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Radical amino acid mutations persist longer in the absence of sex
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/0471250953.bi0605s00openalex-snapshot
Using MODELTEST and PAUP * to Select a Model of Nucleotide Substitution
inferredcites →https://doi.org/10.1002/9781119078845.ch23openalex-snapshot
Diverse Considerations for Successful Phylogenetic Tree Reconstruction: Impacts from Model Misspecification, Recombination, Homoplasy, and Pattern Recognition
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Mitonuclear coevolution as the genesis of speciation and the mitochondrial DNA barcode gap
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The amino acid sequence of chicken muscle desmin provides a common structural model for intermediate filament proteins.
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LIFE HISTORY VARIATION WITHIN POPULATIONS OF AN ASEXUAL PLANT, ERIGERON ANNUUS (ASTERACEAE)
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Probability Models for DNA Sequence Evolution
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Detecting and Analyzing Genetic Recombination Using RDP4
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Very slightly deleterious mutations and the molecular clock
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Are Radical and Conservative Substitution Rates Useful Statistics in Molecular Evolution?
inferredcites →https://doi.org/10.1007/s002390010066openalex-snapshot
Comparative Genomics of Mitochondrial DNA in Members of the Drosophila melanogaster Subgroup
inferredcites →https://doi.org/10.1007/s002399910007openalex-snapshot
Rates of Conservative and Radical Nonsynonymous Nucleotide Substitutions in Mammalian Nuclear Genes
inferredcites →https://doi.org/10.1007/s00497-012-0181-8openalex-snapshot
Differential effects of polyploidy and diploidy on fitness of apomictic Boechera
inferredcites →https://doi.org/10.1007/s10038-008-0260-8openalex-snapshot
Prediction of functional nonsynonymous single nucleotide polymorphisms in human G-protein-coupled receptors
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How different amino acid sequences determine similar protein structures: The structure and evolutionary dynamics of the globins
inferredcites →https://doi.org/10.1016/0022-2836(87)90521-3openalex-snapshot
Determinants of a protein fold
inferredcites →https://doi.org/10.1016/0022-2836(92)90934-copenalex-snapshot
Membrane protein structure prediction
inferredcites →https://doi.org/10.1016/0040-5809(75)90020-9openalex-snapshot
On the number of segregating sites in genetical models without recombination
inferredcites →https://doi.org/10.1016/0169-5347(92)90051-copenalex-snapshot
Population genetics and ecology of Artemia: Insights into parthenogenetic reproduction
inferredcites →https://doi.org/10.1016/j.tig.2004.11.015openalex-snapshot
Genetic instability of C. elegans comes naturally
inferredcites →https://doi.org/10.1016/j.tig.2007.03.008openalex-snapshot
Positive and negative selection on the mitochondrial genome
inferredcites →https://doi.org/10.1016/j.tig.2008.10.009openalex-snapshot
The effects of deleterious mutations on evolution in non-recombining genomes
inferredcites →https://doi.org/10.1016/j.tree.2004.10.003openalex-snapshot
Cytonuclear coevolution: the genomics of cooperation
inferredcites →https://doi.org/10.1016/j.tree.2008.05.011openalex-snapshot
Evolutionary implications of non-neutral mitochondrial genetic variation
inferredcites →https://doi.org/10.1016/j.tree.2015.11.012openalex-snapshot
Sex, Mitochondria, and Genetic Rescue
inferredcites →https://doi.org/10.1016/s0022-2836(65)80134-6openalex-snapshot
Structure and function of haemoglobin
inferredcites →https://doi.org/10.1016/s0168-9525(01)02338-1openalex-snapshot
Natural selection and the evolution of mtDNA-encoded peptides: evidence for intergenomic co-adaptation
inferredcites →https://doi.org/10.1016/s0169-5347(03)00125-3openalex-snapshot
Animal mitochondrial DNA recombination revisited
inferredcites →https://doi.org/10.1016/s0959-437x(00)00254-9openalex-snapshot
Breeding systems and genome evolution
inferredcites →https://doi.org/10.1017/cbo9780511819049.010openalex-snapshot
