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1 protein of the biotin-dependent carboxylase, acetyl coenzyme A carboxylase.
2 nthesis, acting primarily on the activity of acetyl coenzyme A carboxylase.
4 ranscription factor 1c, fatty acid synthase, acetyl coenzyme A carboxylase 2, and carnitine palmitoyl
5 well as increased Ser(92) phosphorylation of acetyl-coenzyme A carboxylase, a downstream target of AM
6 ption from the housekeeping promoter for the acetyl coenzyme A carboxylase (ACC) gene, which encodes
7 eed in cellulo and could be used to identify acetyl coenzyme A carboxylase (ACC) in Pseudomonas aerug
8 reased AMP-activated protein kinase (AMPK)-->acetyl coenzyme A carboxylase (ACC) phosphorylation and
9 the low-density lipoprotein (LDL) receptor, acetyl coenzyme A carboxylase (ACC), and fatty acid synt
15 protein contents of fatty acid synthase and acetyl-coenzyme A carboxylase (ACC), reduced ACC phospho
16 in part by phosphorylating and inactivating acetyl-coenzyme A carboxylase (ACC), the rate-limiting e
19 tty acid biosynthesis in yeast; ACC1 encodes acetyl coenzyme A carboxylase (Acc1), and FAS1 encodes t
21 arboxyl carrier protein isoform 2 (BCCP2) in acetyl-coenzyme A carboxylase (ACCase) function and fatt
22 ns of commercial rates (375 g ha(-1)) of the acetyl-coenzyme A carboxylase (ACCase) inhibiting herbic
26 ase subunit of the heteromeric chloroplastic acetyl-coenzyme A carboxylase (ACCase) of Arabidopsis th
28 carrier protein 2 (BCCP2) inhibited plastid acetyl-coenzyme A carboxylase (ACCase), resulting in alt
32 ls are not sufficient to support heteromeric acetyl-coenzyme A carboxylase activity at a level that i
33 a1 and alpha2 AMPK activity are elevated and acetyl-coenzyme A carboxylase activity is decreased in t
35 downstream targets including phosphorylated acetyl-coenzyme A carboxylase and carnitine palmitoyltra
36 erodimer with the biotin acceptor protein of acetyl-coenzyme A carboxylase and catalyzes posttranslat
37 hosphorylation of downstream target of AMPK, acetyl-coenzyme A carboxylase and inhibition of p70S6 ki
38 ic carbon inside plastids for utilization by acetyl-coenzyme A carboxylase and the fatty acid synthes
39 naling to AMPK substrates, including Raptor, acetyl coenzyme A carboxylase, and PGC-1alpha, is attenu
40 or miR-204-5p which was predicted to inhibit acetyl coenzyme A carboxylase beta, a key fatty acid oxi
42 tations in ACC2, encoding a plastid-targeted acetyl-coenzyme A carboxylase, cause hypersensitivity to
43 sphorylation of the AMPK substrates, p53 and acetyl-coenzyme A carboxylase, changes that correlated w
44 ceded by the accumulation of plastid-encoded acetyl Coenzyme A carboxylase D proteins accounting for
45 l in natural environments, where heteromeric acetyl-coenzyme A carboxylase encoded in part by the chl
48 ary electrophoretic (CE) assay for measuring acetyl coenzyme A carboxylase holoenzyme (holo-ACC) acti
49 horylation of AMPK and its downstream target acetyl coenzyme A carboxylase in response to estradiol (
50 S Ser633 was able to compete with Ser1177 or acetyl-coenzyme A carboxylase Ser79 for AMPKalpha phosph
51 ased phosphorylation of both AMPK-Thr172 and acetyl-coenzyme A carboxylase-Ser79, a downstream enzyme
52 plicated nuclear gene that targets homomeric acetyl-coenzyme A carboxylase to plastids, where the mul
53 carboxyl-carrier subunit of the heteromeric acetyl-coenzyme A carboxylase was isolated and sequenced
54 atory element binding protein 1c), and ACACA(acetyl coenzyme A carboxylase) was not different between
55 Saccharomyces cerevisiae ACC1 gene (encoding acetyl-coenzyme A carboxylase), which has three Gal4 bin
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