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Mitochondrial genome variation affects the mutation rate of the nuclear genome in Drosophila melanogaster
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/1521-1878(200012)22:12<1057::aid-bies3>3.0.co;2-wopenalex-snapshot
The evolution of mutation rates: separating causes from consequences
inferredcites →https://doi.org/10.1016/0027-5107(72)90090-5openalex-snapshot
Genetic control of mutation induction in Drosophila melanogaster I. Sex-chromosome loss in X-rayed mature sperm
inferredcites →https://doi.org/10.1016/0027-5107(79)90107-6openalex-snapshot
Mutagen-sensitive mutants in Drosophila melanogaster
inferredcites →https://doi.org/10.1016/0027-5107(85)90026-0openalex-snapshot
The relationship between reaction kinetics and mutagenic action of monofunctional alkylating agents in higher eukaryotic systems
inferredcites →https://doi.org/10.1016/j.bbabio.2015.06.001openalex-snapshot
Mitochondrial DNA: Radically free of free-radical driven mutations
inferredcites →https://doi.org/10.1016/j.cell.2005.02.001openalex-snapshot
Mitochondria, Oxidants, and Aging
inferredcites →https://doi.org/10.1016/j.cell.2015.10.001openalex-snapshot
Mitochondrial ROS Signaling in Organismal Homeostasis
inferredcites →https://doi.org/10.1016/j.cub.2011.12.009openalex-snapshot
Semaphorin and Eph Receptor Signaling Guide a Series of Cell Movements for Ventral Enclosure in C. elegans
inferredcites →https://doi.org/10.1016/j.cub.2012.07.018openalex-snapshot
Mitochondria, Maternal Inheritance, and Male Aging
inferredcites →https://doi.org/10.1016/j.cub.2012.12.002openalex-snapshot
In vivo male fertility is affected by naturally occurring mitochondrial haplotypes
inferredcites →https://doi.org/10.1016/j.cub.2015.09.012openalex-snapshot
Single Nucleotides in the mtDNA Sequence Modify Mitochondrial Molecular Function and Are Associated with Sex-Specific Effects on Fertility and Aging
inferredcites →https://doi.org/10.1016/j.tree.2004.02.002openalex-snapshot
Mother's curse: the effect of mtDNA on individual fitness and population viability
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/10.1038/hdy.2011.12openalex-snapshot
Cytoplasmic male sterility in Drosophila melanogaster associated with a mitochondrial CYTB variant
inferredcites →https://doi.org/10.1038/nature18618openalex-snapshot
Mitochondrial and nuclear DNA matching shapes metabolism and healthy ageing
inferredcites →https://doi.org/10.1038/nrg2158openalex-snapshot
Mutation rate variation in multicellular eukaryotes: causes and consequences
inferredcites →https://doi.org/10.1038/nrg3366openalex-snapshot
Y-chromosome evolution: emerging insights into processes of Y-chromosome degeneration
inferredcites →https://doi.org/10.1038/srep30016openalex-snapshot
Mitonuclear interactions, mtDNA-mediated thermal plasticity and implications for the Trojan Female Technique for pest control
inferredcites →https://doi.org/10.1046/j.1420-9101.2002.00464.xopenalex-snapshot
Genetic loads under fitness-dependent mutation rates
inferredcites →https://doi.org/10.1073/pnas.101456898openalex-snapshot
Y chromosome polymorphism is a strong determinant of male fitness in Drosophila melanogaster
inferredcites →https://doi.org/10.1073/pnas.1118918109openalex-snapshot
Evidence for elevated mutation rates in low-quality genotypes
inferredcites →https://doi.org/10.1073/pnas.76.4.1967openalex-snapshot
Rapid evolution of animal mitochondrial DNA.
