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Why should mitochondria define species?

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Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1002/0471250953.bi0123s44openalex-snapshot
mtDNA Variation and Analysis Using Mitomap and Mitomaster
inferredcites →https://doi.org/10.1002/9781118659991openalex-snapshot
The Origins of Modern Humans
inferredcites →https://doi.org/10.1002/ajp.22035openalex-snapshot
Species Concept in Primates
inferredcites →https://doi.org/10.1002/bies.200800139openalex-snapshot
Mitochondrial bioenergetics as a major motive force of speciation
inferredcites →https://doi.org/10.1002/bies.200800190openalex-snapshot
The cytoplasmic structure hypothesis for ribosome assembly, vertical inheritance, and phylogeny
inferredcites →https://doi.org/10.1002/bies.200900162openalex-snapshot
Speciation through cytonuclear incompatibility: Insights from yeast and implications for higher eukaryotes
inferredcites →https://doi.org/10.1002/bies.20745openalex-snapshot
The reality and importance of founder speciation in evolution
inferredcites →https://doi.org/10.1002/ece3.2338openalex-snapshot
Mitonuclear coevolution as the genesis of speciation and the mitochondrial DNA barcode gap
inferredcites →https://doi.org/10.1002/ece3.2394openalex-snapshot
Bridging two scholarly islands enriches both: COI DNA barcodes for species identification versus human mitochondrial variation for the study of migrations and pathologies
inferredcites →https://doi.org/10.1002/ece3.398openalex-snapshot
Deep sympatric mitochondrial divergence without reproductive isolation in the common redstart P hoenicurus phoenicurus
inferredcites →https://doi.org/10.1002/path.4809openalex-snapshot
The genetics and pathology of mitochondrial disease
inferredcites →https://doi.org/10.1002/wrna.1287openalex-snapshot
Controlling translation via modulation of tRNA levels
inferredcites →https://doi.org/10.1006/jtbi.2002.3054openalex-snapshot
Red Queen Dynamics of Protein Translation
inferredcites →https://doi.org/10.1007/978-4-431-68302-5_6openalex-snapshot
Recent Evidence for Evolution of the Genetic Code
inferredcites →https://doi.org/10.1007/bf00123984openalex-snapshot
Fluctuation analysis: the effect of plating efficiency
inferredcites →https://doi.org/10.1007/bf02257369openalex-snapshot
Demographic influences on mitochondrial DNA lineage survivorship in animal populations
inferredcites →https://doi.org/10.1007/s00239-015-9675-yopenalex-snapshot
Effects of Codon Usage on Gene Expression: Empirical Studies on Drosophila
inferredcites →https://doi.org/10.1007/s00239-015-9714-8openalex-snapshot
The Code of Silence: Widespread Associations Between Synonymous Codon Biases and Gene Function
inferredcites →https://doi.org/10.1007/s10592-005-9028-2openalex-snapshot
Geographic variability in mitochondrial introgression among hybridizing populations of Golden-winged (Vermivora chrysoptera) and Blue-winged (V.opinus) Warblers
inferredcites →https://doi.org/10.1007/s12064-010-0089-5openalex-snapshot
Saltational symbiosis
inferredcites →https://doi.org/10.1007/s13752-017-0267-5openalex-snapshot
Base Composition, Speciation, and Why the Mitochondrial Barcode Precisely Classifies
inferredcites →https://doi.org/10.1016/0022-5193(65)90083-4openalex-snapshot
Molecules as documents of evolutionary history
inferredcites →https://doi.org/10.1016/j.ajhg.2016.07.022openalex-snapshot
Are Interactions between cis-Regulatory Variants Evidence for Biological Epistasis or Statistical Artifacts?
