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1 sequence, FPIV, important for the budding of parainfluenza virus 5.
2 NASEK was dispensable for viruses, including parainfluenza virus 5 and Coxsackie B virus, that enter
4 ructed chimeras containing the ectodomain of parainfluenza virus 5 F (PIV5 F) and either the MPER, th
5 Here we report the crystal structure of the parainfluenza virus 5 F protein in its prefusion conform
6 ess the functional role of the paramyxovirus parainfluenza virus 5 F protein TM domain, alanine scann
8 rystal structure of a fragment of the simian parainfluenza virus 5 fusion protein (SV5 F), revealing
9 , we show that the FP from the paramyxovirus parainfluenza virus 5 fusogenic protein, F, forms an N-t
10 ng globular head domain of the paramyxovirus parainfluenza virus 5 HN protein is entirely dispensable
11 usion activation, F activation involving the parainfluenza virus 5 HN stalk domain, and properties of
15 hat Cav-1 colocalizes with the paramyxovirus parainfluenza virus 5 (PIV-5) nucleocapsid (NP), matrix
18 Proline substitution in this region of HN of parainfluenza virus 5 (PIV5) and Newcastle disease virus
19 In this work, we generated a recombinant parainfluenza virus 5 (PIV5) containing NP from H5N1 (A/
21 igh similarity to the structure of prefusion parainfluenza virus 5 (PIV5) F, with the main structural
22 Because only the prefusion structure of the parainfluenza virus 5 (PIV5) F-trimer is available, to s
23 MR spectroscopy, we show that the TMD of the parainfluenza virus 5 (PIV5) fusion protein adopts lipid
32 To investigate the role of NP protein in parainfluenza virus 5 (PIV5) particle formation, NP prot
34 serendipitously identified a viral mRNA from parainfluenza virus 5 (PIV5) that activates IFN expressi
36 quence variation of 16 different isolates of parainfluenza virus 5 (PIV5) that were isolated from a n
37 unable to be recognized by measles virus and parainfluenza virus 5 (PIV5) V proteins were tested in s
39 he threonine residue at position 286 of P of parainfluenza virus 5 (PIV5) was found phosphorylated.
40 The V proteins of measles virus (MV) and parainfluenza virus 5 (PIV5) were introduced into HFLC u
41 rotein (prefusion form) of the paramyxovirus parainfluenza virus 5 (PIV5) WR isolate was determined.
48 V), human parainfluenza virus 2 (hPIV2), and parainfluenza virus 5 (PIV5), all members of the genus R
50 that a porcine isolate of the paramyxovirus parainfluenza virus 5 (PIV5), known as SER, requires a l
59 this study, we show that vaccination with a parainfluenza virus 5 recombinant vaccine candidate expr
61 sion (F) protein of the paramxyovirus simian parainfluenza virus 5 (SV5) promotes virus-cell and cell
62 on (F) protein from the paramyxovirus simian parainfluenza virus 5 (SV5) resulted in mutant F protein
63 ined the ability of the paramyxovirus simian parainfluenza virus 5 (SV5) to affect cell cycle progres
64 recently published prefusogenic structure of parainfluenza virus 5/SV5 F places CBF(2) in direct cont
65 ed "stalk exposure model" first proposed for parainfluenza virus 5 to other paramyxoviruses and propo
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