IRESite is an exhaustive, manually annotated nonredundant relational database focused on the IRES elements (Internal Ribosome Entry Site) and containing information not available in the primary public databases. IRES elements were originally found in eukaryotic viruses hijacking initiation of translation of their host. Later on, they were also discovered in 5'-untranslated regions of some eukaryotic mRNA molecules. Currently, IRESite presents up to 92 biologically relevant aspects of every experiment, e. g. the nature of an IRES element, its functionality/defectivity, origin, size, sequence, structure, its relative position with respect to surrounding protein coding regions, positive/negative controls used in the experiment, the reporter ge...
Abstract Background Internal ribosomal entry sites (IRESs) provide alternative, cap-independent tran...
Translation of mRNAs through Internal Ribosome Entry Sites (IRESs) has emerged as a prominent mechan...
AbstractHere we describe a system for promoterless analysis of putative internal ribosome entry site...
IRESite is an exhaustive, manually annotated nonredundant relational database focused on the IRES el...
Published by the Royal Society under the terms of the Creative Commons Attribution License http://cr...
Internal ribosome entry site (IRES) elements are cis-acting RNA regions that promote internal initia...
Certain RNAs are proposed to have an internal ribosome entry site (IRES) in their 5’ untranslated re...
The internal ribosomal entry site (IRES) functions as cap-independent translation initiation sites i...
The standard method of translation initiation, where the ribosome binding onto mRNA is mediated by i...
<div><p>The internal ribosomal entry site (IRES) functions as cap-independent translation initiation...
The synthesis of proteins during eukaryotic translation involves four major phases, where initiation...
Der zentrale Prozess der Realisierung der Erbinformation in Form von Proteinen wird Translation gena...
This article belongs to the Special Issue mRNA Metabolism in Health and Disease 2.0.Many conditions ...
AbstractInternal initiation of protein synthesis in eukaryotes is accomplished by recruitment of rib...
BACKGROUND: The unfolded protein response (UPR) controls the protein folding capacity of the endopla...
Abstract Background Internal ribosomal entry sites (IRESs) provide alternative, cap-independent tran...
Translation of mRNAs through Internal Ribosome Entry Sites (IRESs) has emerged as a prominent mechan...
AbstractHere we describe a system for promoterless analysis of putative internal ribosome entry site...
IRESite is an exhaustive, manually annotated nonredundant relational database focused on the IRES el...
Published by the Royal Society under the terms of the Creative Commons Attribution License http://cr...
Internal ribosome entry site (IRES) elements are cis-acting RNA regions that promote internal initia...
Certain RNAs are proposed to have an internal ribosome entry site (IRES) in their 5’ untranslated re...
The internal ribosomal entry site (IRES) functions as cap-independent translation initiation sites i...
The standard method of translation initiation, where the ribosome binding onto mRNA is mediated by i...
<div><p>The internal ribosomal entry site (IRES) functions as cap-independent translation initiation...
The synthesis of proteins during eukaryotic translation involves four major phases, where initiation...
Der zentrale Prozess der Realisierung der Erbinformation in Form von Proteinen wird Translation gena...
This article belongs to the Special Issue mRNA Metabolism in Health and Disease 2.0.Many conditions ...
AbstractInternal initiation of protein synthesis in eukaryotes is accomplished by recruitment of rib...
BACKGROUND: The unfolded protein response (UPR) controls the protein folding capacity of the endopla...
Abstract Background Internal ribosomal entry sites (IRESs) provide alternative, cap-independent tran...
Translation of mRNAs through Internal Ribosome Entry Sites (IRESs) has emerged as a prominent mechan...
AbstractHere we describe a system for promoterless analysis of putative internal ribosome entry site...