Searching journal content for articles similar to Malko et al. 16 (4): 505.

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  1. ...to accurately predict if an exon is constitutively or alternatively spliced? In this study, we explore evolutionary changes in exon–intron architecture, and examine their influence on alternative splicing. We analyze 17 vertebrate species, employing a -wide, comparative genomic approach. We reconstruct...
  2. ...phenotypes between these two species, such as functional enhancer conservation (46%) (Arnold et al. 2014) and CTCF binding sites (30%) (Ni et al. 2012), but lower than others, such as BEAF-32 (>70%) (Yang et al. 2012) and alternative splicing (∼80%) (Malko 2006).View this table: In this window In a new...
  3. ...), including skipped exon (SE), retained intron (RI), mutually exclusive exons (MX), alternative 5′ (A5), and 3′ (A3) splice sites. Isoform diversity can also be expanded via the inclusion of alternative transcription start sites (TSSs) or transcript end sites (TESs), resulting in differences...
  4. ..., and directed experimental evidence. We report an expanded set of 283 readthrough candidates, including 16 double-readthrough candidates; these were manually curated to rule out alternatives such as A-to-I editing, alternative splicing, dicistronic translation, and selenocysteine incorporation. We report...
  5. ...structure and alternative splicing in fruit flies and malarial mosquito s. Genome Res 16: 505–509. Modrek B, Lee CJ. 2003. Alternative splicing in the human, mouse and rat s is associated with an increased frequency of exon creation and/or loss. Nat Genet 34: 177–180. Mularoni L, Veitia RA, Alba MM. 2007...
  6. ..., was extracted from GenBank. In each case, an alternative splice form that would generate an OBP-like protein was found using FGENESH ( http://genomic.sanger.ac.uk/gf/gf.html ) or Splice Site Prediction by Neural Network ( http://www.fruitfly.org/seq_tools/splice.html ). The 31 OBP-like protein sequences were...
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