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1 d to express rabbit GAPDH in the presence of delta-aminolevulinic acid.
2 condensed with succinyl coenzyme A to yield delta-aminolevulinic acid.
5 nsports oligopeptides and the heme precursor delta-aminolevulinic acid (ALA) by a common mechanism.
8 cid dehydratase (ALAD), an enzyme converting delta-aminolevulinic acid (ALA) into porphobilinogen.
10 w in mutants defective in the genes encoding delta-aminolevulinic acid (ALA) synthase and ferrochelat
11 teria synthesize the tetrapyrrole precursor, delta-aminolevulinic acid (ALA), from glutamate by means
12 e studies to help clarify the roles of heme, delta-aminolevulinic acid (ALA), hemA, and hemM in Esche
15 about the movement of 5-aminolevulinic acid (delta-aminolevulinic acid; ALA) between blood and brain.
16 nt manifests a defect in the biosynthesis of delta-aminolevulinic acid and displays reduced levels of
17 ls of PCT: wild-type mice treated with iron, delta-aminolevulinic acid, and polychlorinated biphenyls
18 dicated, unexpectedly, that it is the enzyme delta-aminolevulinic acid dehydratase (ALA-D) and that i
19 The ALAD gene (chromosome 9q34) codes for delta-aminolevulinic acid dehydratase (ALAD) (E.C. 4.2.1
20 e gene encoding the haem biosynthesis enzyme delta-aminolevulinic acid dehydratase (ALAD) is normally
21 symptoms and its potential modification by a delta-aminolevulinic acid dehydratase (ALAD) polymorphis
24 -independent transcriptional co-regulator of delta-aminolevulinic acid dehydratase (Alad), but not 5-
25 gen (CTX)), and the K59N polymorphism in the delta-aminolevulinic acid dehydratase gene, ALAD, were m
26 veloped for use in the clinical diagnosis of delta-aminolevulinic acid dehydratase-deficient porphyri
29 ociation is modified by polymorphisms in the delta-aminolevulinic acid dehydrogenase (ALAD) gene.
30 phalexin and cefadroxil, the antineoplastics delta-aminolevulinic acid (delta-ALA) and bestatin, and
31 enicity of UVA alone and in combination with delta-aminolevulinic acid (delta-ALA), a precursor of th
32 hase 2, the rate-limiting enzyme upstream of delta-aminolevulinic acid export, failed to restore heme
34 -dextran and given drinking water containing delta-aminolevulinic acid for 21 days, hepatic porphyrin
35 nd human but not rat liver, maximal rates of delta-aminolevulinic acid formation required addition to
38 do not respond adequately to PDT with methyl-delta-aminolevulinic acid (MAL-PDT) and the tumors acqui
39 le in heme synthesis pathway by facilitating delta-aminolevulinic acid production or export from the
42 , due to a deletion in the gene that encodes delta-aminolevulinic acid synthase (HEM1), resulted in d
43 The rate-limiting enzyme in heme synthesis, delta-aminolevulinic acid synthase 2 (ALAS2), was signif
45 l assay of low levels of activity of hepatic delta-aminolevulinic acid synthetase have been studied,
46 succinyl-CoA generation was more labile than delta-aminolevulinic acid synthetase under these conditi
48 n darkness for 14 days, upon the addition of delta-aminolevulinic acid, the level of magnesium-protop
49 ocyte ALA-D is about as active in converting delta-aminolevulinic acid to porphobilinogen and as Zn2+
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