| scholarly article | Q13442814 |
| P50 | author | Lindell Bromham | Q55499685 |
| P2093 | author name string | Lindell Bromham | |
| Xia Hua | |||
| P2860 | cites work | A unified treatment of the probability of fixation when population size and the strength of selection change over time | Q38517913 |
| Antimutator alleles of yeast DNA polymerase gamma modulate the balance between DNA synthesis and excision | Q21134954 | ||
| Mitochondrial DNA, chloroplast DNA and the origins of development in eukaryotic organisms | Q21203765 | ||
| Rates of molecular evolution and diversification in plants: chloroplast substitution rates correlate with species-richness in the Proteaceae | Q21284004 | ||
| Gene Transposition as a Cause of Hybrid Sterility in Drosophila | Q22065882 | ||
| What Is Speciation and How Should We Study It? | Q22066134 | ||
| The frequency of polyploid speciation in vascular plants | Q22066293 | ||
| Natural selection in action during speciation | Q22066356 | ||
| The distribution of fitness effects of new mutations | Q22122013 | ||
| Rates of spontaneous mutation | Q24548000 | ||
| Evolution of the mutation rate | Q24602069 | ||
| Viral mutation rates | Q24611162 | ||
| Rate of de novo mutations and the importance of father's age to disease risk | Q24632353 | ||
| Evolution of mutation rates: phylogenomic analysis of the photolyase/cryptochrome family | Q24642537 | ||
| Radioresistance of Deinococcus radiodurans: functions necessary to survive ionizing radiation are also necessary to survive prolonged desiccation | Q24684819 | ||
| Hybridization and extinction | Q26741109 | ||
| Antimutator variants of DNA polymerases | Q27024636 | ||
| Mitochondrial inverted repeats strongly correlate with lifespan: mtDNA inversions and aging | Q27307958 | ||
| Evolution of mutation rates in bacteria | Q28238561 | ||
| Selforganization of matter and the evolution of biological macromolecules | Q28248277 | ||
| DNA polymerase proofreading: Multiple roles maintain genome stability | Q28249404 | ||
| Relaxation of selective constraint on dog mitochondrial DNA following domestication | Q28249433 | ||
| A constant rate of spontaneous mutation in DNA-based microbes | Q28271032 | ||
| The mismatch repair system (mutS, mutL and uvrD genes) in Pseudomonas aeruginosa: molecular characterization of naturally occurring mutants | Q28492576 | ||
| The large genome constraint hypothesis: evolution, ecology and phenotype | Q28651140 | ||
| Reconstructing the phylogenetic history of long-term effective population size and life-history traits using patterns of amino acid replacement in mitochondrial genomes of mammals and birds | Q28690633 | ||
| Molecular evolution and the latitudinal biodiversity gradient | Q28703531 | ||
| The genome as a life-history character: why rate of molecular evolution varies between mammal species | Q28742524 | ||
| Evolutionary rates of mitochondrial genomes correspond to diversification rates and to contemporary species richness in birds and reptiles | Q28748347 | ||
| Molecular evolutionary rates predict both extinction and speciation in temperate angiosperm lineages | Q28750418 | ||
| Effects of metabolic rate on protein evolution | Q28754488 | ||
| Correlates of substitution rate variation in mammalian protein-coding sequences | Q28755166 | ||
| Accumulation of slightly deleterious mutations in mitochondrial protein-coding genes of large versus small mammals | Q28757218 | ||
| Environmental energy and evolutionary rates in flowering plants | Q28765415 | ||
| Latitude and rates of diversification in birds and butterflies | Q28765975 | ||
| Species richness among birds: body size, life history, sexual selection or ecology? | Q28765995 | ||
| Frequency-dependent selection and the evolution of assortative mating | Q29463194 | ||
| Adaptation from standing genetic variation | Q29614722 | ||
| Mitochondrial DNA mutations, oxidative stress, and apoptosis in mammalian aging | Q29616056 | ||
| DO VARIATIONS IN SUBSTITUTION RATES AND MALE MUTATION BIAS CORRELATE WITH LIFE-HISTORY TRAITS? A STUDY OF 32 MAMMALIAN GENOMES | Q30049175 | ||
| Efficiency of Base Excision Repair of Oxidative DNA Damage and Its Impact on the Risk of Colorectal Cancer in the Polish Population | Q30396620 | ||
| Accumulating Dobzhansky-Muller incompatibilities: reconciling theory and data | Q30946080 | ||
| Geographic range size, life history and rates of diversification in Australian mammals | Q31028235 | ||
