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Nonrandomness of point mutation as reflected in nucleotide substitutions in pseudogenes and its evolutionary implications

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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/bf00267667openalex-snapshot

Mutational specificity of a conditional Escherichia coli mutator, mutD5

inferredcites →https://doi.org/10.1007/bf00281051openalex-snapshot

Mutationsvorg�nge bei der Entstehung von H�moglobinvarianten

inferredcites →https://doi.org/10.1007/bf00395656openalex-snapshot

Sind die Mutationsraten f�r die X-chromosomal recessiven H�mophilieformen in Keimzellen von Frauen niedriger als in Keimzellen von M�nnern?

inferredcites →https://doi.org/10.1007/bf01654100openalex-snapshot

Genetic distance and electrophoretic identity of proteins between taxa

inferredcites →https://doi.org/10.1007/bf01732746openalex-snapshot

Higher frequencies of transitions among point mutations

inferredcites →https://doi.org/10.1007/bf01733904openalex-snapshot

Patterns of nucleotide substitution in pseudogenes and functional genes

inferredcites →https://doi.org/10.1007/bf01734101openalex-snapshot

Mitochondrial DNA sequences of primates: Tempo and mode of evolution

inferredcites →https://doi.org/10.1007/bf01739259openalex-snapshot

Solution to a gene divergence problem under arbitrary stable nucleotide transition probabilities

inferredcites →https://doi.org/10.1007/bf01810830openalex-snapshot

Biases of the estimates of DNA divergence obtained by the restriction enzyme technique

inferredcites →https://doi.org/10.1016/0022-2836(67)90317-8openalex-snapshot

Evidence suggesting a non-random character to nucleotide replacements in naturally occurring mutations

inferredcites →https://doi.org/10.1016/0022-2836(71)90311-1openalex-snapshot

Mutational trends and random processes in the evolution of informational macromolecules

inferredcites →https://doi.org/10.1016/0022-2836(72)90326-9openalex-snapshot

Improved procedures for comparing homologous sequences in molecules of proteins and nucleic acids

inferredcites →https://doi.org/10.1016/0092-8674(78)90040-5openalex-snapshot

The sequence of the chromosomal mouse β-globin major gene: Homologies in capping, splicing and poly(A) sites

inferredcites →https://doi.org/10.1016/0092-8674(80)90125-7openalex-snapshot

Tissue-specific expression of mouse α-amylase genes: Nucleotide sequence of isoenzyme mRNAs from pancreas and salivary gland

inferredcites →https://doi.org/10.1016/0092-8674(80)90238-xopenalex-snapshot

Number and evolutionary conservation of α- and β-tubulin and cytoplasmic β- and γ-actin genes using specific cloned cDNA probes

inferredcites →https://doi.org/10.1016/0092-8674(80)90347-5openalex-snapshot

The 3′ untranslated regions of the duplicated human α-globin genes are unexpectedly divergent

inferredcites →https://doi.org/10.1016/0092-8674(80)90428-6openalex-snapshot

The nucleotide sequence of the human β-globin gene

inferredcites →https://doi.org/10.1016/0092-8674(80)90492-4openalex-snapshot

The nucleotide sequence of a rabbit β-globin pseudogene

inferredcites →https://doi.org/10.1016/0092-8674(81)90089-1openalex-snapshot

Heavy chain variable region contribution to the NPb family of antibodies: somatic mutation evident in a γ2a variable region

inferredcites →https://doi.org/10.1016/0092-8674(81)90301-9openalex-snapshot

Two related pseudogenes are the result of a gene duplication in the goat β-globin locus

inferredcites →https://doi.org/10.1016/0092-8674(81)90419-0openalex-snapshot

Structure and evolution of goat γ-, βC- and βA-globin genes: Three developmentally regulated genes contain inserted elements

inferredcites →https://doi.org/10.1016/0092-8674(82)90185-4openalex-snapshot

Duplication and deletion in the human immunoglobulin ϵ genes

inferredcites →https://doi.org/10.1016/0092-8674(83)90429-4openalex-snapshot

Evolutionary history of a multigene family: An expressed human β-tubulin gene and three processed pseudogenes

inferredcites →https://doi.org/10.1016/b978-0-12-048850-6.50066-1openalex-snapshot

PROBING THE MECHANISM OF TRANSITION AND TRANSVERSION MUTAGENESIS USING THE PHAGE T4 DNA REPLICATION APPARATUS IN VITRO

inferredcites →https://doi.org/10.1016/b978-0-12-048850-6.50069-7openalex-snapshot

BASE MISPAIRING AND NEAREST-NEIGHBOR EFFECTS IN TRANSITION MUTATIONS

inferredcites →https://doi.org/10.1016/b978-0-12-516304-0.50006-4openalex-snapshot