inferredcites →https://doi.org/10.1086/509046openalex-snapshot
The Sorry State of F2 Hybrids: Consequences of Rapid Mitochondrial DNA Evolution in Allopatric Populations
inferredcites →https://doi.org/10.1093/genetics/148.4.1667openalex-snapshot
Rates of Spontaneous Mutation
inferredcites →https://doi.org/10.1093/molbev/msm248openalex-snapshot
Strong Variations of Mitochondrial Mutation Rate across Mammals--the Longevity Hypothesis
inferredcites →https://doi.org/10.1093/molbev/msw226openalex-snapshot
Direct Determination of the Mutation Rate in the Bumblebee Reveals Evidence for Weak Recombination-Associated Mutation and an Approximate Rate Constancy in Insects
inferredcites →https://doi.org/10.1093/molbev/msw244openalex-snapshot
Population Heterogeneity in Mutation Rate Increases the Frequency of Higher-Order Mutants and Reduces Long-Term Mutational Load
inferredcites →https://doi.org/10.1093/nar/gku1099openalex-snapshot
FlyBase: introduction of the Drosophila melanogaster Release 6 reference genome assembly and large-scale migration of genome annotations
inferredcites →https://doi.org/10.1096/fj.02-0752revopenalex-snapshot
Oxidative DNA damage: mechanisms, mutation, and disease
inferredcites →https://doi.org/10.1098/rspb.2005.3182openalex-snapshot
Assessing putative interlocus sexual conflict in Drosophila melanogaster using experimental evolution
inferredcites →https://doi.org/10.1098/rspb.2012.1874openalex-snapshot
The effect of sexual harassment on lethal mutation rate in femaleDrosophila melanogaster
inferredcites →https://doi.org/10.1098/rspb.2013.1521openalex-snapshot
Elevated oxidative damage is correlated with reduced fitness in interpopulation hybrids of a marine copepod
inferredcites →https://doi.org/10.1098/rstb.2013.0440openalex-snapshot
The costs of being male: are there sex-specific effects of uniparental mitochondrial inheritance?
inferredcites →https://doi.org/10.1098/rstb.2013.0443openalex-snapshot
Mitonuclear interactions: evolutionary consequences over multiple biological scales
inferredcites →https://doi.org/10.1111/eva.12297openalex-snapshot
The T rojan F emale T echnique for pest control: a candidate mitochondrial mutation confers low male fertility across diverse nuclear backgrounds in D rosophila melanogaster
inferredcites →https://doi.org/10.1111/evo.12788openalex-snapshot
Intergenomic interactions between mitochondrial and Y-linked genes shape male mating patterns and fertility inDrosophila melanogaster
inferredcites →https://doi.org/10.1111/j.0014-3820.2003.tb01561.xopenalex-snapshot
TOWARD A REALISTIC MODEL OF MUTATIONS AFFECTING FITNESS
inferredcites →https://doi.org/10.1111/j.0014-3820.2006.tb01845.xopenalex-snapshot
WITHIN-POPULATION VARIATION IN CYTOPLASMIC GENES AFFECTS FEMALE LIFE SPAN AND AGING IN DROSOPHILA MELANOGASTER
inferredcites →https://doi.org/10.1111/j.1365-294x.2009.04444.xopenalex-snapshot
Introducing mother’s curse: low male fertility associated with an imported mtDNA haplotype in a captive colony of brown hares
inferredcites →https://doi.org/10.1111/j.1420-9101.2005.00915.xopenalex-snapshot
Sex, mutation and fitness: asymmetric costs and routes to recovery through compensatory evolution
inferredcites →https://doi.org/10.1111/j.1420-9101.2011.02320.xopenalex-snapshot
Fitness-dependent mutation rates in finite populations
inferredcites →https://doi.org/10.1111/j.1474-9726.2008.00428.xopenalex-snapshot
Variation in mitochondrial genotype has substantial lifespan effects which may be modulated by nuclear background
inferredcites →https://doi.org/10.1111/j.1558-5646.2007.00016.xopenalex-snapshot
TEMPERATURE-SPECIFIC OUTCOMES OF CYTOPLASMIC-NUCLEAR INTERACTIONS ON EGG-TO-ADULT DEVELOPMENT TIME IN SEED BEETLES
inferredcites →https://doi.org/10.1111/j.1558-5646.2008.00333.xopenalex-snapshot
MATING DENSITY AND THE STRENGTH OF SEXUAL SELECTION AGAINST DELETERIOUS ALLELES INDROSOPHILA MELANOGASTER
inferredcites →https://doi.org/10.1111/j.1558-5646.2010.01135.xopenalex-snapshot
GENETIC ARCHITECTURE OF METABOLIC RATE: ENVIRONMENT SPECIFIC EPISTASIS BETWEEN MITOCHONDRIAL AND NUCLEAR GENES IN AN INSECT
inferredcites →https://doi.org/10.1111/j.1601-5223.1964.tb01918.xopenalex-snapshot
