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1 distinctly different anatomical adaptations (divergent evolution).
2 t cell types, tissues, or hosts during their divergent evolution.
3 f selection for protein folding stability in divergent evolution.
4 of xenogeneic barriers that are a result of divergent evolution.
5 ences that emerged during a billion years of divergent evolution.
6 A regulators are the result of convergent or divergent evolution.
7 t regional isolation of P. aeruginosa drives divergent evolution.
8 sequences and structures following extensive divergent evolution.
9 architecture of adaptation in ecology-driven divergent evolution.
10 taxa separated by up to 160 million years of divergent evolution.
11 in the creation of new nuclear receptors via divergent evolution.
12 iking example of perhaps both convergent and divergent evolution.
13 that they arose through gene duplication and divergent evolution.
14 ein segments are inserted and deleted during divergent evolution, a set of pairwise alignments contai
17 i also exhibited broadly similar patterns of divergent evolution and enhanced immune evasion in a mon
19 derstanding the connection between causes of divergent evolution and the origin and maintenance of ba
20 e algae groups revealed new insight into the divergent evolution and the universal core of telomerase
22 gonistic coevolution is a cause of rapid and divergent evolution, and is likely to be a major driver
23 MutH is clearly related to these enzymes by divergent evolution, and this suggests that type II rest
25 e effector evolution mechanisms and supports divergent evolution as a major force in driving SUSS eff
26 Nav1.1 channel, despite millions of years of divergent evolution between the two types of channels.
27 stence of this suprafamily demonstrates that divergent evolution can be opportunistic, conscripting a
30 (SCOP) database is considered the result of divergent evolution from a common (beta/alpha)(8)-barrel
31 homology of type I and type II rhodopsins by divergent evolution from a common ancestral protein.
32 oma and relapse/transformed samples suggests divergent evolution from a common progenitor, whereas mo
33 NA and RNA polymerases could have evolved by divergent evolution from an ancestor that shared a commo
34 es in innate immunity represent a process of divergent evolution from an ancient unicellular eukaryot
35 ily, HTS and HTA activity likely arises from divergent evolution in a common structural scaffold with
36 potential for clinical application; however, divergent evolution in ARG1 expression and function in r
37 rther highlights the opportunistic nature of divergent evolution in conscripting the active site of a
38 ecent studies have also revealed patterns of divergent evolution in functional pitcher morphology wit
39 ly of deubiquitinating enzymes that arose by divergent evolution in Legionellales, likely enabling th
40 we review recent research on convergent and divergent evolution in pitcher plant traps, with a focus
41 ogether, our results support the thesis of a divergent evolution in the control of vertebrate reprodu
43 e time interval clearance subjects displayed divergent evolution, indicating different immune respons
45 rotein-like II domain family, have undergone divergent evolution, leading to adaptation of their stru
48 lecular details of the processes involved in divergent evolution of "new" enzymatic functions are ill
49 To tackle this challenge, we examined the divergent evolution of a model bacterial signaling pathw
51 and tetraviruses from a common ancestor and divergent evolution of alphaviruses and flaviviruses fro
52 nucleotides for U12-type splice sites; (iii) divergent evolution of C.elegans 3' splice sites (3'ss)
53 e, and identified SV hotspots underlying the divergent evolution of cellulosic and sweet sorghum.
54 anges in the Antp protein, but likely due to divergent evolution of cofactors, Hox collaborators or t
55 ics play a fundamental role in the long-term divergent evolution of complex multicellularity across t
56 the implications of this conclusion for the divergent evolution of cyanobacterial and plant plastocy
59 acid substitutions likely mimics the natural divergent evolution of enzymatic activities and also hig
64 d the evolutionary processes that led to the divergent evolution of function in this family, we const
65 from ancient gene duplication, resulting in divergent evolution of functionally distinct ATP synthas
66 on, we have examined cases of convergent and divergent evolution of functions performed by disulfide-
69 Together, these results reveal a complex and divergent evolution of glycinergic systems in the major
74 mechanism provides great flexibility for the divergent evolution of new functions mediated by this po
84 e substrate-binding pocket that underlie the divergent evolution of substrate selectivity toward indo
86 ing of enzymes from these clusters suggested divergent evolution of the adenylate-forming superfamily
88 ier study has made a compelling case for the divergent evolution of the eubacterial and archaeal TGTs
89 on 32 (the first to be introduced during the divergent evolution of the family) or 31 converts monome
92 election or random drift, and are subject to divergent evolution of the paralogous sequences after fi
93 roperties contributes in a large part to the divergent evolution of the receptors' function, at least
98 he type I CRISPR-Cascade complex, suggesting divergent evolution of these immune systems from a commo
100 nicillium roqueforti despite the substantial divergent evolution of these two enzymes, while striking
101 ity of NITR sequences among species suggests divergent evolution of this multigene family with a birt
102 fennig introduce character displacement, the divergent evolution of traits in overlapping species.
104 hese results can be understood in light of a divergent evolution scenario that posits correlated dive
106 Male genitalia may experience more rapid, divergent evolution than any other animal character, but
107 diverse enolase superfamily is the result of divergent evolution that conserved enolization of a carb
108 better understand the molecular processes of divergent evolution, the D297G mutant of the l-Ala-d/l-G
109 re separated by over half a billion years of divergent evolution: the zebrafish (Danio rerio) and the
110 life separated by over one billion years of divergent evolution, thus providing an insight into the
111 d B nucleotide-binding motifs) is related by divergent evolution to the cytoplasmic domain of TrwB, t
112 sting a plasticity that may be beneficial in divergent evolution to tune the transport mechanism.
113 tic promiscuity of AP could have facilitated divergent evolution via gene duplication by providing a
114 ts largely from gene duplication followed by divergent evolution, viral proteins frequently achieve i
116 pical distribution among lineages indicating divergent evolution, yet which ecophysiological traits a