Protein Evolution

inferredcites →https://doi.org/10.1016/s0021-9258(19)69903-5openalex-snapshot

Hemoglobin switching in sheep. Isolation of the fetal gamma-globin gene and demonstration that the fetal gamma- and adult beta A-globin genes lie within eight kilobase segments of homologous DNA.

inferredcites →https://doi.org/10.1016/s0021-9258(19)70193-8openalex-snapshot

Molecular basis for substitution mutations. Effect of primer terminal and template residues on nucleotide selection by phage T4 DNA polymerase in vitro.

inferredcites →https://doi.org/10.1017/s0016672300015536openalex-snapshot

Profiles of electrophoretic alleles in natural populations

inferredcites →https://doi.org/10.1017/s0016672300015548openalex-snapshot

Extensions to the model of an infinite number of selectively neutral alleles in a finite population

inferredcites →https://doi.org/10.1038/207259a0openalex-snapshot

Abnormal Haemoglobins and the Genetic Code

inferredcites →https://doi.org/10.1038/263285a0openalex-snapshot

Complementary base pairing and the origin of substitution mutations

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/10.1038/274775a0openalex-snapshot

Molecular basis of base substitution hotspots in Escherichia coli

inferredcites →https://doi.org/10.1038/287117a0openalex-snapshot

Structure of a family of rat amylase genes

inferredcites →https://doi.org/10.1038/290026a0openalex-snapshot

Homology and concerted evolution at the α1 and α2 loci of human α-globin

inferredcites →https://doi.org/10.1038/291201a0openalex-snapshot

Homology between the primary structure of α-fetoprotein, deduced from a complete cDNA sequence, and serum albumin

inferredcites →https://doi.org/10.1038/292267a0openalex-snapshot

Structure of mouse metallothionein-I gene and its mRNA

inferredcites →https://doi.org/10.1038/300330a0openalex-snapshot

The sequences of an expressed rat α-tubulin gene and a pseudogene with an inserted repetitive element

inferredcites →https://doi.org/10.1038/304412a0openalex-snapshot

Nucleotide polymorphism at the alcohol dehydrogenase locus of Drosophila melanogaster

inferredcites →https://doi.org/10.1073/pnas.77.12.7328openalex-snapshot

Nucleotide sequence divergence and functional constraint in mRNA evolution.

inferredcites →https://doi.org/10.1073/pnas.78.1.243openalex-snapshot

Nucleotide sequence of cloned rat serum albumin messenger RNA.

inferredcites →https://doi.org/10.1073/pnas.78.11.7064openalex-snapshot

Allelic forms of rat κ chain genes: Evidence for strong selection at the level of nucleotide sequence

inferredcites →https://doi.org/10.1073/pnas.78.2.1110openalex-snapshot

Nonrandom patterns of codon usage and of nucleotide substitutions in human alpha- and beta-globin genes: an evolutionary strategy reducing the rate of mutations with drastic effects?

inferredcites →https://doi.org/10.1073/pnas.78.6.3521openalex-snapshot

Sequence homology between RNAs encoding rat alpha-fetoprotein and rat serum albumin.

inferredcites →https://doi.org/10.1073/pnas.79.1.71openalex-snapshot

Nucleotide sequence and the encoded amino acids of human serum albumin mRNA.

inferredcites →https://doi.org/10.1073/pnas.79.24.7852openalex-snapshot

Cloning and nucleotide sequence of mouse immunoglobulin epsilon chain cDNA.

inferredcites →https://doi.org/10.1089/dna.1.1983.2.15openalex-snapshot

Molecular Cloning of the Rat Metallothionein 1 (MT-1) mRNA Sequence

inferredcites →https://doi.org/10.1093/genetics/103.2.287openalex-snapshot

HUMAN MITOCHONDRIAL DNA VARIATION AND EVOLUTION: ANALYSIS OF NUCLEOTIDE SEQUENCES FROM SEVEN INDIVIDUALS

inferredcites →https://doi.org/10.1093/nar/10.11.3353openalex-snapshot

Simple DNA sequences in homologous flanking regions near immunoglobulin VHgenes: a role in gene interaction?

inferredcites →https://doi.org/10.1093/nar/10.12.3733openalex-snapshot

Comparative sequence analysis of the mRNAs coding for mouse and rat whey protein

inferredcites →https://doi.org/10.1093/nar/10.19.6041openalex-snapshot

Structure and evolution of the heavy chain from rat immunoglobulin E

inferredcites →https://doi.org/10.1093/oxfordjournals.molbev.a040306openalex-snapshot

Rapid evolution of goat and sheep globin genes following gene duplication.

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.6254144openalex-snapshot

DNA Methylation and Gene Function

inferredcites →https://doi.org/10.1126/science.7434017openalex-snapshot

Silent Nucleotide Substitutions and the Molecular Evolutionary Clock

inferredcites →https://doi.org/10.2307/2407692openalex-snapshot

MOLECULAR POPULATION GENETICS AND EVOLUTION

inferredcites →https://doi.org/10.2307/2412105openalex-snapshot

Atlas of Protein Sequence and Structure, 1972.

inferredcites →https://doi.org/10.2307/2801008openalex-snapshot

Human Haemoglobin Variants and Their Characteristics.

