Evidence for abundant slightly deleterious polymorphisms in bacterial populations
about
Selectionism and neutralism in molecular evolutionWeak selection and protein evolutionThe evolutionary biology of poxvirusesRapid fixation of a distinctive sequence motif in the 3′ noncoding region of the clade of West Nile virus invading North AmericaDistinctive pattern of sequence polymorphism in the NS3 protein of hepatitis C virus type 1b reflects conflicting evolutionary pressuresMore effective purifying selection on RNA viruses than in DNA virusesEvolutionary ecology of virus emergence.The evolution of gene expression QTL in Saccharomyces cerevisiae.Gene genealogies strongly distorted by weakly interfering mutations in constant environments.Detecting the molecular signature of social conflict: theory and a test with bacterial quorum sensing genes.Genome wide analyses reveal little evidence for adaptive evolution in many plant species.Looking for Darwin in all the wrong places: the misguided quest for positive selection at the nucleotide sequence level.Diversity of and selection acting on cylindrospermopsin cyrB gene adenylation domain sequences in Florida.PolyAna: analyzing synonymous and nonsynonymous polymorphic sites.Evolution of adaptive phenotypic traits without positive Darwinian selection.Diversity of the abundant pKLC102/PAGI-2 family of genomic islands in Pseudomonas aeruginosa.The Impact of Selection, Gene Conversion, and Biased Sampling on the Assessment of Microbial Demography.The other side of the nearly neutral theory, evidence of slightly advantageous back-mutations.Pyoverdine receptor: a case of positive Darwinian selection in Pseudomonas aeruginosa.Ongoing purifying selection on intergenic spacers in group A streptococcusNucleotide sequence polymorphism in circovirusesEvolutionary and population genomics of the cavity causing bacteria Streptococcus mutansNear neutrality: leading edge of the neutral theory of molecular evolution.More radical amino acid replacements in primates than in rodents: support for the evolutionary role of effective population size.Relaxation of purifying selection on live attenuated vaccine strains of the family Paramyxoviridae.Synonymous and nonsynonymous polymorphisms versus divergences in bacterial genomes.Small effective population sizes and rare nonsynonymous variants in potyviruses.The pattern and distribution of deleterious mutations in maize.Evolutionary Genetic Analysis Uncovers Multiple Species with Distinct Habitat Preferences and Antibiotic Resistance Phenotypes in the Stenotrophomonas maltophilia Complex.Accumulation of slightly deleterious mutations in the mitochondrial genome: a hallmark of animal domesticationCost of antibiotic resistance and the geometry of adaptation.Large global effective population sizes in Paramecium.Genetic costs of domestication and improvement.Selection on protein-coding genes of natural cyanobacterial populations.Genomic Diversity and Evolution of the Fish Pathogen Flavobacterium psychrophilum.Selection Maintains Low Genomic GC Content in Marine SAR11 Lineages.
P2860
Q22066021-D4E5B9C2-6AFD-4357-8EFC-5CD0CDD0728AQ22305972-29D02736-9FD1-4E7C-927E-CA1C4F5846E9Q24652228-A3468736-66F7-47DB-B5BD-7FBEB26AD4C5Q27485580-F233B89F-672E-4C3F-A9C0-010C20DAFAD5Q27487318-AA09000E-3E4E-4A58-AEF6-974A06A12841Q27489846-8C7D1DCD-F5BD-4478-8283-6B23D295CAF3Q30396932-F5D43847-4651-4CBC-AA66-DF56837D0FC0Q33292681-A96A7F19-E9EE-430E-B725-366C1084222BQ33688892-4B51E4A1-8D00-4B10-AA7E-BB071C6A17D2Q33902818-18FF5AE7-476F-473D-BF91-86FDD67F2075Q34042396-D9B62D2E-51DA-4C4E-ABD8-2A7F62251CF8Q34648294-9D954A9A-7B52-4AA9-81E5-6EE5234080AEQ34739270-42906B26-25E1-4242-932D-7693B0800FF7Q35072675-E08D799E-038B-4FC8-BFA8-1C3F4B859915Q35854956-790FE50C-A836-4B00-90BE-D5E7F4B9D64EQ35855373-66C9A1E9-DBDA-4118-B1B7-BEB3D6EEF0A1Q35941597-4C7A07A7-5B68-4261-9055-4F2A156E44F9Q36089115-EDAAB915-6A77-43DE-9C94-AEE92955F261Q36113710-42FEF056-D355-4B6C-B7FE-E7BFB546DB17Q36138479-B64B6404-0BD2-4633-B104-BB5953B9E795Q36513225-FF42380B-66DC-43FD-96FB-054672902619Q36701991-54E52673-F2F9-4BF0-98A0-9E67B651D640Q37193352-D693899F-3802-4BAC-8A4B-C4E27B6A307DQ37252766-C409C0F6-5AC9-4F4A-865C-23BDE8F73F76Q37255011-18C15790-06D6-443F-BF6D-63D1BEF0C6B8Q37324312-8F56A8E9-69EE-46F0-9C93-4B166DEDA7E6Q37373124-6D077412-D24E-47B8-BFF2-E219AD6D4512Q37460697-83E65871-2860-4E0B-A74F-13D8E4D7EE12Q38598823-3D414C1A-F6C2-4C87-A710-C171E0C36DE6Q41878552-FBF9F699-B064-421C-A19B-3EEA4760CC6AQ42113492-606B5B1D-8198-42B0-AC54-A62876C1A226Q45129391-D645F6D7-D671-43D1-BD34-83D30A097872Q46290705-7BAA11EE-B482-4064-AD50-24ABADD02B12Q48085285-C9955AC8-E230-4338-BC62-17D46134DFB2Q50105020-00BA3CA3-F852-4576-BBE2-B26B95BC82E3Q50441808-4AB9EBDD-B018-47AD-9556-31FEB96427CE
P2860
Evidence for abundant slightly deleterious polymorphisms in bacterial populations
description
2004 nî lūn-bûn
@nan
2004 թուականի Նոյեմբերին հրատարակուած գիտական յօդուած
@hyw
2004 թվականի նոյեմբերին հրատարակված գիտական հոդված
@hy
2004年の論文
@ja
2004年論文
@yue
2004年論文
@zh-hant
2004年論文
@zh-hk
2004年論文
@zh-mo
2004年論文
@zh-tw
2004年论文
@wuu
name
Evidence for abundant slightly deleterious polymorphisms in bacterial populations
@ast
Evidence for abundant slightly deleterious polymorphisms in bacterial populations
@en
Evidence for abundant slightly deleterious polymorphisms in bacterial populations
@nl
type
label
Evidence for abundant slightly deleterious polymorphisms in bacterial populations
@ast
Evidence for abundant slightly deleterious polymorphisms in bacterial populations
@en
Evidence for abundant slightly deleterious polymorphisms in bacterial populations
@nl
prefLabel
Evidence for abundant slightly deleterious polymorphisms in bacterial populations
@ast
Evidence for abundant slightly deleterious polymorphisms in bacterial populations
@en
Evidence for abundant slightly deleterious polymorphisms in bacterial populations
@nl
P2860
P1433
P1476
Evidence for abundant slightly deleterious polymorphisms in bacterial populations
@en
P2093
Austin L Hughes
P2860
P304
P356
10.1534/GENETICS.104.036939
P407
P577
2004-11-15T00:00:00Z