Ronen Shemesh

TL;DR: A computational search for ADAR editing sites in the human transcriptome is described, using millions of available expressed sequences and indicates the role of editing in controlling dsRNA stability.

TL;DR: Polypeptide sequences and polynucleotide sequences are provided in this paper, along with annotative information concerning such sequences and uses for these sequences and their sequences are annotated.

TL;DR: It is demonstrated that at least half of these fusions exist in human tissues, and it is shown that unique splicing patterns dominate the functional and regulatory nature of the resulting transcripts, and found intergenic distance bias in fused compared with nonfused genes.

TL;DR: In this paper, the authors identified and experimentally verified four additional human substrates for ADAR-mediated editing: FLNA, BLCAP, CYFIP2 and IGFBP7.

TL;DR: Four additional candidate human substrates for ADAR-mediated editing are identified and experimentally verified: FLNA, BLCAP, CYFIP2 and IGFBP7, none of these substrates encodes a receptor protein but two of them are strongly expressed in the CNS and seem important for proper nervous system function.