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1 etate and [(14)C]glycerol incorporation into glycerolipids.
2 stid are exported for assembly of eukaryotic glycerolipids.
3 hesis of triacylglycerol and other non-ether glycerolipids.
4 o lipids, a pathway for de novo synthesis of glycerolipids.
5 in the metabolism of endogenous and dietary glycerolipids.
6 incorporation of hydrolyzed fatty acids into glycerolipids.
7 eir close association with various groups of glycerolipids.
8 golipids (GSLs) with lesser amounts of polar glycerolipids.
9 ese data are consistent with a mechanism for glycerolipid acyltransferase catalysis where the invaria
17 a substantial increase in the percentage of glycerolipid and sphingolipids species containing 24:1 a
19 how plants produce and secrete non-membrane glycerolipids and also how to engineer alternative pathw
20 proteins were enzymes that regulate sugars, glycerolipids and cholesterol itself as well as proteins
23 G3P forms the backbone of TAGs and membrane glycerolipids and it can be dephosphorylated to yield gl
25 hat PNPLA3 plays a role in the hydrolysis of glycerolipids and that the I148M substitution causes a l
26 y shunt fatty acids into de novo synthesized glycerolipids and the transfer of lipids into VLDL, resp
29 closely coordinated with that of sterols and glycerolipids and with other processes that occur in the
30 f [3H]oleic acid (OA) or [3H]glycerol to [3H]glycerolipids, and the turnover of these products in PC1
31 pidomic analysis indicates that both PLs and glycerolipids are qualitatively affected by the mutation
32 with age and cataract support the idea that glycerolipids are selectively oxidized over lipids with
34 data together indicate that Bayberry surface glycerolipids are synthesized by a pathway for TAG synth
37 d compound classes, including phospholipids, glycerolipids, bacterial lipoglycans and plant glycolipi
38 alyzed aminolysis of arachidonate-containing glycerolipids, because AEA was produced from synthetic (
40 FAD7, SFD1 and SFD2 are involved in plastid glycerolipid biosynthesis and SAR is also compromised in
44 and lipid homeostasis, probably through the glycerolipid biosynthesis pathway, which may contribute
45 idate phosphatase (PAP) enzymes required for glycerolipid biosynthesis, and also as transcriptional c
46 wild-type hamster GPI restored GPI activity, glycerolipid biosynthesis, and PAP1 activity in GroD1.
47 s highly conserved among acyltransferases in glycerolipid biosynthesis, drastically reduced mitochond
48 ), which catalyzes the first step in de novo glycerolipid biosynthesis, is stimulated by casein kinas
49 interacts with other enzymes involved in ER glycerolipid biosynthesis, suggesting the possibility of
50 e (GPAT) catalyzes the rate-limiting step of glycerolipid biosynthesis, the acylation of glycerol 3-p
51 phosphatase (PAP) enzymes catalyze a step in glycerolipid biosynthesis, the conversion of phosphatida
59 critical roles in trafficking SFAs into the glycerolipid biosynthetic pathway to form saturated phos
61 eficiency appear to include both the loss of glycerolipid building blocks and the accumulation of lip
62 kedly decreased the V(max) of the enzyme for glycerolipids but had only a modest effect on the K(m).
63 indicating reduced synthesis of chloroplast glycerolipids by the prokaryotic pathway of lipid metabo
65 l synthase1 mutant we suggest that a plastid glycerolipid-dependent factor is required in Avr PeX alo
67 he first animal representative of a class of glycerolipid desaturases that have previously been chara
68 g of sphingolipids and increased labeling of glycerolipids dramatically following in vivo labeling wi
70 lso include control of catalytic activity of glycerolipid enzymes by water-soluble precursors, produc
72 tyric acid receptor signaling cascades, plus glycerolipid, fatty acid, and amino acid metabolic pathw
75 gest lipid class, followed by sphingolipids, glycerolipids, fatty acyls, sterol lipids, and prenol li
78 on of FFAR1/GPR40 by an antagonist decreased glycerolipid formation, attenuated fatty acid increases
84 positional diversity, complex lipids such as glycerolipids, glycerophospholipids, saccharolipids, etc
85 and putative identification of fatty acids, glycerolipids, glycerophospholipids, sphingolipids, and
86 main lipid categories including fatty acyls, glycerolipids, glycerophospholipids, sphingolipids, ster
88 categories of lipids: (i) fatty acyls, (ii) glycerolipids, (iii) glycerophospholipids, (iv) cardioli
91 ynthesis and accumulation of fatty acids and glycerolipids in islets and protected against beta cell
94 s incorporated into complex endothelial cell glycerolipids, including monoglycerides, triglycerides,
