| editorial | Q871232 |
| scholarly article | Q13442814 |
| P6179 | Dimensions Publication ID | 1013497374 |
| P356 | DOI | 10.1186/1745-6150-5-14 |
| P932 | PMC publication ID | 2847548 |
| P698 | PubMed publication ID | 20307287 |
| P5875 | ResearchGate publication ID | 42388315 |
| P2093 | author name string | Victor P Shcherbakov | |
| P2860 | cites work | EVOLUTION IN MENDELIAN POPULATIONS | Q5418627 |
| Five rules for the evolution of cooperation | Q22065876 | ||
| Cell evolution and Earth history: stasis and revolution | Q22065915 | ||
| Individuality and adaptation across levels of selection: how shall we name and generalize the unit of Darwinism? | Q22066180 | ||
| The role of extinction in evolution | Q22066197 | ||
| Sexual reproduction as an adaptation to resist parasites (a review) | Q22066201 | ||
| EVOLUTION OF SEXRESOLVING THE PARADOX OF SEX AND RECOMBINATION | Q22121995 | ||
| Adaptive value of sex in microbial pathogens | Q22252364 | ||
| The evolutionary advantage of recombination | Q24533419 | ||
| The theory of speciation via the founder principle | Q24533498 | ||
| Rates of spontaneous mutation | Q24548000 | ||
| Estimate of the mutation rate per nucleotide in humans | Q24548130 | ||
| Multiple pathways of recombination induced by double-strand breaks in Saccharomyces cerevisiae | Q24548535 | ||
| On the conservative nature of intragenic recombination | Q24555721 | ||
| The high spontaneous mutation rate: is it a health risk? | Q24603867 | ||
| Coevolution of robustness, epistasis, and recombination favors asexual reproduction | Q24685529 | ||
| The major evolutionary transitions | Q28235986 | ||
| Origin of sex | Q28263040 | ||
| Reviving the superorganism | Q28280170 | ||
| Why sex and recombination? | Q28283292 | ||
| A phylogenomic inventory of meiotic genes; evidence for sex in Giardia and an early eukaryotic origin of meiosis | Q28304004 | ||
| Remarkably high activities of testicular cytochrome c in destroying reactive oxygen species and in triggering apoptosis | Q28505502 | ||
| Do species populations really start small? New perspectives from the Late Neogene fossil record of African mammals | Q28764961 | ||
| A theory of evolution above the species level | Q28775745 | ||
| The Croonian Lecture, 1991. Genostasis and the limits to evolution | Q43888306 | ||
| On punctuated equilibria | Q47794163 | ||
| Morphological analysis of germ cell apoptosis during postnatal testis development in normal and Hsp 70-2 knockout mice. | Q52197889 | ||
| On sex, mate selection and the red queen. | Q52208683 | ||
| Role of mutator alleles in adaptive evolution. | Q54564129 | ||
| The first sexual lineage and the relevance of facultative sex. | Q55033013 | ||
| Horizontal gene transfer in evolution: facts and challenges. | Q55052335 | ||
| Deleterious mutations as an evolutionary factor: 1. The advantage of recombination | Q56341012 | ||
| Genomes in Flux: The Evolution of Archaeal and Proteobacterial Gene Content | Q56918343 | ||
| Mitochondria and germ-cell death | Q59052600 | ||
| Risky Business: Sexual and Asexual Reproduction in Variable Environments | Q59187049 | ||
| Clades versus Clones in Evolution: Why We Have Sex | Q67318947 | ||
| Population genetic aspects of deleterious cytoplasmic genomes and their effect on the evolution of sexual reproduction | Q68027084 | ||
| Biased conversion as the primary function of recombination | Q70029822 | ||
| Classification of hypotheses on the advantage of amphimixis | Q70503887 | ||
| Speciation as a major reorganization of polygenic balances | Q70615149 | ||
| Emergence and maintenance of sex among diploid organisms aided by assortative mating | Q74236626 | ||
| Tempo and mode of speciation in the sea | Q77420842 | ||
| Direct estimates of human per nucleotide mutation rates at 20 loci causing Mendelian diseases | Q78705444 | ||
| Evolvability | Q79207684 | ||
| Gene co-inheritance and gene transfer | Q80019460 | ||
