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1 V as well as those of its counterpart, human parainfluenza virus type 1.
2 virus (RSV), influenza virus type A (FluA), parainfluenza virus types 1, 2, and 3 (PIV1, PIV2, and P
3 criptase (RT)-PCR assay for the detection of parainfluenza virus types 1, 2, and 3, respiratory syncy
5 iruses, including influenza A and B viruses, parainfluenza virus types 1-3, respiratory syncytial vir
6 ed negative for respiratory syncytial virus, parainfluenza viruses (types 1-3), influenza A and B vir
8 luding influenza virus A, influenza virus B, parainfluenza virus types 1 and 3, respiratory syncytial
9 Hamsters immunized with a recombinant human parainfluenza virus type 1 expressing the fusion F prote
10 nic variation found in a population of human parainfluenza virus type 1 (HPIV-1) during a single loca
12 n to the catalytic binding site, HN of human parainfluenza virus type 1 (hPIV-1) may have a second re
14 hemagglutinin-neuraminidase protein of human parainfluenza virus type 1 (HPIV-1) were used in competi
16 irions in two closely related viruses, human parainfluenza virus type 1 (hPIV1) and Sendai virus (SV)
24 respiratory syncytial virus (RSV) and human parainfluenza virus type 1 (HPIV1) to HPIV4 infect virtu
25 onkeys from challenge with the related human parainfluenza virus type 1 (hPIV1), and SV has advanced
28 he fusion properties of F and HN proteins of parainfluenza virus type 1 (PI1), type 2 (PI2), and type
29 valuation of an attenuated recombinant human parainfluenza virus type 1 (rHPIV1) expressing the membr
33 live virus vaccine, we have used the murine parainfluenza virus type 1 (Sendai virus [SV]) as a xeno
34 tial virus [RSV], influenza A and B viruses, parainfluenza virus types 1 to 3, and adenovirus) was co
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