inferredcites →https://doi.org/10.1016/j.bbabio.2011.09.018openalex-snapshot
Chemiosmotic coupling in oxidative and photosynthetic phosphorylation
inferredcites →https://doi.org/10.1016/j.biocel.2015.03.011openalex-snapshot
Decoding mechanisms by which silent codon changes influence protein biogenesis and function
inferredcites →https://doi.org/10.1016/j.celrep.2016.06.023openalex-snapshot
Differences in Strength and Timing of the mtDNA Bottleneck between Zebrafish Germline and Non-germline Cells
inferredcites →https://doi.org/10.1016/j.cub.2016.03.071openalex-snapshot
Molecular clocks
inferredcites →https://doi.org/10.1016/j.cub.2016.06.034openalex-snapshot
Plumage Genes and Little Else Distinguish the Genomes of Hybridizing Warblers
inferredcites →https://doi.org/10.1016/j.gene.2005.05.001openalex-snapshot
The mitochondrial genome in human adaptive radiation and disease: On the road to therapeutics and performance enhancement
inferredcites →https://doi.org/10.1016/j.jmb.2014.02.009openalex-snapshot
Mitochondrial DNA Variant in COX1 Subunit Significantly Alters Energy Metabolism of Geographically Divergent Wild Isolates in Caenorhabditis elegans
inferredcites →https://doi.org/10.1016/j.jmb.2015.09.003openalex-snapshot
Overcoming Challenges in Engineering the Genetic Code
inferredcites →https://doi.org/10.1016/j.molcel.2015.05.035openalex-snapshot
Codon Bias as a Means to Fine-Tune Gene Expression
inferredcites →https://doi.org/10.1016/j.tcb.2013.07.003openalex-snapshot
Inheritance of the fittest mitochondria in yeast
inferredcites →https://doi.org/10.1016/s0022-2836(66)80022-0openalex-snapshot
Codon—anticodon pairing: The wobble hypothesis
inferredcites →https://doi.org/10.1016/s0092-8674(03)00510-5openalex-snapshot
Ira Herskowitz (1946–2003)
inferredcites →https://doi.org/10.1017/s0016672300014634openalex-snapshot
The hitch-hiking effect of a favourable gene
inferredcites →https://doi.org/10.1017/s0016672308009579openalex-snapshot
The hitch-hiking effect of a favourable gene
inferredcites →https://doi.org/10.1023/b:bire.0000019187.19019.e6openalex-snapshot
NOBEL LECTURE: Worms, Life and Death
inferredcites →https://doi.org/10.1038/164150a0openalex-snapshot
Origin of Bacterial Variants
inferredcites →https://doi.org/10.1038/267275a0openalex-snapshot
Preponderance of synonymous changes as evidence for the neutral theory of molecular evolution
inferredcites →https://doi.org/10.1038/325031a0openalex-snapshot
Mitochondrial DNA and human evolution
inferredcites →https://doi.org/10.1038/325728a0openalex-snapshot
Coevolution of codon usage and transfer RNA abundance
inferredcites →https://doi.org/10.1038/462272aopenalex-snapshot
Biodiversity: On the origin of bar codes
inferredcites →https://doi.org/10.1038/494035copenalex-snapshot
Species splitting puts conservation at risk
inferredcites →https://doi.org/10.1038/535218aopenalex-snapshot
How China is rewriting the book on human origins
inferredcites →https://doi.org/10.1038/539140aopenalex-snapshot
Scientific language is becoming more informal
inferredcites →https://doi.org/10.1038/hdy.2009.188openalex-snapshot
Swarms of diversity at the gene cox1 in Antarctic krill
inferredcites →https://doi.org/10.1038/nature11433openalex-snapshot
Codon-usage-based inhibition of HIV protein synthesis by human schlafen 11
inferredcites →https://doi.org/10.1038/nature13691openalex-snapshot
Another explanation for apparent epistasis
inferredcites →https://doi.org/10.1038/nature15393openalex-snapshot
A global reference for human genetic variation
inferredcites →https://doi.org/10.1038/nature15394openalex-snapshot
An integrated map of structural variation in 2,504 human genomes
inferredcites →https://doi.org/10.1038/nature18618openalex-snapshot
Mitochondrial and nuclear DNA matching shapes metabolism and healthy ageing
inferredcites →https://doi.org/10.1038/nature18902openalex-snapshot
Mitochondrial DNA in evolution and disease
inferredcites →https://doi.org/10.1038/nature20483openalex-snapshot
Replacing the cell's power plants
