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Suppression of ribosomal pausing by eIF5A is necessary to maintain the fidelity of start codon selection
PubMed Full text in PMC Similar studies
Suppression of ribosomal pausing by eIF5A is necessary to maintain the fidelity of start codon selection (CRISPR screen)
PubMed Full text in PMC Similar studies SRA Run Selector
Suppression of ribosomal pausing by eIF5A is necessary to maintain the fidelity of start codon selection (RNA-sequencing)
PubMed Full text in PMC Similar studies Analyze with GEO2RSRA Run Selector
Suppression of ribosomal pausing by eIF5A is necessary to maintain the fidelity of start codon selection (Ribosome profiling)
Snapshot of translation in mammalian cells that are depleted of polyamines or replete with polyamines
Ribosome profiling study of eIF5A depletion strain
Study of ribosome dynamics after eIF5A depletion in budding yeast
Ribosome profiling in archaea reveals leaderless translation, novel translational initiation sites, and ribosome pausing at single codon resolution
Bi-directional ribosome scanning controls the stringency of start codon selection
The RNA helicase Ded1p suppresses translation initiation from near-cognate start codons
Genome-wide survey of ribosome collision
Genome-wide survey of ribosome collision [eif5A siRNA]
Genome-wide survey of ribosome collision [anisomycin]
Genome-wide survey of ribosome collision [monosome/disome]
Defining codon-mediated mRNA decay and No-go decay in zebrafish embryos
Ribosome profiling reveals sequence-independent post-initiation pausing as a signature of translation
Translational control through differential ribosome pausing during amino acid limitation in mammalian cells
Transcriptome-wide sites of collided ribosomes reveal sequence determinants of translational pausing in vivo
Competition between translation initiation factor eIF5 and its mimic protein 5MP determines non-AUG initiation rate genome-wide
Lso2 is a conserved ribosome-bound protein required for translational recovery in yeast
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