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  1. ...nucleotide. Cell 133: 116–127. Mitrovich QM, Tuch BB, Guthrie C, Johnson AD. 2007. Computational and experimental approaches double the number of known introns in the pathogenic yeast Candida albicans. Genome Res 17: 492–502. Mortazavi A, Williams BA, McCue K, Schaeffer L, Wold B. 2008. Mapping...
  2. ...additional Lachancea species. With 10 fully sequenced, assembled, and annotated s, the Lachancea clade is themost densely sampled yeast genus at the genomic level within the Saccharomycetaceae family. Second, we developed a new computational method called AnChro, to reconstruct ancestral organization...
  3. ...of Otago, Dunedin, New Zealand Abstract The ALS (agglutinin-like sequence) gene family encodes proteins that play a role in adherence of the yeast Candida albicans to endothelial and epithelial cells. The proteins are proposed as virulence factors for this important fungal pathogen...
  4. ...-rich) region immediately upstream of the TSS, with a peak close to the −8 position, in all scanning-model yeasts except Candida albicans (Fig. 4A; Supplemental Fig. S9). We also detected a similar A-rich region at the same location in S. cerevisiae in all growth conditions examined based on published TSS maps...
  5. ...effective approach—also the most difficult—is large-scale experimental gene disruption. Such screens represent a massive investment of time and resources, and they are not always feasible. For instance, traditional essentiality screens are difficult in Candida albicans because of its partial-diploid nature...
  6. ...subdivision of hemiascomycetes consists of species that translate CTG codons as serine rather than leucine, a reassignment believed to have occurred more than 170 million years ago (Miranda et al. 2006). This subdivision has been intensely studied because it contains the pathogenic yeastCandida albicans...
  7. ...for scarcer POL translation (Clare et al. 1988; Jacks et al. 1988). Alternatively, the s of the Candida albicans Ty1/Copia element, Tca2, and of Moloney murine leukaemia retrovirus (MLV) encode for a stop codon betweenGAG and POL (Yoshinaka et al. 1985; Matthews et al. 1997), and POL suboptimal translation...
  8. ...costs associated with resistance mutations could be compensated and greater phenotypic plasticity could be acquired. [Supplemental material is available for this article.] Genome variation in the eukaryotic pathogen Plasmodium falciparum underpins both fundamental biology, such as the ability...
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