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Synonymous substitution rates in Drosophila: Mitochondrial versus nuclear genes
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1007/bf00057504openalex-snapshot
Molecular evolution of the Rh3 gene in Drosophila
inferredcites →https://doi.org/10.1007/bf00167113openalex-snapshot
New methods for estimating the numbers of synonymous and nonsynonymous substitutions
inferredcites →https://doi.org/10.1007/bf00173193openalex-snapshot
The importance of base composition in the correct assessment of genetic distance
inferredcites →https://doi.org/10.1007/bf00173196openalex-snapshot
A method for estimating the numbers of synonymous and nonsynonymous substitutions per site
inferredcites →https://doi.org/10.1007/bf01731581openalex-snapshot
A simple method for estimating evolutionary rates of base substitutions through comparative studies of nucleotide sequences
inferredcites →https://doi.org/10.1007/bf01734101openalex-snapshot
Mitochondrial DNA sequences of primates: Tempo and mode of evolution
inferredcites →https://doi.org/10.1007/bf02099755openalex-snapshot
The mitochondrial DNA molecule ofDrosophila yakuba: Nucleotide sequence, gene organization, and genetic code
inferredcites →https://doi.org/10.1007/bf02100221openalex-snapshot
Molecular clock of silent substitution: At least six-fold preponderance of silent changes in mitochondrial genes over those in nuclear genes
inferredcites →https://doi.org/10.1007/bf02100996openalex-snapshot
Mitochondrial DNA evolution in themelanogaster species subgroup ofDrosophila
inferredcites →https://doi.org/10.1007/bf02111289openalex-snapshot
Tempo and mode of sequence evolution in mitochondrial DNA of HawaiianDrosophila
inferredcites →https://doi.org/10.1007/bf02407308openalex-snapshot
Unbiased estimation of the rates of synonymous and nonsynonymous substitution
inferredcites →https://doi.org/10.1007/bf02603075openalex-snapshot
On the rate of DNA sequence evolution inDrosophila
inferredcites →https://doi.org/10.1007/bf02931754openalex-snapshot
Pattern of synonymous and nonsynonymous substitutions: An indicator of mechanisms of molecular evolution
inferredcites →https://doi.org/10.1007/pl00006256openalex-snapshot
Codon Usage Bias and tRNA Abundance in Drosophila
inferredcites →https://doi.org/10.1016/0169-5347(94)90176-7openalex-snapshot
Thermal habit, metabolic rate and the evolution of mitochondrial DNA
inferredcites →https://doi.org/10.1016/s0169-5347(00)89195-8openalex-snapshot
Is mitochondrial DNA a strictly neutral marker?
inferredcites →https://doi.org/10.1073/pnas.80.2.492openalex-snapshot
Interspecific cytoplasmic gene flow in the absence of nuclear gene flow: evidence from Drosophila.
inferredcites →https://doi.org/10.1073/pnas.83.23.9090openalex-snapshot
Rates of nucleotide substitution in Drosophila mitochondrial DNA and nuclear DNA are similar.
inferredcites →https://doi.org/10.1073/pnas.90.9.4087openalex-snapshot
Body size, metabolic rate, generation time, and the molecular clock.
inferredcites →https://doi.org/10.1073/pnas.94.15.7784openalex-snapshot
Evolution of codon usage bias in Drosophila
inferredcites →https://doi.org/10.1093/genetics/118.4.671openalex-snapshot
Rates and patterns of scnDNA and mtDNA divergence within the Drosophila melanogaster subgroup.
inferredcites →https://doi.org/10.1093/genetics/129.4.1111openalex-snapshot
Lack of polymorphism on the Drosophila fourth chromosome resulting from selection.
inferredcites →https://doi.org/10.1093/genetics/130.4.855openalex-snapshot
Rates of synonymous substitution and base composition of nuclear genes in Drosophila.
inferredcites →https://doi.org/10.1093/genetics/134.3.847openalex-snapshot
Codon usage bias and base composition of nuclear genes in Drosophila.
