus polymerase is recruited to nucleotides 1 to 11 at the 3' end of the nucleocapsid and can scan to access internal signals |
Q35305398 | Examples of expression systems based on animal RNA viruses: alphaviruses and influenza virus |
Q40748329 | Expression of a foreign gene by recombinant canine distemper virus recovered from cloned DNAs |
Q35733629 | Extent of terminal complementarity modulates the balance between transcription and replication of vesicular stomatitis virus RNA. |
Q39603387 | Fidelity of leader and trailer sequence usage by the respiratory syncytial virus and avian pneumovirus replication complexes |
Q39869698 | Functional cDNA clones of the human respiratory syncytial (RS) virus N, P, and L proteins support replication of RS virus genomic RNA analogs and define minimal trans-acting requirements for RNA replication. |
Q38525112 | G gene-deficient single-round rabies viruses for neuronal circuit analysis |
Q36002362 | Gene rearrangement attenuates expression and lethality of a nonsegmented negative strand RNA virus |
Q41195146 | Genetic engineering of animal RNA viruses |
Q33647014 | Highly diverse intergenic regions of the paramyxovirus simian virus 5 cooperate with the gene end U tract in viral transcription termination and can influence reinitiation at a downstream gene |
Q33795744 | Identification of a bovine coronavirus packaging signal |
Q39612159 | Identification of a minimal size requirement for termination of vesicular stomatitis virus mRNA: implications for the mechanism of transcription. |
Q34343423 | Identification of an upstream sequence element required for vesicular stomatitis virus mRNA transcription |
Q40128579 | Identification of nonessential regions of the nsp2 replicase protein of porcine reproductive and respiratory syndrome virus strain VR-2332 for replication in cell culture |
Q40842194 | Identification of nucleocapsid binding sites within coronavirus-defective genomes |
Q33785124 | Identification of the respiratory syncytial virus proteins required for formation and passage of helper-dependent infectious particles. |
Q30435339 | Importance of hydrogen bond contacts between the N protein and RNA genome of vesicular stomatitis virus in encapsidation and RNA synthesis |
Q45789668 | In vitro and in vivo comparison of hammerhead, hairpin, and hepatitis delta virus self-processing ribozyme cassettes |
Q35750036 | In vivo delivery of cytoplasmic RNA virus-derived miRNAs |
Q40396501 | Inducible vesicular stomatitis virus (VSV) L cell line for packaging of recombinant VSV. |
Q40793123 | Infectious rabies viruses from cloned cDNA. |
Q34744464 | Infectivity of a human respiratory syncytial virus lacking the SH, G, and F proteins is efficiently mediated by the vesicular stomatitis virus G protein |
Q42984861 | Interferon alpha-2b inhibits negative-strand RNA and protein expression from full-length HCV1a infectious clone |
Q45728516 | Leader RNA binding ability of Chandipura virus P protein is regulated by its phosphorylation status: a possible role in genome transcription-replication switch. |
Q40043258 | Long-term replication of Sendai virus defective interfering particle nucleocapsids in stable helper cell lines |
Q40570398 | Mapping the site of guanylylation on VP1, the protein primer for infectious pancreatic necrosis virus RNA synthesis |
Q27015752 | Marburg Virus Reverse Genetics Systems |
Q38125018 | Master sensors of pathogenic RNA - RIG-I like receptors |
Q40234004 | Matrix protein of VSV New Jersey serotype containing methionine to arginine substitutions at positions 48 and 51 allows near-normal host cell gene expression |
Q42591165 | Mechanism of RNA synthesis initiation by the vesicular stomatitis virus polymerase |
Q36650409 | Minigenomes, transcription and replication competent virus-like particles and beyond: reverse genetics systems for filoviruses and other negative stranded hemorrhagic fever viruses |
Q35878577 | Mutational analyses of the intergenic dinucleotide and the transcriptional start sequence of vesicular stomatitis virus (VSV) define sequences required for efficient termination and initiation of VSV transcripts |
