Searching journal content for articles similar to Hughes and Friedman 13 (5): 794.

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  1. ...; Bochtler and Fernandes 2021). 6mA studies in eukaryotes are complicated by varying abundance and divergent functions across species. In protists, green algae, and basal fungi, 6mA is abundant, enriched at the ApT dinucleotide, and associated with genes, all of which are consistent with its role...
  2. ...that could help detect signals of adaptation in an overall noisy data set. Such models exist, for instance, to detect selective signatures in the evolution of the protein-coding gene (Shapiro and Alm 2008) but, to our knowledge, have not been developed for metabolic networks or presence/absence signatures...
  3. ...in transcription and regulation of gene Figure 2. Median expression levels for single-copy (yellow) and duplicate genes (shades of blue) across all organs in the mouse . Duplicate genes are grouped into age classes. Expression evolution of mammalian duplicate genes Genome Research 1463 www..org expression...
  4. ...) Intron gain/loss rate ratio. Intron evolution in Neurospora Genome Research 103 www..org with the RT-mRNA as an intron loss mechanism for these particular genes. No statistically significant differences were detected in the number of short direct repeats for the lost introns (inferred by the sequence...
  5. ...-alleles at 37°C in vitro for 11 of 11 RH strain pairs. Genes are ordered by decreasing significance of the Y-allele advantage. Error bars, 61 SE. Fraser et al. 1934 Genome Research www..org Prud’homme et al. 2007; Wray 2007; Rebeiz et al. 2009, Manceau et al. 2011). Since unicellular species such as yeast...
  6. ....e., after the divergence from lineage of egg-layingmonotremes), and hence are younger than previously thought (Potrzebowski et al. 2008). Notably, tracing the evolutionary origin of individual X-derived retrogenes also identified striking cases of independent parallel exports of key housekeeping genes...
  7. .... This observation has been confirmed by the lack of a homolog of the S. cerevisiae FOX2 gene (which encodes a multifunctional β-oxidation protein) in the s of either of these two fungi. The lack of β-oxidation has been noted before in the case of E. cuniculi and is not surprising, since this unicellular eukaryote...
  8. .... Abstract Inferring the gene content of ancestral genomes is a fundamental challenge in molecular evolution. Due to the statistical nature of this problem, ancestral genomes inferred by the maximum likelihood (ML) or the maximum-parsimony (MP) methods are prone to considerable error rates. In general...
  9. ...beyond sequence per se, such as gene composition and gene order, have been used to construct “ trees” that, generally, combine the phylogenetic signal with signals reflecting the lifestyles of the compared organisms, for example, parallel gene loss in parasites ( Snel et al. 1999 , 2005 ; Wolf et al...
  10. ...://ncbi.nlm.nih.gov/pub/aravind/expansions , and http://www..org .] The eukaryotic crown group (the unresolved assemblage of lineages in the eukaryotic tree, which includes plants, animals, fungi, and some protists, as opposed to early branching eukaryotes, which are all unicellular protists), although only representing the proverbial tip...
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