inferredcites →https://doi.org/10.1093/genetics/136.1.155openalex-snapshot
Evolutionary inferences from DNA variation at the 6-phosphogluconate dehydrogenase locus in natural populations of drosophila: selection and geographic differentiation.
inferredcites →https://doi.org/10.1093/genetics/138.3.741openalex-snapshot
Neutral and non-neutral evolution of Drosophila mitochondrial DNA.
inferredcites →https://doi.org/10.1093/genetics/138.3.757openalex-snapshot
Unraveling selection in the mitochondrial genome of Drosophila.
inferredcites →https://doi.org/10.1093/genetics/143.1.375openalex-snapshot
Nucleotide Variation at the Gpdh Locus in the Genus Drosophila
inferredcites →https://doi.org/10.1093/nar/14.11.4519openalex-snapshot
RNA mapping on Drosophila mitochondrial DNA: precursors and template strands
inferredcites →https://doi.org/10.1093/oxfordjournals.molbev.a025634openalex-snapshot
Excess amino acid polymorphism in mitochondrial DNA: contrasts among genes from Drosophila, mice, and humans
inferredcites →https://doi.org/10.1093/oxfordjournals.molbev.a040003openalex-snapshot
Evolution of the Zfx and Zfy genes: rates and interdependence between the genes.
inferredcites →https://doi.org/10.1093/oxfordjournals.molbev.a040023openalex-snapshot
Estimation of the number of nucleotide substitutions in the control region of mitochondrial DNA in humans and chimpanzees.
inferredcites →https://doi.org/10.1093/oxfordjournals.molbev.a040052openalex-snapshot
Molecular drift of the bride of sevenless (boss) gene in Drosophila.
inferredcites →https://doi.org/10.1093/oxfordjournals.molbev.a040145openalex-snapshot
Polymorphism and divergence at the prune locus in Drosophila melanogaster and D. simulans.
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/oxfordjournals.molbev.a040410openalex-snapshot
Simple methods for estimating the numbers of synonymous and nonsynonymous nucleotide substitutions.
inferredcites →https://doi.org/10.1093/oxfordjournals.molbev.a040464openalex-snapshot
Analysis of nucleotide substitutions of mitochondrial DNAs in Drosophila melanogaster and its sibling species.
inferredcites →https://doi.org/10.1093/oxfordjournals.molbev.a040525openalex-snapshot
"Silent" sites in Drosophila genes are not neutral: evidence of selection among synonymous codons.
inferredcites →https://doi.org/10.1093/oxfordjournals.molbev.a040752openalex-snapshot
Estimation of the number of nucleotide substitutions when there are strong transition-transversion and G+C-content biases.
inferredcites →https://doi.org/10.1093/oxfordjournals.molbev.a040763openalex-snapshot
The rate and pattern of nucleotide substitution in Drosophila mitochondrial DNA.
inferredcites →https://doi.org/10.1111/j.1558-5646.1994.tb02222.xopenalex-snapshot
USING HITCHHIKING GENES TO STUDY ADAPTATION AND DIVERGENCE DURING SPECIATION WITHIN THE DROSOPHILA MELANOGASTER SPECIES COMPLEX
inferredcites →https://doi.org/10.1111/j.1558-5646.1997.tb02430.xopenalex-snapshot
MITOCHONDRIAL DNA PHYLOGENIES FOR THEDROSOPHILA OBSCURAGROUP
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Incoming claims: where this work appears in other papers’ reference lists and arguments.
