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  1. ...of 22 RNA editing in gut-brain interactions remains unexplored. Comparative transcriptomic 23 analyses were performed between heads of germ-free (GF) versus conventional (CV) 24 honey bees. A total of 1,528 A-to-I editing sites are identified in honey bee heads, among 25 which nonsynonymous editing...
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  2. ...the RNA products and the corresponding genomic sequences. A-to-I editing is also known as A-to-G editing because inosine is subsequently recognized as guanosine (G) by the cellular translation machinery. Since nonsynonymous A-to-G RNA editing events can result in amino acid changes at the RNA level (even...
  3. ...authors: Michael.Jantsch@meduniwien.ac.at, Konstantin.Licht@meduniwien.ac.atAbstractPre-mRNA-splicing and adenosine to inosine (A-to-I) RNA-editing occur mostly cotranscriptionally. During A-to-I editing, a genomically encoded adenosine is deaminated to inosine by adenosine deaminases acting on RNA (ADARs...
  4. ...from miRNA sequencing data of The Cancer Genome Atlas and identified 19 adenosine-to-inosine (A-to-I) RNA editing hotspots. We independently validated 15 of them by perturbation experiments in several cancer cell lines. These miRNA editing events show extensive correlations with key clinical variables...
  5. ...in the noncoding regions. By RNA-seq analyses, a large number of A-to-I RNA editing events have been identified in the transcriptomes of humans (Li et al. 2009; Bahn et al. 2012; Peng et al. 2012; Ramaswami et al. 2013; Sakurai et al. 2014) and other animals (Danecek et al. 2012; St Laurent et al. 2013; Chen et al...
  6. ...RNA modification types, such as m6A, yield relatively modest basecalling “error” signatures (Begik et al. 2021), leading to a relatively high number of false positives and false negatives when predicting them in a transcriptome-wide fashion (Liu et al. 2019).Basecalling “errors” in nanopore sequencing...
  7. ...-to-Gmismatches generated by inevitablemapping errors, unidentified SNPs, and sequencing noise. Combined with the sites identified by the conventional ICE method, we report here the identification of 19,791 novel editing sites in the human transcriptome and 1258 mRNAs in which A-to-I editing had not previously been...
  8. ...and Kawahara 2021). Notably, Z-RNA structures influence the adenine-to-inosine (A-to-I) editing ability of ADAR with downstream effects on autoimmune diseases and encephalopathy (Koeris et al. 2005; de Reuver et al. 2021; Nakahama et al. 2021; Tang et al. 2021; Zillinger and Bartok 2021; Jiao et al. 2022...
  9. ...) RNA editing and its impact on alternative splicing. We observed that >95% A-to-I RNA editing events occurred in the chromatin-associated RNA prior to polyadenylation. We report about 500 editing sites in the 3′ acceptor sequences that can alter splicing of the associated exons. These exons are highly...
  10. ...content. Adenosine-to-inosine (A-to-I) RNA editing by ADAR proteins converts a genomically encoded adenosine into inosine. It is known that most RNA editing in human takes place in the primate-specific Alu sequences, but the extent of this phenomenon and its effect on transcriptome diversity are not yet...
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