Q33794492 | Mutations in the 5' trailer region of a respiratory syncytial virus minigenome which limit RNA replication to one step |
Q30436296 | Mutations in the C-terminal loop of the nucleocapsid protein affect vesicular stomatitis virus RNA replication and transcription differentially |
Q35845259 | Mutations within noncoding terminal sequences of model RNAs of Sendai virus: influence on reporter gene expression |
Q30411593 | Newly identified phosphorylation site in the vesicular stomatitis virus P protein is required for viral RNA synthesis |
Q36181607 | Novel insights into the regulation of the viral polymerase complex of neurotropic Borna disease virus |
Q41829930 | Opposing effects of inhibiting cap addition and cap methylation on polyadenylation during vesicular stomatitis virus mRNA synthesis |
Q33815341 | Optimal replication activity of vesicular stomatitis virus RNA polymerase requires phosphorylation of a residue(s) at carboxy-terminal domain II of its accessory subunit, phosphoprotein P. |
Q33639525 | Overlapping signals for transcription and replication at the 3' terminus of the vesicular stomatitis virus genome. |
Q27026528 | PRRSV structure, replication and recombination: Origin of phenotype and genotype diversity |
Q33673962 | Paramyxovirus replication and pathogenesis. Reverse genetics transforms understanding |
Q33813672 | Phenotypic consequences of rearranging the P, M, and G genes of vesicular stomatitis virus |
Q34193706 | Phosphorylation of vesicular stomatitis virus phosphoprotein P is indispensable for virus growth |
Q35897834 | Phosphorylation within the amino-terminal acidic domain I of the phosphoprotein of vesicular stomatitis virus is required for transcription but not for replication |
Q33782279 | Polyadenylation of vesicular stomatitis virus mRNA dictates efficient transcription termination at the intercistronic gene junctions |
Q33844261 | Polymerase slippage at vesicular stomatitis virus gene junctions to generate poly(A) is regulated by the upstream 3'-AUAC-5' tetranucleotide: implications for the mechanism of transcription termination |
Q35999993 | Positive strands to the rescue again: a segmented negative-strand RNA virus derived from cloned cDNAs |
Q40663332 | Positive- and negative-acting signals combine to determine differential RNA replication from the paramyxovirus simian virus 5 genomic and antigenomic promoters |
Q40886502 | Poxvirus vectors: cytoplasmic expression of transferred genes |
Q34301926 | Presence of an encephalomyocarditis virus internal ribosome entry site sequence in avian infectious bronchitis virus defective RNAs abolishes rescue by helper virus |
Q33707803 | Production of infectious human respiratory syncytial virus from cloned cDNA confirms an essential role for the transcription elongation factor from the 5' proximal open reading frame of the M2 mRNA in gene expression and provides a capability for va |
Q43753378 | RNA induced polymerization of the Borna disease virus nucleoprotein |
Q27487321 | RNA polymerase I-mediated expression of viral RNA for the rescue of infectious virulent and avirulent Rift Valley fever viruses |
Q35865852 | RNA replication by a respiratory syncytial virus RNA analog does not obey the rule of six and retains a nonviral trinucleotide extension at the leader end. |
Q35845933 | RNA replication by respiratory syncytial virus (RSV) is directed by the N, P, and L proteins; transcription also occurs under these conditions but requires RSV superinfection for efficient synthesis of full-length mRNA |
Q39549066 | RNA replication for the paramyxovirus simian virus 5 requires an internal repeated (CGNNNN) sequence motif |
Q39606043 | RNA replication from the simian virus 5 antigenomic promoter requires three sequence-dependent elements separated by sequence-independent spacer regions |
Q40451218 | RNA viruses as vectors for the expression of heterologous proteins. |
Q45752770 | Rapid and efficient recovery of Sendai virus from cDNA: factors influencing recombinant virus rescue |