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Analysis of a Shift in Codon Usage in Drosophila
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Relative Rates of Nucleotide Substitution in Frogs
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Effect of Divergence Time and Recombination Rate on Molecular Evolution of Drosophila INE-1 Transposable Elements and Other Candidates for Neutrally Evolving Sites
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Comparative Genomics of Drosophila mtDNA: Novel Features of Conservation and Change Across Functional Domains and Lineages
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Complex Patterns of Plastid 16S rRNA Gene Evolution in Nonphotosynthetic Green Algae
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Nature of selective constraints on synonymous codon usage of rice differs in GC-poor and GC-rich genes
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inferred← citeshttps://doi.org/10.1016/j.gene.2008.01.010openalex-snapshot
The heterochromatic copies of the LTR retrotransposons as a record of the genomic events that have shaped the Drosophila melanogaster genome
inferred← citeshttps://doi.org/10.1016/j.gene.2010.08.002openalex-snapshot
Molecular phylogenetic study in genus Hydra
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inferred← citeshttps://doi.org/10.1016/j.mito.2018.06.004openalex-snapshot
Is there a mutation gradient along vertebrate mitochondrial genome mediated by genome replication?
inferred← citeshttps://doi.org/10.1016/j.ympev.2003.10.002openalex-snapshot
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Computational Molecular Evolution
inferred← citeshttps://doi.org/10.1093/acprof:oso/9780198567028.002.0004openalex-snapshot
Copyright Page
inferred← citeshttps://doi.org/10.1093/acprof:oso/9780198567028.003.0001openalex-snapshot
Models of nucleotide substitution
inferred← citeshttps://doi.org/10.1093/acprof:oso/9780198567028.003.0002openalex-snapshot
Models of amino acid and codon substitution
inferred← citeshttps://doi.org/10.1093/acprof:oso/9780198567028.003.0003openalex-snapshot
Phylogeny reconstruction: overview
inferred← citeshttps://doi.org/10.1093/acprof:oso/9780198567028.003.0004openalex-snapshot
Maximum likelihood methods
inferred← citeshttps://doi.org/10.1093/acprof:oso/9780198567028.003.0005openalex-snapshot
Bayesian methods
inferred← citeshttps://doi.org/10.1093/acprof:oso/9780198567028.003.0006openalex-snapshot
Comparison of methods and tests on trees
inferred← citeshttps://doi.org/10.1093/acprof:oso/9780198567028.003.0007openalex-snapshot
Molecular clock and estimation of species divergence times
inferred← citeshttps://doi.org/10.1093/acprof:oso/9780198567028.003.0008openalex-snapshot
Neutral and adaptive protein evolution
inferred← citeshttps://doi.org/10.1093/acprof:oso/9780198567028.003.0009openalex-snapshot
Simulating molecular evolution
inferred← citeshttps://doi.org/10.1093/acprof:oso/9780198567028.003.0010openalex-snapshot
Perspectives
inferred← citeshttps://doi.org/10.1093/acprof:oso/9780199602605.001.0001openalex-snapshot
Molecular Evolution
inferred← citeshttps://doi.org/10.1093/acprof:oso/9780199602605.002.0003openalex-snapshot
Copyright Page
inferred← citeshttps://doi.org/10.1093/acprof:oso/9780199602605.003.0001openalex-snapshot
Models of nucleotide substitution
inferred← citeshttps://doi.org/10.1093/acprof:oso/9780199602605.003.0002openalex-snapshot
Models of amino acid and codon substitution
inferred← citeshttps://doi.org/10.1093/acprof:oso/9780199602605.003.0003openalex-snapshot
Phylogeny reconstruction: overview
inferred← citeshttps://doi.org/10.1093/acprof:oso/9780199602605.003.0004openalex-snapshot
Maximum likelihood methods
