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On finding all suboptimal foldings of an RNA molecule.
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Improved predictions of secondary structures for RNA.
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A guide for probing native small nuclear RNA and ribonucleoprotein structures.
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Predicting optimal and suboptimal secondary structure for RNA.
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'Hairpin' catalytic RNA model: evidence for helices and sequence requirement for substrate RNA.
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A site-specific self-cleavage reaction performed by a novel RNA in Neurospora mitochondria.
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Nucleotide sequence and structural analysis of two satellite RNAs associated with chicory yellow mottle virus.
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Architecture of ribosomal RNA: constraints on the sequence of "tetra-loops".
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Effects of GA mismatches on the structure and thermodynamics of RNA internal loops.
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Melting and chemical modification of a cyclized self-splicing group I intron: similarity of structures in 1 M Na+, in 10 mM Mg2+, and in the presence of substrate.
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Structural features that give rise to the unusual stability of RNA hairpins containing GNRA loops.
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Evidence that genomic and antigenomic RNA self-cleaving elements from hepatitis delta virus have similar secondary structures.
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Context dependence of hydrogen bond free energy revealed by substitutions in an RNA hairpin.
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Small catalytic RNAs.
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Substrate selection rules for the hairpin ribozyme determined by in vitro selection, mutation, and analysis of mismatched substrates.
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Reaction conditions and kinetics of self-cleavage of a ribozyme derived from Neurospora VS RNA.
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Essential nucleotide sequences and secondary structure elements of the hairpin ribozyme.
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A major family of motifs involving G.A mismatches in ribosomal RNA.
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Three-dimensional structure of a hammerhead ribozyme.
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The VS catalytic RNA replicates by reverse transcription as a satellite of a retroplasmid.
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Nucleotide sequence requirements for self-cleavage of Neurospora VS RNA.
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Major groove accessibility of RNA.
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The molecular mechanism of thermal unfolding of Escherichia coli formylmethionine transfer RNA.
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Reactions at the termini of tRNA with T4 RNA ligase.
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Direct chemical method for sequencing RNA.
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Rapid and efficient site-specific mutagenesis without phenotypic selection.
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