inferredcites →https://doi.org/10.1038/nature20592openalex-snapshot
Mitochondrial replacement in human oocytes carrying pathogenic mitochondrial DNA mutations
inferredcites →https://doi.org/10.1038/ncomms10457openalex-snapshot
Novel base-pairing interactions at the tRNA wobble position crucial for accurate reading of the genetic code
inferredcites →https://doi.org/10.1038/s41559-016-0001openalex-snapshot
Tipping points in the dynamics of speciation
inferredcites →https://doi.org/10.1038/srep08297openalex-snapshot
Interbreeding among deeply divergent mitochondrial lineages in the American cockroach (Periplaneta americana)
inferredcites →https://doi.org/10.1038/srep35275openalex-snapshot
Molecular evolution of a widely-adopted taxonomic marker (COI) across the animal tree of life
inferredcites →https://doi.org/10.1046/j.1365-2958.1996.6201335.xopenalex-snapshot
Modulation of lambda integrase synthesis by rare arginine tRNA
inferredcites →https://doi.org/10.1063/1.3050879openalex-snapshot
The Structure of Scientific Revolutions
inferredcites →https://doi.org/10.1073/pnas.072660299openalex-snapshot
Conflicting levels of selection in the accumulation of mitochondrial defects in Saccharomyces cerevisiae
inferredcites →https://doi.org/10.1073/pnas.0803076105openalex-snapshot
Many species in one: DNA barcoding overestimates the number of species when nuclear mitochondrial pseudogenes are coamplified
inferredcites →https://doi.org/10.1073/pnas.1409328111openalex-snapshot
Maternal age effect and severe germ-line bottleneck in the inheritance of human mitochondrial DNA
inferredcites →https://doi.org/10.1073/pnas.1502900112openalex-snapshot
How clonal are Neisseria species? The epidemic clonality model revisited
inferredcites →https://doi.org/10.1073/pnas.1508087112openalex-snapshot
In the light of evolution IX: Clonal reproduction: Alternatives to sex
inferredcites →https://doi.org/10.1073/pnas.1604338113openalex-snapshot
In the light of evolution X: Comparative phylogeography
inferredcites →https://doi.org/10.1073/pnas.1605856113openalex-snapshot
Emergent rules for codon choice elucidated by editing rare arginine codons in Escherichia coli
inferredcites →https://doi.org/10.1073/pnas.1619993114openalex-snapshot
A null model for microbial diversification
inferredcites →https://doi.org/10.1073/pnas.221274498openalex-snapshot
Chromosomal inversions and the reproductive isolation of species
inferredcites →https://doi.org/10.1073/pnas.36.12.708openalex-snapshot
Experiments with the Chemostat on Spontaneous Mutations of Bacteria
inferredcites →https://doi.org/10.1073/pnas.82.15.4905openalex-snapshot
Molecular mechanism of codon recognition by tRNA species with modified uridine in the first position of the anticodon.
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.94.15.7748openalex-snapshot
Phylogenetics and the origin of species
inferredcites →https://doi.org/10.1073/pnas.98.3.944openalex-snapshot
Molecular clocks
inferredcites →https://doi.org/10.1080/10635150600969898openalex-snapshot
DNA Barcoding Will Often Fail to Discover New Animal Species over Broad Parameter Space
inferredcites →https://doi.org/10.1080/10635150701701083openalex-snapshot
Species Concepts and Species Delimitation
inferredcites →https://doi.org/10.1086/668166openalex-snapshot
A Symbiotic View of Life: We Have Never Been Individuals
inferredcites →https://doi.org/10.1093/aibsbulletin/2.2.14-bopenalex-snapshot
Genetics and the Origin of Species
inferredcites →https://doi.org/10.1093/gbe/evr040openalex-snapshot
Evolutionary Patterns of the Mitochondrial Genome in Metazoa: Exploring the Role of Mutation and Selection in Mitochondrial Protein–Coding Genes
inferredcites →https://doi.org/10.1093/gbe/evv226openalex-snapshot
Mitochondrial Involvement in Vertebrate Speciation? The Case of Mito-nuclear Genetic Divergence in Chameleons
inferredcites →https://doi.org/10.1093/genetics/124.1.175openalex-snapshot
Fluctuation analysis: the probability distribution of the number of mutants under different conditions.
