Our latest manuscript, related to #RNA#RibosomeProfiling#RiboSeq, was online @NatureComms!
We reported that a compound DMDA-PatA functions as an mRNA-selective translation inhibitor, clamping target DEAD-box RNA binding proteins on GNG motifs.
https://t.co/hZIS9YneZu
We are happy to announce that our latest manuscript, related to #RNA#RibosomeProfiling#RiboSeq, was published in @NatureComms !
We reported a new method to measure ribosome stoichiometry (ribosome number) and kinetics in a genome-wide manner.
https://t.co/09oN93IOS5
We are happy to announce that our latest manuscript, related to #RNA#RibosomeProfiling#RiboSeq, was published published with @SpringerNature in @NatureSMB !
We reported the translation factor eIF4A1 has a repressive role in stressed cells.
https://t.co/cdrKMB1qig
My first tweet!! 🥳 And I’m excited to share that @MarinaMikhaylo8’s and my last project on axonal transport has been published in @J_Cell_Sci! Grateful for the amazing teamwork with our collaborators along the way! Thank you @peris_leticia, @yuhao_han, @yannespopp, @MoutinMJ 🙏
Cellular repair of DNA breaks enables editing of the human genome.
Do human cells repair RNA breaks, and can we use it to edit transcriptomes?
Our work with @ANemudraia and @WiedenheftLab is now online in @ScienceMagazine!
#ScienceResearch
https://t.co/L5qKw1tYrl
Finally! Our paper showing that dCas13 is a great tool for gene knockdown with high selectivity via translational repression is out on @NatureComms! Congrats, @anto_apos and the team (@IwasakiLabRIKEN, @YoshihoIkeuchi lab, Tsuiji lab in Aichi Gakuin U)!
https://t.co/6ETCwqQAOD