scholarly article | Q13442814 |
P6179 | Dimensions Publication ID | 1046083466 |
P356 | DOI | 10.1186/1745-6150-8-24 |
P932 | PMC publication ID | 4231362 |
P698 | PubMed publication ID | 24139515 |
P5875 | ResearchGate publication ID | 258057905 |
P2093 | author name string | Adi Livnat | |
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How malaria has affected the human genome and what human genetics can teach us about malaria | Q21032480 | ||
Emergence of young human genes after a burst of retroposition in primates | Q21092789 | ||
A map of recent positive selection in the human genome | Q21563624 | ||
Perspective: A Critique of Sewall Wright's Shifting Balance Theory of Evolution | Q22064589 | ||
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Darwinian alchemy: Human genes from noncoding DNA | Q22065773 | ||
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Massive Horizontal Gene Transfer in Bdelloid Rotifers | Q22065861 | ||
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Climbing Mount Probable: Mutation as a Cause of Nonrandomness in Evolution | Q22066030 | ||
On the immortality of television sets: "function" in the human genome according to the evolution-free gospel of ENCODE | Q22066047 | ||
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Genomic evidence for ameiotic evolution in the bdelloid rotifer Adineta vaga | Q22122134 | ||
An integrated encyclopedia of DNA elements in the human genome | Q22122150 | ||
Mapping and sequencing of structural variation from eight human genomes | Q22122215 | ||
Selfish DNA: the ultimate parasite | Q22122417 | ||
Selfish genes, the phenotype paradigm and genome evolution | Q22122418 | ||
Hominoid-specific de novo protein-coding genes originating from long non-coding RNAs | Q34426574 | ||
Non-B DNA structure-induced genetic instability and evolution | Q34473652 | ||
Evolutionary fate of retroposed gene copies in the human genome | Q34480366 | ||
Mutationism and the dual causation of evolutionary change | Q34523907 | ||
Animals mix it up too: the distribution of self-fertilization among hermaphroditic animals | Q34579910 | ||
Regulating general mutation rates: examination of the hypermutable state model for Cairnsian adaptive mutation. | Q34617476 | ||
Human SNP variability and mutation rate are higher in regions of high recombination | Q34750287 | ||
Molecular mechanisms for genomic disorders | Q34762662 | ||
Collective evolution and the genetic code | Q34771128 | ||
A clarification of pollen discounting and its joint effects with inbreeding depression on mating system evolution | Q34834572 | ||
The biogenesis and function of PIWI proteins and piRNAs: progress and prospect | Q34990505 | ||
Gene duplication and other evolutionary strategies: from the RNA world to the future | Q35167114 | ||
Characterization of a spontaneous mutation to a beta-thalassemia allele | Q35200973 | ||
Mutation rate distribution inferred from coincident SNPs and coincident substitutions | Q35211692 | ||
A chromosomal rearrangement hotspot can be identified from population genetic variation and is coincident with a hotspot for allelic recombination | Q35221469 | ||
Natural selection and the emergence of a mutation phenotype: an update of the evolutionary synthesis considering mechanisms that affect genome variation | Q35550595 | ||
An evolutionary reduction principle for genetic modifiers | Q35614856 | ||
Complex human chromosomal and genomic rearrangements | Q35731269 | ||
Evidence for de novo evolution of testis-expressed genes in the Drosophila yakuba/Drosophila erecta clade | Q35846239 | ||
Sexual selection, genetic conflict, selfish genes, and the atypical patterns of gene expression in spermatogenic cells | Q35967889 | ||
Extensive parallelism in protein evolution | Q36062958 | ||
Genome-wide genetic variations are highly correlated with proximal DNA methylation patterns | Q36130844 | ||
Echoes from the past--are we still in an RNP world? | Q36225256 | ||
PERSPECTIVE: THE THEORIES OF FISHER AND WRIGHT IN THE CONTEXT OF METAPOPULATIONS: WHEN NATURE DOES MANY SMALL EXPERIMENTS. | Q36387730 | ||
Evolution of recombination in a constant environment | Q36403048 | ||
TRIMCyp expression in Old World primates Macaca nemestrina and Macaca fascicularis | Q36491100 | ||
Independent genesis of chimeric TRIM5-cyclophilin proteins in two primate species | Q36491115 | ||
Positive selection in the evolution of cancer | Q36500617 | ||
Structural variation of the human genome | Q36509260 | ||
Alternative RNA splicing regulation in the testis | Q36664932 | ||
Non-B DNA conformations, mutagenesis and disease | Q36817656 | ||
Mechanisms for human genomic rearrangements | Q36975128 | ||
Analysis of copy number variants and segmental duplications in the human genome: Evidence for a change in the process of formation in recent evolutionary history | Q36995330 | ||