inferred← citeshttps://doi.org/10.1093/acprof:oso/9780199602605.003.0005openalex-snapshot
Comparison of phylogenetic methods and tests on trees
inferred← citeshttps://doi.org/10.1093/acprof:oso/9780199602605.003.0006openalex-snapshot
Bayesian theory
inferred← citeshttps://doi.org/10.1093/acprof:oso/9780199602605.003.0007openalex-snapshot
Bayesian computation (MCMC)
inferred← citeshttps://doi.org/10.1093/acprof:oso/9780199602605.003.0008openalex-snapshot
Bayesian phylogenetics
inferred← citeshttps://doi.org/10.1093/acprof:oso/9780199602605.003.0009openalex-snapshot
Coalescent theory and species trees
inferred← citeshttps://doi.org/10.1093/acprof:oso/9780199602605.003.0010openalex-snapshot
Molecular clock and estimation of species divergence times
inferred← citeshttps://doi.org/10.1093/acprof:oso/9780199602605.003.0011openalex-snapshot
Neutral and adaptive protein evolution
inferred← citeshttps://doi.org/10.1093/acprof:oso/9780199602605.003.0012openalex-snapshot
Simulating molecular evolution
inferred← citeshttps://doi.org/10.1093/biolinnean/blw045openalex-snapshot
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inferred← citeshttps://doi.org/10.1093/genetics/153.3.1395openalex-snapshot
The Effect of Tandem Substitutions on the Correlation Between Synonymous and Nonsynonymous Rates in Rodents
inferred← citeshttps://doi.org/10.1093/genetics/157.1.295openalex-snapshot
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inferred← citeshttps://doi.org/10.1093/jisesa/iev056openalex-snapshot
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inferred← citeshttps://doi.org/10.1093/molbev/msk025openalex-snapshot
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inferred← citeshttps://doi.org/10.1093/mutage/gex004openalex-snapshot
Cellular and population level processes influence the rate, accumulation and observed frequency of inherited and somatic mtDNA mutations
inferred← citeshttps://doi.org/10.1093/oxfordjournals.molbev.a003958openalex-snapshot
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inferred← citeshttps://doi.org/10.1093/oxfordjournals.molbev.a004014openalex-snapshot
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inferred← citeshttps://doi.org/10.1093/oxfordjournals.molbev.a004056openalex-snapshot
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inferred← citeshttps://doi.org/10.1093/oxfordjournals.molbev.a026236openalex-snapshot
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inferred← citeshttps://doi.org/10.1093/oxfordjournals.molbev.a026391openalex-snapshot
Comparative Evolution of the Mitochondrial Cytochrome b Gene and Nuclear β-Fibrinogen Intron 7 in Woodpeckers
inferred← citeshttps://doi.org/10.1101/2022.11.03.515082openalex-snapshot
Synonymous and non-synonymous transitions/transversions vividly disclose purifying selection in Escherichia coli coding sequences
inferred← citeshttps://doi.org/10.1101/851139openalex-snapshot
On the inference of a southern origin of the North American firefly Photinus pyralis
inferred← citeshttps://doi.org/10.1101/gr.178701openalex-snapshot
Analysis of Conserved Noncoding DNA in Drosophila Reveals Similar Constraints in Intergenic and Intronic Sequences
inferred← citeshttps://doi.org/10.1101/gr.6255407openalex-snapshot
RCPdb: An evolutionary classification and codon usage database for repeat-containing proteins
inferred← citeshttps://doi.org/10.1111/evo.12295openalex-snapshot
INTROGRESSION IN THEDROSOPHILA SUBOBSCURA—D. MADEIRENSISSISTER SPECIES: EVIDENCE OF GENE FLOW IN NUCLEAR GENES DESPITE MITOCHONDRIAL DIFFERENTIATION
inferred← citeshttps://doi.org/10.1111/j.0014-3820.2002.tb00187.xopenalex-snapshot
EVOLUTION OF WOLBACHIA-INDUCED CYTOPLASMIC INCOMPATIBILITY IN DROSOPHILA SIMULANS AND D. SECHELLIA