Phylogeny inference based on parsimony and other methods using PAUP
inferredcites →https://doi.org/10.1017/s0016672300010156openalex-snapshot
The effect of linkage on limits to artificial selection
inferredcites →https://doi.org/10.1017/s0016672300014634openalex-snapshot
The hitch-hiking effect of a favourable gene
inferredcites →https://doi.org/10.1017/s0016672307008920openalex-snapshot
Effective population size and tests of neutrality at cytoplasmic genes inArabidopsis
inferredcites →https://doi.org/10.1038/328519a0openalex-snapshot
Evidence from a New Zealand snail for the maintenance of sex by parasitism
inferredcites →https://doi.org/10.1038/341660a0openalex-snapshot
RNA editing in wheat mitochondria results in the conservation of protein sequences
inferredcites →https://doi.org/10.1038/351652a0openalex-snapshot
Adaptive protein evolution at the Adh locus in Drosophila
inferredcites →https://doi.org/10.1038/hdy.2012.13openalex-snapshot
Male offspring production by asexual Potamopyrgus antipodarum, a New Zealand snail
inferredcites →https://doi.org/10.1038/ismej.2017.69openalex-snapshot
Experimental evolution and the dynamics of adaptation and genome evolution in microbial populations
inferredcites →https://doi.org/10.1038/nature04195openalex-snapshot
The importance of sequence diversity in the aggregation and evolution of proteins
inferredcites →https://doi.org/10.1038/nmeth.2109openalex-snapshot
jModelTest 2: more models, new heuristics and parallel computing
inferredcites →https://doi.org/10.1038/nrg2146openalex-snapshot
The distribution of fitness effects of new mutations
inferredcites →https://doi.org/10.1038/sj.hdy.6800772openalex-snapshot
The conversion of variance and the evolutionary potential of restricted recombination
inferredcites →https://doi.org/10.1073/pnas.76.10.5269openalex-snapshot
Mathematical model for studying genetic variation in terms of restriction endonucleases.
inferredcites →https://doi.org/10.1073/pnas.85.17.6414openalex-snapshot
Effects of linkage on rates of molecular evolution.
inferredcites →https://doi.org/10.1073/pnas.92.22.10432openalex-snapshot
Transfer RNA editing in land snail mitochondria.
inferredcites →https://doi.org/10.1073/pnas.98.1.105openalex-snapshot
An amino acid code for protein folding
inferredcites →https://doi.org/10.1080/00222930050122147openalex-snapshot
Testing for the accumulation of deleterious mutations in asexual eukaryote genomes using molecular sequences
inferredcites →https://doi.org/10.1083/jcb.107.1.89openalex-snapshot
Differential effects of mutations in three domains on folding, quaternary structure, and intracellular transport of vesicular stomatitis virus G protein.
inferredcites →https://doi.org/10.1093/bib/bbn017openalex-snapshot
MEGA: A biologist-centric software for evolutionary analysis of DNA and protein sequences
inferredcites →https://doi.org/10.1093/gbe/evq086openalex-snapshot
Effective Population Size and the Efficacy of Selection on the X Chromosomes of Two Closely Related Drosophila Species
inferredcites →https://doi.org/10.1093/genetics/133.3.693openalex-snapshot
Statistical tests of neutrality of mutations.
inferredcites →https://doi.org/10.1093/genetics/134.4.1289openalex-snapshot
The effect of deleterious mutations on neutral molecular variation.
inferredcites →https://doi.org/10.1093/genetics/136.4.1469openalex-snapshot
Muller's ratchet under epistatic selection.
inferredcites →https://doi.org/10.1093/genetics/156.2.879openalex-snapshot
Consequences of Recombination on Traditional Phylogenetic Analysis
inferredcites →https://doi.org/10.1093/jhered/esx041openalex-snapshot
Genetic Variation for Mitochondrial Function in the New Zealand Freshwater Snail Potamopyrgus antipodarum
inferredcites →https://doi.org/10.1093/molbev/msi084openalex-snapshot
Widespread Recombination in Published Animal mtDNA Sequences1
inferredcites →https://doi.org/10.1093/molbev/msj058openalex-snapshot
Tracing Hybrid Incompatibilities to Single Amino Acid Substitutions
inferredcites →https://doi.org/10.1093/molbev/msn231openalex-snapshot
An Investigation of the Statistical Power of Neutrality Tests Based on Comparative and Population Genetic Data
inferredcites →https://doi.org/10.1093/molbev/msn279openalex-snapshot