Evolutionary Rate at the Molecular Level | Q22122432 | ||
De novo origination of a new protein-coding gene in Saccharomyces cerevisiae | Q22305974 | ||
On the evolution of cells | Q24530769 | ||
A molecular approach to the study of genic heterozygosity in natural populations. II. Amount of variation and degree of heterozygosity in natural populations of Drosophila pseudoobscura | Q24533326 | ||
Modification of linkage intensity by natural selection | Q24533341 | ||
Hypervariable sites in the mtDNA control region are mutational hotspots | Q24538895 | ||
Extensive outcrossing and androdioecy in a vertebrate species that otherwise reproduces as a self-fertilizing hermaphrodite | Q24550968 | ||
Novel genes derived from noncoding DNA in Drosophila melanogaster are frequently X-linked and exhibit testis-biased expression | Q24550970 | ||
The genomic and transcriptomic landscape of a HeLa cell line | Q24632989 | ||
Is evolution Darwinian or/and Lamarckian? | Q24651873 | ||
Paired-end mapping reveals extensive structural variation in the human genome | Q24653260 | ||
Replication stalling at unstable inverted repeats: interplay between DNA hairpins and fork stabilizing proteins | Q24655285 | ||
On the origin of new genes in Drosophila | Q24655674 | ||
Independent evolution of an antiviral TRIMCyp in rhesus macaques | Q24656091 | ||
Functional bias and spatial organization of genes in mutational hot and cold regions in the human genome | Q24796018 | ||
A scan for positively selected genes in the genomes of humans and chimpanzees | Q24796729 | ||
Evolutionarily conserved and diverged alternative splicing events show different expression and functional profiles | Q24810664 | ||
Bias of selection on human copy-number variants | Q25257186 | ||
A de novo originated gene depresses budding yeast mating pathway and is repressed by the protein encoded by its antisense strand | Q27933502 | ||
Molecular basis for dominantly inherited inclusion body beta-thalassemia | Q28118609 | ||
On the possibility of constructive neutral evolution | Q28141783 | ||
Gene Regulation for Higher Cells: A Theory | Q28256064 | ||
A DNA replication mechanism for generating nonrecurrent rearrangements associated with genomic disorders | Q28262802 | ||
Evolution and tinkering | Q28276084 | ||
Why sex and recombination? | Q28283292 | ||
Common west African HLA antigens are associated with protection from severe malaria | Q28288693 | ||
Origin of primate orphan genes: a comparative genomics approach | Q28303276 | ||
CpG islands and the regulation of transcription | Q28315762 | ||
Emergence of a new gene from an intergenic region | Q28509330 | ||
RNA-based gene duplication: mechanistic and evolutionary insights | Q28681186 | ||
Transformation of a transposon into a derived prolactin promoter with function during human pregnancy | Q28727133 | ||
The mutational spectrum of non-CpG DNA varies with CpG content | Q28751110 | ||
On "genomenclature": a comprehensive (and respectful) taxonomy for pseudogenes and other "junk DNA" | Q34204541 | ||
Frameshift mutations and the genetic code. This paper is dedicated to Professor Theodosius Dobzhansky on the occasion of his 66th birthday | Q34229913 | ||
DNA methylation and the frequency of CpG in animal DNA. | Q34252001 | ||
POLYMORPHISM AND NATURAL SELECTION IN HUMAN POPULATIONS. | Q34259628 | ||
De novo mutations in human genetic disease | Q34288731 | ||
Evolving responsively: adaptive mutation | Q34297067 | ||
Phylogenetic patterns of emergence of new genes support a model of frequent de novo evolution | Q34329311 | ||
Ten years of genetics and genomics: what have we achieved and where are we heading? | Q34416724 | ||
Evolution of a TRIM5-CypA splice isoform in old world monkeys | Q28755216 | ||
CpG dinucleotides and the mutation rate of non-CpG DNA | Q28757270 | ||
A novel testis ubiquitin-binding protein gene arose by exon shuffling in hominoids | Q28757273 | ||
Caenorhabditis phylogeny predicts convergence of hermaphroditism and extensive intron loss | Q28775792 | ||
Cleistogamy: A tool for the study of floral morphogenesis, function and evolution | Q29013970 | ||
A POPULATION GENETIC THEORY OF CANALIZATION. | Q29038294 | ||
Genome architecture, rearrangements and genomic disorders | Q29614721 | ||
A fine-scale map of recombination rates and hotspots across the human genome | Q29614885 | ||
Inferring nonneutral evolution from human-chimp-mouse orthologous gene trios | Q29616015 | ||
Recent segmental duplications in the human genome | Q29616016 | ||
THE RELATION OF RECOMBINATION TO MUTATIONAL ADVANCE | Q29616118 | ||
Cancer/testis antigens, gametogenesis and cancer | Q29616129 | ||
DNA methylation landscapes: provocative insights from epigenomics | Q29617144 | ||
