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1 ptor binding and toxicity toward gypsy moth (Lymantria dispar).
2 binding proteins (PBPs) from the gypsy moth, Lymantria dispar.
3 by 4-fold, while retaining activity against Lymantria dispar.
4 n-specific toxin, bound purified gypsy moth (Lymantria dispar) aminopeptidase N (APN) biphasically.
5 ight trajectories of a moth and a butterfly (Lymantria dispar and Pieris rapae), hindwing removal cau
6 ased survival and weight gain of gypsy moth (Lymantria dispar) caterpillars, suggesting that aldoxime
7 giensis toxin against the forest insect pest Lymantria dispar (gypsy moth), unfortunately it is also
8 9, populations of North American gypsy moth, Lymantria dispar, in seven contiguous northeastern state
12 he population growth rate of the gypsy moth, Lymantria dispar (L.), along its invasion front in Virgi
15 AMVsod is expressed late during infection of Lymantria dispar (Ld652) cells and produces a discrete n
16 nonpermissive for AcMNPV, was identified in Lymantria dispar M nuclear polyhedrosis virus (LdMNPV).
17 ingle gene, hrf-1, from another baculovirus, Lymantria dispar M nucleopolyhedrovirus, is able to prec
19 MNPV (OpMNPV) GP64 and F, thogotovirus GP75, Lymantria dispar MNPV (LdMNPV) F, human immunodeficiency
20 lyses of the genome of one of these viruses, Lymantria dispar MNPV (LdMNPV), revealed a single open r
22 tified two enhancin genes (E1 and E2) in the Lymantria dispar multinucleocapsid NPV (LdMNPV) and show
23 usly identified an enhancin gene (E1) in the Lymantria dispar multinucleocapsid nucleopolyhedrovirus
25 high frequency during serial passage of the Lymantria dispar nucleopolyhedrovirus (LdMNPV) in the L.
27 c in outbreak populations of the gypsy moth, Lymantria dispar, throughout many forested and residenti
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