What points at this work

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

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Large Differentiation of Extremely Threatened Chinese Pangolins Provide New Genomic Cues for Their Conservation

inferred← citeshttps://doi.org/10.1001/archneurol.2012.54openalex-snapshot

Autosomal Dominant Familial Dyskinesia and Facial Myokymia

inferred← citeshttps://doi.org/10.1002/(sici)1098-1004(1996)8:1<23::aid-humu3>3.0.co;2-qopenalex-snapshot

Single base-pair substitutions in pathology and evolution: Two sides to the same coin

inferred← citeshttps://doi.org/10.1002/(sici)1098-1004(1997)9:6<537::aid-humu7>3.0.co;2-zopenalex-snapshot

Large majority of single-nucleotide mutations along the dystrophin gene can be explained by more than one mechanism of mutagenesis

inferred← citeshttps://doi.org/10.1002/(sici)1099-0526(199903/04)4:4<61::aid-cplx8>3.0.co;2-nopenalex-snapshot

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Spectrum of Mutations in the Human Genome Inferred by Single Nucleotide Polymorphisms

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Spectrum of Point Mutations in the Human Genome and Major Subpopulations

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Reconstruction of molecular phylogeny of extant hominoids from DNA sequence data

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Rare missense variants in DVL1, one of the human counterparts of the Drosophila dishevelled gene, do not confer increased risk for neural tube defects

inferred← citeshttps://doi.org/10.1002/em.10065openalex-snapshot

p53 As a mutagen test in breast cancer

inferred← citeshttps://doi.org/10.1002/humu.10018openalex-snapshot

Mutations in the factor IX gene (F9) during the past 150 years have relative rates similar to ancient mutations

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Worldwide haplotype diversity and coding sequence variation at human bitter taste receptor loci

inferred← citeshttps://doi.org/10.1002/humu.20694openalex-snapshot

6-mercaptopurine and 9-(2-phosphonyl-methoxyethyl) adenine (PMEA) transport altered by two missense mutations in the drug transporter gene ABCC4

inferred← citeshttps://doi.org/10.1002/jez.b.21144openalex-snapshot

PCR survey of hox genes in the goldfish Carassius auratus auratus

inferred← citeshttps://doi.org/10.1002/mgg3.1479openalex-snapshot

Multimodal imaging and genetic characteristics of Chinese patients with USH2A ‐associated nonsyndromic retinitis pigmentosa

inferred← citeshttps://doi.org/10.1002/pro.5560070319openalex-snapshot

Serial increase in the thermal stability of 3‐isopropylmalate dehydrogenase from Bacillus subtilis by experimental evolution

inferred← citeshttps://doi.org/10.1006/jmbi.1995.0535openalex-snapshot

Distinctive Sequence Features in Protein Coding Genic Non-coding, and Intergenic Human DNA

inferred← citeshttps://doi.org/10.1006/jmbi.1997.1104openalex-snapshot

HIV genetic variation is directed and restricted by DNA precursor availability

inferred← citeshttps://doi.org/10.1006/jmbi.1999.3275openalex-snapshot

Tendency for local repetitiveness in amino acid usages in modern proteins

inferred← citeshttps://doi.org/10.1006/meth.1998.0604openalex-snapshot

Evolutionary Analysis of RNA Editing Enzymes

inferred← citeshttps://doi.org/10.1006/viro.1997.8676openalex-snapshot

Naturally Occurring Hepatitis B Virus Genomes Bearing the Hallmarks of Retroviral G → A Hypermutation

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Fractals and Wavelets: What Can We Learn on Transcription and Replication from Wavelet-Based Multifractal Analysis of DNA Sequences?

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Fractals and Wavelets: What Can We Learn on Transcription and Replication from Wavelet-Based Multifractal Analysis of DNA Sequences?

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Codon Bias and the Context Dependency of Nucleotide Substitutions in the Evolution of Plastid DNA

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Molecular Evolution of 18S rDNA in Angiosperms: Implications for Character Weighting in Phylogenetic Analysis

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Evolution of DNA Sequences

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Computational Methods of Identification of Pseudogenes Based on Functionality: Entropy and GC Content

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Drugs, the human genome, and individual-based medicine

inferred← citeshttps://doi.org/10.1007/978-3-642-29764-9_2openalex-snapshot

Improving the Semantics of a Conceptual Schema of the Human Genome by Incorporating the Modeling of SNPs

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Reconstructing the Evolution of Proteins

inferred← citeshttps://doi.org/10.1007/978-3-642-75256-8_1openalex-snapshot

Evolution and Structural Theory: The Frontier Between Chemistry and Biology

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Molecular Systematics at the Species Boundary: Exploiting Conserved and Variable Regions of the Mitochondrial Genome of Animals via Direct Sequencing from Amplified DNA