inferredcites →https://doi.org/10.1093/genetics/128.4.657openalex-snapshot
Twenty-five years ago in Genetics: electrophoresis in the development of evolutionary genetics: milestone or millstone?
inferredcites →https://doi.org/10.1093/genetics/129.3.897openalex-snapshot
The selection-mutation-drift theory of synonymous codon usage.
inferredcites →https://doi.org/10.1093/genetics/144.1.369openalex-snapshot
Dynamics of Plant Mitochondrial Genome: Model of a Three-Level Selection Process
inferredcites →https://doi.org/10.1093/genetics/144.4.1331openalex-snapshot
D obzhansky , B ateson , and the Genetics of Speciation
inferredcites →https://doi.org/10.1093/genetics/151.4.1621openalex-snapshot
Beneficial Mutations, Hitchhiking and the Evolution of Mutation Rates in Sexual Populations
inferredcites →https://doi.org/10.1093/genetics/170.1.1openalex-snapshot
Bottlenecks, Genetic Polymorphism and SpeciationThis article is dedicated to the memory of Takeo Maruyama.
inferredcites →https://doi.org/10.1093/genetics/28.6.491openalex-snapshot
MUTATIONS OF BACTERIA FROM VIRUS SENSITIVITY TO VIRUS RESISTANCE
inferredcites →https://doi.org/10.1093/genetics/74.3.421openalex-snapshot
ON THE ORIGIN OF MITOCHONDRIAL MUTANTS: EVIDENCE FOR INTRACELLULAR SELECTION OF MITOCHONDRIA IN THE ORIGIN OF ANTIBIOTIC-RESISTANT CELLS IN YEAST
inferredcites →https://doi.org/10.1093/genetics/82.3.547openalex-snapshot
THE EFFECTS OF HITCHHIKING ON A GENE FOR RECOMBINATION
inferredcites →https://doi.org/10.1093/genetics/94.4.1011openalex-snapshot
THE THEORY OF SPECIATION VIA THE FOUNDER PRINCIPLE
inferredcites →https://doi.org/10.1093/hmg/ddw207openalex-snapshot
The Yin and Yang of codon usage
inferredcites →https://doi.org/10.1093/jhered/esv020openalex-snapshot
Problems and Cautions With Sequence Mismatch Analysis and Bayesian Skyline Plots to Infer Historical Demography
inferredcites →https://doi.org/10.1093/molbev/msh031openalex-snapshot
Evolution of Interacting Proteins in the Mitochondrial Electron Transport System in a Marine Copepod
inferredcites →https://doi.org/10.1093/molbev/msn159openalex-snapshot
Rapidly Evolving Mitochondrial Genome and Directional Selection in Mitochondrial Genes in the Parasitic Wasp Nasonia (Hymenoptera: Pteromalidae)
inferredcites →https://doi.org/10.1093/molbev/msu056openalex-snapshot
The Relation between Recombination Rate and Patterns of Molecular Evolution and Variation in Drosophila melanogaster
inferredcites →https://doi.org/10.1093/nar/gks1007openalex-snapshot
MODOMICS: a database of RNA modification pathways—2013 update
inferredcites →https://doi.org/10.1093/nar/gku390openalex-snapshot
A complete landscape of post-transcriptional modifications in mammalian mitochondrial tRNAs
inferredcites →https://doi.org/10.1093/ve/vev005openalex-snapshot
Evolutionary reversion of live viral vaccines: Can genetic engineering subdue it?
