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1 that PBCV-1 DC should be reclassified as an arginine decarboxylase.
2 spondin 1-(THBS 1), interleukin 6 (IL6), and arginine decarboxylase 2 (ADC2)) were down-regulated.
5 and functional presence of L-ornithine or L-arginine decarboxylase activity in proteins from phyla A
6 e in high amounts does not affect the native arginine decarboxylase activity, (c) Orn biosynthesis oc
7 rotoplast isolation show a rapid increase in arginine decarboxylase activity, a massive accumulation
9 S-mutagenized M2 seedlings for low levels of arginine decarboxylase (ADC) activity and identified sev
10 ture determination of bacterial biosynthetic arginine decarboxylase (ADC) and carboxynorspermidine de
14 ted viral (AAV) vector carrying the gene for arginine decarboxylase (ADC) prevented the development o
15 ently, conversion of arginine to agmatine by arginine decarboxylase (ADC) was considered important on
16 e enzymes, ornithine decarboxylase (ODC) and arginine decarboxylase (ADC), and the enzymatic activiti
17 arboxylase (ODC), pyruvoyl-dependent ODC and arginine decarboxylase (ADC), arginase, S-adenosylmethio
18 Polyamine (PA) titers and the activities of arginine decarboxylase (ADC, EC 4.1.1.19) and ornithine
19 is, Arabidopsis is reliant on the additional arginine decarboxylase (ADC; EC 4.1.1.9) pathway, found
20 2.5 acid challenge, the structural gene for arginine decarboxylase (adiA), and the regulator cysB, c
21 that agmatine, a metabolite of arginine via arginine decarboxylase (an arginine pathway distinct fro
22 tive pathways for polyamine biosynthesis via arginine decarboxylase and agmatinase were activated to
23 tive adcAB operon, which encodes a catabolic arginine decarboxylase and an antiporter protein, and PA
24 A and speC code for the biosynthetic enzymes arginine decarboxylase and ornithine decarboxylase, resp
28 determined the structure of the acid-induced arginine decarboxylase by X-ray crystallography to 2.4 A
29 e outer membrane porin (CPn1033 or aaxA), an arginine decarboxylase (CPn1032 or aaxB), and a putative
30 ily, the Paramecium bursaria Chlorella virus arginine decarboxylase (cvADC), shares about 40% amino a
33 de diverged homologs of a pyruvoyl-dependent arginine decarboxylase enzyme that nonpathogenic euryarc
35 distantly related to the bacterial and plant arginine decarboxylases from their common beta/alpha-fol
36 luding aspartate semialdehyde dehydrogenase, arginine decarboxylase gene activator, GTP cyclohydrolas
37 yridoxal 5'-phosphate-dependent ornithine or arginine decarboxylase genes, required to produce putres
38 The reaction mechanism of Yersinia pestis arginine decarboxylase has been investigated using a ser
39 eria in close proximity to homologues of the arginine decarboxylase in a gene arrangement pattern sim
44 ly, we reported that the speA gene, encoding arginine decarboxylase, is required for swarming in the
45 tory system affecting nitric oxide synthase, arginine decarboxylase, kyotorphin synthase, and arginin
48 wn here, these organisms have a new class of arginine decarboxylase (PvlArgDC) formed by the self-cle
49 specific 'suicide' inhibitor of the enzyme (arginine decarboxylase) responsible for their osmoticall
50 h encodes a pyridoxal 5'-phosphate-dependent arginine decarboxylase, restoring arginine-dependent aci
51 potentially from the AdoMetDC/SpeD-derived L-arginine decarboxylases, revealing unsuspected polyamine
53 es involved in polyamine biosynthesis--speA (arginine decarboxylase), speB (agmatine ureohydrolase),
56 The construction of the rhamnose-regulated arginine decarboxylase system allowed us to render S. Ty
58 pyridoxal 5'-phosphate or pyruvoyl-dependent arginine decarboxylases that catalyze the first step in
60 o the cytoplasm, providing the substrate for arginine decarboxylases, which consume a cellular proton