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The Age and Evolution of the DRB Pseudogenes

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Evolution of nuclear rDNA its sequences in the Cladophora albida/sericea clade (Chlorophyta)

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The influence of nearest neighbors on the rate and pattern of spontaneous point mutations

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Properties of a general model of DNA evolution under no-strand-bias conditions

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New methods for estimating the numbers of synonymous and nonsynonymous substitutions

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Constraints on mutability in a multiallelic gene family

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Neighboring base composition is strongly correlated with base substitution bias in a region of the chloroplast genome

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Estimating the pattern of nucleotide substitution

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Patterns of nucleotide substitutions inferred from the phylogenies of the class I major histocompatibility complex genes

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Evolutionary consequences of nonrandom damage and repair of chromatin domains

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Evolution of V genes: DNA sequence structure of functional germline genes and pseudogenes

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The mutational spectrum of single base-pair substitutions causing human genetic disease: patterns and predictions

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NS 1 gene sequences from eight dengue-2 viruses and their evolutionary relationships with other dengue-2 viruses

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Robustness of maximum likelihood tree estimation against different patterns of base substitutions

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An evolutionary perspective on synonymous codon usage in unicellular organisms

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The number of nucleotides required to determine the branching order of three species, with special reference to the human-chimpanzee-gorilla divergence

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Property and efficiency of the maximum likelihood method for molecular phylogeny

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Evolution of cytochrome c genes and pseudogenes

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Mutation pattern of human immunodeficiency virus genes

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The distribution of the dinucleotide CpG and cytosine methylation in the vitellogenin gene family

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Extreme differences in charge changes during protein evolution

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Pattern of nucleotide substitution and the extent of purifying selection in retroviruses

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Strand symmetry of mutation rates in theβ-globin region

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An analysis of codon usage in mammals: Selection or mutation bias?

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Nucleic acid composition, codon usage, and the rate of synonymous substitution in protein-coding genes

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Molecular evolutionary rates of oncogenes

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Evolutionary change of restriction sites under unequal rates of nucleotide substitution among the three positions of codons

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On transition bias in mitochondrial genes of pocket gophers

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The evolution of long interspersed repeated DNA (L1, LINE 1) as revealed by the analysis of an ancient rodent L1 DNA family

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Potential problems in estimating the male-to-female mutation rate ratio from DNA sequence data

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Pattern of synonymous and nonsynonymous substitutions: An indicator of mechanisms of molecular evolution

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Contribution of Mutation and RNA Recombination to the Evolution of a Plant Pathogenic RNA

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Mutation Pattern Variation Among Regions of the Primate Genome

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The Influence of Specific Neighboring Bases on Substitution Bias in Noncoding Regions of the Plant Chloroplast Genome

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Theoretical minimal RNA rings designed according to coding constraints mimic deamination gradients

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The α-gliadin gene family. II. DNA and protein sequence variation, subfamily structure, and origins of pseudogenes

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Cost-Minimization of Amino Acid Usage

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Reduced Polymorphism in the Chimpanzee Semen Coagulating Protein, Semenogelin I

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Processed Pseudogenes, Processed Genes, and Spontaneous Mutations in the Arabidopsis Genome

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Rates of Conservative and Radical Nonsynonymous Nucleotide Substitutions in Mammalian Nuclear Genes

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Disparate Evolution of Paralogous Introns in the Xdh Gene of Drosophila

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The Codon-Degeneracy Model of Molecular Evolution

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Ss-bCNGa: a unique member of the bacterial cyclic nucleotide gated (bCNG) channel family that gates in response to mechanical tension

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Cytonuclear disequilibria in wild populations of rabbit ( Oryctolagus cuniculus L. ) suggest unequal allele turnover rates at the b locus ( IGKC1 )

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A novel Cx50 (GJA8) p.H277Y mutation associated with autosomal dominant congenital cataract identified with targeted next-generation sequencing

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Profiles of accepted mutation: from neutrality in a pseudogene to disease-causing mutation on its homologous gene

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Examination of the selective pressures on a live PRRS vaccine virus

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The Structure and Diversity of α1-Acid Glycoprotein/Orosomucoid Gene in Africans

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Voltage-Gated Sodium Channel NaV1.2: Structural Perspective of the Genetic Variability

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Molecular evolution of paclitaxel biosynthetic genes TS and DBAT of Taxus species

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Molecular evolution of the membrane associated progesterone receptor in the Brachionus plicatilis (Rotifera, Monogononta) species complex

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Comparison of Ribosomal DNA ITS Regions Among Hippophae rhamnoides ssp. sinensis from Different Geographic Areas in China

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The study of neighboring nucleotide composition and transition/transversion bias

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Population genomic landscapes and insights for conservation of the critically endangered island-endemic Chinese pangolin in Taiwan

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The rates and patterns of insertions, deletions and substitutions in mouse and rat inferred from introns

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Prediction of sites under adaptive evolution in flavin-containing monooxygenases: Selection pattern revisited

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Fractals and Wavelets : What Can We Learn on Transcription and Replication from Wavelet-Based Multifractal Analysis of DNA Sequences ?

