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1 so prevented by the transgenic expression of spermine synthase.
3 nt these alterations were due to the loss of spermine synthase activity, since this chromosomal delet
5 e is formed from spermidine by the action of spermine synthase, an aminopropyltransferase, whose gene
6 y-CAG/SpmS mice had extremely high levels of spermine synthase and contained spermine in all tissues
7 to reside in the ACL5 gene, which encodes a spermine synthase and whose expression is specific to pr
13 with a recessively expressed mutation of the spermine synthase gene, leading to spermine deficiency,
15 we identified the SPE4 gene, which codes for spermine synthase, on the right arm of chromosome XII of
16 tion Snyder-Robinson syndrome that both lack spermine synthase show clearly that the correct spermine
20 mapped and analyzed another gene 5' of PEX, spermine synthase (SpS), which encodes a ubiquitous enzy
23 transgenic line that ubiquitously expresses spermine synthase under the control of a composite cytom
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