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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.
3                                              delta-Aminolevulinic acid (5-ALA) was used to induce apo
4                                  During AIP, delta-aminolevulinic acid (ALA) accumulates and promotes
5 nsports oligopeptides and the heme precursor delta-aminolevulinic acid (ALA) by a common mechanism.
6                                              delta-Aminolevulinic acid (ALA) causes cells to accumula
7                                  Addition of delta-aminolevulinic acid (ALA) in darkness drastically
8 cid dehydratase (ALAD), an enzyme converting delta-aminolevulinic acid (ALA) into porphobilinogen.
9                           The heme precursor delta-aminolevulinic acid (ALA) is taken up by the dipep
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
13 sociated with increased urinary excretion of delta-aminolevulinic acid (ALA).
14 ed from the universal tetrapyrrole precursor delta-aminolevulinic acid (ALA).
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
22                 The heme biosynthesis enzyme delta-aminolevulinic acid dehydratase (ALAD) requires ma
23               We report a new assay of human delta-aminolevulinic acid dehydratase (ALAD), an enzyme
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
27 % inhibition of the heme biosynthetic enzyme delta-aminolevulinic acid dehydratase.
28 ated gene encoding the heme synthesis enzyme delta-aminolevulinic acid dehydratase.
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
33                                              delta-Aminolevulinic acid-fed antisense Arabidopsis plan
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
36 st before assay did not increase the rate of delta-aminolevulinic acid formation.
37          2) The incorporation of radioactive delta-aminolevulinic acid into heme A is reduced in yah1
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
40               Addition of the heme precursor delta-aminolevulinic acid restored the cytochrome conten
41 ining proteins, whereas supplementation with delta-aminolevulinic acid reversed these defects.
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
44              Overexpression of mitochondrial delta-aminolevulinic acid synthase 2, the rate-limiting
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
47                                              delta-Aminolevulinic acid, the biosynthetic precursor of
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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