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Extreme variations in the ratios of non‐synonymous to synonymous nucleotide substitution rates in signal peptide evolution

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A conserved intron in the V‐ATPase A subunit genes of plants and algae

inferred← citeshttps://doi.org/10.1016/0022-2836(89)90501-9openalex-snapshot

Chromosome localization-dependent compositional bias of point mutations in Alu repetitive sequences

inferred← citeshttps://doi.org/10.1016/0022-2836(91)80109-8openalex-snapshot

Secondary structure as a constraint on the evolution of a plant viral satellite RNA

inferred← citeshttps://doi.org/10.1016/0022-2836(92)90465-vopenalex-snapshot

Extreme divergence of a novel wheat thionin generated by a mutational burst specifically affecting the mature protein domain of the precursor

inferred← citeshttps://doi.org/10.1016/0022-2836(94)90009-4openalex-snapshot

Wide variations in neighbor-dependent substitution rates

inferred← citeshttps://doi.org/10.1016/0027-5107(87)90042-xopenalex-snapshot

Rate of base substitution in mammalian nuclear DNA is dependent on local sequence context

inferred← citeshttps://doi.org/10.1016/0027-5107(92)90109-fopenalex-snapshot

Local sequence dependence of rate of base replacement in mammals

inferred← citeshttps://doi.org/10.1016/0042-6822(92)90082-zopenalex-snapshot

The sequence of the genome of adenovirus type 5 and its comparison with the genome of adenovirus type 2

inferred← citeshttps://doi.org/10.1016/0076-6879(90)83042-8openalex-snapshot

[40] Statistical tests of molecular phylogenies

inferred← citeshttps://doi.org/10.1016/0097-8485(92)80043-yopenalex-snapshot

The pattern of substitution mutation in different nearest-neighbor environments of the human genome

inferred← citeshttps://doi.org/10.1016/0097-8485(93)85005-wopenalex-snapshot

On the robustness of maximum entropy relationships for complexity distributions of nucleotide sequences

inferred← citeshttps://doi.org/10.1016/0166-3542(96)00944-8openalex-snapshot

Nucleotide substitution patterns can predict the requirements for drug-resistance of HIV-1 proteins

inferred← citeshttps://doi.org/10.1016/0167-5699(93)90144-aopenalex-snapshot

Discriminating intrinsic and actigen-selected mutational hotspots in immunoglobulin V genes

inferred← citeshttps://doi.org/10.1016/0169-5347(96)10009-4openalex-snapshot

The excess of transitions among nucleotide substitutions: new methods of estimating transition bias underscore its significance

inferred← citeshttps://doi.org/10.1016/0303-2647(92)90047-3openalex-snapshot

The uncertainty principle as an evolutionary engine

inferred← citeshttps://doi.org/10.1016/0378-1119(91)90056-hopenalex-snapshot

Cloning and nucleotide sequence of the chimpanzee c-myc gene

inferred← citeshttps://doi.org/10.1016/0378-1119(92)90520-yopenalex-snapshot

Gibbon and marmoset c-myc nucleotide sequences

inferred← citeshttps://doi.org/10.1016/0888-7543(88)90085-7openalex-snapshot

The spider monkey ψη-globin gene and surrounding sequences: Recent or ancient insertions of LINEs and SINEs?

inferred← citeshttps://doi.org/10.1016/0888-7543(92)90448-2openalex-snapshot

Sequence organization of variant mouse 4.5 S RNA genes and pseudogenes

inferred← citeshttps://doi.org/10.1016/1050-3862(94)90051-5openalex-snapshot

Selection of oligonucleotide probes and experimental conditions for multiplex hybridization experiments

inferred← citeshttps://doi.org/10.1016/b978-0-12-398760-0.50017-1openalex-snapshot

ESTIMATION OF THE NUMBERS OF SYNONYMOUS AND NONSYNONYMOUS SUBSTITUTIONS BETWEEN PROTEIN CODING GENES11This work was supported by NIH grant GM30998.

inferred← citeshttps://doi.org/10.1016/b978-0-12-816125-8.00023-7openalex-snapshot