inferredcites →https://doi.org/10.1096/fj.15-273714openalex-snapshot
A synonymous codon change alters the drug sensitivity of ΔF508 cystic fibrosis transmembrane conductance regulator
inferredcites →https://doi.org/10.1098/rspb.2002.2218openalex-snapshot
Biological identifications through DNA barcodes
inferredcites →https://doi.org/10.1098/rspb.2016.1735openalex-snapshot
When COI barcodes deceive: complete genomes reveal introgression in hairstreaks
inferredcites →https://doi.org/10.1098/rstb.2003.1397openalex-snapshot
Do species populations really start small? New perspectives from the Late Neogene fossil record of African mammals
inferredcites →https://doi.org/10.1098/rstb.2015.0321openalex-snapshot
From writing to reading the encyclopedia of life
inferredcites →https://doi.org/10.1101/gad.229724.113openalex-snapshot
Hallmarks of a new era in mitochondrial biochemistry
inferredcites →https://doi.org/10.1111/evo.12080openalex-snapshot
GENETIC AND DEVELOPMENTAL BASIS OF F2HYBRID BREAKDOWN INNASONIAPARASITOID WASPS
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.13037openalex-snapshot
“Darwin's corollary” and cytoplasmic incompatibility induced by Cardinium may contribute to speciation in Encarsia wasps (Hymenoptera: Aphelinidae)
inferredcites →https://doi.org/10.1111/j.0014-3820.2002.tb01364.xopenalex-snapshot
DIVERGENCE OF MITOCHONDRIAL DNA IS NOT CORROBORATED BY NUCLEAR DNA, MORPHOLOGY, OR BEHAVIOR IN DROSOPHILA SIMULANS
inferredcites →https://doi.org/10.1111/j.1365-294x.2009.04380.xopenalex-snapshot
Mitochondrial DNA as a marker of molecular diversity: a reappraisal
inferredcites →https://doi.org/10.1111/j.1365-294x.2011.05055.xopenalex-snapshot
Hybrid origin of Audubon’s warbler
inferredcites →https://doi.org/10.1111/j.1558-5646.1995.tb02308.xopenalex-snapshot
INFERRING PHYLOGENIES FROM mt DNA VARIATION: MITOCHONDRIAL-GENE TREES VERSUS NUCLEAR-GENE TREES
inferredcites →https://doi.org/10.1111/j.1558-5646.2007.00239.xopenalex-snapshot
MITOCHONDRIAL INTROGRESSION AND INCOMPLETE LINEAGE SORTING THROUGH SPACE AND TIME: PHYLOGENETICS OF CROTAPHYTID LIZARDS
inferredcites →https://doi.org/10.1111/j.1755-0998.2011.03049.xopenalex-snapshot
Searching for evidence of selection in avian DNA barcodes
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.12678openalex-snapshot
Sequential adaptive introgression of the mitochondrial genome in D rosophila yakubaand D rosophila santomea
inferredcites →https://doi.org/10.1111/mec.12685openalex-snapshot
Pool and conquer: new tricks for (c)old problems
inferredcites →https://doi.org/10.1111/mec.13443openalex-snapshot
Reproductive clonality in protozoan pathogens—truth or artifact? A comment on Ramírez and Llewellyn
inferredcites →https://doi.org/10.1126/science.1088434openalex-snapshot
Effects of Purifying and Adaptive Selection on Regional Variation in Human mtDNA
inferredcites →https://doi.org/10.1126/science.1090727openalex-snapshot
Unifying the Epidemiological and Evolutionary Dynamics of Pathogens
inferredcites →https://doi.org/10.1126/science.1122033openalex-snapshot
Population Size Does Not Influence Mitochondrial Genetic Diversity in Animals
inferredcites →https://doi.org/10.1126/science.1198878openalex-snapshot
Classic Selective Sweeps Were Rare in Recent Human Evolution
inferredcites →https://doi.org/10.1126/science.129.3364.1649openalex-snapshot
Genes and Antibodies
inferredcites →https://doi.org/10.1126/science.133.3449.307openalex-snapshot
Immunological Recognition of Self
inferredcites →https://doi.org/10.1126/science.278.5339.804openalex-snapshot
Y Chromosome Shows That Adam Was an African
inferredcites →https://doi.org/10.1126/science.aag0822openalex-snapshot
Spatiotemporal microbial evolution on antibiotic landscapes
inferredcites →https://doi.org/10.1128/jb.63.3.399-406.1952openalex-snapshot
REPLICA PLATING AND INDIRECT SELECTION OF BACTERIAL MUTANTS
inferredcites →https://doi.org/10.1128/mbio.00981-15openalex-snapshot
Selective Sweeps and Parallel Pathoadaptation Drive Pseudomonas aeruginosa Evolution in the Cystic Fibrosis Lung
inferredcites →https://doi.org/10.1128/mmbr.56.1.229-264.1992openalex-snapshot
Recent evidence for evolution of the genetic code.