Cyclophilin A retrotransposition into TRIM5 explains owl monkey resistance to HIV-1 | Q29618920 | ||
Positive selection for the male functionality of a co-retroposed gene in the hominoids | Q30875924 | ||
Constant and hypervariable regions in conotoxin propeptides | Q33254000 | ||
Evolution of hydra, a recently evolved testis-expressed gene with nine alternative first exons in Drosophila melanogaster | Q33290219 | ||
The impact of recombination on nucleotide substitutions in the human genome | Q33332585 | ||
A microhomology-mediated break-induced replication model for the origin of human copy number variation | Q33404060 | ||
Cryptic variation in the human mutation rate | Q33405561 | ||
Cellular inheritance | Q33524161 | ||
A human-specific de novo protein-coding gene associated with human brain functions | Q33550753 | ||
Human triallelic sites: evidence for a new mutational mechanism? | Q33628441 | ||
Speciation of cone snails and interspecific hyperdivergence of their venom peptides. Potential evolutionary significance of introns | Q33692316 | ||
RNAs from all categories generate retrosequences that may be exapted as novel genes or regulatory elements | Q33778366 | ||
Discrete DNA sites regulate global distribution of meiotic recombination | Q33814609 | ||
An Alu Transposition Model for the Origin and Expansion of Human Segmental Duplications | Q33906041 | ||
New words in human mutagenesis. | Q33947155 | ||
Selection, generalized transmission and the evolution of modifier genes. I. The reduction principle | Q33953545 | ||
The population genetics of the haemoglobinopathies | Q33953606 | ||
Mechanisms of DNA double-strand break repair and their potential to induce chromosomal aberrations | Q33962417 | ||
Copy number variation in human health, disease, and evolution | Q34019142 | ||
Heterogeneous duplications in patients with Pelizaeus-Merzbacher disease suggest a mechanism of coupled homologous and nonhomologous recombination | Q34137518 | ||
Origins, evolution, and phenotypic impact of new genes. | Q34153587 | ||
Covert sex. | Q34159054 | ||
Ancient asexual scandals. | Q34159189 | ||
Primate CpG islands are maintained by heterogeneous evolutionary regimes involving minimal selection | Q34188001 | ||
Some Genetic Aspects of Sex | Q56235384 | ||
Enzyme Polymorphisms in Man | Q56267425 | ||
Complex gene rearrangements caused by serial replication slippage | Q57263791 | ||
Role of genomic architecture in PLP1 duplication causing Pelizaeus-Merzbacher disease | Q57537928 | ||
The structure and evolution of centromeric transition regions within the human genome | Q57690476 | ||
On the Origin of Species by Means of Natural Selection, or the Preservation of Favoured Races in the Struggle for Life | Q58704769 | ||
High genetic polymorphism of hemoglobin disorders in Laos | Q59389515 | ||
Evolution of Sex Determination in the Conchostracan Shrimp Eulimnadia texana | Q63379861 | ||
So much "junk" DNA in our genome | Q70462013 | ||
Selection against harmful mutations in large sexual and asexual populations | Q70563103 | ||
A general model for the evolution of recombination | Q71859154 | ||
Directional selection and the evolution of sex and recombination | Q72912312 | ||
Genomic disorders: structural features of the genome can lead to DNA rearrangements and human disease traits | Q77572380 | ||
Phenotype variability of the dominant beta-thalassemia induced in four Dutch families by the rare cd121 (G-->T) mutation | Q77754379 | ||
SOME ASPECTS OF EVOLUTION | Q81119764 | ||
The accessory burrows of digger wasps | Q81129148 | ||
Self-fertilization and the escape from pollen limitation in variable pollination environments | Q81150328 | ||
Allee effect and self-fertilization in hermaphrodites: reproductive assurance in demographically stable populations | Q81371878 | ||
The genetic mechanism of sex determination in the conchostracan shrimp Eulimnadia texana | Q83791627 | ||
Genomes on the edge: programmed genome instability in ciliates | Q37051931 | ||
Complex rearrangements in patients with duplications of MECP2 can occur by fork stalling and template switching | Q37201006 | ||
Understanding what determines the frequency and pattern of human germline mutations | Q37347927 | ||
Molecular evolution of the antiretroviral TRIM5 gene. | Q37399926 | ||
On the problems of a closed marriage: celebrating Darwin 200. | Q37455570 | ||
A Trim5-cyclophilin A fusion protein found in owl monkey kidney cells can restrict HIV-1. | Q37513372 | ||
Genetic recombination as a major cause of mutagenesis in the human globin gene clusters | Q37561798 | ||
Triggers for genomic rearrangements: insights into genomic, cellular and environmental influences | Q37806625 | ||
Variation in the mutation rate across mammalian genomes | Q37942062 | ||