| Correlates of species richness in mammals: body size, life history, and ecology | Q31156969 | ||
| Increased transmission of mutations by low-condition females: evidence for condition-dependent DNA repair | Q33319616 | ||
| Speciation through sensory drive in cichlid fish. | Q33373657 | ||
| Slower tempo of microevolution in island birds: implications for conservation biology | Q33453868 | ||
| Standing variation and new mutations both contribute to a fast response to selection for flowering time in maize inbreds. | Q33521759 | ||
| Mutation rate is linked to diversification in birds | Q33741325 | ||
| Standing genetic variation in contingency loci drives the rapid adaptation of Campylobacter jejuni to a novel host | Q33808990 | ||
| The evolution of mutation rates: separating causes from consequences | Q33925698 | ||
| The population genetics of speciation: the evolution of hybrid incompatibilities | Q33964957 | ||
| Studies on Hybrid Sterility. II. Localization of Sterility Factors in Drosophila Pseudoobscura Hybrids | Q33972480 | ||
| Mutator suppression and escape from replication error-induced extinction in yeast | Q34055320 | ||
| Limits to natural selection | Q34085649 | ||
| Ring species as bridges between microevolution and speciation | Q34113581 | ||
| The mitochondrial theory of aging and its relationship to reactive oxygen species damage and somatic mtDNA mutations | Q34245297 | ||
| Adaptive evolution: evaluating empirical support for theoretical predictions | Q34312048 | ||
| Nonhuman genetics. Strong male bias drives germline mutation in chimpanzees | Q34424599 | ||
| Evolution of high mutation rates in experimental populations of E. coli | Q34429727 | ||
| High frequency of hypermutable Pseudomonas aeruginosa in cystic fibrosis lung infection. | Q34508854 | ||
| Antimutator mutants in bacteriophage T4 and Escherichia coli | Q34603796 | ||
| Life History Traits, Protein Evolution, and the Nearly Neutral Theory in Amniotes | Q38899662 | ||
| Longevity Is Linked to Mitochondrial Mutation Rates in Rockfish: A Test Using Poisson Regression | Q40864140 | ||
| Gene Expression Evolves under a House-of-Cards Model of Stabilizing Selection. | Q41030787 | ||
| Relative rates of nucleotide substitution at the rbcL locus of monocotyledonous plants | Q41097072 | ||
| Exploring the Relationships between Mutation Rates, Life History, Genome Size, Environment, and Species Richness in Flowering Plants | Q41157013 | ||
| Heritable genetic variation via mutation-selection balance: Lerch's zeta meets the abdominal bristle | Q41596066 | ||
| Reproductive isolation caused by colour pattern mimicry | Q42054153 | ||
| Gain of deleterious function causes an autoimmune response and Bateson-Dobzhansky-Muller incompatibility in rice | Q43169538 | ||
| Chromosomal evidence of incipient speciation in the Afrotropical malaria mosquito Anopheles funestus | Q43933378 | ||
| Interaction between selection and biased gene conversion in mammalian protein-coding sequence evolution revealed by a phylogenetic covariance analysis | Q44396836 | ||
| Genomic evidence for large, long-lived ancestors to placental mammals | Q44542979 | ||
| Divergent evolution of duplicate genes leads to genetic incompatibilities within A. thaliana | Q44749998 | ||
| Error thresholds and the constraints to RNA virus evolution | Q44997148 | ||
| Mitochondrial DNA as a tool for reconstructing past life-history traits in mammals | Q45369038 | ||
| Percolation on the fitness hypercube and the evolution of reproductive isolation | Q46236098 | ||
| Divergence in DNA photorepair efficiency among genotypes from contrasting UV radiation environments in nature. | Q46642412 | ||
| Joint reconstruction of divergence times and life-history evolution in placental mammals using a phylogenetic covariance model | Q47198891 | ||
| Are radical and conservative substitution rates useful statistics in molecular evolution? | Q47281908 | ||
| Strong variations of mitochondrial mutation rate across mammals--the longevity hypothesis | Q47285264 | ||
| Species richness in agamid lizards: chance, body size, sexual selection or ecology? | Q47436466 | ||
| Determinants of rate variation in mammalian DNA sequence evolution | Q48057174 | ||
| Testing for "snowballing" hybrid incompatibilities in Solanum: impact of ancestral polymorphism and divergence estimates. | Q48113622 | ||
| Ecology predicts large-scale patterns of phylogenetic diversification in birds. | Q50786137 | ||
