戻る
「早戻しボタン」を押すと検索画面に戻ります。 [閉じる]

コーパス検索結果 (１語後でソート)

通し番号をクリックするとPubMedの該当ページを表示します
1 so prevented by the transgenic expression of spermine synthase.
2 from both spermidine synthase (2.5.1.16) and spermine synthase (2.5.1.22).
3 nt these alterations were due to the loss of spermine synthase activity, since this chromosomal delet
4         This mutant has neither spermine nor spermine synthase activity.
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
8 nzymes analyzed (ODC, polyamine oxidase, and spermine synthase) and reduction of spermine.
9 ertility in male mice and that regulation of spermine synthase content is not required.
10 onally identify for the first time bacterial spermine synthases, derived from phyla Bacillota, Rhodot
11                   Mutant strains lacking the spermine synthase-encoding gene SPS1 progressed through
12 transgenic mice (CAG/SpmS mice) that express spermine synthase from the ubiquitous CAG promoter.
13 s a rare disease associated with a defective spermine synthase gene and low intracellular spermine le
14 ects of the Gy and Hyp mutations on both the spermine synthase gene and the Pex gene.
15                  Four missing introns of the spermine synthase gene were identified in Gy male mice,
16 with a recessively expressed mutation of the spermine synthase gene, leading to spermine deficiency,
17                                              Spermine synthase is an aminopropyltransferase that adds
18                           Since the gene for spermine synthase is immediately upstream of the homolog
19 we identified the SPE4 gene, which codes for spermine synthase, on the right arm of chromosome XII of
20 tion Snyder-Robinson syndrome that both lack spermine synthase show clearly that the correct spermine
21  caused by a significant decrease or loss of spermine synthase (SMS) activity.
22 caused by a loss-of-function mutation in the spermine synthase (SMS) gene.
23                                              Spermine synthase (SMS) is an enzyme which function is t
24                Loss-of-function mutations in spermine synthase (SMS), a polyamine biosynthesis enzyme
25                         Here, we report that spermine synthase (SMS), a polyamine biosynthetic enzyme
26  protease inhibitor, directly interacts with spermine synthase (SMS), impeding its lysosome-mediated
27 n Ancestor, thus their biosynthetic enzymes, spermine synthase (SpmSyn) and thermospermine synthase (
28  mapped and analyzed another gene 5' of PEX, spermine synthase (SpS), which encodes a ubiquitous enzy
29 n in polyamine content due to the absence of spermine synthase, the product of the SpmS gene.
30 ersed by the production of spermine from the spermine synthase transgene.
31  transgenic line that ubiquitously expresses spermine synthase under the control of a composite cytom
32                             A pseudogene for spermine synthase was also identified in the mouse genom