inferred← citeshttps://doi.org/10.1111/j.0014-3820.2005.tb01754.xopenalex-snapshot
EVOLUTIONARY HISTORY OF CONTAGIOUS ASEXUALITY IN DAPHNIA PULEX
inferred← citeshttps://doi.org/10.1111/j.0014-3820.2006.tb01178.xopenalex-snapshot
USING COALESCENT SIMULATIONS TO TEST THE IMPACT OF QUATERNARY CLIMATE CYCLES ON DIVERGENCE IN AN ALPINE PLANT-INSECT ASSOCIATION
inferred← citeshttps://doi.org/10.1111/j.1095-8312.2011.01836.xopenalex-snapshot
Genetically separate populations of the ocean-skater Halobates sericeus (Heteroptera: Gerridae) have been maintained since the late Pleistocene
inferred← citeshttps://doi.org/10.1111/j.1096-0031.2004.00014.xopenalex-snapshot
Character‐state space versus rate of evolution in phylogenetic inference
inferred← citeshttps://doi.org/10.1111/j.1096-0031.2006.00139.xopenalex-snapshot
Molecular evolution and radiation of dung beetles in Madagascar
inferred← citeshttps://doi.org/10.1111/j.1365-2427.2010.02571.xopenalex-snapshot
Spatial population genetic structure reveals strong natal site fidelity in Echinocladius martini (Diptera: Chironomidae) in northeast Queensland, Australia
inferred← citeshttps://doi.org/10.1111/j.1365-2583.2005.00595.xopenalex-snapshot
Genetic variability in the three genomes of Nasonia : nuclear, mitochondrial and Wolbachia
inferred← citeshttps://doi.org/10.1111/j.1365-294x.2006.02941.xopenalex-snapshot
Evolutionary relationships of Drosophila mojavensis geographic host races and their sister species Drosophila arizonae
inferred← citeshttps://doi.org/10.1111/j.1365-294x.2010.04639.xopenalex-snapshot
Host-associated genetic differentiation in a seed parasitic weevil Rhinusa antirrhini (Coleptera: Curculionidae) revealed by mitochondrial and nuclear sequence data
inferred← citeshttps://doi.org/10.1111/j.1420-9101.2008.01607.xopenalex-snapshot
No resistance to male‐killing Wolbachia after thousands of years of infection
inferred← citeshttps://doi.org/10.1111/j.1442-9993.2009.01932.xopenalex-snapshot
Deeply divergent mitochondrial lineages reveal patterns of local endemism in chironomids of the Australian Wet Tropics
inferred← citeshttps://doi.org/10.1111/j.1558-5646.2007.00076.xopenalex-snapshot
DISCORDANT DIVERGENCE TIMES AMONG Z-CHROMOSOME REGIONS BETWEEN TWO ECOLOGICALLY DISTINCT SWALLOWTAIL BUTTERFLY SPECIES
inferred← citeshttps://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
inferred← citeshttps://doi.org/10.1111/j.1744-7410.2010.00207.xopenalex-snapshot
Gene and species trees reveal mitochondrial and nuclear discordance in the Drosophila cardini group (Diptera: Drosophilidae)
inferred← citeshttps://doi.org/10.1111/j.1755-0998.2009.02637.xopenalex-snapshot
Evaluation of mitochondrial genes as DNA barcode for Basidiomycota
inferred← citeshttps://doi.org/10.1111/mec.12678openalex-snapshot
Sequential adaptive introgression of the mitochondrial genome in D rosophila yakubaand D rosophila santomea
inferred← citeshttps://doi.org/10.1111/syen.12431openalex-snapshot
How well do multispecies coalescent methods perform with mitochondrial genomic data? A case study of butterflies and moths (Insecta: Lepidoptera)
inferred← citeshttps://doi.org/10.1134/s1063074019050055openalex-snapshot
Molecular Phylogeny of Gobies (Teleostei, Gobiidae) from Iranian Water Bodies with a New Record
inferred← citeshttps://doi.org/10.1146/annurev.ecolsys.37.091305.110018openalex-snapshot
Incorporating Molecular Evolution into Phylogenetic Analysis, and a New Compilation of Conserved Polymerase Chain Reaction Primers for Animal Mitochondrial DNA
inferred← citeshttps://doi.org/10.1146/annurev.genet.35.102401.091106openalex-snapshot
Does Nonneutral Evolution Shape Observed Patterns of DNA Variation in Animal Mitochondrial Genomes?
