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1 nding of the pH-driven alteration of Sindbis virus structure.
2 on the viral envelope, and disruption of the virus structure.
3 he protein involved in its assembly into the virus structure.
4 ation of the Trp-38 side chain in the native virus structure.
5 tion shows PKD1 bound with minimal change in virus structure.
6 ndicating that the vp3 gene is important for virus structure.
7 tricacies, interactions, and beauty of these virus structures.
8 ranged major capsid proteins yet observed in virus structures.
9 ement has not yet been observed in any known virus structures.
10                                          The virus structure also reveals an altered association betw
11 d for over 20 years and contains a number of virus structure analysis tools.
12 he technologies and specific applications to virus structure and function.
13 ies have led to the determination of several virus structures at near-atomic resolution (3.3 - 4.6 A)
14                     The study of filamentous virus structure by Raman spectroscopy requires accurate
15      The availability of and ease with which virus structures can now be predicted is likely to drive
16 equivalence are then examined in some larger virus structures containing multiple subunit types and a
17 principle allow researchers to perform X-ray virus structure determination for single particles at ro
18                        By high-resolution in-virus structure determination of MA, we show that MA doe
19 lography has been the standard technique for virus structure determinations.
20 nular areas devoid of cellular organelles or virus structures except for occasional short crescent-sh
21                                    Many more virus structures followed, but soon it became essential
22   At the time of this writing, there are 931 virus structures from 62 different virus families in the
23                          Recently, dozens of virus structures have been solved to resolutions between
24 ly genetically encoded, and most pleomorphic virus structures have no selective advantage in vitro.
25                It was less easy to interpret virus structure in chemically fixed or cryosectioned mat
26           Comparison of wild-type and mutant virus structures in conjunction with bioinformatics esta
27 nce as a pathogen, little is known about the virus structure, in part because of its intrinsic struct
28 ext-generation vaccines target less variable virus structures, including the haemagglutinin stem.
29                       Fitting of the Fab and virus structures into the cryoEM densities identified th
30 rstand in terms of a simple pattern based on virus structure or tissue tropism.
31  differences in pandemic versus non-pandemic virus structures, replication properties and virus-host
32 ion electron microscopy images and the known virus structures showed high affinity and mutual orderin
33 inding permitted a more detailed view of the virus structure than was previously possible, leading to
34 lecular virology, immunity and pathogenesis, virus structure, the viral use and abuse of cellular pat
35 of icosahedrally ordered RNA observed in any virus structure to date.
36                                The resulting virus structure will provide a framework for continuing
37 Comparison between our infectious bronchitis virus structure with published RTC structures from other
38 tion of these cell lines with respect to (i) virus structure within and reactivated from the cell lin