inferredcites →https://doi.org/10.1139/g89-009openalex-snapshot
The neutral theory of molecular evolution and the world view of the neutralists
inferredcites →https://doi.org/10.1146/annurev.es.18.110187.002421openalex-snapshot
INTRASPECIFIC PHYLOGEOGRAPHY: The Mitochondrial DNA Bridge Between Population Genetics and Systematics
inferredcites →https://doi.org/10.1146/annurev.genet.39.110304.095751openalex-snapshot
A Mitochondrial Paradigm of Metabolic and Degenerative Diseases, Aging, and Cancer: A Dawn for Evolutionary Medicine
inferredcites →https://doi.org/10.1186/1471-2148-13-83openalex-snapshot
Mitochondrial lineage sorting in action – historical biogeography of the Hyles euphorbiae complex (Sphingidae, Lepidoptera) in Italy
inferredcites →https://doi.org/10.1186/s11658-016-0025-xopenalex-snapshot
Codon bias and the folding dynamics of the cystic fibrosis transmembrane conductance regulator
inferredcites →https://doi.org/10.1186/s12862-014-0262-4openalex-snapshot
Analysis of codon usage bias of mitochondrial genome in Bombyx moriand its relation to evolution
inferredcites →https://doi.org/10.1261/rna.058180.116openalex-snapshot
Codon optimality controls differential mRNA translation during amino acid starvation
inferredcites →https://doi.org/10.1261/rna.731007openalex-snapshot
The wobble hypothesis revisited: Uridine-5-oxyacetic acid is critical for reading of G-ending codons
inferredcites →https://doi.org/10.1371/journal.pbio.0020312openalex-snapshot
Identification of Birds through DNA Barcodes
inferredcites →https://doi.org/10.1371/journal.pgen.1000959openalex-snapshot
All About Mitochondrial Eve: An Interview with Rebecca Cann
inferredcites →https://doi.org/10.1371/journal.pgen.1005920openalex-snapshot
Hybrid Dysgenesis in Drosophila simulans Associated with a Rapid Invasion of the P-Element
inferredcites →https://doi.org/10.1371/journal.pone.0054339openalex-snapshot
Mitochondrial DNA Variants Mediate Energy Production and Expression Levels for CFH, C3 and EFEMP1 Genes: Implications for Age-Related Macular Degeneration
inferredcites →https://doi.org/10.1371/journal.pone.0100755openalex-snapshot
DNA Barcoding Works in Practice but Not in (Neutral) Theory
inferredcites →https://doi.org/10.1371/journal.pone.0103131openalex-snapshot
How Often Do They Have Sex? A Comparative Analysis of the Population Structure of Seven Eukaryotic Microbial Pathogens
inferredcites →https://doi.org/10.1515/9781400858712openalex-snapshot
The Evolution of Individuality
inferredcites →https://doi.org/10.1534/genetics.104.031153openalex-snapshot
Accuracy and Power of Statistical Methods for Detecting Adaptive Evolution in Protein Coding Sequences and for Identifying Positively Selected Sites
inferredcites →https://doi.org/10.1534/genetics.104.91769openalex-snapshot
Mitochondria as Chi
inferredcites →https://doi.org/10.1534/genetics.112.143396openalex-snapshot
Clonal Interference in the Evolution of Influenza
inferredcites →https://doi.org/10.1534/genetics.115.176677openalex-snapshot
Adaptation, Clonal Interference, and Frequency-Dependent Interactions in a Long-Term Evolution Experiment with Escherichia coli
inferredcites →https://doi.org/10.1554/0014-3820(2002)056[0527:domdin]2.0.co;2openalex-snapshot
DIVERGENCE OF MITOCHONDRIAL DNA IS NOT CORROBORATED BY NUCLEAR DNA, MORPHOLOGY, OR BEHAVIOR IN DROSOPHILA SIMULANS
inferredcites →https://doi.org/10.1642/0004-8038(2001)118[0231:avimgo]2.0.co;2openalex-snapshot
Anomalous Variation in Mitochondrial Genomes of White-crowned (Zonotrichia leucophrys) and Golden-crowned (Z. atricapilla) Sparrows: Pseudogenes, Hybridization, or Incomplete Lineage Sorting?
