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1 ants die at the transition from the first to second instar.
2 le (otd) are expressed throughout the entire second instar eye-antennal disc, conferring a default fa
3 e lymph glands of third-instar, but never of second-instar hosts, are almost always accompanied by di
4 instar, reduced MMP was already apparent at second instar in the cell bodies, axons and neuromuscula
7 emizygous for our emb alleles can develop to second instar larvae but persist at this stage and consi
9 netic screen utilizing transgenic Drosophila second instar larvae expressing an actin, green fluoresc
11 in gene targeting, die as small, immobilized second instar larvae with severely deformed musculature.
13 lies die around the transition from first to second instar larvae, and homozygous importin alpha3 mut
15 ity of irradiated combination formulation on second-instar larvae Ephestia Kuehniella was 68.89%, whi
17 hila germline cystocytes generated either in second instar larval ovaries or in adults over-producing
18 loping larvae leaves the timing of first and second instar molts largely unchanged, but triples durat
20 and L mutually antagonize each other during second instar of larval development to restrict their fu
22 (ex) driven by a heat pulse during the early second instar resulted in a severe phenotype that includ
23 e its expression is specifically elevated in second-instar wing discs during wing margin formation.
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