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1 c pathway, including fatty acid synthase and glycerol-3-phosphate acyltransferase.
2 acid synthase, acetyl-CoA carboxylase 1, and glycerol-3-phosphate acyltransferase.
3 c enzymes, including fatty acid synthase and glycerol-3-phosphate acyltransferase.
4 l-3-phosphate dehydrogenase, and plsB, an sn-glycerol-3-phosphate acyltransferase.
5 in homology modeling of both the AGPATs with glycerol-3-phosphate acyltransferase 1 (GPAT1) revealed
6 s impair insulin signaling, we overexpressed glycerol-3-phosphate acyltransferase-1 (GPAT1) in primar
7 osis by upregulating target genes, including glycerol-3-phosphate acyltransferase-1 (Gpat1), which ca
8 vitro studies suggest that the mitochondrial glycerol-3-phosphate acyltransferase-1 (mtGPAT1) isoform
10 ulating oleoyl-CoA utilization by microsomal glycerol-3-phosphate acyltransferase 3.2-fold and protec
15 in the model plant Arabidopsis thaliana: the glycerol-3-phosphate acyltransferase 6 (GPAT6) and a mem
16 t a dual functionality of pathogen-inducible GLYCEROL-3-PHOSPHATE ACYLTRANSFERASE 6 (GPAT6) in contro
17 mutation in the soluble chloroplastic enzyme glycerol-3-phosphate acyltransferase (ACT1) completely r
18 loss of both dihydroxyacetone phosphate and glycerol-3-phosphate acyltransferase activities in yeast
19 AT resulted in a complete loss of Leishmania glycerol-3-phosphate acyltransferase activity and a majo
20 shmania major promastigotes express a single glycerol-3-phosphate acyltransferase activity important
21 istent with this, inhibition of ER-localized glycerol-3-phosphate acyltransferase activity protected
24 on of LPT1 had a minimal effect on 1-acyl-sn-glycerol-3-phosphate acyltransferase activity, but overe
27 enzymes: glycerol 3-phosphate dehydrogenase, glycerol 3-phosphate acyltransferase and lysophosphatidi
28 alyses revealed that LmGAT is a low-affinity glycerol-3-phosphate acyltransferase and exhibits higher
29 act1, which encodes the chloroplast acyl-ACP:glycerol-3-phosphate acyltransferase, and one in lpat1,
30 ose-6-phosphate dehydrogenase, malic enzyme, glycerol-3-phosphate acyltransferase, and stearoyl-CoA d
31 oelii glycerol 3-phosphate dehydrogenase and glycerol 3-phosphate acyltransferase are expressed only
32 identified a genetic locus in mitochondrial glycerol-3-phosphate acyltransferase associated with inc
33 e homozygous mutant deficient of the plastid glycerol-3-phosphate acyltransferase; both mutations blo
34 mice; however, the activities of microsomal glycerol-3-phosphate acyltransferase, diacylglycerol acy
35 erichia coli, LPA acyltransferase (1-acyl-sn-glycerol-3-phosphate acyltransferase; EC 2.3.1.51) catal
37 egulator (GCKR), tribbles homolog 1 (TRIB1), glycerol-3-phosphate acyltransferase (GPAM), mitochondri
38 -relevant key nodes, including mitochondrial glycerol-3-phosphate acyltransferase (GPAM), were expose
40 key enzymes in the Kennedy pathway, such as glycerol 3-phosphate acyltransferase (GPAT), lysophospha
41 ansferases essential for cutin biosynthesis, glycerol-3-phosphate acyltransferase (GPAT) 4 and GPAT8.
45 t that LpxL shares distant homology with the glycerol-3-phosphate acyltransferase (GPAT) family, incl
46 Arabidopsis (Arabidopsis thaliana) has eight glycerol-3-phosphate acyltransferase (GPAT) genes that a
47 tion, enzymatic activity of liver microsomal glycerol-3-phosphate acyltransferase (GPAT) increased 4-
51 G biosynthesis, including those that encoded glycerol-3-phosphate acyltransferase (GPAT), acyl-CoA:di
53 sequences from various acyltransferases [sn-glycerol-3-phosphate acyltransferase (GPAT), lysophospha
56 fatty acid synthase (FAS) and mitochondrial glycerol-3-phosphate acyltransferase (GPAT)-involved in
59 Microsomal and mitochondrial isoforms of glycerol-3-phosphate acyltransferase (GPAT; E.C. 2.3.1.1
61 opersicum 'Micro-Tom'; the wild type and the GLYCEROL-3-PHOSPHATE ACYLTRANSFERASE [GPAT6] and CUTIN S
65 nzymes involved in both TAG synthesis, Gpam (glycerol-3-phosphate acyltransferase, mitochondrial), Dg
66 s rs2792751 in GPAM/GPAT1, the gene encoding glycerol-3-phosphate acyltransferase, mitochondrial, and
68 ave previously shown rat liver mitochondrial glycerol-3-phosphate acyltransferase (mtGAT), which cata
69 Second-site mutations in the ACT1-encoded glycerol-3-phosphate acyltransferase or GLY1-encoded gly
70 epresentative members of this family, the sn-glycerol-3-phosphate acyltransferase (PlsB) and the bifu
73 sD was most closely related to the 1-acyl-sn-glycerol-3-phosphate acyltransferase (plsC) gene family
74 SF binds constitutively to the mitochondrial glycerol 3-phosphate acyltransferase promoter during fas
75 cooperative activation of the mitochondrial glycerol-3-phosphate acyltransferase promoter by USF and
76 xotrophs, and this lipid export requires the glycerol-3-phosphate acyltransferase RAM2, a direct targ
78 s based on competition between Ole1p and the glycerol-3-phosphate acyltransferase Sct1p/Gat2p for the
79 e PlsB26 protein had a significantly reduced glycerol-3-phosphate acyltransferase specific activity c
80 y the transfer of fatty acids to glycerol by glycerol-3-phosphate acyltransferases, which facilitate