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1 SPV and B19 are 50% identical at the nucleotide level, a
2 SPV capsid protein was expressed in insect cells, and SP
3 SPV capsid proteins, like those of B19, self-assembled t
4 SPV is an important pathogen in surgically manipulated c
5 SPV pre-mRNAs contain three introns, compared to two fou
8 ransfection of cloned SPV into COS cells and SPV infection of the human erythroid progenitor line UT-
9 d protein was expressed in insect cells, and SPV was cultured in human and macaque bone marrow mononu
10 iremia, measured by dot blot and/or PCR, and SPV-specific antibodies were determined retrospectively.
14 of exposed handlers (n=65) were found to be SPV seropositive, compared with 35% of nonexposed indivi
15 f transcripts of SPV and B19 is similar, but SPV also has coding strategies in common with other parv
17 s generated following transfection of cloned SPV into COS cells and SPV infection of the human erythr
22 that the splicing pattern of transcripts of SPV and B19 is similar, but SPV also has coding strategi
26 The transcription map of simian parvovirus (SPV), an Erythrovirus similar to Parvovirus B19, was inv
28 introduced into a colony, clinically silent SPV infection could be readily transmitted within the en
34 on was spliced were abundant and encoded the SPV 14-kDa protein (analogous to the B19 11-kDa protein)
41 he Food and Drug Administration, the Toronto SPV and the Freestyle valve (Medtronic, Minneapolis, MN)
42 the Baylor College of Medicine, the Toronto SPV stentless valve has been our stentless xenograft val
44 tion of the Toronto stentless porcine valve (SPV) (St. Jude, Minneapolis, MN), recently approved by t
45 Analysis of spatial phylogenetic variation (SPV) within the SCYLV isolates could not be assessed by
47 observations of Saturn's south polar vortex (SPV) showing that it shares some properties with terrest
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