| Separate sexes and the mitochondrial theory of ageing. | Q51016046 | ||
| Testing the metabolic theory of ecology: allometric scaling exponents in mammals. | Q51186337 | ||
| A trade-off between oxidative stress resistance and DNA repair plays a role in the evolution of elevated mutation rates in bacteria. | Q51489925 | ||
| Domestication relaxed selective constraints on the yak mitochondrial genome. | Q51612400 | ||
| A Test of the Snowball Theory for the Rate of Evolution of Hybrid Incompatibilities | Q51619902 | ||
| A generation time effect on the rate of molecular evolution in invertebrates. | Q51639783 | ||
| Inverse relationship between longevity and evolutionary rate of mitochondrial proteins in mammals and birds. | Q51855791 | ||
| Large punctuational contribution of speciation to evolutionary divergence at the molecular level. | Q51931944 | ||
| Generation time, life history and the substitution rate of neutral mutations. | Q34669070 | ||
| Kr/Kc but not dN/dS correlates positively with body mass in birds, raising implications for inferring lineage-specific selection | Q34686560 | ||
| Amplification of DNA from preserved specimens shows blowflies were preadapted for the rapid evolution of insecticide resistance. | Q34695409 | ||
| Oxidative damage to DNA related to survivorship and carotenoid-based sexual ornamentation in the common yellowthroat | Q34992147 | ||
| Biochemical characterization of RecA variants that contribute to extreme resistance to ionizing radiation. | Q35019564 | ||
| Challenges and complexities in estimating both the functional impact and the disease risk associated with the extensive genetic variation in human DNA repair genes | Q35114513 | ||
| Adaptive divergence in the monkey flower Mimulus guttatus is maintained by a chromosomal inversion | Q35603045 | ||
| Cancer and neurologic degeneration in xeroderma pigmentosum: long term follow-up characterises the role of DNA repair. | Q35605167 | ||
| Mitochondria: are they the seat of senescence? | Q35668395 | ||
| How closely does genetic diversity in finite populations conform to predictions of neutral theory? Large deficits in regions of low recombination | Q35765322 | ||
| The Adaptive Significance of Natural Genetic Variation in the DNA Damage Response of Drosophila melanogaster | Q35947736 | ||
| Metabolic rate does not calibrate the molecular clock | Q36024200 | ||
| The Pace of Hybrid Incompatibility Evolution in House Mice. | Q36050102 | ||
| Molecular Evolutionary Consequences of Island Colonization | Q36064489 | ||
| Genome analyses substantiate male mutation bias in many species | Q36144620 | ||
| Life-history traits drive the evolutionary rates of mammalian coding and noncoding genomic elements | Q36300009 | ||
| Extraordinary genome stability in the ciliate Paramecium tetraurelia | Q36437010 | ||
| Mutation rate variation in multicellular eukaryotes: causes and consequences | Q36885382 | ||
| The microbiology of mutability | Q36917147 | ||
| Linking global patterns in biodiversity to evolutionary dynamics using metabolic theory | Q36933530 | ||
| Energy, ageing, fidelity and sex: oocyte mitochondrial DNA as a protected genetic template | Q36937111 | ||
| Review. The strength and genetic basis of reproductive isolating barriers in flowering plants | Q37024107 | ||
| Mitochondrial whims: metabolic rate, longevity and the rate of molecular evolution | Q37186291 | ||
| Why do species vary in their rate of molecular evolution? | Q37186348 | ||
| The evolution of hybrid incompatibilities along a phylogeny. | Q37241461 | ||
| Spontaneous mutational and standing genetic (co)variation at dinucleotide microsatellites in Caenorhabditis briggsae and Caenorhabditis elegans | Q37398959 | ||
| The molecular evolutionary basis of species formation | Q37669190 | ||
| Somatic mitochondrial DNA mutations in mammalian aging | Q37720726 | ||
| Hybrid incompatibility genes: remnants of a genomic battlefield? | Q37771756 | ||
| Bacterial hypermutation in cystic fibrosis, not only for antibiotic resistance | Q37794342 | ||
| Magic traits in speciation: 'magic' but not rare? | Q37877005 | ||
| Variation in the mutation rate across mammalian genomes | Q37942062 | ||
| Divergence hitchhiking and the spread of genomic isolation during ecological speciation-with-gene-flow | Q37971462 | ||
| Testing the metabolic theory of ecology | Q38038914 | ||
