| scholarly article | Q13442814 |
| P2093 | author name string | Jeff Gore | |
| Andrea Velenich | |||
| P2860 | cites work | Universally sloppy parameter sensitivities in systems biology models | Q21145658 |
| Sucrose utilization in budding yeast as a model for the origin of undifferentiated multicellularity | Q21563533 | ||
| Genome evolution and adaptation in a long-term experiment with Escherichia coli | Q22122199 | ||
| Non-adaptive origins of interactome complexity | Q24607502 | ||
| An epistatic ratchet constrains the direction of glucocorticoid receptor evolution | Q27657553 | ||
| The genetic landscape of a cell | Q28131628 | ||
| What is flux balance analysis? | Q28275348 | ||
| Simpson's Paradox in a Synthetic Microbial System | Q29300436 | ||
| Escherichia coli K-12 undergoes adaptive evolution to achieve in silico predicted optimal growth | Q29397612 | ||
| Darwinian evolution can follow only very few mutational paths to fitter proteins | Q29616042 | ||
| In silico predictions of Escherichia coli metabolic capabilities are consistent with experimental data | Q29618471 | ||
| Emergent bistability by a growth-modulating positive feedback circuit | Q30495631 | ||
| Plasticity of the cis-regulatory input function of a gene | Q33239285 | ||
| The cost of expression of Escherichia coli lac operon proteins is in the process, not in the products | Q33317948 | ||
| Growth landscape formed by perception and import of glucose in yeast | Q33348349 | ||
| Death and cannibalism in a seasonal environment facilitate bacterial coexistence | Q33385515 | ||
| A mixture of "cheats" and "co-operators" can enable maximal group benefit | Q33698025 | ||
| Reciprocal sign epistasis between frequently experimentally evolved adaptive mutations causes a rugged fitness landscape | Q33892372 | ||
| Nonlinear fitness landscape of a molecular pathway | Q33981298 | ||
| Optimality and evolution of transcriptionally regulated gene expression | Q33994101 | ||
| Evolutionary accessibility of mutational pathways | Q34005257 | ||
| Sequence space and the ongoing expansion of the protein universe | Q34116384 | ||
| Reciprocal sign epistasis is a necessary condition for multi-peaked fitness landscapes. | Q34155513 | ||
| Metabolic trade-offs and the maintenance of the fittest and the flattest | Q34173698 | ||
| Cooperation and Hamilton's rule in a simple synthetic microbial system | Q34175797 | ||
| Ecosystems biology of microbial metabolism | Q34185936 | ||
| Extreme genome reduction in symbiotic bacteria | Q34230656 | ||
| Optimality and evolutionary tuning of the expression level of a protein | Q34437723 | ||
| The biochemical architecture of an ancient adaptive landscape | Q34461523 | ||
| Empirical fitness landscapes reveal accessible evolutionary paths | Q34606034 | ||
| From fitness landscapes to seascapes: non-equilibrium dynamics of selection and adaptation. | Q34949551 | ||
| Structure of deviations from optimality in biological systems. | Q35013239 | ||
| Competitive interactions in Escherichia coli populations: the role of bacteriocins | Q35018612 | ||
| The decoupling between genetic structure and metabolic phenotypes in Escherichia coli leads to continuous phenotypic diversity | Q35137906 | ||
| Bacterial growth laws and their applications | Q35154086 | ||
| Social conflict drives the evolutionary divergence of quorum sensing | Q35170708 | ||
| Synthetic cooperation in engineered yeast populations | Q35629292 | ||
| Evolutionary paths to antibiotic resistance under dynamically sustained drug selection | Q36500996 | ||
| A synthetic Escherichia coli predator-prey ecosystem | Q36663520 | ||
| Defined spatial structure stabilizes a synthetic multispecies bacterial community | Q36984976 | ||
| Synthetic control of a fitness tradeoff in yeast nitrogen metabolism | Q37074216 | ||
| The cost of gene expression underlies a fitness trade-off in yeast | Q37134524 | ||
| Tuning gene expression to changing environments: from rapid responses to evolutionary adaptation | Q37203938 | ||
| Evolutionary selection between alternative modes of gene regulation | Q37211321 | ||
| Sloppiness, robustness, and evolvability in systems biology | Q37213575 | ||
| Dynamics in the mixed microbial concourse | Q37814778 | ||
| The frequency of fitness peak shifts is increased at expanding range margins due to mutation surfing | Q39217959 | ||
| Diminishing returns epistasis among beneficial mutations decelerates adaptation | Q39954065 | ||
| Snowdrift game dynamics and facultative cheating in yeast | Q41200215 | ||
| The rate at which asexual populations cross fitness valleys | Q41491337 | ||
| Regulatory revolution: evolving the "anti-LacI" repressor | Q41987123 | ||
| Growth rate-dependent global effects on gene expression in bacteria | Q42062295 | ||
| Shifts in growth strategies reflect tradeoffs in cellular economics | Q42242972 | ||
| Emergent cooperation in microbial metabolism | Q42397954 | ||
| Cost of unneeded proteins in E. coli is reduced after several generations in exponential growth | Q43077744 | ||
| Negative epistasis between beneficial mutations in an evolving bacterial population | Q44010374 | ||
| Multiple peaks and reciprocal sign epistasis in an empirically determined genotype-phenotype landscape. | Q45401948 | ||
| Interdependence of cell growth and gene expression: origins and consequences. | Q45940657 | ||
| The Prisoner's Dilemma and polymorphism in yeast SUC genes. | Q51002601 | ||
| Phenotypic diversity, population growth, and information in fluctuating environments. | Q51965535 | ||
| Tradeoffs and optimality in the evolution of gene regulation. | Q53412988 | ||
| Hidden randomness between fitness landscapes limits reverse evolution. | Q54359491 | ||
| Mutational reversions during adaptive protein evolution | Q80447790 | ||
| P433 | issue | 3-4 | |
| P304 | page(s) | 323-328 | |
| P577 | publication date | 2012-06-08 | |
| P1433 | published in | Current Opinion in Chemical Biology | Q15758415 |
| P1476 | title | Synthetic approaches to understanding biological constraints | |
| P478 | volume | 16 |
| Q42379846 | Detecting the Collapse of Cooperation in Evolving Networks |
| Q35923572 | Dynamic control and quantification of bacterial population dynamics in droplets |
| Q36820204 | Range expansion promotes cooperation in an experimental microbial metapopulation. |
| Q34526498 | Scaling laws governing stochastic growth and division of single bacterial cells |
| Q42202304 | Secreting and sensing the same molecule allows cells to achieve versatile social behaviors |
| Q40587253 | The strength of genetic interactions scales weakly with mutational effects |
| Q51064344 | Universality in stochastic exponential growth. |
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