Jonathan D. Dinman

The frameshift signal of HIV-1 involves a potential intramolecular triplex RNA structure.

New targets for antivirals: the ribosomal A-site and the factors that interact with it.

An "integrated model" of programmed ribosomal frameshifting.

The 9-A solution: how mRNA pseudoknots promote efficient programmed -1 ribosomal frameshifting.

Delayed rRNA processing results in significant ribosome biogenesis and functional defects.

Decreased peptidyltransferase activity correlates with increased programmed -1 ribosomal frameshifting and viral maintenance defects in the yeast Saccharomyces cerevisiae.

An in vivo dual-luciferase assay system for studying translational recoding in the yeast Saccharomyces cerevisiae.

A programmed -1 ribosomal frameshift signal can function as a cis-acting mRNA destabilizing element.

Evidence against a direct role for the Upf proteins in frameshifting or nonsense codon readthrough.

Systematic analysis of bicistronic reporter assay data.

Torsional restraint: a new twist on frameshifting pseudoknots.

A three-stemmed mRNA pseudoknot in the SARS coronavirus frameshift signal.

Structural and functional analysis of 5S rRNA in Saccharomyces cerevisiae.

Identification of functionally important amino acids of ribosomal protein L3 by saturation mutagenesis.

Comparative study of the effects of heptameric slippery site composition on -1 frameshifting among different eukaryotic systems.

Specific effects of ribosome-tethered molecular chaperones on programmed -1 ribosomal frameshifting.

Efficient expression of the 15-kDa form of infectious pancreatic necrosis virus VP5 by suppression of a UGA codon.

An arc of unpaired "hinge bases" facilitates information exchange among functional centers of the ribosome.

Identification of functional, endogenous programmed -1 ribosomal frameshift signals in the genome of Saccharomyces cerevisiae.

Ribosomal protein L3: influence on ribosome structure and function.

Optimization of ribosome structure and function by rRNA base modification.

Ribosomal protein L3: gatekeeper to the A site.

Programmed Ribosomal Frameshifting Goes Beyond Viruses: Organisms from all three kingdoms use frameshifting to regulate gene expression, perhaps signaling a paradigm shift.

Differentiating between near- and non-cognate codons in Saccharomyces cerevisiae.

Integration of residue-specific acid cleavage into proteomic workflows.

Human ribosomal protein L13a is dispensable for canonical ribosome function but indispensable for efficient rRNA methylation.

5S rRNA: Structure and Function from Head to Toe.

Evaluation of microwave-accelerated residue-specific acid cleavage for proteomic applications.

rRNA mutants in the yeast peptidyltransferase center reveal allosteric information networks and mechanisms of drug resistance.

Structure/function analysis of yeast ribosomal protein L2.

A new kinetic model reveals the synergistic effect of E-, P- and A-sites on +1 ribosomal frameshifting.

The role of programmed-1 ribosomal frameshifting in coronavirus propagation.

PRFdb: a database of computationally predicted eukaryotic programmed -1 ribosomal frameshift signals.

Yeast ribosomal protein L10 helps coordinate tRNA movement through the large subunit.

The 3' proximal translational enhancer of Turnip crinkle virus binds to 60S ribosomal subunits.

Ribosomal protein L3 functions as a 'rocker switch' to aid in coordinating of large subunit-associated functions in eukaryotes and Archaea.

The eukaryotic ribosome: current status and challenges.

Expanding the ribosomal universe.

Achieving a golden mean: mechanisms by which coronaviruses ensure synthesis of the correct stoichiometric ratios of viral proteins.

Enhanced purity, activity and structural integrity of yeast ribosomes purified using a general chromatographic method.

A molecular clamp ensures allosteric coordination of peptidyltransfer and ligand binding to the ribosomal A-site.

A flexible loop in yeast ribosomal protein L11 coordinates P-site tRNA binding.

The many paths to frameshifting: kinetic modelling and analysis of the effects of different elongation steps on programmed -1 ribosomal frameshifting.

Endogenous ribosomal frameshift signals operate as mRNA destabilizing elements through at least two molecular pathways in yeast.

Ribosome binding to a 5' translational enhancer is altered in the presence of the 3' untranslated region in cap-independent translation of turnip crinkle virus.

Mutations of highly conserved bases in the peptidyltransferase center induce compensatory rearrangements in yeast ribosomes.

The central core region of yeast ribosomal protein L11 is important for subunit joining and translational fidelity.

A rapid, inexpensive yeast-based dual-fluorescence assay of programmed--1 ribosomal frameshifting for high-throughput screening.

An extensive network of information flow through the B1b/c intersubunit bridge of the yeast ribosome.

Evolution of a helper virus-derived, ribosome binding translational enhancer in an untranslated satellite RNA of Turnip crinkle virus.

rRNA pseudouridylation defects affect ribosomal ligand binding and translational fidelity from yeast to human cells.

Control of gene expression by translational recoding.