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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
13 derstanding the connection between causes of divergent evolution and the origin and maintenance of ba
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
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
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
32 e time interval clearance subjects displayed divergent evolution, indicating different immune respons
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
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
44 acid substitutions likely mimics the natural divergent evolution of enzymatic activities and also hig
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-
54 Together, these results reveal a complex and divergent evolution of glycinergic systems in the major
58 mechanism provides great flexibility for the divergent evolution of new functions mediated by this po
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
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
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
78 hese results can be understood in light of a divergent evolution scenario that posits correlated dive
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
89 pical distribution among lineages indicating divergent evolution, yet which ecophysiological traits a
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