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1 t regional isolation of P. aeruginosa drives divergent evolution.
2 sequences and structures following extensive divergent evolution.
3 architecture of adaptation in ecology-driven divergent evolution.
4 f selection for protein folding stability in divergent evolution.
5 ences that emerged during a billion years of divergent evolution.
6 in the creation of new nuclear receptors via divergent evolution.
7 A regulators are the result of convergent or divergent evolution.
8 iking example of perhaps both convergent and divergent evolution.
9 that they arose through gene duplication and divergent evolution.
10 ein segments are inserted and deleted during divergent evolution, a set of pairwise alignments contai
11 e derived from a common precursor with later divergent evolution along genus lines.
12 ese duplicated genes and genomes can undergo divergent evolution and evolve new functions.
13 derstanding the connection between causes of divergent evolution and the origin and maintenance of ba
14                         Our demonstration of divergent evolution and the widespread occurrence of the
15 gonistic coevolution is a cause of rapid and divergent evolution, and is likely to be a major driver
16  MutH is clearly related to these enzymes by divergent evolution, and this suggests that type II rest
17     Molecular details of both convergent and divergent evolution are beginning to emerge.
18 Nav1.1 channel, despite millions of years of divergent evolution between the two types of channels.
19 stence of this suprafamily demonstrates that divergent evolution can be opportunistic, conscripting a
20                 In spite of a long period of divergent evolution, conserved gene synteny was observed
21                              This example of divergent evolution demonstrates that point mutations ar
22  (SCOP) database is considered the result of divergent evolution from a common (beta/alpha)(8)-barrel
23 homology of type I and type II rhodopsins by divergent evolution from a common ancestral protein.
24 oma and relapse/transformed samples suggests divergent evolution from a common progenitor, whereas mo
25 NA and RNA polymerases could have evolved by divergent evolution from an ancestor that shared a commo
26 es in innate immunity represent a process of divergent evolution from an ancient unicellular eukaryot
27 ily, HTS and HTA activity likely arises from divergent evolution in a common structural scaffold with
28 rther highlights the opportunistic nature of divergent evolution in conscripting the active site of a
29 ecent studies have also revealed patterns of divergent evolution in functional pitcher morphology wit
30  we review recent research on convergent and divergent evolution in pitcher plant traps, with a focus
31 t potentially attractive starting points for divergent evolution in the laboratory.
32 e time interval clearance subjects displayed divergent evolution, indicating different immune respons
33                             This pattern of 'divergent evolution' means that the majority of 'actiona
34                                 We develop a divergent evolution model based on the lattice space whi
35 lecular details of the processes involved in divergent evolution of "new" enzymatic functions are ill
36    To tackle this challenge, we examined the divergent evolution of a model bacterial signaling pathw
37                 The results suggest that, in divergent evolution of all such domains, stabilization i
38  and tetraviruses from a common ancestor and divergent evolution of alphaviruses and flaviviruses fro
39 nucleotides for U12-type splice sites; (iii) divergent evolution of C.elegans 3' splice sites (3'ss)
40 anges in the Antp protein, but likely due to divergent evolution of cofactors, Hox collaborators or t
41  the implications of this conclusion for the divergent evolution of cyanobacterial and plant plastocy
42                                              Divergent evolution of de novo enzymes in this way could
43                                              Divergent evolution of dio2 paralogs supports organ-spec
44 acid substitutions likely mimics the natural divergent evolution of enzymatic activities and also hig
45                                              Divergent evolution of enzyme function is commonly expla
46 digm for elucidating Nature's strategies for divergent evolution of enzyme function.
47 K. mikimotoi, and have detected evidence for divergent evolution of fucoxanthin plastid genomes.
48            The molecular pathway for natural divergent evolution of function in the superfamily is un
49 d the evolutionary processes that led to the divergent evolution of function in this family, we const
50  from ancient gene duplication, resulting in divergent evolution of functionally distinct ATP synthas
51 on, we have examined cases of convergent and divergent evolution of functions performed by disulfide-
52                                   The rapid, divergent evolution of genitalia is a general trend in a
53                     We develop models of the divergent evolution of genomes; the elementary object of
54 Together, these results reveal a complex and divergent evolution of glycinergic systems in the major
55                                              Divergent evolution of HIV and DIPs appears likely since
56                                        Thus, divergent evolution of lentiviruses may have resulted in
57                                Moreover, the divergent evolution of M6P/IGF2R imprinting predicts tha
58 mechanism provides great flexibility for the divergent evolution of new functions mediated by this po
59                             The data support divergent evolution of nodaviruses, picornaviruses, and
60 ith the insect mushroom body despite obvious divergent evolution of overall shape.
61              These findings suggest that the divergent evolution of packaging signals aids with the s
62 boxylase in fold type III, thus suggesting a divergent evolution of PLP-dependent enzymes.
63                                          The divergent evolution of protein sequences from genomic da
64                                          The divergent evolution of proteins in cellular signaling pa
65                            Our findings show divergent evolution of the ankB allele in exploiting eit
66 ier study has made a compelling case for the divergent evolution of the eubacterial and archaeal TGTs
67 on 32 (the first to be introduced during the divergent evolution of the family) or 31 converts monome
68                        Our data suggests the divergent evolution of the gut microbiota in the pandas.
69 election or random drift, and are subject to divergent evolution of the paralogous sequences after fi
70 roperties contributes in a large part to the divergent evolution of the receptors' function, at least
71     Thus, despite the apparently accelerated divergent evolution of the RfaH proteins, the mechanism
72 n 19, a residue also introduced early in the divergent evolution of the seminal RNase gene.
73  differ in structure and function because of divergent evolution of their amino acid sequences.
74 he type I CRISPR-Cascade complex, suggesting divergent evolution of these immune systems from a commo
75 nicillium roqueforti despite the substantial divergent evolution of these two enzymes, while striking
76 ity of NITR sequences among species suggests divergent evolution of this multigene family with a birt
77                                              Divergent evolution of two group O (C181 or Y181) and th
78 hese results can be understood in light of a divergent evolution scenario that posits correlated dive
79  been common during the 900 million years of divergent evolution separating Fugu and human.
80    Male genitalia may experience more rapid, divergent evolution than any other animal character, but
81 diverse enolase superfamily is the result of divergent evolution that conserved enolization of a carb
82 better understand the molecular processes of divergent evolution, the D297G mutant of the l-Ala-d/l-G
83 re separated by over half a billion years of divergent evolution: the zebrafish (Danio rerio) and the
84  life separated by over one billion years of divergent evolution, thus providing an insight into the
85 d B nucleotide-binding motifs) is related by divergent evolution to the cytoplasmic domain of TrwB, t
86 tic promiscuity of AP could have facilitated divergent evolution via gene duplication by providing a
87 ts largely from gene duplication followed by divergent evolution, viral proteins frequently achieve i
88 ing iron and 2-oxoglutarate, consistent with divergent evolution within the extended family.
89 pical distribution among lineages indicating divergent evolution, yet which ecophysiological traits a

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