Long-term experimental evolution in Escherichia coli. XI. Rejection of non-transitive interactions as cause of declining rate of adaptation.
about
Adaptive molecular evolution for 13,000 phage generations: a possible arms race.Clonal interference and the periodic selection of new beneficial mutations in Escherichia coliThe causes of epistasisAdaptation, Clonal Interference, and Frequency-Dependent Interactions in a Long-Term Evolution Experiment with Escherichia coliCryptic fitness advantage: diploids invade haploid populations despite lacking any apparent advantage as measured by standard fitness assaysIncreased susceptibility to repeated freeze-thaw cycles in Escherichia coli following long-term evolution in a benign environmentE. coli microcosms indicate a tight link between predictability of ecosystem dynamics and diversityUnderstanding the evolutionary fate of finite populations: the dynamics of mutational effects.Identification and dynamics of a beneficial mutation in a long-term evolution experiment with Escherichia coliInitial mutations direct alternative pathways of protein evolutionDifferences in accumulation and virulence determine the outcome of competition during Tobacco etch virus coinfection.Reciprocal sign epistasis between frequently experimentally evolved adaptive mutations causes a rugged fitness landscape.Microbial domestication signatures of Lactococcus lactis can be reproduced by experimental evolution.Metabolic erosion primarily through mutation accumulation, and not tradeoffs, drives limited evolution of substrate specificity in Escherichia coliMeasuring selection coefficients below 10(-3): method, questions, and prospects.Complex genetic changes in strains of Saccharomyces cerevisiae derived by selection in the laboratoryWhat Can Phages Tell Us about Host-Pathogen Coevolution?Experimental observations of rapid Maize streak virus evolution reveal a strand-specific nucleotide substitution bias.The genetics of adaptation for eight microvirid bacteriophages.The dynamics of adaptation on correlated fitness landscapesExperimental evolution and the dynamics of adaptation and genome evolution in microbial populations.The impact of high-order epistasis in the within-host fitness of a positive-sense plant RNA virus.Evolution of organismal stoichiometry in a long-term experiment with Escherichia coli.On measuring selection in experimental evolution.Multiple genetic pathways to similar fitness limits during viral adaptation to a new host.Negative epistasis between beneficial mutations in an evolving bacterial population.Additive Phenotypes Underlie Epistasis of Fitness Effects.Sustained fitness gains and variability in fitness trajectories in the long-term evolution experiment with Escherichia coli.Genome properties and the limits of adaptation in bacteriophages.Phenotypic and Genomic Evolution during a 20,000-Generation Experiment with the Bacterium Escherichia coliExperimental evolution of bacteria across 60,000 generations, and what it might mean for economics and human decision-makingExperimental Design, Population Dynamics, and Diversity in Microbial Experimental EvolutionFitness effects of altering gene expression noise in
P2860
Q24545052-DB2D8E9B-1446-4C43-9B34-6F6726872C8BQ24545892-E3A038DC-6644-4D68-BED6-3F71A6321A34Q26860873-DA448E77-F732-4B72-B68E-490A8F57BDA8Q28647522-9794B119-D32B-41A4-83B5-0A3DC99AE0E9Q28741669-98F4E9D3-8406-48A9-A0D7-BDA1C22B2969Q28764749-1665E7FF-66B4-4422-AC70-57E894417650Q33250075-E6B25485-4F05-48D9-BEC3-C093BF3F2E0FQ33281050-AF9FFD50-6843-4F5C-B064-94CBA9C84B41Q33521105-E332025B-79C6-4623-8227-B24B55B2E887Q33847781-978701E8-4952-4D33-95C0-0430C0A3C592Q33851358-AF23F747-34B3-4176-8A3B-D152EABB1EFEQ33892372-56BC0844-AFD1-40B8-A001-7F8C149655FDQ34232235-2C060497-AF79-4A4C-A94D-12730238E90EQ34405876-7ACF8293-207C-4842-B327-1474C751938AQ35644806-CB0B35B8-33E1-446E-9D02-68C87EFEB9FEQ36052336-4C2060F3-BB29-40B9-A903-B9E94457AD0EQ36424693-6798490A-A9F9-4851-B421-4CCAFBF5F474Q36948120-926D0015-6EF1-4145-9689-12222D7B88DAQ37353497-802BBA14-8B63-4BE9-BEC9-D371EB60B244Q37399576-E32FB941-D16A-4A1A-BFE7-41D54C774922Q38683209-4E99489E-A009-4CF2-84BC-FA62B1DC7CDCQ41012991-0C25F341-4D57-40B0-A1A2-32162EC1968DQ41227508-74648065-8A1F-48B3-9F5A-5F0E74BD71E3Q42076622-2954C2F9-3072-4E78-BD36-956410968D82Q42205511-AA7C9A8C-742F-4084-BBF0-1CBC405045D6Q44010374-CFC6DB0B-E38B-4DF1-B157-8206F2E09DD6Q47587442-33201A3C-504C-4EBA-9CFD-B3B4E963B795Q53247059-7304CBC4-0A98-43A9-BDD6-DA3FA9DF2C25Q54505889-8D80B181-F27D-43D5-8A35-F0963CA53F51Q56431644-9AA5513A-702C-423F-993C-014206BC9319Q56919932-5D83FBD0-8874-4857-B355-98861F2AAA53Q57174769-850CA6DA-65B5-403C-9CFC-C5FE3A9B6943Q58733567-292BA60E-F7F4-4565-946D-15B27BD347EC
P2860
Long-term experimental evolution in Escherichia coli. XI. Rejection of non-transitive interactions as cause of declining rate of adaptation.
description
2002 nî lūn-bûn
@nan
2002 թուականի Հոկտեմբերին հրատարակուած գիտական յօդուած
@hyw
2002 թվականի հոտեմբերին հրատարակված գիտական հոդված
@hy
2002年の論文
@ja
2002年論文
@yue
2002年論文
@zh-hant
2002年論文
@zh-hk
2002年論文
@zh-mo
2002年論文
@zh-tw
2002年论文
@wuu
name
Long-term experimental evoluti ...... f declining rate of adaptation
@nl
Long-term experimental evoluti ...... declining rate of adaptation.
@ast
Long-term experimental evoluti ...... declining rate of adaptation.
@en
type
label
Long-term experimental evoluti ...... f declining rate of adaptation
@nl
Long-term experimental evoluti ...... declining rate of adaptation.
@ast
Long-term experimental evoluti ...... declining rate of adaptation.
@en
prefLabel
Long-term experimental evoluti ...... f declining rate of adaptation
@nl
Long-term experimental evoluti ...... declining rate of adaptation.
@ast
Long-term experimental evoluti ...... declining rate of adaptation.
@en
P2860
P356
P1476
Long-term experimental evoluti ...... declining rate of adaptation.
@en
P2093
J Arjan G M de Visser
P2860
P2888
P356
10.1186/1471-2148-2-19
P407
P577
2002-10-30T00:00:00Z
P5875
P6179
1030137210