scholarly article | Q13442814 |
P6179 | Dimensions Publication ID | 1090828583 |
P356 | DOI | 10.1038/S41559-017-0228-1 |
P932 | PMC publication ID | 5540182 |
P698 | PubMed publication ID | 28782044 |
P50 | author | Balázs Papp | Q30518275 |
P2093 | author name string | Csaba Pál | |
P2860 | cites work | Rapid evolutionary escape by large populations from local fitness peaks is likely in nature. | Q52565464 |
Adaptive evolution of bacterial metabolic networks by horizontal gene transfer. | Q54474627 | ||
Environmental change exposes beneficial epistatic interactions in a catalytic RNA. | Q55436455 | ||
Irremediable Complexity? | Q58033712 | ||
The genetical theory of natural selection | Q61661297 | ||
Developmental Constraints and Evolution: A Perspective from the Mountain Lake Conference on Development and Evolution | Q61795275 | ||
Open issues in genetic programming | Q62680490 | ||
Exploiting the co-evolution of interacting proteins to discover interaction specificity | Q73073424 | ||
Stability-mediated epistasis constrains the evolution of an influenza protein | Q21128791 | ||
Facilitated variation: how evolution learns from past environments to generalize to new environments | Q21145369 | ||
The look-ahead effect of phenotypic mutations | Q21203773 | ||
A catalog of neutral and deleterious polymorphism in yeast | Q21563326 | ||
Historical contingency and the evolution of a key innovation in an experimental population of Escherichia coli | Q22066316 | ||
From The Origin of Species to the origin of bacterial flagella | Q22121991 | ||
The genetic theory of adaptation: a brief history | Q22122021 | ||
On the Evolution of Biochemical Syntheses | Q24522220 | ||
Protein stability promotes evolvability | Q24546311 | ||
Evolvability | Q24595167 | ||
Beyond directed evolution—semi-rational protein engineering and design | Q24604225 | ||
The rate of establishment of complex adaptations | Q24619467 | ||
Mutational processes molding the genomes of 21 breast cancers | Q24620915 | ||
Exploring protein fitness landscapes by directed evolution | Q24630945 | ||
Stepwise formation of the bacterial flagellar system | Q24683633 | ||
An epistatic ratchet constrains the direction of glucocorticoid receptor evolution | Q27657553 | ||
Increased mutagenesis and unique mutation signature associated with mitotic gene conversion | Q27934880 | ||
The evolutionary origin of complex features | Q28203090 | ||
Chaperonin overexpression promotes genetic variation and enzyme evolution | Q28247346 | ||
Programming cells by multiplex genome engineering and accelerated evolution | Q28253066 | ||
Environmental changes bridge evolutionary valleys | Q28272911 | ||
The 'evolvability' of promiscuous protein functions | Q28295483 | ||
Ancestral genes can control the ability of horizontally acquired loci to confer new traits | Q28479229 | ||
Fluctuating selection: the perpetual renewal of adaptation in variable environments | Q28748404 | ||
Scaling expectations for the time to establishment of complex adaptations | Q28749184 | ||
Evolution of increased complexity in a molecular machine | Q29545093 | ||
A systematic survey of loss-of-function variants in human protein-coding genes | Q29615756 | ||
Darwinian evolution can follow only very few mutational paths to fitter proteins | Q29616042 | ||
Neutral genetic drift can alter promiscuous protein functions, potentially aiding functional evolution | Q30479736 | ||
Genome shuffling leads to rapid phenotypic improvement in bacteria | Q30809181 | ||
Saltational evolution: hopeful monsters are here to stay | Q47644946 | ||
Evolvability as a function of purifying selection in TEM-1 β-lactamase | Q50438672 | ||
PERSPECTIVE: COMPLEX ADAPTATIONS AND THE EVOLUTION OF EVOLVABILITY. | Q51606245 | ||
On the Potential Origins of the High Stability of Reconstructed Ancestral Proteins. | Q51642957 | ||
How perfect can protein interactomes be? | Q51786485 | ||
The evolution of genetic networks by non-adaptive processes. | Q51905685 | ||
Guidelines: From artificial evolution to computational evolution: a research agenda. | Q51935923 | ||
Formation of regulatory modules by local sequence duplication | Q31036385 | ||
Intense neutral drifts yield robust and evolvable consensus proteins | Q33336905 | ||
Ohno's model revisited: measuring the frequency of potentially adaptive mutations under various mutational drifts | Q33358606 | ||
The puzzle of the Krebs citric acid cycle: assembling the pieces of chemically feasible reactions, and opportunism in the design of metabolic pathways during evolution. | Q33367704 | ||
Rapid diversification of cell signaling phenotypes by modular domain recombination | Q33556382 | ||
Adaptive evolution of complex innovations through stepwise metabolic niche expansion. | Q33622451 | ||
Deletional bias across the three domains of life. | Q33633504 | ||
Variation and evolution of the citric-acid cycle: a genomic perspective. | Q33677040 | ||
Applying neutral drift to the directed molecular evolution of a β-glucuronidase into a β-galactosidase: Two different evolutionary pathways lead to the same variant | Q33891617 | ||