inferred← citeshttps://doi.org/10.1155/2012/329434openalex-snapshot
DNA Barcoding and Molecular Phylogeny ofDrosophila liniand Its Sibling Species
inferred← citeshttps://doi.org/10.11606/d.6.2009.tde-28012010-105230openalex-snapshot
Estudos taxonômicos de espécies do gênero Culex (Diptera: Culicidae) da região neotropical, utilizando a subunidade I do gene mitocondrial citocromo oxidase
inferred← citeshttps://doi.org/10.1186/1471-2148-6-24openalex-snapshot
No variation and low synonymous substitution rates in coral mtDNA despite high nuclear variation
inferred← citeshttps://doi.org/10.1186/1471-2148-7-95openalex-snapshot
The influence of body size and net diversification rate on molecular evolution during the radiation of animal phyla
inferred← citeshttps://doi.org/10.1186/1471-2148-8-33openalex-snapshot
Independent Origins of New Sex-Linked Chromosomes in the melanica and robusta Species Groups of Drosophila
inferred← citeshttps://doi.org/10.1186/gb-2001-2-11-research0049openalex-snapshot
Optimality of the genetic code with respect to protein stability and amino-acid frequencies
inferred← citeshttps://doi.org/10.1196/annals.1396.011openalex-snapshot
Comparative Analysis of Mitochondrial Genotype and Aging
inferred← citeshttps://doi.org/10.1201/9781420092592-7openalex-snapshot
Decapod phylogenetics and molecular evolution
inferred← citeshttps://doi.org/10.1266/ggs.74.117openalex-snapshot
Paleo-demography of the Drosophila melanogaster subgroup. Application of the maximum likelihood method.
inferred← citeshttps://doi.org/10.1266/ggs.76.209openalex-snapshot
A statistical analysis of nucleotide substitutions in the Drosophila Adh region reflects irregularities in molecular clocks.
inferred← citeshttps://doi.org/10.1266/ggs.79.293openalex-snapshot
Molecular phylogeny of the nasuta subgroup of Drosophila based on 12S rRNA, 16S rRNA and CoI mitochondrial genes, RAPD and ISSR polymorphisms
inferred← citeshttps://doi.org/10.12782/specdiv.11.57openalex-snapshot
Molecular Phylogeny of the Indo-Australian Glyphodes and its Allied Genera (Insecta: Lepidoptera: Crambidae: Spilomelinae) Inferred from Mitochondrial COI and COII and Nuclear EF-1α Gene Sequences
inferred← citeshttps://doi.org/10.1371/journal.pone.0032593openalex-snapshot
Mitochondrial Pseudogenes in the Nuclear Genomes of Drosophila
inferred← citeshttps://doi.org/10.1371/journal.pone.0100558openalex-snapshot
The Complete Nucleotide Sequence of the Mitochondrial Genome of Bactrocera minax (Diptera: Tephritidae)
inferred← citeshttps://doi.org/10.14411/eje.2024.015openalex-snapshot
Evidence of a South American origin for the Drosophila repleta group (Diptera: Drosophilidae)
inferred← citeshttps://doi.org/10.1534/genetics.104.033597openalex-snapshot
Multilocus Analysis of Introgression Between Two Sympatric Sister Species of Drosophila: Drosophila yakuba and D. santomea
inferred← citeshttps://doi.org/10.1534/genetics.105.047399openalex-snapshot
Evolutionary Rates and Expression Level in Chlamydomonas
inferred← citeshttps://doi.org/10.1534/genetics.106.058792openalex-snapshot
The period Gene Thr-Gly Polymorphism in Australian and African Drosophila melanogaster Populations: Implications for Selection
inferred← citeshttps://doi.org/10.1603/me09293openalex-snapshot
Taxonomic and Phylogenetic Relationships Between Species of the Genus Culex (Diptera: Culicidae) From Brazil Inferred From the Cytochrome c Oxidase I Mitochondrial Gene
