http://biowww.net/ Wed, 07 Jan 2009 10:12:59 +0100 FeedCreator 1.7.2 http://biowww.net/methods/detail-289.html RNase mitochondrial RNA processing (RNase MRP) mutants have been shown to have an exit-from-mitosis defect that is caused by an increase in Molecular and Cellular Biology.2003:24(3):945 ... Schmitt Mark E. http://biowww.net/methods/detail-290.html A technique is described to identify the rare sequences within an RNA molecule that are available for efficient interaction with complementary DNA probes: the target RNA is digested by RNase H in the presence of a random pool of complementary DNA fragments gen ... AtkinsJ F http://biowww.net/methods/detail-291.html Nucleic Acids Research.1996:24(3):532 ... CechT R http://biowww.net/methods/detail-294.html Existing computational methods for RNA secondary-structure prediction tacitly assume RNA to only encode functional RNA structures. However, experimental studies have revealed that some RNA sequences, e.g. compact viral genomes, can simultaneously encode functi ... HeinJotun http://biowww.net/methods/detail-295.html The problem of systematic and objective identification of canonical and non-canonical base pairs in RNA three-dimensional (3D) structures was studied. A probabilistic approach was applied, and an algorithm and its implementation in a computer program that dete ... MajorFrançois http://biowww.net/methods/detail-296.html Post-transcriptional methylation of ribose at position O-2' is one of the most common and conserved types of RNA modification. Details of the functional roles of these methylations are far from clear, although in tRNA they are involved at position 34 in regula ... McCloskeyJ A http://biowww.net/methods/detail-297.html We have developed a sequencing method based on the RNA polymerase chain termination reaction with rhodamine dye attached to 3′-deoxynucleoside triphosphate (3′-dNTP). This method enables us to conduct a rapid isothermal sequencing reaction in & ... HayashizakiYoshihide http://biowww.net/methods/detail-298.html Many RNAs need Mg2+to produce stable tertiary structures. Here we describe a simple method to measure the rate and activation parameters of tertiary structure unfolding that exploits this Mg2+dependence. Our approach is based on mixing an RNA solution with exc ... GlickG D http://biowww.net/methods/detail-299.html A new method for rapid purification and structural analysis of oligoribonucleotides of 19 and 20 nt is applied to RNA hairpins SL3 and SL2, which are stable secondary structures present on the ψ recognition element of HIV-1. This approach uses ion-pair ... FabrisDaniele