A Rapid Method for Sequencing the 5′‐ and 3′‐Termini of Double‐Stranded RNA Viral Templates using RLM‐RACE
- 1 September 2003
- journal article
- research article
- Published by Wiley in Journal of Phytopathology
- Vol. 151 (9) , 525-527
- https://doi.org/10.1046/j.1439-0434.2003.00755.x
Abstract
No abstract availableKeywords
This publication has 12 references indexed in Scilit:
- Nucleotide sequence and genome organization of Cucurbit yellow stunting disorder virus RNA1Archiv für die gesamte Virusforschung, 2003
- Complete Genome Sequence and Analyses of the Subgenomic RNAs of Sweet Potato Chlorotic Stunt Virus Reveal Several New Features for the Genus CrinivirusJournal of Virology, 2002
- Molecular Characterization of the Cucurbit Yellow Stunting Disorder Virus Coat Protein GenePhytopathology®, 1999
- Sequence-independent amplification and cloning of large dsRNA virus genome segments by poly(dA)-oligonucleotide ligationJournal of Virological Methods, 1998
- Differentiation between cucurbit yellow stunting disorder virus and beet pseudo‐yellows virus by a reverse transcription‐polymerase chain reaction assayPlant Pathology, 1998
- Cherry Chlorotic Rusty Spot: Description of a New Viruslike Disease from Cherry and Studies on its Etiologic AgentPlant Disease, 1996
- Mapping the 5′ and 3′ ends ofTetrahymena thermophilamRNAs using RNA ligase mediated amplification of cDNA ends (RLM-RACE)Nucleic Acids Research, 1993
- Double-Stranded RNA from Plants Infected with ClosterovirusesPhytopathology®, 1983
- Cloning the double-stranded RNA genes of reovirus: sequence of the cloned S2 gene.Proceedings of the National Academy of Sciences, 1982
- Sequences at the 3′ ends of yeast viral dsRNAs: proposed transcriptase and replicase initiation sitesNucleic Acids Research, 1981