N 6 -Methyladenosine (m 6 A) is an abundant post-transcriptional RNA modification that
influences multiple aspects of gene expression. In addition to recruiting proteins, m 6 A can …

RNA modifications are crucial factors for efficient protein synthesis. All classes of RNAs that
are involved in translation are modified to different extents. Recently, mRNA modifications …

We present the access to [5‐ 19 F, 5‐ 13 C]‐uridine and ‐cytidine phosphoramidites for the
production of site‐specifically modified RNAs up to 65 nucleotides (nts). The amidites were …

The HIV-1 Rev response element (RRE) RNA element mediates the nuclear export of intron
containing viral RNAs by forming an oligomeric complex with the viral protein Rev. Stem IIB …

Fluorine labeling of ribonucleic acids (RNA) in conjunction with 19 F NMR spectroscopy has
emerged as a powerful strategy for spectroscopic analysis of RNA structure and dynamics, …

Nuclear export complexes composed of rev response element (RRE) ribonucleic acid (RNA)
and multiple molecules of rev protein are promising targets for the development of …

tRNA superwobbling, used by certain bacteria and organelles, is an intriguing decoding
concept in which a single tRNA isoacceptor is used to decode all synonymous codons of a four-…

N 6 -methyladenosine (m 6 A) is a ubiquitous RNA post-transcriptional modification found in
coding as well as non-coding RNAs. m 6 A has also been found in viral RNAs where it is …

Watson–Crick like G‐U mismatches with tautomeric G enol or U enol bases can evade fidelity
checkpoints and thereby contribute to translational errors. The 5‐oxyacetic acid uridine (…

Although group II intron ribozymes are intensively studied the question how structural dynamics
affects splicing catalysis has remained elusive. We report for the first time that the group …