More on selection for and against recombination | Q37952264 | ||
Transposable element recruitments in the mammalian placenta: impacts and mechanisms. | Q38023371 | ||
CpG mutation rates in the human genome are highly dependent on local GC content | Q38515926 | ||
Why are some genetic diseases common? Distinguishing selection from other processes by molecular analysis of globin gene variants | Q39006484 | ||
PERSPECTIVE: A CRITIQUE OF SEWALL WRIGHT'S SHIFTING BALANCE THEORY OF EVOLUTION. | Q39343164 | ||
Molecular basis and prenatal diagnosis of beta-thalassemia | Q39524584 | ||
Role of Mre11 in chromosomal nonhomologous end joining in mammalian cells | Q39820516 | ||
Mobile genetic elements in animal cells and their biological significance | Q40112136 | ||
On the evolutionary costs of self-incompatibility: incomplete reproductive compensation due to pollen limitation. | Q40471076 | ||
The Directed Mutation Controversy and Neo-Darwinism | Q40484446 | ||
Genomes were forged by massive bombardments with retroelements and retrosequences | Q40751648 | ||
The genomic distribution and local context of coincident SNPs in human and chimpanzee. | Q41198612 | ||
Population genetic perspectives on the evolution of recombination. | Q41291263 | ||
On the specificity of adaptive mutations. | Q41819829 | ||
RNA-mediated genome rearrangement: hypotheses and evidence | Q42174640 | ||
Allelic recombination and de novo deletions in sperm in the human beta-globin gene region | Q42681194 | ||
Transposon-mediated rewiring of gene regulatory networks contributed to the evolution of pregnancy in mammals. | Q42772867 | ||
What introns have to tell us: hierarchy in genome evolution | Q43498395 | ||
Heterogeneity of the transition/transversion ratio in Drosophila and Hominidae genomes. | Q43721710 | ||
The evolution of self-fertilization and inbreeding depression under pollen discounting and pollen limitation | Q44057266 | ||
Hypermutability of HoxA13A and functional divergence from its paralog are associated with the origin of a novel developmental feature in zebrafish and related taxa (Cypriniformes). | Q44523359 | ||
The ENCODE project: missteps overshadowing a success | Q45180939 | ||
A novel fusion gene, TRIM5-Cyclophilin A in the pig-tailed macaque determines its susceptibility to HIV-1 infection | Q46825405 | ||
GROUP SELECTION, SEX, AND FOSSILS. | Q47683049 | ||
Genome structural variation and sporadic disease traits | Q48085036 | ||
Natural inheritance | Q51508521 | ||
Prior selfing and the selfing syndrome in animals: an experimental approach in the freshwater snail Biomphalaria pfeifferi. | Q51714159 | ||
Cancer/testis (CT) antigens - a new link between gametogenesis and cancer | Q52105492 | ||
Conservation of hotspots for recombination in low-copy repeats associated with the NF1 microdeletion. | Q52840662 | ||
The testis as a conduit for genomic plasticity: an advanced interdisciplinary workshop. | Q52853747 | ||
Selection for linkage modification. I. Random mating populations. | Q52969891 | ||
Direct and indirect consequences of meiotic recombination: implications for genome evolution. | Q53092704 | ||
BAR DUPLICATION. | Q55044538 | ||
Weismann Rules! OK? Epigenetics and the Lamarckian temptation | Q55879436 | ||
The cost of natural selection | Q55897487 | ||
The Evolutionary Enigma of Mixed Mating Systems in Plants: Occurrence, Theoretical Explanations, and Empirical Evidence | Q56082823 | ||
Behavioral Homology and Phylogeny | Q56083577 | ||
The Cleistogamous Breeding System: A Review of Its Frequency, Evolution, and Ecology in Angiosperms | Q56171575 | ||
A Mathematical Theory of Saving | Q56172383 | ||
P433 | issue | 1 | |
P407 | language of work or name | English | Q1860 |
P304 | page(s) | 24 | |
P577 | publication date | 2013-10-18 | |
P1433 | published in | Biology Direct | Q1954915 |
P1476 | title | Interaction-based evolution: how natural selection and nonrandom mutation work together | |
P478 | volume | 8 |
Q34526653 | Algorithms, complexity, and the sciences |
Q46013855 | Evolution and Learning: Used Together, Fused Together. A Response to Watson and Szathmáry. |
Q47834821 | Genome evolution is driven by gene expression-generated biophysical constraints through RNA-directed genetic variation: A hypothesis |
Q36337880 | How evolution learns to generalise: Using the principles of learning theory to understand the evolution of developmental organisation. |
Q94672157 | Linking gut microbiota with the human diseases |
Q35236703 | Public health evolutionary biology of antimicrobial resistance: priorities for intervention |
Q33676605 | Simplification, Innateness, and the Absorption of Meaning from Context: How Novelty Arises from Gradual Network Evolution |
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