scholarly article | Q13442814 |
P2093 | author name string | J Adams | |
C N Vargas | |||
R B Helling | |||
Julian Adams | |||
Robert B Helling | |||
Christopher N Vargas | |||
P2860 | cites work | The control by respiration of the uptake of α-methyl glucoside in Escherichia coli K12 | Q66898793 |
The role of energy-spilling reactions in the growth of Klebsiella aerogenes NCTC 418 in aerobic chemostat culture | Q68246250 | ||
The generation of a ColE1-Apr cloning vehicle which allows detection of inserted DNA | Q68326869 | ||
The maintenance of Plasmid-containing organisms in populations of Escherichia coli | Q70209628 | ||
Tumors; a mixed bag of cells | Q70264698 | ||
The clonal evolution of tumor cell populations | Q28271546 | ||
Experiments with the Chemostat on spontaneous mutations of bacteria | Q33711073 | ||
Metabolic Regulation in Glucose-Limited Chemostat Cultures of Escherichia coli | Q33773089 | ||
Physiological characterization of adaptive clones in evolving populations of the yeast, Saccharomyces cerevisiae | Q33950972 | ||
Direct selection of L-arabinose negative mutants of Escherichia coli strain B@rl. | Q33979380 | ||
Structure of evolving populations of Saccharomyces cerevisiae: adaptive changes are frequently associated with sequence alterations involving mobile elements belonging to the Ty family | Q37400309 | ||
Stimulation of glycolysis and amino acid uptake in NRK-49F cells by transforming growth factor beta and epidermal growth factor | Q37679055 | ||
Evolution of tumours and the impact of molecular oncology | Q39494403 | ||
Transport of α-methyl glucoside in mutants of Escherichia coli K12 deficient in Ca2+, Mg2+-activated adenosine triphosphatase | Q39733671 | ||
Transport of α-methyl glucoside in a cytochrome-deficient mutant ofEscherichia coliK-12 | Q39768940 | ||
Phosphoenolpyruvate:carbohydrate phosphotransferase system of bacteria | Q39830391 | ||
The population genetics of Escherichia coli | Q40080341 | ||
Frequency-Dependent Selection for Plasmid-Containing Cells of ESCHERICHIA COLI. | Q42107041 | ||
Selective neutrality of 6PGD allozymes in E. coli and the effects of genetic background. | Q42990028 | ||
Glucose transport in Salmonella typhimurium and Escherichia coli | Q50214406 | ||
THE GLUCOSE PERMEASE SYSTEM IN BACTERIA | Q50268113 | ||
Frequency of fixation of adaptive mutations is higher in evolving diploid than haploid yeast populations | Q59092867 | ||
P433 | issue | 3 | |
P407 | language of work or name | English | Q1860 |
P921 | main subject | Escherichia coli | Q25419 |
P304 | page(s) | 349-358 | |
P577 | publication date | 1987-07-01 | |
P1433 | published in | Genetics | Q3100575 |
P1476 | title | Evolution of Escherichia coli during growth in a constant environment | |
Evolution of <i>Escherichia coli</i> During Growth in a Constant Environment | |||
P478 | volume | 116 |
Q57803669 | A shared coevolutionary history does not alter the outcome of coalescence in experimental populations of Pseudomonas fluorescens |
Q64076456 | A yield-cost tradeoff governs s decision between fermentation and respiration in carbon-limited growth |
Q68167329 | Adaptation and major chromosomal changes in populations of Saccharomyces cerevisiae |
Q57465837 | Adaptation limits ecological diversification and promotes ecological tinkering during the competition for substitutable resources |
Q39960085 | Adaptation of Salmonella typhimurium mutants containing uncoupled enzyme IIGlc to glucose-limited conditions |
Q42161738 | Adaptation of model genetically engineered microorganisms to lake water: growth rate enhancements and plasmid loss |
Q24545052 | Adaptive molecular evolution for 13,000 phage generations: a possible arms race |
Q90442733 | An enormous potential for niche construction through bacterial cross-feeding in a homogeneous environment |
Q33563144 | Beware batch culture: Seasonality and niche construction predicted to favor bacterial adaptive diversification |
Q28533513 | Community flux balance analysis for microbial consortia at balanced growth |
Q57169429 | Construction and Characterization of Synthetic Bacterial Community for Experimental Ecology and Evolution |
Q35736793 | Crowded growth leads to the spontaneous evolution of semistable coexistence in laboratory yeast populations. |
Q34609402 | Design and use of multiplexed chemostat arrays |
Q24794895 | Differences in codon bias cannot explain differences in translational power among microbes |
Q55283806 | Different adaptive strategies in E. coli populations evolving under macronutrient limitation and metal ion limitation. |
Q42738443 | Divergence and redundancy of transport and metabolic rate-yield strategies in a single Escherichia coli population |
Q37814778 | Dynamics in the mixed microbial concourse |
Q35782830 | Dynamics of Simple Food Webs |
Q33515252 | E Unibus Plurum: genomic analysis of an experimentally evolved polymorphism in Escherichia coli |
Q35124389 | Ecological perspectives on synthetic biology: insights from microbial population biology. |
Q60503746 | Effective models and the search for quantitative principles in microbial evolution |
Q36373474 | Emergence of microbial diversity due to cross-feeding interactions in a spatial model of gut microbial metabolism. |