THE EFFECT OF TEMPERATURE DURING IRRADIATION ON INDUCED MUTATION FREQUENCY IN DROSOPHILA MELANOGASTER SPERM
inferredcites →https://doi.org/10.1111/jeb.12468openalex-snapshot
A meta‐analysis of the strength and nature of cytoplasmic genetic effects
inferredcites →https://doi.org/10.1111/jeb.12702openalex-snapshot
Context‐dependent effects of Y chromosome and mitochondrial haplotype on male locomotive activity in Drosophila melanogaster
inferredcites →https://doi.org/10.1111/jeb.12822openalex-snapshot
Evolutionary implications of mitochondrial genetic variation: mitochondrial genetic effects on OXPHOS respiration and mitochondrial quantity change with age and sex in fruit flies
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.1201157openalex-snapshot
Experimental Evidence Supports a Sex-Specific Selective Sieve in Mitochondrial Genome Evolution
inferredcites →https://doi.org/10.1126/science.289.5488.2342openalex-snapshot
High Direct Estimate of the Mutation Rate in the Mitochondrial Genome of Caenorhabditis elegans
inferredcites →https://doi.org/10.1146/annurev-biochem-060408-093701openalex-snapshot
Somatic Mitochondrial DNA Mutations in Mammalian Aging
inferredcites →https://doi.org/10.1186/1471-2148-9-54openalex-snapshot
The erratic mitochondrial clock: variations of mutation rate, not population size, affect mtDNA diversity across birds and mammals
inferredcites →https://doi.org/10.1186/1471-2164-15-330openalex-snapshot
Mito-nuclear interactions as drivers of gene movement on and off the X-chromosome
inferredcites →https://doi.org/10.1371/journal.pbio.0060030openalex-snapshot
Increased Transmission of Mutations by Low-Condition Females: Evidence for Condition-Dependent DNA Repair
inferredcites →https://doi.org/10.1371/journal.pbio.1002419openalex-snapshot
Low Genetic Quality Alters Key Dimensions of the Mutational Spectrum
inferredcites →https://doi.org/10.1371/journal.pgen.1002028openalex-snapshot
Ultra-Deep Sequencing of Mouse Mitochondrial DNA: Mutational Patterns and Their Origins
inferredcites →https://doi.org/10.1371/journal.pgen.1003974openalex-snapshot
Oxidative Stress Is Not a Major Contributor to Somatic Mitochondrial DNA Mutations
inferredcites →https://doi.org/10.1534/genetics.105.052050openalex-snapshot
Intergenomic Epistasis for Fitness: Within-Population Interactions Between Cytoplasmic and Nuclear Genes in Drosophila melanogaster
inferredcites →https://doi.org/10.1534/genetics.106.056200openalex-snapshot
Increase of the Spontaneous Mutation Rate in a Long-Term Experiment With Drosophila melanogaster
inferredcites →https://doi.org/10.1534/genetics.112.143321openalex-snapshot
DNA Repair Pathway Choice Is Influenced by the Health of Drosophila melanogaster
inferredcites →https://doi.org/10.1534/genetics.113.151670openalex-snapshot
Rates and Genomic Consequences of Spontaneous Mutational Events in Drosophila melanogaster
inferredcites →https://doi.org/10.1534/genetics.116.187286openalex-snapshot
Mitonuclear Epistasis for Development Time and Its Modification by Diet in Drosophila
inferredcites →https://doi.org/10.1554/06-210.1openalex-snapshot
DISRUPTION OF MITOCHONDRIAL FUNCTION IN INTERPOPULATION HYBRIDS OF TIGRIOPUS CALIFORNICUS
inferredcites →https://doi.org/10.18637/jss.v033.i02openalex-snapshot
MCMC Methods for Multi-Response Generalized Linear Mixed Models: The MCMCglmm R Package
inferredcites →https://doi.org/10.3109/19401736.2015.1106496openalex-snapshot
Complete mitochondrial genome sequences of thirteen globally sourced strains of fruit fly ( Drosophila melanogaster ) form a powerful model for mitochondrial research
inferredcites →https://doi.org/10.7554/elife.16923openalex-snapshot
A mitochondrial DNA hypomorph of cytochrome oxidase specifically impairs male fertility in Drosophila melanogaster
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.2478/jvetres-2019-0015openalex-snapshot
Mitochondrial theory of skeletal muscle ageing –new facts, new doubts
inferred← citeshttps://doi.org/10.5204/thesis.eprints.210165openalex-snapshot
Multigenerational mtGenome analysis for identification of historical military remains
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