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1 nine different organisms to form a ten-step de novo pathway.
2 s PGC1alpha deficiency or AKI attenuates the de novo pathway.
3 ucleotide triphosphate pools produced by the de novo pathway.
4 trioles have an activity that suppresses the de novo pathway.
5 o regulate the expression or activity of the de novo pathway.
6 ge pathway of ceramide formation and not the de novo pathway.
7 to occur primarily due to activation of the de novo pathway.
8 eramide in LNCaP cells is independent of the de novo pathway.
9 f DHFR and/or other enzymes along the purine de novo pathway.
10 the gene that encodes the third step in the de novo pathway, 3-dehydroquinate dehydratase (DHQ), was
12 eaction sits at the branch point between the de novo pathway and the salvage pathway, and has been sh
13 ays in hemopoietic and other cells that lack de novo pathways and are the route of cellular uptake fo
14 on of AT2 receptor induces the activation of de novo pathway, and a metabolite of this pathway, possi
15 ition of intracellular PA generation through de novo pathways attenuates sepsis-induced acute lung in
18 phosphate (dCTP) can be produced both by the de novo pathway (DNP) and by the nucleoside salvage path
19 es mediating ceramide generation through the de novo pathway (e.g. serine palmitoyltransferase) and v
21 ased activity of PDX3 as well as of the B(6) de novo pathway enzyme PDX1, correlating with increased
22 ite complementation." First, the trypanosome de novo pathway enzymes GDP-mannose dehydratase (GMD) an
23 the FX locus, which encodes an enzyme in the de novo pathway for GDP-fucose synthesis, exhibit a virt
25 phenolate mofetil (MMF), an inhibitor of the de novo pathway for purine biosynthesis, decreases rejec
28 athway, which provides an alternative to the de novo pathway for the biosynthesis of purine nucleotid
30 NAD biosynthesis, remarkably, they have one de novo pathway gene, nadC, encoding quinolinate phospho
31 reased expression of salvage and some of the de novo pathway genes was observed in both the pdx3 and
32 ittle change in expression of the vitamin B6 de novo pathway genes, but significant increases in expr
33 oxylase enzymes that convert PS to PE in the de novo pathway, has diminished PE levels like those of
35 reduction in fatty acids synthesized by the de novo pathway in L2 MECs of bitransgenic versus contro
38 pids and specifically those generated in the de novo pathway in the cell cycle arrest response to hea
39 oss-talk between phospholipid remodeling and de novo pathways involves ubiquitin-lysosomal processing
40 hosphates generated from receptor-linked and de novo pathways is crucial to the maintenance of approp
42 cidal effect as sudden NAD starvation of the de novo pathway mutant in both actively growing and nonr
43 roceramide desaturase as a key enzyme in the de novo pathway of ceramide generation was investigated
45 of ceramide was blocked by inhibitors of the de novo pathway of SL synthesis, beta-chloro-L-alanine a
47 rine nucleotide biosynthesis, mutants in the de novo pathway that disable the feedback inhibition of
48 dicating that most GDP-fucose is formed by a de novo pathway that involves the bioconversion of GDP-m
49 ose isomerase occupies a key position on the de novo pathway to GDP-mannose from glucose, just before
53 modifying natural pathways and establishing de novo pathways with enzymes from a variety of organism
54 osynthesized in this autotroph either by the de novo pathway, with chorismate as an intermediate, or
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