Near Neutrality, Rate Heterogeneity, and Linkage Govern Mitochondrial Genome Evolution in Atlantic Cod (Gadus morhua) and Other Gadine Fish
inferredcites →https://doi.org/10.1093/molbev/msp119openalex-snapshot
Estimating the Rate of Adaptive Molecular Evolution in the Presence of Slightly Deleterious Mutations and Population Size Change
inferredcites →https://doi.org/10.1093/molbev/msp300openalex-snapshot
Accelerated Mutation Accumulation in Asexual Lineages of a Freshwater Snail
inferredcites →https://doi.org/10.1093/molbev/msr093openalex-snapshot
Positive and Negative Selection in Murine Ultraconserved Noncoding Elements
inferredcites →https://doi.org/10.1093/molbev/msr211openalex-snapshot
Mitochondrial–Nuclear Interactions and Accelerated Compensatory Evolution: Evidence from the Primate Cytochrome c Oxidase Complex
inferredcites →https://doi.org/10.1093/molbev/msr237openalex-snapshot
Deleterious Mutation Accumulation in Asexual Timema Stick Insects
inferredcites →https://doi.org/10.1093/molbev/mss228openalex-snapshot
Evidence for Compensatory Evolution of Ribosomal Proteins in Response to Rapid Divergence of Mitochondrial rRNA
inferredcites →https://doi.org/10.1093/molbev/mst010openalex-snapshot
MAFFT Multiple Sequence Alignment Software Version 7: Improvements in Performance and Usability
inferredcites →https://doi.org/10.1093/molbev/msu345openalex-snapshot
Recurrent Loss of Sex Is Associated with Accumulation of Deleterious Mutations in Oenothera
inferredcites →https://doi.org/10.1093/molbev/msv206openalex-snapshot
The Roles of Compensatory Evolution and Constraint in Aminoacyl tRNA Synthetase Evolution
inferredcites →https://doi.org/10.1093/nar/22.20.4354openalex-snapshot
Convenient single-step, one tube purification of PCR products for direct sequencing
inferredcites →https://doi.org/10.1093/nar/gkg123openalex-snapshot
MitoDrome: a database of Drosophila melanogaster nuclear genes encoding proteins targeted to the mitochondrion
inferredcites →https://doi.org/10.1093/oxfordjournals.jbchem.a135454openalex-snapshot
The Folding Type of a Protein Is Relevant to the Amino Acid Composition
inferredcites →https://doi.org/10.1093/oxfordjournals.jhered.a111354openalex-snapshot
The Mutational Meltdown in Asexual Populations
inferredcites →https://doi.org/10.1093/oxfordjournals.molbev.a025930openalex-snapshot
The rate heterogeneity of nonsynonymous substitutions in mammalian mitochondrial genes
inferredcites →https://doi.org/10.1093/oxfordjournals.molbev.a040343openalex-snapshot
A new method for estimating synonymous and nonsynonymous rates of nucleotide substitution considering the relative likelihood of nucleotide and codon changes.
inferredcites →https://doi.org/10.1093/sysbio/sys029openalex-snapshot
MrBayes 3.2: Efficient Bayesian Phylogenetic Inference and Model Choice Across a Large Model Space
inferredcites →https://doi.org/10.1098/rspb.2008.1758openalex-snapshot
The causes of mutation accumulation in mitochondrial genomes
inferredcites →https://doi.org/10.1101/gr.1299703openalex-snapshot
Single Nucleotide Variation Analysis in 65 Candidate Genes for CNS Disorders in a Representative Sample of the European Population
inferredcites →https://doi.org/10.1111/evo.12554openalex-snapshot
Fitness decline in spontaneous mutation accumulation lines of Caenorhabditis elegans with varying effective population sizes
inferredcites →https://doi.org/10.1111/evo.12718openalex-snapshot
Gene flow betweenDrosophila yakubaandDrosophila santomeain subunit V of cytochromecoxidase: A potential case of cytonuclear cointrogression
inferredcites →https://doi.org/10.1111/evo.12808openalex-snapshot
Conservative and compensatory evolution in oxidative phosphorylation complexes of angiosperms with highly divergent rates of mitochondrial genome evolution
inferredcites →https://doi.org/10.1111/j.0014-3820.2004.tb01648.xopenalex-snapshot
GEOGRAPHIC DIFFERENCES IN SPECIES BOUNDARIES AMONG MEMBERS OF THE MONTASTRAEA ANNULARIS COMPLEX BASED ON MOLECULAR AND MORPHOLOGICAL MARKERS
inferredcites →https://doi.org/10.1111/j.1365-294x.2004.02292.xopenalex-snapshot
Pleistocene glaciation is implicated in the phylogeographical structure of Potamopyrgus antipodarum, a New Zealand snail
