Herein, we detail a novel reverse-transcription (RT) assay to directly detect chemical adducts on RNA. We optimize a fluorescence quenching assay to detect RT polymerization and employ our approach to detect N1-alkylation of inosine, an important post-transcriptional modification, using a phenylacrylamide as a model compound. We anticipate our approach can be expanded to identify novel reagents that form adducts with RNA and further explored to understand the relationship between RT processivity and natural post-transcriptional modifications in RNA
By using single-molecule multiparameter fluorescence detection, fluorescence resonance energy transf...
Nanopore direct RNA sequencing (dRNA-Seq) reads reveal RNA modifications through consistent error pr...
The combination of Reverse Transcription (RT) and high-throughput sequencing has emerged as a powerf...
Inosine at the “wobble” position (I34) is one of the few essential posttranscriptional modifications...
Oxidative base damage In DNA and metabolic defects In the recognition and removal of such damage pla...
We have developed a simple method to measure RNA synthesis in real time. In this technique, transcri...
The first chemical modification to RNA was discovered nearly 60 years ago; to date, more than 100 ch...
New chemical probes have been designed to facilitate the identification of adenosine-to-inosine (A-t...
RNA is a highly regulatory biomolecule within the cell. RNA has been identified in many biological f...
The natural chemical modifications of messenger RNA (mRNA) in living organisms have shown essential ...
International audienceReverse transcription (RT) of RNA templates containing RNA modifications leads...
RNA detection has become one of the most robust parts in molecular biology, medical diagnostics and ...
By using single-molecule multiparameter fluorescence detection, fluorescence resonance energy transf...
Optimized and stringent chemical methods to profile nascent RNA expression are still in demand. Here...
Inosine (I) is a nucleoside that is a result of the deamination of adenosine (A). It is ubiquitous i...
By using single-molecule multiparameter fluorescence detection, fluorescence resonance energy transf...
Nanopore direct RNA sequencing (dRNA-Seq) reads reveal RNA modifications through consistent error pr...
The combination of Reverse Transcription (RT) and high-throughput sequencing has emerged as a powerf...
Inosine at the “wobble” position (I34) is one of the few essential posttranscriptional modifications...
Oxidative base damage In DNA and metabolic defects In the recognition and removal of such damage pla...
We have developed a simple method to measure RNA synthesis in real time. In this technique, transcri...
The first chemical modification to RNA was discovered nearly 60 years ago; to date, more than 100 ch...
New chemical probes have been designed to facilitate the identification of adenosine-to-inosine (A-t...
RNA is a highly regulatory biomolecule within the cell. RNA has been identified in many biological f...
The natural chemical modifications of messenger RNA (mRNA) in living organisms have shown essential ...
International audienceReverse transcription (RT) of RNA templates containing RNA modifications leads...
RNA detection has become one of the most robust parts in molecular biology, medical diagnostics and ...
By using single-molecule multiparameter fluorescence detection, fluorescence resonance energy transf...
Optimized and stringent chemical methods to profile nascent RNA expression are still in demand. Here...
Inosine (I) is a nucleoside that is a result of the deamination of adenosine (A). It is ubiquitous i...
By using single-molecule multiparameter fluorescence detection, fluorescence resonance energy transf...
Nanopore direct RNA sequencing (dRNA-Seq) reads reveal RNA modifications through consistent error pr...
The combination of Reverse Transcription (RT) and high-throughput sequencing has emerged as a powerf...