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1 nct from the previously identified mammalian diacylglycerol acyltransferase.
2 ng a number of mutant mouse models, identify diacylglycerol acyltransferase 1 (DGAT1) as an important
3 the neutral lipid synthesis enzyme acyl-CoA:diacylglycerol acyltransferase 1 (DGAT1) functions as th
4 accumulation, and co-expression of FUS3 and diacylglycerol acyltransferase 1 (DGAT1) further increas
5 acylglycerol (TG) synthesis enzyme acyl CoA: diacylglycerol acyltransferase 1 (DGAT1) in WAT and in a
6 ery and optimization of a series of acyl CoA:diacylglycerol acyltransferase 1 (DGAT1) inhibitors base
13 he triglyceride-synthesizing enzyme acyl CoA:diacylglycerol acyltransferase 1 (DGAT1) plays a critica
18 er cells through a process dependent on host diacylglycerol acyltransferase 1 (DGAT1), an enzyme that
20 transferase 1 and 2 enzymes and the acyl-CoA:diacylglycerol acyltransferase 1 and 2 enzymes, exhibite
21 ic diacylglycerol acyltransferase 2, but not diacylglycerol acyltransferase 1, thus inhibiting hepati
24 dentify the triglyceride-synthesizing enzyme diacylglycerol acyltransferase-1 (DGAT1) as a key host f
30 we investigated the role of acyl-coenzyme A:diacylglycerol acyltransferase 2 (DGAT2) in glucose and
31 ology of imidazopyridine-based inhibitors of diacylglycerol acyltransferase 2 (DGAT2) is described.
33 Coexpression of RcPDAT1A and RcDGAT2 (for diacylglycerol acyltransferase 2) with RcFAH12 restored
34 in selectively and directly inhibits hepatic diacylglycerol acyltransferase 2, but not diacylglycerol
37 es in acyl-CoA synthetase long 1 (ACSL1) and diacylglycerol acyltransferase-2 (DGAT2), and (b) decrea
38 c activity, increased expression of acyl CoA:diacylglycerol acyltransferase-2 in the liver, and eleva
39 by expressing a codon-optimized version of a diacylglycerol acyltransferase 2A from the soil fungus U
40 contrast, adipocyte acyl-CoA synthetase and diacylglycerol acyltransferase activities in postmenopau
41 Long chain acyl-CoA synthetase (ACS) and diacylglycerol acyltransferase activities, CD36, fatty a
43 r triacylglycerols than controls but similar diacylglycerol acyltransferase activity, triacylglycerol
46 cloning of a gene encoding acyl coenzyme A : diacylglycerol acyltransferase, an enzyme that catalyses
47 sted that parts of the hepatic activities of diacylglycerol acyltransferase and acyl cholesterol acyl
48 attributed to decreased expression of sn-1,2 diacylglycerol acyltransferase and mitochondrial acyl-Co
49 similar to the recently identified acyl-CoA diacylglycerol acyltransferase and, when deleted, result
50 osomal glycerol-3-phosphate acyltransferase, diacylglycerol acyltransferase, and ethanolamine phospho
52 nce that FATP1/acyl-CoA synthetase and DGAT2/diacylglycerol acyltransferase are components of a trigl
53 es fatty acid esterification at the level of diacylglycerol acyltransferase by determining fatty acyl
54 DosR kinases, nitroreductases (acg; Rv3131), diacylglycerol acyltransferase (DGAT) (Rv3130c), and man
56 t MGAT2 also possessed an intrinsic acyl-CoA:diacylglycerol acyltransferase (DGAT) activity, which co
61 cerol synthesis is catalyzed by the acyl-CoA:diacylglycerol acyltransferase (DGAT) enzymes, DGAT1 and
64 ning and disruption of the gene for acyl-CoA:diacylglycerol acyltransferase (DGAT) have shown that al
68 glycerol-3-phosphate acyltransferase (GPAT), diacylglycerol acyltransferase (DGAT), and hormone-sensi
70 rotein similar to mammalian acyl coenzyme A: diacylglycerol acyltransferase (DGAT), which converts di
72 A pool, making these PUFAs available for the diacylglycerol acyltransferase (DGAT)-catalyzed reaction
73 g chemical and genetic approaches to disrupt diacylglycerol acyltransferase (DGAT)-dependent LD bioge
74 by lecithin:retinol acyltransferase (LRAT), diacylglycerol acyltransferase (DGAT)1 also does this.
77 hosphatidic acid acyltransferases (LPAT) and diacylglycerol acyltransferases (DGAT) that are required
79 and oleic-acid contents encodes an acyl-CoA:diacylglycerol acyltransferase (DGAT1-2), which catalyze
80 ellular properties of tung type 1 and type 2 diacylglycerol acyltransferases (DGAT1 and DGAT2), two u
81 e identified several genes encoding acyl-CoA:diacylglycerol acyltransferases (DGATs) and phospholipid
83 onoacylglycerol acyltransferases (MGATs) and diacylglycerol acyltransferases (DGATs) catalyze the two
84 A construct containing a Yarrowia lipolytica diacylglycerol acyltransferase gene (DGAT1) to increase
86 , in vitro, and in vivo activities of type-2 diacylglycerol acyltransferases in Nannochloropsis ocean
87 the endoplasmic reticulum, and that certain diacylglycerol acyltransferases may be the candidate enz
88 for components involved in TAG accumulation (diacylglycerol acyltransferases or major lipid droplet p
90 , and physiological analyses of phospholipid:diacylglycerol acyltransferase (PDAT) in the green micro
92 ROL ACYLTRANSFERASE1 (DGAT1) or PHOSPHOLIPID:DIACYLGLYCEROL ACYLTRANSFERASE (PDAT) on seed lipid comp
94 ol acyltransferases (DGATs) and phospholipid:diacylglycerol acyltransferases (PDATs) from the flax ge
95 ic proteins (CD36, acyl-CoA synthetases, and diacylglycerol acyltransferase) predict differences in F
97 monstrate that inhibition of acyl-coenzyme A:diacylglycerol acyltransferase, the enzyme that catalyze
98 haracterization of Chlamydomonas reinhardtii diacylglycerol acyltransferase type two (DGTT) enzymes a
99 y enzymes long chain acyl-CoA synthetase and diacylglycerol acyltransferase, which were similar in ti
100 patic specific inhibition of acyl-coenzyme A:diacylglycerol acyltransferase with antisense oligonucle
101 acyl wax ester synthase, wax ester synthase/diacylglycerol acyltransferase (WS/DGAT), recently descr
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