inferredcites →https://doi.org/10.1111/j.1365-294x.2012.05664.xopenalex-snapshot
The biogeography of mitochondrial and nuclear discordance in animals
inferredcites →https://doi.org/10.1111/j.1469-8137.2005.01492.xopenalex-snapshot
Inheritance and recombination of mitochondrial genomes in plants, fungi and animals
inferredcites →https://doi.org/10.1111/j.1558-5646.1993.tb01266.xopenalex-snapshot
MULLER'S RATCHET AND MUTATIONAL MELTDOWNS
inferredcites →https://doi.org/10.1111/j.1558-5646.1998.tb02014.xopenalex-snapshot
INTENSE SELECTION OF MITE CLONES IN A HETEROGENEOUS ENVIRONMENT
inferredcites →https://doi.org/10.1111/j.1558-5646.2010.01077.xopenalex-snapshot
MITOCHONDRIAL-NUCLEAR EPISTASIS AFFECTS FITNESS WITHIN SPECIES BUT DOES NOT CONTRIBUTE TO FIXED INCOMPATIBILITIES BETWEEN SPECIES OF DROSOPHILA
inferredcites →https://doi.org/10.1111/j.1558-5646.2011.01360.xopenalex-snapshot
WIDE VARIATION IN PLOIDY LEVEL AND GENOME SIZE IN A NEW ZEALAND FRESHWATER SNAIL WITH COEXISTING SEXUAL AND ASEXUAL LINEAGES
inferredcites →https://doi.org/10.1111/j.1601-5223.1992.tb00169.xopenalex-snapshot
Genetic variation in coexisting sexual diploid and parthenogenetic triploid forms of Fridericia galba (Enchytraeidae, Oligochaeta) in a heterogeneous environment
inferredcites →https://doi.org/10.1111/mec.12006openalex-snapshot
A disproportionate role for mt DNA in D obzhansky– M uller incompatibilities?
inferredcites →https://doi.org/10.1111/mec.12422openalex-snapshot
Discordance between nuclear and mitochondrial genomes in sexual and asexual lineages of the freshwater snail P otamopyrgus antipodarum
inferredcites →https://doi.org/10.1111/mec.13959openalex-snapshot
The on‐again, off‐again relationship between mitochondrial genomes and species boundaries
inferredcites →https://doi.org/10.1126/science.181.4096.223openalex-snapshot
Principles that Govern the Folding of Protein Chains
inferredcites →https://doi.org/10.1126/science.185.4154.862openalex-snapshot
Amino Acid Difference Formula to Help Explain Protein Evolution
inferredcites →https://doi.org/10.1126/science.3892686openalex-snapshot
Aromatic-Aromatic Interaction: A Mechanism of Protein Structure Stabilization
inferredcites →https://doi.org/10.1201/b17795-7openalex-snapshot
The Influence of Re combination on the Estimation of Selection from Coding Sequence Alignments
inferredcites →https://doi.org/10.1371/journal.pgen.1000083openalex-snapshot
Assessing the Evolutionary Impact of Amino Acid Mutations in the Human Genome
inferredcites →https://doi.org/10.1371/journal.pgen.1006550openalex-snapshot
Mutation Accumulation in an Asexual Relative of Arabidopsis
inferredcites →https://doi.org/10.1371/journal.pone.0085845openalex-snapshot
Response to Phosphorus Limitation Varies among Lake Populations of the Freshwater Snail Potamopyrgus antipodarum
inferredcites →https://doi.org/10.1534/g3.114.016493openalex-snapshot
Similar Efficacies of Selection Shape Mitochondrial and Nuclear Genes in Both Drosophila melanogaster and Homo sapiens
inferredcites →https://doi.org/10.1534/genetics.107.080523openalex-snapshot
Cytonuclear Genic Incompatibilities Cause Increased Mortality in Male F2 Hybrids ofNasonia giraultiandN. vitripennis
inferredcites →https://doi.org/10.1534/genetics.109.109736openalex-snapshot
Coalescent Simulation of Intracodon Recombination
inferredcites →https://doi.org/10.1534/genetics.109.113423openalex-snapshot
The Effect of Recombination on the Reconstruction of Ancestral Sequences
inferredcites →https://doi.org/10.2307/2266021openalex-snapshot
Evidence for a Cost of Sex in the Freshwater Snail Potamopyrgus Antipodarum
inferredcites →https://doi.org/10.2307/4615733openalex-snapshot
A Simple Sequentially Rejective Multiple Test Procedure
inferredcites →https://doi.org/10.5962/bhl.title.27468openalex-snapshot
The genetical theory of natural selection
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.1093/jhered/esx041openalex-snapshot
Genetic Variation for Mitochondrial Function in the New Zealand Freshwater Snail Potamopyrgus antipodarum
inferred← citeshttps://doi.org/10.1111/mec.13959openalex-snapshot
The on‐again, off‐again relationship between mitochondrial genomes and species boundaries
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