Bioinformatic Approaches for Repurposing and Repositioning Antibiotics, Antiprotozoals, and Antivirals

inferred← citeshttps://doi.org/10.1016/b978-012053640-5/50006-9openalex-snapshot

The maturation of the antibody response

inferred← citeshttps://doi.org/10.1016/b978-012220360-2/50006-4openalex-snapshot

The Fidelity of Cellular and Viral polymerases and its manipulation for Hypermutagenesis

inferred← citeshttps://doi.org/10.1016/j.ajhg.2009.03.006openalex-snapshot

Autosomal-Dominant Distal Myopathy Associated with a Recurrent Missense Mutation in the Gene Encoding the Nuclear Matrix Protein, Matrin 3

inferred← citeshttps://doi.org/10.1016/j.ajhg.2011.01.008openalex-snapshot

Hexosamine Biosynthetic Pathway Mutations Cause Neuromuscular Transmission Defect

inferred← citeshttps://doi.org/10.1016/j.ajhg.2012.04.002openalex-snapshot

A Human Homeotic Transformation Resulting from Mutations in PLCB4 and GNAI3 Causes Auriculocondylar Syndrome

inferred← citeshttps://doi.org/10.1016/j.ajhg.2012.05.018openalex-snapshot

HOXB1 Founder Mutation in Humans Recapitulates the Phenotype of Hoxb1 Mice

inferred← citeshttps://doi.org/10.1016/j.biosystems.2017.03.001openalex-snapshot

A binary representation of the genetic code

inferred← citeshttps://doi.org/10.1016/j.biosystems.2020.104116openalex-snapshot

Deamination gradients within codons after 1<−>2 position swap predict amino acid hydrophobicity and parallel β-sheet conformational preference

inferred← citeshttps://doi.org/10.1016/j.cub.2018.12.008openalex-snapshot

The Genomic Footprints of the Fall and Recovery of the Crested Ibis

inferred← citeshttps://doi.org/10.1016/j.gene.2005.03.003openalex-snapshot

Molecular evolution of growth hormone gene family in old world monkeys and hominoids

inferred← citeshttps://doi.org/10.1016/j.gene.2005.05.019openalex-snapshot

An investigation of the variation in the transition bias among various animal mitochondrial DNA

inferred← citeshttps://doi.org/10.1016/j.gene.2005.08.024openalex-snapshot

Sequence context analysis of 8.2 million single nucleotide polymorphisms in the human genome

inferred← citeshttps://doi.org/10.1016/j.gene.2005.10.025openalex-snapshot

Evolutionary conservation and mutational spectrum of BMPR2 gene

inferred← citeshttps://doi.org/10.1016/j.gene.2013.09.114openalex-snapshot

Extraordinarily low evolutionary rates of short wavelength-sensitive opsin pseudogenes

inferred← citeshttps://doi.org/10.1016/j.gene.2014.05.019openalex-snapshot

Signatures of natural selection in the mitochondrial genomes of Tachycineta swallows and their implications for latitudinal patterns of the ‘pace of life’

inferred← citeshttps://doi.org/10.1016/j.gene.2017.10.001openalex-snapshot

Presence of a consensus DNA motif at nearby DNA sequence of the mutation susceptible CG nucleotides

inferred← citeshttps://doi.org/10.1016/j.gene.2023.147373openalex-snapshot

MicroRNA sequence variation can impact interactions with target mRNA in cattle

inferred← citeshttps://doi.org/10.1016/j.jtbi.2006.02.004openalex-snapshot

Error propagation across levels of organization: From chemical stability of ribosomal RNA to developmental stability

inferred← citeshttps://doi.org/10.1016/j.meegid.2021.105030openalex-snapshot

Evolutionary analysis of the anti-viral STAT2 gene of primates and rodents: Signature of different stages of an arms race

inferred← citeshttps://doi.org/10.1016/j.physrep.2010.10.001openalex-snapshot

Multi-scale coding of genomic information: From DNA sequence to genome structure and function

inferred← citeshttps://doi.org/10.1016/j.pld.2023.06.005openalex-snapshot

Conservation genomic investigation of an endangered conifer, Thuja sutchuenensis, reveals low genetic diversity but also low genetic load

inferred← citeshttps://doi.org/10.1016/j.pld.2024.04.001openalex-snapshot

Genomic divergence and mutation load in the Begonia masoniana complex from limestone karsts

inferred← citeshttps://doi.org/10.1016/j.vas.2023.100303openalex-snapshot

Analysis of RBD-ACE2 interactions in livestock species as a factor in the spread of SARS-CoV-2 among animals

inferred← citeshttps://doi.org/10.1016/j.ygcen.2021.113791openalex-snapshot

Molecular evolutionary insights from PRLR in mammals

inferred← citeshttps://doi.org/10.1016/j.ygeno.2004.06.015openalex-snapshot

The influence of neighboring-nucleotide composition on single nucleotide polymorphisms (SNPs) in the mouse genome and its comparison with human SNPs

inferred← citeshttps://doi.org/10.1016/j.ygeno.2005.09.012openalex-snapshot

Sequence context analysis in the mouse genome: Single nucleotide polymorphisms and CpG island sequences

inferred← citeshttps://doi.org/10.1016/j.ygeno.2006.06.003openalex-snapshot

Mutational spectrum in the recent human genome inferred by single nucleotide polymorphisms

inferred← citeshttps://doi.org/10.1016/j.ympev.2008.04.030openalex-snapshot

Exploring tree-building methods and distinct molecular data to recover a known asymmetric phage phylogeny

inferred← citeshttps://doi.org/10.1016/s0021-9258(18)68333-4openalex-snapshot

Molecular cloning and characterization of human atrial and ventricular myosin alkali light chain cDNA clones.