| Is metabolic rate a universal 'pacemaker' for biological processes? | Q38215131 | ||
| NATURAL SELECTION AND RANDOM GENETIC DRIFT IN PHENOTYPIC EVOLUTION. | Q38400597 | ||
| Evolution and speciation on holey adaptive landscapes. | Q52257646 | ||
| Reproductive isolation between divergent races of pea aphids on two hosts. II. Selection against migrants and hybrids in the parental environments. | Q52584508 | ||
| Comment on "A test of the snowball theory for the rate of evolution of hybrid incompatibilities". | Q52727585 | ||
| Elevated rates of nonsynonymous substitution in island birds. | Q52930817 | ||
| Life history and the male mutation bias. | Q52957068 | ||
| Role of mutator alleles in adaptive evolution. | Q54564129 | ||
| Elevated UV-B radiation reduces genome stability in plants. | Q55034050 | ||
| Life history influences rates of climatic niche evolution in flowering plants. | Q55052250 | ||
| Can reinforcement complete speciation? | Q55055500 | ||
| Mild environmental stress elicits mutations affecting fitness in Chlamydomonas. | Q55691280 | ||
| Contemporary evolution meets conservation biology | Q55870320 | ||
| Mutation Accumulation and the Extinction of Small Populations | Q55967297 | ||
| The Nearly Neutral Theory of Molecular Evolution | Q55968685 | ||
| Latitudinal Gradients in Species Diversity: The Search for the Primary Cause | Q56387730 | ||
| EVOLUTION OF TEMPORAL ISOLATION IN THE WILD: GENETIC DIVERGENCE IN TIMING OF MIGRATION AND BREEDING BY INTRODUCED CHINOOK SALMON POPULATIONS | Q56594945 | ||
| The Role of Reinforcement in Speciation: Theory and Data | Q56689884 | ||
| Evolution and Ecology of Species Range Limits | Q56772618 | ||
| Extremophilic Acinetobacter Strains from High-Altitude Lakes in Argentinean Puna: Remarkable UV-B Resistance and Efficient DNA Damage Repair | Q56918859 | ||
| Costs and Benefits of High Mutation Rates: Adaptive Evolution of Bacteria in the Mouse Gut | Q56944626 | ||
| Inclusion of a near-complete fossil record reveals speciation-related molecular evolution | Q57006653 | ||
| Body size does not predict species richness among the metazoan phyla | Q57006967 | ||
| EVOLUTIONARY RATES AND SPECIES DIVERSITY IN FLOWERING PLANTS | Q57069444 | ||
| On the Origin of Species by Means of Natural Selection, or the Preservation of Favoured Races in the Struggle for Life | Q58704769 | ||
| Rate and Pattern of Mutation at Microsatellite Loci in Maize | Q59388952 | ||
| Host-parasite arms race in mutation modifications: indefinite escalation despite a heavy load? | Q71932257 | ||
| Rates of conservative and radical nonsynonymous nucleotide substitutions in mammalian nuclear genes | Q73400097 | ||
| Risk of population extinction from fixation of deleterious and reverse mutations | Q77392703 | ||
| Population size and molecular evolution on islands | Q81278519 | ||
| Population extinction and the genetics of adaptation | Q81709194 | ||
| The evolution of low mutation rates in experimental mutator populations of Saccharomyces cerevisiae | Q84444250 | ||
| An evolutionary comparative scan for longevity-related oxidative stress resistance mechanisms in homeotherms | Q84556747 | ||
| Hybrid Incompatibility “Snowballs” Between Solanum Species | Q85041068 | ||
| Association between genetic variants of DNA repair genes and coronary artery disease | Q86027990 | ||
| PHENOTYPIC EVOLUTION BY NEUTRAL MUTATION | Q88179642 | ||
| A Dynamical Theory of Speciation on Holey Adaptive Landscapes | Q88192097 | ||
| COMPETITION BETWEEN HIGH AND LOW MUTATING STRAINS OF ESCHERICHIA COLI | Q88206326 | ||
| SPECIATION BY POLYPLOIDY IN TREEFROGS: MULTIPLE ORIGINS OF THE TETRAPLOID, HYLA VERSICOLOR | Q88206762 | ||
| P407 | language of work or name | English | Q1860 |
| P304 | page(s) | 12 | |
| P577 | publication date | 2017-02-07 | |
| P1433 | published in | Frontiers in Genetics | Q2499875 |
| P1476 | title | Darwinism for the Genomic Age: Connecting Mutation to Diversification | |
| P478 | volume | 8 |
| Q48323029 | Phylogenetic estimates of diversification rate are affected by molecular rate variation. |
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| Q46179578 | Plant size: a key determinant of diversification? |
| Q49245617 | Protein evolution depends on multiple distinct population size parameters |
| Q92484446 | Sexual selection, body mass and molecular evolution interact to predict diversification in birds |
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