inferred← citeshttps://doi.org/10.1636/ha09-49.1openalex-snapshot
The phylogenetic utility of the nuclear protein-coding gene EF-1α for resolving recent divergences in Opiliones, emphasizing intron evolution
inferred← citeshttps://doi.org/10.1643/0045-8511(2007)7[101:meamas]2.0.co;2openalex-snapshot
Morphological, Ecological, and Molecular Analyses Separate Muraena augusti from Muraena helena as a Valid Species
inferred← citeshttps://doi.org/10.18174/121409openalex-snapshot
Lake Tana's piscivorous Barbus (Cyprinidae, Ethiopia) ecology - evolution - exploitation
inferred← citeshttps://doi.org/10.21203/rs.3.rs-7648095/v1openalex-snapshot
Analysis of codon usage bias between Ophiocordyceps sinensis and Thitarodes xiaojinensis
inferred← citeshttps://doi.org/10.3389/fmicb.2020.00863openalex-snapshot
The Mitochondrial Genome of the Phytopathogenic Fungus Bipolaris sorokiniana and the Utility of Mitochondrial Genome to Infer Phylogeny of Dothideomycetes
inferred← citeshttps://doi.org/10.3390/nu7042897openalex-snapshot
The Queuine Micronutrient: Charting a Course from Microbe to Man
inferred← citeshttps://doi.org/10.3390/oceans1030011openalex-snapshot
Molecular Phylogenetics of Trapezia Crabs in the Central Mexican Pacific
inferred← citeshttps://doi.org/10.3410/f.1033418.380706openalex-snapshot
Faculty Opinions recommendation of The period gene Thr-Gly polymorphism in Australian and African Drosophila melanogaster populations: implications for selection.
inferred← citeshttps://doi.org/10.3906/biy-1003-65openalex-snapshot
Utilization of cytochrome oxidase I in Cephus pygmeus (L.) (Hymenoptera: Cephidae)
inferred← citeshttps://doi.org/10.4172/jpb.1000025openalex-snapshot
Analysis of Synonymous Codon Usage Bias in Pseudomonas Syringae Phages: Implication in Phage Therapy for Halo Blight Disease
inferred← citeshttps://doi.org/10.5352/jls.2010.20.4.481openalex-snapshot
The Rates of Synonymous and Nonsynonymous Substitutions in Sorbus aucuparia Using Nuclear and Chloroplast Genes
inferred← citeshttps://doi.org/10.6026/97320630081096openalex-snapshot
Synonymous codon usage in chloroplast genome of Coffea arabica
inferred← citeshttps://doi.org/10.70675/2212b624z1a62z4646za085zddbbf2fb57efopenalex-snapshot
Organisation génétique des populations d'esturgeon européen Acipenser sturio : passé, présent, futur
inferred← citeshttps://doi.org/10.70675/907af94cze6c1z4c6bza835z94679c54a0f7openalex-snapshot
Diversity and dynamics of Wolbachia-host associations in arthropods from the Society archipelago, French Polynesia
inferred← citeshttps://doi.org/10.7287/peerj.749v0.1/reviews/1openalex-snapshot
Peer Review #1 of "The effects of island forest restoration on open habitat specialists: the endangered weevil Hadramphus spinipennis Broun and its host-plant Aciphylla dieffenbachii Kirk (v0.1)"
inferred← citeshttps://doi.org/10.7287/peerj.749v0.1/reviews/2openalex-snapshot
Peer Review #2 of "The effects of island forest restoration on open habitat specialists: the endangered weevil Hadramphus spinipennis Broun and its host-plant Aciphylla dieffenbachii Kirk (v0.1)"
inferred← citeshttps://doi.org/10.7717/peerj.749openalex-snapshot
The effects of island forest restoration on open habitat specialists: the endangered weevil Hadramphus spinipennis Broun and its host-plant Aciphylla dieffenbachii Kirk
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