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1 nct from the previously identified mammalian diacylglycerol acyltransferase.
2 g functions to produce TAGs, namely acyl-CoA:diacylglycerol acyltransferase 1 (DGAT1) and phospholipi
3 ng a number of mutant mouse models, identify diacylglycerol acyltransferase 1 (DGAT1) as an important
4 the neutral lipid synthesis enzyme acyl-CoA:diacylglycerol acyltransferase 1 (DGAT1) functions as th
5 accumulation, and co-expression of FUS3 and diacylglycerol acyltransferase 1 (DGAT1) further increas
6 acylglycerol (TG) synthesis enzyme acyl CoA: diacylglycerol acyltransferase 1 (DGAT1) in WAT and in a
7 ery and optimization of a series of acyl CoA:diacylglycerol acyltransferase 1 (DGAT1) inhibitors base
14 he triglyceride-synthesizing enzyme acyl CoA:diacylglycerol acyltransferase 1 (DGAT1) plays a critica
19 ructures of the TG-synthesis enzyme acyl-CoA:diacylglycerol acyltransferase 1 (DGAT1), a membrane bou
20 er cells through a process dependent on host diacylglycerol acyltransferase 1 (DGAT1), an enzyme that
23 transferase 1 and 2 enzymes and the acyl-CoA:diacylglycerol acyltransferase 1 and 2 enzymes, exhibite
24 ic diacylglycerol acyltransferase 2, but not diacylglycerol acyltransferase 1, thus inhibiting hepati
27 dentify the triglyceride-synthesizing enzyme diacylglycerol acyltransferase-1 (DGAT1) as a key host f
32 mbrane-associated, lipid metabolizing enzyme diacylglycerol acyltransferase 2 (DGAT2) as a model syst
34 we investigated the role of acyl-coenzyme A:diacylglycerol acyltransferase 2 (DGAT2) in glucose and
35 ology of imidazopyridine-based inhibitors of diacylglycerol acyltransferase 2 (DGAT2) is described.
37 Coexpression of RcPDAT1A and RcDGAT2 (for diacylglycerol acyltransferase 2) with RcFAH12 restored
38 in selectively and directly inhibits hepatic diacylglycerol acyltransferase 2, but not diacylglycerol
41 es in acyl-CoA synthetase long 1 (ACSL1) and diacylglycerol acyltransferase-2 (DGAT2), and (b) decrea
42 ons in the triacylglycerol synthesis enzyme, diacylglycerol acyltransferase-2 (Dgat2), cause yolk sac
43 c activity, increased expression of acyl CoA:diacylglycerol acyltransferase-2 in the liver, and eleva
44 by expressing a codon-optimized version of a diacylglycerol acyltransferase 2A from the soil fungus U
45 Instead, Arabidopsis chloroplast-localized DIACYLGLYCEROL ACYLTRANSFERASE 3 (DGAT3) promoted fungal
46 contrast, adipocyte acyl-CoA synthetase and diacylglycerol acyltransferase activities in postmenopau
47 Long chain acyl-CoA synthetase (ACS) and diacylglycerol acyltransferase activities, CD36, fatty a
49 r triacylglycerols than controls but similar diacylglycerol acyltransferase activity, triacylglycerol
52 cloning of a gene encoding acyl coenzyme A : diacylglycerol acyltransferase, an enzyme that catalyses
53 sted that parts of the hepatic activities of diacylglycerol acyltransferase and acyl cholesterol acyl
54 attributed to decreased expression of sn-1,2 diacylglycerol acyltransferase and mitochondrial acyl-Co
55 similar to the recently identified acyl-CoA diacylglycerol acyltransferase and, when deleted, result
56 osomal glycerol-3-phosphate acyltransferase, diacylglycerol acyltransferase, and ethanolamine phospho
58 nce that FATP1/acyl-CoA synthetase and DGAT2/diacylglycerol acyltransferase are components of a trigl
59 mutant dgat1-1 (in which phosphatidylcholine:diacylglycerol acyltransferase (AtPDAT1) is the major TA
60 es fatty acid esterification at the level of diacylglycerol acyltransferase by determining fatty acyl
61 DosR kinases, nitroreductases (acg; Rv3131), diacylglycerol acyltransferase (DGAT) (Rv3130c), and man
65 t MGAT2 also possessed an intrinsic acyl-CoA:diacylglycerol acyltransferase (DGAT) activity, which co
68 lysophosphatidate acyltransferase (LPAT) and diacylglycerol acyltransferase (DGAT) but can also be pr
71 lglycerol synthesis is catalysed by acyl-CoA diacylglycerol acyltransferase (DGAT) enzymes(2-4), the
72 seeds, two evolutionarily unrelated acyl-CoA:diacylglycerol acyltransferase (DGAT) enzymes, DGAT1 and
73 cerol synthesis is catalyzed by the acyl-CoA:diacylglycerol acyltransferase (DGAT) enzymes, DGAT1 and
77 ning and disruption of the gene for acyl-CoA:diacylglycerol acyltransferase (DGAT) have shown that al
81 glycerol-3-phosphate acyltransferase (GPAT), diacylglycerol acyltransferase (DGAT), and hormone-sensi
82 3-phosphate acyltransferase (GPAT), acyl-CoA:diacylglycerol acyltransferase (DGAT), and phospholipid:
84 rotein similar to mammalian acyl coenzyme A: diacylglycerol acyltransferase (DGAT), which converts di
86 A pool, making these PUFAs available for the diacylglycerol acyltransferase (DGAT)-catalyzed reaction
87 g chemical and genetic approaches to disrupt diacylglycerol acyltransferase (DGAT)-dependent LD bioge
88 Mechanistically, cell cycle arrest induces diacylglycerol acyltransferase (DGAT)-dependent lipid dr
90 by lecithin:retinol acyltransferase (LRAT), diacylglycerol acyltransferase (DGAT)1 also does this.
