sameAs
Reconstructing the early evolution of Fungi using a six-gene phylogenyBiopython: freely available Python tools for computational molecular biology and bioinformaticsThe archaebacterial origin of eukaryotesDistribution and phylogenetic significance of the 71-kb inversion in the plastid genome in Funariidae (Bryophyta)Newly resolved relationships in an early land plant lineage: Bryophyta class Sphagnopsida (peat mosses)Assembling the fungal tree of life: progress, classification, and evolution of subcellular traitsConflicting phylogenies for early land plants are caused by composition biases among synonymous substitutionsThe primary divisions of life: a phylogenomic approach employing composition-heterogeneous methodsComparative analysis of zebrafish bone morphogenetic proteins 2, 4 and 16: molecular and evolutionary perspectives.Molecular Taxonomic Profiling of Bacterial Communities in a Gilthead Seabream (Sparus aurata) HatcheryGlobal patterns in peatmoss biodiversity.First molecular estimate of cyclostome bryozoan phylogeny confirms extensive homoplasy among skeletal characters used in traditional taxonomy.Peatmoss (Sphagnum) diversification associated with Miocene Northern Hemisphere climatic cooling?Analyses of charophyte chloroplast genomes help characterize the ancestral chloroplast genome of land plantsCompositional biases among synonymous substitutions cause conflict between gene and protein trees for plastid origins.An archaeal origin of eukaryotes supports only two primary domains of life.Effects of sample handling and cultivation bias on the specificity of bacterial communities in keratose marine spongesPhylogenetically and spatially close marine sponges harbour divergent bacterial communitiesDiversity of the candidate phylum Poribacteria in the marine sponge Aplysina fulvaExtant diversity of bryophytes emerged from successive post-Mesozoic diversification bursts.Metatranscriptomes reveal functional variation in diatom communities from the Antarctic Peninsula.Organellar phylogenomics of an emerging model system: Sphagnum (peatmoss).Absence of N-terminal acetyltransferase diversification during evolution of eukaryotic organisms.Three geographically separate domestications of Asian rice.Phylogeny and evolution of medical species of Candida and related taxa: a multigenic analysis.Increased diversification rates follow shifts to bisexuality in liverworts.A transcriptome resource for the copepod Calanus glacialis across a range of culture temperatures.Mitochondrial phylogenomics of early land plants: mitigating the effects of saturation, compositional heterogeneity, and codon-usage bias.Evolution of multiple paralogous adenosine kinase genes in the moss genus Hygroamblystegium: phylogenetic implications.Evolutionary conservation of TFIIH subunits: implications for the use of zebrafish as a model to study TFIIH function and regulation.Phylogeny and morphological evolution of the amblystegiaceae (Bryopsida).A 20-state empirical amino-acid substitution model for green plant chloroplasts.Identification of a fish short-chain dehydrogenase/reductase associated with bone metabolism.The Interrelationships of Land Plants and the Nature of the Ancestral Embryophyte.WASABI: an automated sequence processing system for multigene phylogenies.A congruent phylogenomic signal places eukaryotes within the Archaea.Chloroplast Phylogeny of Asplenioid Ferns based on rbcL and trnL-F Spacer Sequences (Polypodiidae, Aspleniaceae) and its Implications for BiogeographyMultilocus genetic analyses provide insight into speciation and hybridization in aquatic grasses, genusRuppiaGeographical range in liverworts: does sex really matter?Nuclear protein phylogenies support the monophyly of the three bryophyte groups (Bryophyta Schimp.)
P50
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P50
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