Searching journal content for articles similar to Sakurai et al. 24 (3): 522.

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  1. ...establish a more 411 comprehensive functional landscape of A-to-I RNA editing in the light of adaptive 412 evolution, and complete the complex connectome of gut-brain interaction. 413 Taken together, using honey bees as a model, we delicately demonstrate the complex 414 and dynamic transcriptomic diversity...
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  2. ...Te-Lun Mai and Trees-Juen Chuang Genomics Research Center, Academia Sinica, Taipei 11529, Taiwan Corresponding author: trees@gate.sinica.edu.twAbstractAdenosine-to-inosine (A-to-I) RNA editing is a very common co-/posttranscriptional modification that can lead to A-to-G changes at the RNA level...
  3. ...different brain tissues. We therefore demonstrate that splicing efficiency is a major factor controlling tissue-specific differences in editing levels.Adenosine to inosine editing (A-to-I editing) deaminates adenosines in double-stranded RNAs leading to nucleotide differences between RNA and DNA (Licht...
  4. ...of individual missense A-to-I RNA editing events in cancer development (Chen et al. 2013; Galeano et al. 2013; Han et al. 2014). More recently, we and other groups have systematically characterized the RNA-editing genomic landscape in various cancer types using mRNA-seq data from The Cancer Genome Atlas (TCGA...
  5. ...-stranded RNA (dsRNA) (Bass 2006). A-to-I RNA editing is widespread, with modifications occurring in more than half of the human transcriptome (Bazak et al. 2014). As inosine (I) and guanosine (G) base pair similarly, RNA editing in coding regions of genes can alter the amino acid sequence of proteins...
  6. ...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...
  7. ...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...
  8. ...Corresponding author: hahundle@indiana.eduAbstractAdenosine (A) to inosine (I) RNA editing contributes to transcript diversity and modulates gene expression in a dynamic, cell type–specific manner. During mammalian brain development, editing of specific adenosines increases, whereas the expression of A-to-I...
  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. ..., Guangzhou 510275, PR China ↵2 Co-first authors, listed alphabetically Corresponding authors: zhangrui3@mail.sysu.edu.cn, gnannan3@mail.sysu.edu.cnAbstractAdenosine-to-inosine (A-to-I) RNA editing regulates miRNA biogenesis and function. To date, fewer than 160 miRNA editing sites have been identified. Here...
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