94 hosphatidic acid acyltransferases (LPAT) and diacylglycerol acyltransferases (DGAT) that are required
95 odeling involves a unique TAG lipase and two diacylglycerol acyltransferases (DGAT) that are selectiv
98 and oleic-acid contents encodes an acyl-CoA:diacylglycerol acyltransferase (DGAT1-2), which catalyze
99 ellular properties of tung type 1 and type 2 diacylglycerol acyltransferases (DGAT1 and DGAT2), two u
100 ed in storage lipid biosynthesis, two type-1 diacylglycerol acyltransferases (DGAT1) from rice were c
101 ogastat (PF-06865571), a systemically acting diacylglycerol acyltransferase (DGAT2) inhibitor that ha
102 e identified several genes encoding acyl-CoA:diacylglycerol acyltransferases (DGATs) and phospholipid
104 onoacylglycerol acyltransferases (MGATs) and diacylglycerol acyltransferases (DGATs) catalyze the two
105 ipid phosphate phosphohydrolases (LPINs) and diacylglycerol acyltransferases (DGATs), are involved in
106 A construct containing a Yarrowia lipolytica diacylglycerol acyltransferase gene (DGAT1) to increase
108 e-limiting steps of TAG biosynthesis, type-2 diacylglycerol acyltransferase genes (DGTTs), triggered
109 ession of genes encoding heteromeric ACCase, diacylglycerol acyltransferase, glyceraldehyde-3-phospha
111 , in vitro, and in vivo activities of type-2 diacylglycerol acyltransferases in Nannochloropsis ocean
112 oexpressing RcLPCAT with castor phospholipid:diacylglycerol acyltransferase increased novel FA and to
113 the endoplasmic reticulum, and that certain diacylglycerol acyltransferases may be the candidate enz
114 lized the Arabidopsis (Arabidopsis thaliana) diacylglycerol acyltransferase mutant dgat1-1 (in which
115 for components involved in TAG accumulation (diacylglycerol acyltransferases or major lipid droplet p
117 , and physiological analyses of phospholipid:diacylglycerol acyltransferase (PDAT) in the green micro
119 ROL ACYLTRANSFERASE1 (DGAT1) or PHOSPHOLIPID:DIACYLGLYCEROL ACYLTRANSFERASE (PDAT) on seed lipid comp
120 to provide PUFA substrates for phospholipid:diacylglycerol acyltransferase (PDAT) to synthesize TAG.
121 rol acyltransferase (DGAT), and phospholipid:diacylglycerol acyltransferase (PDAT), were strengthened
124 the absence of DGAT1 activity, phospholipid:diacylglycerol acyltransferase (PDAT1) plays an importan
125 ol acyltransferases (DGATs) and phospholipid:diacylglycerol acyltransferases (PDATs) from the flax ge
127 ic proteins (CD36, acyl-CoA synthetases, and diacylglycerol acyltransferase) predict differences in F
129 monstrate that inhibition of acyl-coenzyme A:diacylglycerol acyltransferase, the enzyme that catalyze
131 haracterization of Chlamydomonas reinhardtii diacylglycerol acyltransferase type two (DGTT) enzymes a
132 y enzymes long chain acyl-CoA synthetase and diacylglycerol acyltransferase, which were similar in ti
134 patic specific inhibition of acyl-coenzyme A:diacylglycerol acyltransferase with antisense oligonucle
135 acyl wax ester synthase, wax ester synthase/diacylglycerol acyltransferase (WS/DGAT), recently descr