inferred← citeshttps://doi.org/10.1016/s0022-5193(86)80164-3openalex-snapshot

The evolution of electrophoretic mobility of proteins

inferred← citeshttps://doi.org/10.1016/s0022-5193(88)80243-1openalex-snapshot

Free fitness that always increases in evolution

inferred← citeshttps://doi.org/10.1016/s0027-5107(03)00014-9openalex-snapshot

SNP and haplotype variation in the human genome

inferred← citeshttps://doi.org/10.1016/s0065-2660(08)60458-7openalex-snapshot

The Drosophila Alcohol Dehydrogenase Gene–Enzyme System

inferred← citeshttps://doi.org/10.1016/s0167-4781(03)00144-1openalex-snapshot

The human mitochondrial translation initiation factor 2 gene (MTIF2): transcriptional analysis and identification of a pseudogene

inferred← citeshttps://doi.org/10.1016/s0378-1119(03)00379-2openalex-snapshot

Amino acid substitutions in the human genome: evolutionary implications of single nucleotide polymorphisms

inferred← citeshttps://doi.org/10.1016/s0378-1119(03)00670-xopenalex-snapshot

Investigating single nucleotide polymorphism (SNP) density in the human genome and its implications for molecular evolution

inferred← citeshttps://doi.org/10.1016/s0378-1119(03)00697-8openalex-snapshot

High mutation rates in human and ape pseudoautosomal genes

inferred← citeshttps://doi.org/10.1016/s0378-1119(97)00516-7openalex-snapshot

Trash DNA is what gets thrown away: high rate of DNA loss in Drosophila

inferred← citeshttps://doi.org/10.1016/s0378-4347(99)00571-xopenalex-snapshot

Allelic discrimination by denaturing high-performance liquid chromatography

inferred← citeshttps://doi.org/10.1016/s0888-7543(03)00009-0openalex-snapshot

Distribution analysis of nonsynonymous polymorphisms within the G-protein-coupled receptor gene family

inferred← citeshttps://doi.org/10.1016/s0921-8777(01)00108-2openalex-snapshot

Human germline mutation in the factor IX gene

inferred← citeshttps://doi.org/10.1017/s0016672300030676openalex-snapshot

The role of DNA replication and isochores in generating mutation and silent substitution rate variance in mammals

inferred← citeshttps://doi.org/10.1021/ci5001136openalex-snapshot

Combination of Genetic Screening and Molecular Dynamics as a Useful Tool for Identification of Disease-Related Mutations: ZASP PDZ Domain G54S Mutation Case

inferred← citeshttps://doi.org/10.1021/mp400193ropenalex-snapshot

Functional Analysis of Novel Variants in the Organic Cation/Ergothioneine Transporter 1 Identified in Singapore Populations

inferred← citeshttps://doi.org/10.1023/a:1005808615763openalex-snapshot

Structural analyses of plastid-derived 16S rRNAs in holoparasitic angiosperms

inferred← citeshttps://doi.org/10.1023/a:1005901413475openalex-snapshot

Molecular evolution of cdc2 pseudogenes in spruce (Picea)

inferred← citeshttps://doi.org/10.1023/a:1016076215168openalex-snapshot

DNA loss and evolution of genome size in Drosophila

inferred← citeshttps://doi.org/10.1038/35002070openalex-snapshot

Rapid evolution of male reproductive genes in the descent of man

inferred← citeshttps://doi.org/10.1038/icb.1996.44openalex-snapshot

Gene family use and somatic mutation in primary and secondary fluorescein‐specific IgM antibody responses

inferred← citeshttps://doi.org/10.1038/nbt1286openalex-snapshot

Improving catalytic function by ProSAR-driven enzyme evolution

inferred← citeshttps://doi.org/10.1038/ng.886openalex-snapshot

Increased exonic de novo mutation rate in individuals with schizophrenia

inferred← citeshttps://doi.org/10.1038/ng1103openalex-snapshot

Transcription-associated mutational asymmetry in mammalian evolution

inferred← citeshttps://doi.org/10.1038/npg.els.0005118openalex-snapshot

Pseudogenes and their Evolution

inferred← citeshttps://doi.org/10.1038/s41439-025-00312-4openalex-snapshot

Two novel pathogenic PDX1 variants in two Japanese patients with maturity-onset diabetes of the young

inferred← citeshttps://doi.org/10.1038/s41467-026-68867-6openalex-snapshot

Genomic consequences of residual recombination in a hybrid apomictic hickory complex