Q39551144 | Rapid delivery of foreign genes into plants by direct rub-inoculation with intact plasmid DNA of a tomato bushy stunt virus gene vector |
Q24310706 | Recognition of 5' triphosphate by RIG-I helicase requires short blunt double-stranded RNA as contained in panhandle of negative-strand virus |
Q40650685 | Recognition of cis-acting elements of infectious haematopoietic necrosis virus and viral hemorrhagic septicemia virus by homologous and heterologous helper proteins |
Q34337129 | Recombinant vesicular stomatitis viruses from DNA. |
Q35705123 | Recovery of human metapneumovirus genetic lineages a and B from cloned cDNA. |
Q40817409 | Recovery of infectious classical swine fever virus (CSFV) from full-length genomic cDNA clones by a swine kidney cell line expressing bacteriophage T7 RNA polymerase. |
Q35869559 | Recovery of infectious respiratory syncytial virus expressing an additional, foreign gene. |
Q33784805 | Redesign and genetic dissection of the rhabdoviruses |
Q39548712 | Regulation of RNA synthesis by the genomic termini of vesicular stomatitis virus: identification of distinct sequences essential for transcription but not replication |
Q36749435 | Repeatable Population Dynamics among Vesicular Stomatitis Virus Lineages Evolved under High Co-infection |
Q39870009 | Replication and amplification of novel vesicular stomatitis virus minigenomes encoding viral structural proteins |
Q39549502 | Replication and packaging of transmissible gastroenteritis coronavirus-derived synthetic minigenomes |
Q35984283 | Replication of the genomic RNA of a positive-strand RNA animal virus from negative-sense transcripts |
Q39594181 | Rescue of Newcastle disease virus from cloned cDNA: evidence that cleavability of the fusion protein is a major determinant for virulence |
Q39875441 | Rescue of a synthetic chloramphenicol acetyltransferase RNA into influenza virus-like particles obtained from recombinant plasmids |
Q41130981 | Rescue of measles virus using a replication-deficient vaccinia-T7 vector |
Q33804946 | Rescue of mumps virus from cDNA. |
Q34301750 | Rescue of recombinant Marburg virus from cDNA is dependent on nucleocapsid protein VP30 |
Q39878135 | Rescue of rinderpest virus from cloned cDNA. |
Q36645648 | Rescue of synthetic analogs of genomic RNA and replicative-intermediate RNA of human parainfluenza virus type 3. |
Q40038834 | Rescue of synthetic genomic RNA analogs of rabies virus by plasmid-encoded proteins. |
Q40015599 | Rescue of synthetic minireplicons establishes the absence of the NS1 and NS2 genes from avian pneumovirus |
Q39897567 | Respiratory syncytial virus inhibits lung epithelial Na+ channels by up-regulating inducible nitric-oxide synthase. |
Q43719139 | Reverse Genetics Meets the Nonsegmented Negative-Strand RNA Viruses |
Q38363535 | Reverse genetics of Mononegavirales: How they work, new vaccines, and new cancer therapeutics |
Q33784788 | Reverse genetics of nodaviruses |
Q35552101 | Ribozyme-based gene-inactivation systems require a fine comprehension of their substrate specificities; the case of delta ribozyme |
Q33843270 | Role of the hypervariable hinge region of phosphoprotein P of vesicular stomatitis virus in viral RNA synthesis and assembly of infectious virus particles |
Q35877758 | Role of the intergenic dinucleotide in vesicular stomatitis virus RNA transcription |
Q30421666 | Second-site mutations selected in transcriptional regulatory sequences compensate for engineered mutations in the vesicular stomatitis virus nucleocapsid protein |
Q60031926 | Segment-specific terminal sequences of Bunyamwera bunyavirus regulate genome replication |
Q30438147 | Selection for gene junction sequences important for VSV transcription |
Q39873145 | Sindbis virus DNA-based expression vectors: utility for in vitro and in vivo gene transfer. |
Q37191937 | Single-amino-acid alterations in a highly conserved central region of vesicular stomatitis virus N protein differentially affect the viral nucleocapsid template functions |