inferredcites →https://doi.org/10.2183/pjab.86.11openalex-snapshot
Unique features of animal mitochondrial translation systems - The non-universal genetic code, unusual features of the translational apparatus and their relevance to human mitochondrial diseases -
inferredcites →https://doi.org/10.2307/j.ctvjsf433openalex-snapshot
The Structure of Evolutionary Theory
inferredcites →https://doi.org/10.3109/19401736.2012.710203openalex-snapshot
Influence of certain forces on evolution of synonymous codon usage bias in certain species of three basal orders of aquatic insects
inferredcites →https://doi.org/10.3389/fgene.2014.00158openalex-snapshot
Transfer RNA and human disease
inferredcites →https://doi.org/10.3390/ijms16034518openalex-snapshot
tRNA Biology in Mitochondria
inferredcites →https://doi.org/10.4161/rna.27361openalex-snapshot
Diversity of human tRNA genes from the 1000-genomes project
inferredcites →https://doi.org/10.5860/choice.39-6411openalex-snapshot
The structure of evolutionary theory
inferredcites →https://doi.org/10.5860/choice.51-6166openalex-snapshot
The Origins of modern humans: biology reconsidered
inferredcites →https://doi.org/10.5962/bhl.title.21095openalex-snapshot
The methods and scope of genetics
inferredcites →https://doi.org/10.7208/chicago/9780226018898.001.0001openalex-snapshot
Relentless Evolution
inferredcites →https://doi.org/10.7554/elife.11473openalex-snapshot
Population genomics reveals the origin and asexual evolution of human infective trypanosomes

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

inferred← citeshttps://doi.org/10.1016/j.tig.2020.03.002openalex-snapshot
Mitonuclear Compensatory Coevolution
inferred← citeshttps://doi.org/10.1111/jav.02822openalex-snapshot
Phylogeography and demographic history of the black kite Milvus migrans , a widespread raptor in Eurasia, Australia and Africa
inferred← citeshttps://doi.org/10.1111/mec.15078openalex-snapshot
Species‐level predation network uncovers high prey specificity in a Neotropical army ant community
inferred← citeshttps://doi.org/10.1134/s2079086419040042openalex-snapshot
Estimates of Genetic Introgression, Gene Tree Reticulation, Taxon Divergence, and Sustainability of DNA Barcoding Based on Genetic Molecular Markers
inferred← citeshttps://doi.org/10.1134/s2079086421010060openalex-snapshot
Philosophy of Evolutionary Biology
inferred← citeshttps://doi.org/10.1139/gen-2020-0192openalex-snapshot
A complement to DNA barcoding reference library for identification of fish from the Northeast Pacific
inferred← citeshttps://doi.org/10.1163/15685381-20191186openalex-snapshot
Mitochondrial lineages or discrete species? Assessing diversity within Timon tangitanus (Lacertidae) using mitochondrial and nuclear DNA sequences
inferred← citeshttps://doi.org/10.1371/journal.pone.0286314openalex-snapshot
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inferred← citeshttps://doi.org/10.26508/lsa.202101307openalex-snapshot
pSATdb: a database of mitochondrial common, polymorphic, and unique microsatellites
inferred← citeshttps://doi.org/10.3389/fevo.2019.00342openalex-snapshot
The Mitochondrial Genome–on Selective Constraints and Signatures at the Organism, Cell, and Single Mitochondrion Levels
inferred← citeshttps://doi.org/10.3389/fevo.2021.565649openalex-snapshot
Is Global Microbial Biodiversity Increasing, Decreasing, or Staying the Same?
inferred← citeshttps://doi.org/10.3390/ani11051473openalex-snapshot
Some Examples of the Use of Molecular Markers for Needs of Basic Biology and Modern Society
inferred← citeshttps://doi.org/10.3390/d14100805openalex-snapshot
The Mitogenome Structure of Righteye Flounders (Pleuronectidae): Molecular Phylogeny and Systematics of the Family in East Asia
inferred← citeshttps://doi.org/10.5944/endoxa.46.2020.28983openalex-snapshot
Adán y Eva. Una antropología darwinista
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