inferred← citeshttps://doi.org/10.1038/s41588-018-0167-zopenalex-snapshot

Predicting the clinical impact of human mutation with deep neural networks

inferred← citeshttps://doi.org/10.1038/s41598-017-04457-3openalex-snapshot

Mitochondrial haplotypes influence metabolic traits across bovine inter- and intra-species cybrids

inferred← citeshttps://doi.org/10.1038/s41598-017-06056-8openalex-snapshot

Origin and dispersal of early domestic pigs in northern China

inferred← citeshttps://doi.org/10.1038/s42003-022-03757-3openalex-snapshot

Whole-genome resequencing of Chinese pangolins reveals a population structure and provides insights into their conservation

inferred← citeshttps://doi.org/10.1038/s42003-024-07036-1openalex-snapshot

Signatures of local adaptation and maladaptation to future climate in wild Zizania latifolia

inferred← citeshttps://doi.org/10.1038/s42003-026-09846-xopenalex-snapshot

Population genomics of Quercus gilva provides insights into the conservation of fengshui forests

inferred← citeshttps://doi.org/10.1038/srep13118openalex-snapshot

Mitochondrial Haplotypes Influence Metabolic Traits in Porcine Transmitochondrial Cybrids

inferred← citeshttps://doi.org/10.1038/srep27272openalex-snapshot

Purifying selection shapes the coincident SNP distribution of primate coding sequences

inferred← citeshttps://doi.org/10.1073/pnas.0404142101openalex-snapshot

Bayesian Markov chain Monte Carlo sequence analysis reveals varying neutral substitution patterns in mammalian evolution

inferred← citeshttps://doi.org/10.1073/pnas.0730857100openalex-snapshot

Natural variation in human membrane transporter genes reveals evolutionary and functional constraints

inferred← citeshttps://doi.org/10.1073/pnas.0912499106openalex-snapshot

Mutation patterns in cancer genomes

inferred← citeshttps://doi.org/10.1073/pnas.200348197openalex-snapshot

Worldwide DNA sequence variation in a 10-kilobase noncoding region on human chromosome 22

inferred← citeshttps://doi.org/10.1073/pnas.2233252100openalex-snapshot

Functional constraints and frequency of deleterious mutations in noncoding DNA of rodents

inferred← citeshttps://doi.org/10.1073/pnas.2304096120openalex-snapshot

Genomic analysis reveals a cryptic pangolin species

inferred← citeshttps://doi.org/10.1073/pnas.2406343121openalex-snapshot

Large-scale genome sequencing of giant pandas improves the understanding of population structure and future conservation initiatives

inferred← citeshttps://doi.org/10.1073/pnas.82.23.8114openalex-snapshot

DNA methylation at asymmetric sites is associated with numerous transition mutations.

inferred← citeshttps://doi.org/10.1073/pnas.85.10.3499openalex-snapshot

Spectrum of spontaneous mutation at the APRT locus of Chinese hamster ovary cells: an analysis at the DNA sequence level.

inferred← citeshttps://doi.org/10.1073/pnas.90.6.2385openalex-snapshot

Passenger transgenes reveal intrinsic specificity of the antibody hypermutation mechanism: clustering, polarity, and specific hot spots.

inferred← citeshttps://doi.org/10.1073/pnas.91.2.827openalex-snapshot

Weak male-driven molecular evolution in rodents.

inferred← citeshttps://doi.org/10.1073/pnas.92.21.9717openalex-snapshot

Neighboring base composition and transversion/transition bias in a comparison of rice and maize chloroplast noncoding regions.

inferred← citeshttps://doi.org/10.1073/pnas.93.24.13919openalex-snapshot

Transcription-induced mutations: Increase in C to T mutations in the nontranscribed strand during transcription in Escherichia coli

inferred← citeshttps://doi.org/10.1073/pnas.94.11.5722openalex-snapshot

Molecular evolution of angiosperm mitochondrial introns and exons

inferred← citeshttps://doi.org/10.1073/pnas.94.21.11422openalex-snapshot

Accelerated evolution as a consequence of transitions to mutualism

inferred← citeshttps://doi.org/10.1073/pnas.95.9.5088openalex-snapshot

The role of robustness and changeability on the origin and evolution of genetic codes

inferred← citeshttps://doi.org/10.1073/pnas.96.4.1475openalex-snapshot

Patterns of nucleotide substitution in Drosophila and mammalian genomes

inferred← citeshttps://doi.org/10.1080/106351500750049734openalex-snapshot

Quantification of Homoplasy for Nucleotide Transitions and Transversions and a Reexamination of Assumptions in Weighted Phylogenetic Analysis

inferred← citeshttps://doi.org/10.1084/jem.168.2.475openalex-snapshot

Mutational hot spots in Ig V region genes of human follicular lymphomas.

inferred← citeshttps://doi.org/10.1084/jem.169.6.2007openalex-snapshot

Early onset of somatic mutation in immunoglobulin VH genes during the primary immune response.

showing the first 200 of 359

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