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2 ked the cell movements and ability to propel latex spheres along their surfaces that are characterist
6 and 1.0 mum using monodisperse (polystyrene latex spheres) and polydisperse (red-fluorescent spheres
8 mutants restored motility, ability to propel latex spheres, and sensitivity to bacteriophage infectio
14 f PEG surface packing on monodisperse 200 nm latex spheres indicates that the size of the hydrophobic
15 hlights the report by Terray et al., who use latex spheres manipulated by optical traps to pump fluid
16 when tethered cells or cells carrying small latex spheres on flagellar stubs were shifted from H(2)O
17 preading, cell motility, the ability to move latex spheres, phage sensitivity, and the ability to dig
20 method was developed using 2-um polystyrene latex spheres (PSLs) to investigate skin contamination (
21 ing emissions, and monodispersed polystyrene latex spheres under controlled laboratory conditions and