Research Article
More than one way to splice an RNA: Branching without a bulge and splicing without branching in group II introns
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- 01 October 1998, pp. 1186-1202
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Structure and stability of variants of the sarcin-ricin loop of 28S rRNA: NMR studies of the prokaryotic SRL and a functional mutant
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- 01 October 1998, pp. 1203-1215
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PRP16, a DEAH-box RNA helicase, is recruited to the spliceosome primarily via its nonconserved N-terminal domain
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- 01 October 1998, pp. 1216-1229
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Programmed frameshifting in the synthesis of mammalian antizyme is +1 in mammals, predominantly +1 in fission yeast, but −2 in budding yeast
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- 01 October 1998, pp. 1230-1238
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Protein–RNA interactions in the U5 snRNP of Saccharomyces cerevisiae
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- 01 October 1998, pp. 1239-1250
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Cryoenzymology of the hammerhead ribozyme
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- 01 October 1998, pp. 1251-1258
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The RNA recognition motif of yeast translation initiation factor Tif3/eIF4B is required but not sufficient for RNA strand-exchange and translational activity
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- 01 October 1998, pp. 1259-1267
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Spb4p, an essential putative RNA helicase, is required for a late step in the assembly of 60S ribosomal subunits in Saccharomyces cerevisiae
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- 01 October 1998, pp. 1268-1281
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Metal ion probing of rRNAs: Evidence for evolutionarily conserved divalent cation binding pockets
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- 01 October 1998, pp. 1282-1294
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Correlation between bending of the VM region and pathogenicity of different Potato Spindle Tuber Viroid strains
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- 01 October 1998, pp. 1295-1303
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Identification and functional analysis of hPRP17, the human homologue of the PRP17/CDC40 yeast gene involved in splicing and cell cycle control
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- 01 October 1998, pp. 1304-1312
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METHOD
T7 RNA polymerase produces 5′ end heterogeneity during in vitro transcription from certain templates
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- 01 October 1998, pp. 1313-1317
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