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1 ack of genetic interactions between gish and rutabaga.
2 ocess that requires a learning-related gene, rutabaga.
3 hort-term memory formation, namely dunce and rutabaga.
4 -term synaptic plasticity, such as dunce and rutabaga.
9 tasks, and demonstrates that defects of the rutabaga and dunce products interact synergistically in
10 genes of the cAMP signaling pathway, such as rutabaga and NF1, suggesting that RDL works up stream of
22 hored by the adenylyl cyclase encoded by the rutabaga gene, is indispensable for olfactory memory for
27 n was necessary and sufficient to rescue the rutabaga memory deficit, which rules out a developmental
29 ion at least as strong as those of dunce and rutabaga, memory mutants with defective cAMP metabolism
31 restore short-term or long-term memory to a rutabaga mutant with expression of rutabaga in different
34 d seizure satellites were both suppressed by rutabaga mutations that disrupt Ca(2+)/CaM-dependent ade
38 ) or long-term memory (LTM) was evaluated in rutabaga (rut) and dunce (dnc) mutants using aversive ph
39 Drosophila memory mutants dunce (dnc) and rutabaga (rut) are known to have altered intracellular c
40 Mutants of the Drosophila dunce (dnc) and rutabaga (rut) genes, which encode a cAMP-specific phosp
42 eport that cAMP signals misrelated in either rutabaga (rut) or dunce (dnc) mutants separate between c
43 xpression of an adenylate cyclase encoded by rutabaga (rut), is sufficient to strengthen synaptic tra
44 s in Drosophila memory mutants revealed that rutabaga (rut)-dependent cAMP signals couple in a diverg
47 d plasticity, including the adenylyl cyclase Rutabaga, the Ig-CAM Fasciclin II, the transcription fac
48 nd that this plasticity was dependent on the Rutabaga type I adenylyl cyclase, linking cAMP-dependent
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