| Multilevel selection, cooperation, and altruism : Reflections on unto others: The evolution and psychology of unselfish behavior | Q85636767 | ||
| THE MAINTENANCE OF SEX BY PARASITISM AND MUTATION ACCUMULATION UNDER EPISTATIC FITNESS FUNCTIONS | Q88206848 | ||
| Recent development of the neutral theory viewed from the Wrightian tradition of theoretical population genetics | Q28775811 | ||
| Species selection on variability | Q28775904 | ||
| THE RELATION OF RECOMBINATION TO MUTATIONAL ADVANCE | Q29616118 | ||
| Accelerated mutation accumulation in asexual lineages of a freshwater snail | Q30432860 | ||
| Macroevolution is more than repeated rounds of microevolution | Q30659534 | ||
| The dynamics of Phanerozoic marine animal diversity agrees with the hyperbolic growth model | Q33276851 | ||
| Mutual policing and repression of competition in the evolution of cooperative groups | Q33366828 | ||
| Darwinian evolution in the light of genomics | Q33408694 | ||
| Reactivation of Irradiated Bacteriophage by Transfer of Self-Reproducing Units | Q33749275 | ||
| The evolution of mutation rates: separating causes from consequences | Q33925698 | ||
| High Negative Interference over Short Segments of the Genetic Structure of Bacteriophage T4. | Q33976870 | ||
| The mutational load with epistatic gene interactions in fitness | Q33983691 | ||
| Recent advances in understanding of the evolution and maintenance of sex. | Q34159194 | ||
| Deleterious mutations and the evolution of sexual reproduction | Q34164458 | ||
| Extension of covariance selection mathematics | Q34227739 | ||
| Mutation load and rapid adaptation favour outcrossing over self-fertilization. | Q34279988 | ||
| George Price's contributions to evolutionary genetics. | Q34288456 | ||
| Punctuated equilibrium comes of age. | Q34344229 | ||
| Commuting the death sentence: how oocytes strive to survive | Q34443613 | ||
| Programmed and altruistic ageing | Q34469684 | ||
| Digital genetics: unravelling the genetic basis of evolution | Q34485612 | ||
| Evolution of genetic variability and the advantage of sex and recombination in changing environments. | Q34607759 | ||
| Functional and ecological impacts of horizontal gene transfer in eukaryotes | Q34613589 | ||
| Regulating general mutation rates: examination of the hypermutable state model for Cairnsian adaptive mutation. | Q34617476 | ||
| Diploidy and the selective advantage for sexual reproduction in unicellular organisms | Q35012141 | ||
| Establishment of oocyte population in the fetal ovary: primordial germ cell proliferation and oocyte programmed cell death | Q36094983 | ||
| A genome-wide view of the spectrum of spontaneous mutations in yeast. | Q36756806 | ||
| Programmed genetic instability: a tumor-permissive mechanism for maintaining the evolvability of higher species through methylation-dependent mutation of DNA repair genes in the male germ line | Q36766892 | ||
| The cellular, developmental and population-genetic determinants of mutation-rate evolution | Q36936869 | ||
| Self-structuring in spatial evolutionary ecology | Q37028295 | ||
| Spontaneous mutation | Q37041840 | ||
| Why are sex and recombination so common? | Q37193328 | ||
| Signs of sex: what we know and how we know it. | Q37413715 | ||
| Imprinting of genome precludes parthenogenesis, but uniparental embryos can be rescued to reproduce | Q39544116 | ||
| Sexual imprinting, learning and speciation | Q41675453 | ||
| The generation of complexity in evolution: A thermodynamic and information-theoretical discussion | Q41748181 | ||
| P433 | issue | 1 | |
| P407 | language of work or name | English | Q1860 |
| P304 | page(s) | 14 | |
| P577 | publication date | 2010-03-22 | |
| P1433 | published in | Biology Direct | Q1954915 |
| P1476 | title | Biological species is the only possible form of existence for higher organisms: the evolutionary meaning of sexual reproduction | |
| P478 | volume | 5 |
Search more.