Area of research
Molecular Biology · Genetics
Research interest
Research interests include RNA and protein synthesis mechanisms, RNA modifications and cancer, Bacterial Genetics and Biotechnology, and Bacteriophages and microbial interactions.
Guidelines for minimal reporting requirements, design and interpretation of experiments involving the use of eukaryotic dual gene expression reporters (MINDR)
Translon: a single term for translated regions
Evaluating ribosomal frameshifting in CCR5 mRNA decoding
Lack of evidence for ribosomal frameshifting in ATP7B mRNA decoding
Monitoring translation in all reading frames downstream of weak stop codons provides mechanistic insights into the impact of nucleotide and cellular contexts
Tissue-specific dynamic codon redefinition in <i>Drosophila</i>
The energy landscape of −1 ribosomal frameshifting
AMD1 mRNA employs ribosome stalling as a mechanism for molecular memory formation
Stop codon readthrough generates a C-terminally extended variant of the human vitamin D receptor with reduced calcitriol response
Pyrrolysine in archaea: a 22nd amino acid encoded through a genetic code expansion
Translational autoregulation of BZW1 and BZW2 expression by modulating the stringency of start codon selection
Avoidance of reporter assay distortions from fused dual reporters
Translation Initiation from Conserved Non-AUG Codons Provides Additional Layers of Regulation and Coding Capacity
Systematic analysis of the <i>PTEN</i> 5′ leader identifies a major AUU initiated proteoform
Transcriptional slippage in the positive‐sense RNA virus family Potyviridae
Coupling of mRNA Structure Rearrangement to Ribosome Movement during Bypassing of Non-coding Regions
A Nascent Peptide Signal Responsive to Endogenous Levels of Polyamines Acts to Stimulate Regulatory Frameshifting on Antizyme mRNA
Evidence of efficient stop codon readthrough in four mammalian genes
Cryptic MHC class I-binding peptides are revealed by aminoglycoside-induced stop codon read-through into the 3′ UTR
Sepp1UF forms are N-terminal selenoprotein P truncations that have peroxidase activity when coupled with thioredoxin reductase-1
High-efficiency translational bypassing of non-coding nucleotides specified by mRNA structure and nascent peptide
Analysis of tetra- and hepta-nucleotides motifs promoting -1 ribosomal frameshifting in Escherichia coli
Discontinuous Triplet Decoding with or without Re-Pairing by Peptidyl tRNA
rRNA:mRNA pairing alters the length and the symmetry of mRNA-protected fragments in ribosome profiling experiments
An Overlapping Protein-Coding Region in Influenza A Virus Segment 3 Modulates the Host Response
Production of Selenoprotein P (Sepp1) by Hepatocytes Is Central to Selenium Homeostasis
Ribosomal frameshifting used in influenza A virus expression occurs within the sequence UCC_UUU_CGU and is in the +1 direction
Alternative reading frame selection mediated by a tRNA-like domain of an internal ribosome entry site