Evolution of a metabolic pathway for degradation of a toxic xenobiotic: the patchwork approach | Q33904333 | ||
Deletional bias and the evolution of bacterial genomes | Q33955011 | ||
Stability effects of mutations and protein evolvability | Q34019441 | ||
A time-invariant principle of genome evolution | Q34059478 | ||
Network-level architecture and the evolutionary potential of underground metabolism. | Q34060771 | ||
A structural perspective of compensatory evolution | Q34079015 | ||
Permissive secondary mutations enable the evolution of influenza oseltamivir resistance | Q34118992 | ||
The rate of fitness-valley crossing in sexual populations. | Q34141931 | ||
Cryptic genetic variation promotes rapid evolutionary adaptation in an RNA enzyme | Q34189506 | ||
Evolutionary biochemistry: revealing the historical and physical causes of protein properties. | Q34358160 | ||
Horizontal gene transfer, genome innovation and evolution | Q34447824 | ||
Evolution of hormone-receptor complexity by molecular exploitation | Q34511638 | ||
Enzyme engineering by targeted libraries | Q34592014 | ||
Evolutionary meandering of intermolecular interactions along the drift barrier | Q34926385 | ||
From fitness landscapes to seascapes: non-equilibrium dynamics of selection and adaptation. | Q34949551 | ||
Should evolutionary geneticists worry about higher-order epistasis? | Q35035921 | ||
Deep mutational scanning: a new style of protein science | Q35541240 | ||
Protein evolution. Pervasive degeneracy and epistasis in a protein-protein interface. | Q35556345 | ||
Evolving new protein-protein interaction specificity through promiscuous intermediates. | Q35811852 | ||
GroEL and the maintenance of bacterial endosymbiosis | Q35864149 | ||
The evolution of multimeric protein assemblages | Q35919899 | ||
The Evolutionary Potential of Phenotypic Mutations | Q35921425 | ||
A highly precise and portable genome engineering method allows comparison of mutational effects across bacterial species | Q35925574 | ||
Varying environments can speed up evolution | Q35941090 | ||
Delayed commitment to evolutionary fate in antibiotic resistance fitness landscapes | Q35994748 | ||
Evolution of Robustness to Protein Mistranslation by Accelerated Protein Turnover | Q36257601 | ||
Breaking evolutionary constraint with a tradeoff ratchet | Q36354875 | ||
The genomic landscape and evolutionary resolution of antagonistic pleiotropy in yeast | Q36442608 | ||
Pervasive multinucleotide mutational events in eukaryotes | Q36553453 | ||
Evolutionary assembly patterns of prokaryotic genomes | Q36959159 | ||
Estimating the mutation load in human genomes | Q37121904 | ||
Adaptation in protein fitness landscapes is facilitated by indirect paths | Q37175865 | ||
Asymmetric relationships between proteins shape genome evolution. | Q37207176 | ||
Evolution of biomolecular networks: lessons from metabolic and protein interactions | Q37620156 | ||
Systems-biology approaches for predicting genomic evolution | Q37909892 | ||
The aneuploidy paradox: costs and benefits of an incorrect karyotype | Q37923163 | ||
Cumulative impact of chaperone-mediated folding on genome evolution | Q38061175 | ||
Evolutionary constraints in variable environments, from proteins to networks | Q38208066 | ||
Protein mistranslation: friend or foe? | Q38229416 | ||
The White-Knight Hypothesis, or Does the Environment Limit Innovations? | Q39015834 | ||
A global genetic interaction network maps a wiring diagram of cellular function | Q39318959 | ||
PERSPECTIVE: A CRITIQUE OF SEWALL WRIGHT'S SHIFTING BALANCE THEORY OF EVOLUTION. | Q39343164 | ||
An evolutionary biochemist's perspective on promiscuity | Q40354235 | ||
Intermolecular epistasis shaped the function and evolution of an ancient transcription factor and its DNA binding sites | Q41342939 | ||
Bacterial evolution of antibiotic hypersensitivity. | Q41867646 | ||
Evolution of protein complexes by duplication of homomeric interactions | Q41955358 | ||
Aneuploidy underlies rapid adaptive evolution of yeast cells deprived of a conserved cytokinesis motor | Q42033067 | ||
Limits of neutral drift: lessons from the in vitro evolution of two ribozymes. | Q42929210 | ||
Latent evolutionary potentials under the neutral mutational drift of an enzyme | Q43177884 | ||
Evolutionary dynamics of prokaryotic transcriptional regulatory networks | Q44136796 | ||
Compensatory evolution in mitochondrial tRNAs navigates valleys of low fitness | Q44504962 | ||
P433 | issue | 8 | |
P304 | page(s) | 1084-1092 | |
P577 | publication date | 2017-07-21 | |
P1433 | published in | Nature Ecology and Evolution | Q39049712 |
P1476 | title | Evolution of complex adaptations in molecular systems. | |
P478 | volume | 1 |
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Q89891674 | Readthrough errors purge deleterious cryptic sequences, facilitating the birth of coding sequences |
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