Searching journal content for articles similar to Dahary et al. 15 (3): 364.

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  1. ...lymphoblastoid cell lines revealed that the majority of expressed sense–antisense genes exhibited alternative splicing events that were correlated to the expression of the antisense gene. Most of these events occurred in areas of sense–antisense (SAS) gene overlap, which were significantly enriched in both exons...
  2. ...( Kapranov et al. 2005 ), including transcripts generated from many so-called overlapping genes and anti-sense genes ( Kiyosawa et al. 2003 ; Imanishi et al. 2004 ; Dahary et al. 2005 ). Newly identified additional PAPs (and thus first exons) have expanded the transcript regions (from TSSs to transcript...
  3. ...compared Tag-seq data to LongSAGE data and observed improved representation of several classes of rare transcripts, including transcription factors, antisense transcripts, and intronic sequences, the latter possibly representing novel exons or genes. We observed increases in the diversity, abundance...
  4. ...transcript through what appears to be a mechanism of transcription interference. Diploid cells with IME4 antisense transcription have reduced sense transcripts and do not enter meiosis. Furthermore, human diseases ranging from breast cancer and lymphoma to thalassemia have been linked to naturally occurring...
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  5. ...overlap in their 3′ UTRs ( Shendure and Church 2002 ; Yelin et al. 2003 ) and in light of accumulating evidence for the importance of antisense transcription in various kinds of transcriptional and post-transcriptional regulation ( Lavorgna et al. 2004 ; Dahary et al. 2005 ). However, we have not observed...
  6. ...aligned to the , containing at least one RNA sequence. We next searched for clusters reporting on fusion between two genes. To avoid cases in which such clusters are caused by natural antisense overlaps, we used the “Antisensor” algorithm ( Yelin et al. 2003 ) to identify and separate such clusters...
  7. ...conserved phylogenetically, while others are recurrently involved in chromosomal rearrangement, resulting in breakpoint reuse. Both gene order conservation and breakpoint reuse can result from the existence of functional constraints on where chromosomal breakpoints occur or from the existence of regions...
  8. ...in testes may have biological implications, and this observation is in accordance with previous reports ( Kleene et al. 1998 ; Reymond et al. 2002 ; Marques et al. 2005 ) and especially a recent finding that transcription of human retrocopies mainly (and/or initially) occurs in testes ( Vinckenbosch et al...
  9. ...investment required, suffers from the problem that not all proteins can be easily expressed and purified. An alternative method would be to randomly fragment DNA enriched in coding sequences, and to rely on the variable expression of different polypeptides to provide overlapping fragmented representation...
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