Q27469662 | Stable high-level expression of heterologous genes in vitro and in vivo by noncytopathic DNA-based Kunjin virus replicon vectors |
Q33639235 | The 5' terminal trailer region of vesicular stomatitis virus contains a position-dependent cis-acting signal for assembly of RNA into infectious particles. |
Q39870549 | The L protein of Rift Valley fever virus can rescue viral ribonucleoproteins and transcribe synthetic genome-like RNA molecules |
Q27313335 | The Length of Vesicular Stomatitis Virus Particles Dictates a Need for Actin Assembly during Clathrin-Dependent Endocytosis |
Q30440689 | The VSV polymerase can initiate at mRNA start sites located either up or downstream of a transcription termination signal but size of the intervening intergenic region affects efficiency of initiation |
Q37749473 | The chase for the RIG-I ligand--recent advances |
Q39581526 | The length and sequence composition of vesicular stomatitis virus intergenic regions affect mRNA levels and the site of transcript initiation |
Q40038247 | The membrane-associated and secreted forms of the respiratory syncytial virus attachment glycoprotein G are synthesized from alternative initiation codons |
Q33782056 | The product of the respiratory syncytial virus M2 gene ORF1 enhances readthrough of intergenic junctions during viral transcription |
Q41729114 | The replicative complex of paramyxoviruses: structure and function. |
Q36651219 | The rule of six, a basic feature for efficient replication of Sendai virus defective interfering RNA. |
Q72434991 | The termini of VSV DI particle RNAs are sufficient to signal RNA encapsidation, replication, and budding to generate infectious particles |
Q33785253 | Three of the four nucleocapsid proteins of Marburg virus, NP, VP35, and L, are sufficient to mediate replication and transcription of Marburg virus-specific monocistronic minigenomes |
Q33870273 | Transcription and RNA replication of tacaribe virus genome and antigenome analogs require N and L proteins: Z protein is an inhibitor of these processes |
Q34034236 | Transcription and replication initiate at separate sites on the vesicular stomatitis virus genome |
Q34816770 | Transcriptional control of the RNA-dependent RNA polymerase of vesicular stomatitis virus |
Q40392626 | Transient expression in insect cells using a recombinant baculovirus synthesising bacteriophage T7 RNA polymerase. |
Q39870396 | Translation but not the encoded sequence is essential for the efficient propagation of the defective interfering RNAs of the coronavirus mouse hepatitis virus |
Q33818839 | Translation from the 5' untranslated region (UTR) of mRNA 1 is repressed, but that from the 5' UTR of mRNA 7 is stimulated in coronavirus-infected cells |
Q37646064 | Two RNA polymerase complexes from vesicular stomatitis virus-infected cells that carry out transcription and replication of genome RNA. |
Q33908729 | Utilization of homotypic and heterotypic proteins of vesicular stomatitis virus by defective interfering particle genomes for RNA replication and virion assembly: implications for the mechanism of homologous viral interference |
Q27481497 | Vesicular Stomatitis Virus mRNA Capping Machinery Requires Specific cis-Acting Signals in the RNA |
Q91767093 | Viral replicons as valuable tools for drug discovery |
Q39550387 | Virus promoters determine interference by defective RNAs: selective amplification of mini-RNA vectors and rescue from cDNA by a 3' copy-back ambisense rabies virus |
Q40267817 | Visualization of intracellular transport of vesicular stomatitis virus nucleocapsids in living cells. |
Q45711001 | Yeast as a model host to study replication and recombination of defective interfering RNA of Tomato bushy stunt virus |
Q39882283 | cis-Acting signals involved in termination of vesicular stomatitis virus mRNA synthesis include the conserved AUAC and the U7 signal for polyadenylation |
Q36648578 | cis-acting requirements for the replication of flock house virus RNA 2. |
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