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1 quired the capacity for homoacetogenesis via lateral gene transfer.
2 somal islands that may have been acquired by lateral gene transfer.
3 y of AP2 domains supports the possibility of lateral gene transfer.
4 , as well as the entire cassette, evolved by lateral gene transfer.
5 c respiration may have been acquired through lateral gene transfer.
6 maripaludis may have acquired cysS by a late lateral gene transfer.
7 able mutational rates, site variability, and lateral gene transfer.
8 ved from a combination of common descent and lateral gene transfer.
9 inary fission and lacks all natural means of lateral gene transfer.
10 change, mating pair formation and widespread lateral gene transfer.
11 occurrences in eukaryotes are the result of lateral gene transfer.
12 ce cell-type specialization were acquired by lateral gene transfer.
13 acteria community organization and mediating lateral gene transfer.
14 of distinct virulence elements acquired via lateral gene transfer.
15 , one protozoan, and cyanophages, suggesting lateral gene transfer.
16 stical support for acquisition as islands by lateral gene transfer.
17 en in this small subset of diatoms through a lateral gene transfer.
18 otAB stator, the latter possibly acquired by lateral gene transfer.
19 om other bacteria and are likely acquired by lateral gene transfer.
20 ze, almost 20% of the genome is derived from lateral gene transfer.
21 revious niche with greater opportunities for lateral gene transfer.
22 0 sequence was recently acquired by means of lateral gene transfer.
23 halophilic archaea and bacteria may indicate lateral gene transfer.
24 cus I were acquired by independent events of lateral gene transfer.
25 SBS/NAAAR appear to have been transmitted by lateral gene transfer.
26 e, provides evidence for several examples of lateral gene transfer.
27 onstraints are there on gene duplication and lateral gene transfer?
29 rotransposition, duplication-divergence, and lateral gene transfer, all of which involve recruitment
31 s; and (3) that continuous, lineage-specific lateral gene transfer, although it sometimes occurs, doe
35 domains must have included several events of lateral gene transfer and gene loss as well as lineage-s
36 but it is possible that the combined rate of lateral gene transfer and gene loss is higher than that
37 ds are all consistent with the hypothesis of lateral gene transfer and not ancient gene duplication.
39 from complete genome sequencing results that lateral gene transfer and recombination are essential co
41 uire and eliminate blocks of DNA sequence by lateral gene transfer and spontaneous deletion, respecti
42 coding sequences might have been acquired by lateral gene transfer and the number of hemerythrin-like
43 converting the uninitiated to their cause by lateral gene transfer, and enforcing cooperative behavio
44 have been acquired in part by phage-mediated lateral gene transfer, and some are differentially expre
45 pproximately 7 to 15 represent genes where a lateral gene transfer appears to have generated homoplas
48 terial species, which rules out interspecies lateral gene transfer as the origin of lux-rib2 in P. le
49 ferences revealed nine potential examples of lateral gene transfer associated with metal efflux prote
50 l "crystallized," i.e., became refractory to lateral gene transfer, at different stages of "cooling,"
51 this method is resilient to some effects of lateral gene transfer because transfers of genes are mas
52 oson and represents a possible mechanism for lateral gene transfer between Archaea or possibly betwee
53 yotes, supplemented by possible instances of lateral gene transfer between bacteria and eukaryotes.
55 the DnaK trees suggested the possibility of lateral gene transfer between Firmicutes and Methanosarc
56 rsification at the species level by allowing lateral gene transfer between strains that are too dista
58 e sequences, however, increasingly implicate lateral gene transfer, both from prokaryotes to eukaryot
59 e complex signaling network used to regulate lateral gene transfer can be resolved as individual sign
64 e, which we hypothesize may be a result of a lateral gene transfer event, and an unidentified 456 ami
67 ermotoga maritima MSB8 presents evidence for lateral gene transfer events between bacterial and archa
69 the Bcep781 group phages can also engage in lateral gene transfer events with otherwise unrelated ph
70 uplication and secondary losses, interdomain lateral gene transfer events, alteration of cellular loc
76 nd a type II membrane protein has evolved by lateral gene transfer for the esterification of many bac
77 . brevicollis was believed to have arisen by lateral gene transfer from a prokaryote, and is a fusion
79 ion, we conclude that chy1 probably arose by lateral gene transfer from an actinomycete bacterium.
81 h various means, including gene duplication, lateral gene transfer from bacteria that are not their c
82 olic pathways that likely transpired through lateral gene transfer from bacteria, and amplification o
85 om separate and different sources, involving lateral gene transfer from eubacteria, than did all othe
87 t in either bacteria or spiders, followed by lateral gene transfer from one lineage to the other.
88 ed that all three genes had been acquired by lateral gene transfer from the low-moles-percent G+C gra
89 omes are usually ascribed to gene loss or to lateral gene transfer from unrelated cellular organisms.
90 e acquired via a minimum of four independent lateral gene transfers from C(4) taxa that diverged from
97 the mutation rate and the scope and level of lateral gene transfer, i.e., evolutionary temperature, d
98 ights into eukaryotic evolution, the role of lateral gene transfer in amebic biology and the adaptati
101 gens, and have established the importance of lateral gene transfer in generating structural diversity
109 idered to be obstructed by the potential for lateral gene transfer (LGT) among lineages at virtually
111 ledge of the extent and functional impact of lateral gene transfer (LGT) from prokaryotes to eukaryot
112 Genetic recombinants that resulted from lateral gene transfer (LGT) have been detected in sexual
113 sequences has demonstrated the importance of lateral gene transfer (LGT) in prokaryotic evolution.
115 exually transmitted infections suggests that lateral gene transfer (LGT) is an important means by whi
118 aeal genomes are known to have acquired, via lateral gene transfer (LGT), several genes from eubacter
123 quivalog' families, where both orthology and lateral gene transfer may be part of the evolutionary hi
124 many of the clustered regions suggests that lateral gene transfer may have occurred between thermoph
127 Phylogenetic analyses suggested that two lateral gene transfers occurred in the DapL genes, one f
129 hylogenomic analysis identifies evidence for lateral gene transfer of bacterial genes into the E. his
131 of alleles between hosts, indicating limited lateral gene transfer of these alleles despite host prox
135 lastp hits in Methanocaldococcus jannaschii, lateral gene transfer or gene loss has apparently result
136 se of their ability to pick up new traits by lateral gene transfer, our gut microbes also enable adap
137 1950s-era prototype and vaccine strains by a lateral gene transfer, substituting the coding region fo
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