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1 origin in the duplication of a gene encoding deoxyhypusine synthase.
2 were evaluated as donor substrates for human deoxyhypusine synthase.
3 a specific lysine residue (Lys329) in human deoxyhypusine synthase.
4 a) of the conserved lysine residues in human deoxyhypusine synthase.
5 slation elongation factor eIF5A, mediated by deoxyhypusine synthase.
6 e spermidine biosynthetic pathway but retain deoxyhypusine synthase.
7 erythroid progenitors, by the inhibition of deoxyhypusine synthase, abrogates erythropoiesis but not
9 endently by duplication of the gene encoding deoxyhypusine synthase, an enzyme involved in the posttr
10 pusine formation by a selective inhibitor of deoxyhypusine synthase and by its depletion with RNA int
11 two sequential enzymatic steps catalyzed by deoxyhypusine synthase and deoxyhypusine hydroxylase (DO
12 se models for the hypusine-modifying enzymes deoxyhypusine synthase and deoxyhypusine hydroxylase as
16 We discovered that homozygous depletion of deoxyhypusine synthase and/or deoxyhypusine hydroxylase
18 ivity, formation of different complexes with deoxyhypusine synthase, and Km values (1.5 +/- 0.2 vs. 8
29 is a two-step reaction involving the enzymes deoxyhypusine synthase (DHPS) and deoxyhypusine hydroxyl
30 sination, which is catalyzed by two enzymes, deoxyhypusine synthase (DHPS) and deoxyhypusine hydroxyl
31 s catalyzed by two enzymatic steps involving deoxyhypusine synthase (DHPS) and deoxyhypusine hydroxyl
33 two sequential enzymatic steps catalyzed by deoxyhypusine synthase (DHPS) and deoxyhypusine hydroxyl
34 eIF5A post-translationally via two enzymes, deoxyhypusine synthase (DHPS) and deoxyhypusine hydroxyl
35 s and Main Results: Hypusine forming enzymes-deoxyhypusine synthase (DHPS) and deoxyhypusine hydroxyl
36 nd mouse models with inducible knockdowns of deoxyhypusine synthase (DHPS) and eIF5A to investigate t
41 In-vivo inhibition of elF5A hypusination by deoxyhypusine synthase (DHS) inhibitor "GC7" was studied
44 f eukaryotic initiation factor 5A (eIF5A) by deoxyhypusine synthase, employing spermidine as a butyla
45 SS, we identified sequences encoding HSS and deoxyhypusine synthase from various species of the Convo
46 of transcript levels have shown that HSS and deoxyhypusine synthase have also diverged with respect t
47 s suggest a previously unrecognized role for deoxyhypusine synthase in promoting T cell proliferation
50 Th17, and Treg), but those treated with the deoxyhypusine synthase inhibitor GC7 showed a dose-depen
51 ctive metabolite that functions similarly to deoxyhypusine synthase inhibitors but has other unidenti
54 chain of the deoxyhypusine residue prevents deoxyhypusine synthase-mediated reversal of the modifica
55 xyhypusine residue, was incubated with human deoxyhypusine synthase, NAD, and 1,3-diaminopropane, [3H
57 t here at 2.2 A a new Form II crystal of the deoxyhypusine synthase:NAD holoenzyme grown at low ionic
61 tion in the single copy gene, yDHS, encoding deoxyhypusine synthase results in the loss of viability
63 of human DOHH along with eIF5A precursor and deoxyhypusine synthase was required for overproduction o
64 nsion of this prozyme paradigm to the enzyme deoxyhypusine synthase, which is required for spermidine
65 differentiation by providing substrates for deoxyhypusine synthase, which synthesizes the amino acid