Q42031695 | Enrichment and elimination of mutY mutators in Escherichia coli populations |
Q54203976 | Escherichia coli cultures maintain stable subpopulation structure during long-term evolution. |
Q35756922 | Evolution of coexistence in a crowded microplate well |
Q36456226 | Evolution of microbial diversity during prolonged starvation |
Q28752472 | Evolution of resource cycling in ecosystems and individuals |
Q24545715 | Evolution of specialists in an experimental microcosm |
Q39751889 | Evolutionary engineering of Saccharomyces cerevisiae for anaerobic growth on xylose |
Q27330287 | Evolutionary pressures on microbial metabolic strategies in the chemostat |
Q51316362 | Evolutionary rescue and the coexistence of generalist and specialist competitors: an experimental test. |
Q33811779 | Ex uno plures: clonal reinforcement drives evolution of a simple microbial community |
Q57174769 | Experimental Design, Population Dynamics, and Diversity in Microbial Experimental Evolution |
Q34611032 | Experimental analysis of molecular events during mutational periodic selections in bacterial evolution. |
Q34464683 | FREQ-Seq: a rapid, cost-effective, sequencing-based method to determine allele frequencies directly from mixed populations |
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Q38165448 | Intra-tumor heterogeneity: lessons from microbial evolution and clinical implications |
Q34570453 | Laboratory-dependent bacterial ecology: a cautionary tale |
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Q34607657 | Mutational adaptation of Escherichia coli to glucose limitation involves distinct evolutionary pathways in aerobic and oxygen-limited environments. |
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Q57460084 | Neutral and selective dynamics in a synthetic microbial community |
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Q33967085 | On genetic map functions |
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Q33736264 | Parallel and divergent genotypic evolution in experimental populations of Ralstonia sp |
Q28708794 | Parallel evolutionary dynamics of adaptive diversification in Escherichia coli |
Q39567512 | Pathway choice in glutamate synthesis in Escherichia coli. |
Q42651561 | Perceiving molecular evolution processes in Escherichia coli by comprehensive metabolite and gene expression profiling |
Q36055368 | Pervasive Selection for Cooperative Cross-Feeding in Bacterial Communities. |
Q54308248 | Plasmid macro-evolution: selection of deletions during adaptation in a nutrient-limited environment |
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Q34613893 | Profiles of adaptation in two similar viruses |
Q79691116 | Protein carbon content evolves in response to carbon availability and may influence the fate of duplicated genes |
Q35209137 | Quantifying the effects of the division of labor in metabolic pathways |
Q28607257 | Replaying Evolution to Test the Cause of Extinction of One Ecotype in an Experimentally Evolved Population |
Q35010326 | Resource availability and competition shape the evolution of survival and growth ability in a bacterial community |
Q34682045 | SIZE DOESN'T MATTER: MICROBIAL SELECTION EXPERIMENTS ADDRESS ECOLOGICAL PHENOMENA. |
Q36824400 | Selection intensity for codon bias and the effective population size of Escherichia coli |
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Q51180623 | Spatial structure leads to ecological breakdown and loss of diversity. |
Q39678201 | Speed versus efficiency in microbial growth and the role of parallel pathways |
Q36236273 | Stability of Cross-Feeding Polymorphisms in Microbial Communities |
Q35959844 | Stock culture heterogeneity rather than new mutational variation complicates short-term cell physiology studies of Escherichia coli K-12 MG1655 in continuous culture. |
Q39916365 | Stoichiometric flux balance models quantitatively predict growth and metabolic by-product secretion in wild-type Escherichia coli W3110. |
Q39492823 | Survival response and rearrangement of plasmid DNA of Lactococcus lactis during long-term starvation |
Q35629336 | Synthetic ecology: a model system for cooperation |
Q22122206 | The Beagle in a bottle |
Q49588422 | The Experimental Study of Bacterial Evolution and Its Implications for the Modern Synthesis of Evolutionary Biology |
Q33533638 | The ecology of nasal colonization of Streptococcus pneumoniae, Haemophilus influenzae and Staphylococcus aureus: the role of competition and interactions with host's immune response |
Q35544067 | The enduring utility of continuous culturing in experimental evolution |
Q51700308 | The evolution of contact-dependent inhibition in non-growing populations of Escherichia coli. |
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Q33769826 | The repeatability of adaptive radiation during long-term experimental evolution of Escherichia coli in a multiple nutrient environment |
Q26864257 | The spectrum of adaptive mutations in experimental evolution |
Q54482596 | Unparallel diversification in bacterial microcosms. |
Q36844784 | Unraveling microbial interactions in food fermentations: from classical to genomics approaches |
Q39896249 | Why does Escherichia coli have two primary pathways for synthesis of glutamate? |
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