95 d sphingomyelin, increased with age, whereas glycerolipids, including phosphatidylcholine and two pho
96 ocked the incorporation of [3H]glycerol into glycerolipids, incorporation of [14C]oleate into TG, but
97 the fatty acyl content of various classes of glycerolipids indicated that the Spr2 gene product catal
100 rst step in assembly of membrane and storage glycerolipids is acylation of glycerol-3-phosphate (G3P)
101 ation between gene expression and changes in glycerolipid levels during the Arabidopsis thaliana resp
102 between the coordination of transcripts and glycerolipid levels in a changing environment and the ef
103 ysis indicates coordinate regulation between glycerolipid metabolism and a broad spectrum of metaboli
105 overy of PDCT is important for understanding glycerolipid metabolism in plants and other organisms, a
108 This may indicate a block in the downstream glycerolipid metabolism pathway in GPD3 overexpression l
110 te application of T-87 cells for analysis of glycerolipid metabolism, including tests of gene functio
116 kidney tissue fatty acid, phospholipid, and glycerolipid metabolisms prior to and after the onset of
119 hether DGLA could be mobilized from cellular glycerolipids, neutrophils were stimulated with ionophor
126 utant, which is defective in the prokaryotic glycerolipid pathway, PDAT1 overexpression enhances TAG
129 oss all eight lipid categories: fatty acyls, glycerolipids, phosphoglycerolipids, polyketides, prenol
130 and biochemical analyses have revealed that glycerolipids play important roles in cell signaling, me
131 een important for evolution of extracellular glycerolipid polymers and adaptation of plants to a terr
136 ple analytical techniques, we determined the glycerolipid profile of P. tricornutum grown with variou
141 c acid, mono- and diacylglycerols, and other glycerolipids, some implicated in augmenting insulin sec
142 ailability, this study analyzed the membrane glycerolipid species in soybean root hairs and in roots
143 nces of >600 individual glycerophospholipid, glycerolipid, sphingolipid and sterol lipids between a p
144 zes the initial and rate-controlling step in glycerolipid synthesis and aids in partitioning acyl-CoA
146 oxyacetone phosphate (acyl-DHAP) pathway for glycerolipid synthesis is commonly believed to be involv
148 to-oncoprotein c-Fos has an emerging role in glycerolipid synthesis regulation; by interacting with k
149 Expression of several genes that regulate glycerolipid synthesis was not changed by GW7647 treatme
150 for the generation of diacylglycerol during glycerolipid synthesis, and exhibits dual functions in t
151 r redox and ATP production, gluconeogenesis, glycerolipid synthesis, and fatty acid oxidation in panc
152 ndrial enzyme catalyzing the initial step in glycerolipid synthesis, are induced during the different
153 rst two steps of the prokaryotic pathway for glycerolipid synthesis, so we investigated whether other
154 acylglycerol mobilization and precursors for glycerolipid synthesis, suggesting that lipid metabolism
167 separate gene, catalyze the initial step in glycerolipid synthesis; in liver, the major isoforms are
168 A comparison of microsomal and peroxisomal glycerolipid synthetic pathways, using D-[3-(3)H, U-(14)
169 PNPLA3 was observed against the three major glycerolipids, TAG, diacylglycerol, and monoacylglycerol
170 f 15 other sphingolipids, phospholipids, and glycerolipids tested, have been termed "sphingosine-depe
172 aine lipids are ether-linked, nonphosphorous glycerolipids that resemble the more commonly known phos
173 in synthesis of triacylglycerol and related glycerolipids, the possible functions of different isoen
174 tracts were treated with 0.1 N KOH to remove glycerolipids, the sphingoid base 1-phosphates were conv
175 he newly synthesized fatty acids first enter glycerolipids through PC acyl editing, largely at the sn
176 d phospholipase A (pPLA) hydrolyzes membrane glycerolipids to produce monoacyl compounds and free fat
177 the drug inhibited both de novo synthesis of glycerolipids via the glycerol-3-phosphate pathway and t
178 support the hypothesis that the synthesis of glycerolipids via the monoacylglycerol pathway may be hi
180 and ether- species), cholesteryl esters, and glycerolipids were associated with future cardiovascular
181 perimentally that esterified carotenoids and glycerolipids were not removed, indicating a much more s
182 s starvation, 140 molecular species of polar glycerolipids were quantitatively profiled in rosettes a
183 lipids, sphingolipids, free fatty acids, and glycerolipids) which were mapped to their corresponding
185 hermophila resulted the detection of various glycerolipids with an ether bond, indicating reconstitut
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