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1 BCDO2), the only known mammalian xanthophyll cleavage enzyme.
2 that only mouse BCO2 is an active zeaxanthin cleavage enzyme.
3 nase, and Gcv3, the H protein of the glycine cleavage enzyme.
4 dehydrogenases and the H subunit of glycine cleavage enzyme.
5 eaved to acetoacetate plus acetyl-CoA by HMG cleavage enzyme.
6 ogenase associates with recombinant carotene cleavage enzyme.
7 of cholesterol to the cholesterol side-chain cleavage enzyme.
8 e delivery and intracellular activity of DNA cleavage enzymes.
9 plicable for directed evolution of other DNA cleavage enzymes.
10 y conserved motifs found in other carotenoid cleavage enzymes.
11 umvent resistance conferred by endopeptidase cleavage enzymes.
12 nal transduction down-regulates beta amyloid cleavage enzyme 1 (BACE1) activity, reduces Abeta genera
14 brane aspartyl protease termed beta-site APP cleavage enzyme 1 (BACE1) that cleaves the amyloid-beta
17 ARS-CoV-2, is regulated by a metalloprotease cleavage enzyme, a disintegrin and metalloprotease domai
18 etotic hyperglycinemia and deficient glycine cleavage enzyme activity, but without mutations in AMT,
21 tochrome P450scc (cytochrome P450 side chain cleavage enzyme) and aldosterone synthase, it did inhibi
22 myloid precursor protein (APP), beta-amyloid cleavage enzyme, and presenilin-1, a component of the ga
24 al membrane where the cholesterol side-chain cleavage enzyme carries out the first committed step in
27 n of unknown proteins, sucrose transport and cleavage enzymes, cysteine and methionine biosynthesis e
29 rotease-substrate cleavage assay, termed the cleavage enzyme- cytometric bead array (CE-CBA), which r
30 anded substrate specificity of aromatic ring-cleavage enzymes during fungal evolution, as well as a c
31 g Steroidogenic Factor 1 and P450 Side Chain Cleavage enzyme expression in Ptch1-expressing precursor
32 gonizes the function of ADAM10, an essential cleavage enzyme for the activation of the Notch signalin
34 d over; the latter process is mediated by PG cleavage enzymes, for example, the endopeptidases (EPs).
36 cently reported cDNA sequence for a carotene cleavage enzyme from Drosophila, we identified a cDNA en
37 on of the prodrug synthesis, elongation, and cleavage enzymes from the colibactin biosynthetic pathwa
40 uced expression of the endogenous side chain cleavage enzyme gene, and consequently, promote steroido
42 e recombinant enzyme suggested that carotene cleavage enzyme interacts with other proteins present wi
43 , MAX3/CCD7 and MAX4/CCD8, encode carotenoid cleavage enzymes involved in generating a branch-inhibit
45 idization studies demonstrated that carotene cleavage enzyme is expressed prominently in maternal tis
46 -carotene oxygenase 2 (BCO2) is a carotenoid cleavage enzyme located in the inner mitochondrial membr
48 inantly contain LHRH1-5-like peptide and its cleavage enzyme, metalloendopeptidase E.C.3.4.24.15 (EP2
49 rve both the phosphoryl transfer and the C-C cleavage enzymes of the PEP mutase superfamily, is propo
50 ptional (ORF12) regulator, an intradiol ring cleavage enzyme (ORF3), a maleylacetate reductase (ORF10
51 colocalizes with the cholesterol side-chain cleavage enzyme P450(scc) in both mouse and human brains
52 11A1 is the classical cholesterol side chain cleavage enzyme (P450(scc)) that removes six carbons of
53 ic acute regulatory protein, P450 side chain cleavage enzyme, P450 aromatase, 3beta-hydroxysteroid de
54 egulatory protein (StAR) and P450 side-chain cleavage enzyme (P450scc), without affecting P450 aromat
56 gene encoding a novel carbon-phosphorus bond cleavage enzyme, phosphonoacetate hydrolase, from Pseudo
57 aseolus vulgaris) that the gene encoding the cleavage enzyme (PvNCED1) is up-regulated by water stres
59 y is found to the archaeal Holliday junction cleavage enzymes, strongly suggesting a role in DNA repl
60 logue of the known pimeloyl-ACP methyl ester cleavage enzymes suggesting that it encodes a novel enzy
61 expressing the human cholesterol side-chain cleavage enzyme system and wild-type and mutant MLN64 pr
63 etabolism through its involvement in glycine cleavage enzyme system, intersecting two vital roles for
65 11A1 gene encodes the cholesterol side chain cleavage enzyme that catalyzes the initial and rate-limi
67 ses (SPCs) are a family of calcium-dependent cleavage enzymes that act on dibasic sites of various pe
68 doglycan synthases as well as membrane-bound cleavage enzymes that control where new peptidoglycan is
70 ases, dioxygenases and other downstream ring-cleavage enzymes-that funnel carbon to central metabolis
73 phnA) encodes a novel carbon-phosphorus bond cleavage enzyme whose expression is independent of the p
75 benefits and drawbacks of three types of DNA cleavage enzymes (zinc finger endonucleases, transcripti