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1 equilibrium parameters is demonstrated for a triglyceride lipase.
2 ats is dependent on the action of pancreatic triglyceride lipase.
3 f insulin signaling and mice lacking adipose triglyceride lipase.
4 ytes by inhibiting the expression of adipose triglyceride lipase.
5 inflammation, and an upregulation of adipose triglyceride lipase.
6 acellular triacylglycerol hydrolase, adipose triglyceride lipase.
7 olysis of triglyceride by activating adipose triglyceride lipase.
8 t triacylglycerol lipase 3 and human adipose triglyceride lipase.
9  activity and the protein content of adipose triglyceride lipase, acetyl-CoA carboxylase 2 and AMP-ac
10  inhibitor of all known iPLA2s, inhibits the triglyceride lipase activity of each of the three isofor
11 IPRP2 lid domain or beta5-loop had decreased triglyceride lipase activity similar to that of PNLIPRP2
12 substantial phospholipase activity, but less triglyceride lipase activity.
13 7 cells had phospholipase A1 activity but no triglyceride lipase activity.
14 holipase activity is similar to its level of triglyceride lipase activity.
15 ferase 1) and degrade LD via ATGL (adipocyte triglyceride lipase) after FA loading.
16 ctivities, including coactivation of adipose triglyceride lipase and acylation of lysophosphatidic ac
17 -containing 2 (PNPLA2) family that possesses triglyceride lipase and acylglycerol transacylase activi
18 e lipase activation without altering adipose triglyceride lipase and CGI-58 expression in adipocytes.
19 ships of structure to function of pancreatic triglyceride lipase and colipase.
20 sue cultures increased expression of adipose triglyceride lipase and genes regulated by FFA, and incr
21              Elevated expressions of adipose triglyceride lipase and hormone sensitive lipase in adip
22 n association with the activation of adipose triglyceride lipase and hormone-sensitive lipase.
23  and lipolytic mechanism of human pancreatic triglyceride lipase and of colipase, another pancreatic
24  ability of endothelial cells to secrete the triglyceride lipase and phospholipase activities charact
25 eatic protein that interacts with pancreatic triglyceride lipase and that is required for lipase acti
26 testine by the pancreatic enzyme, pancreatic triglyceride lipase, and intestinal brush border enzyme,
27 The expression of OXPAT/perilipin-5, adipose triglyceride lipase, and stearoyl-CoA desaturase protein
28 estine and drives fat loss via the adipocyte triglyceride lipase ATGL-1.
29 apillary lumen, and the discovery of adipose triglyceride lipase (ATGL) and comparative gene identifi
30  levels of the key lipolytic enzymes adipose triglyceride lipase (ATGL) and hormone sensitive lipase
31  via activation of cytosolic lipases adipose triglyceride lipase (ATGL) and hormone-sensitive lipase
32    This study examined the role that adipose triglyceride lipase (ATGL) and hormone-sensitive lipase
33             Recent studies show that adipose triglyceride lipase (ATGL) and hormone-sensitive lipase
34                                      Adipose triglyceride lipase (ATGL) and its coactivator comparati
35       Recent studies have identified adipose triglyceride lipase (ATGL) as a major lipase in adipose
36 5-fold in association with increased adipose triglyceride lipase (ATGL) at the LD surface.
37 work designated as the "lipolysome." Adipose triglyceride lipase (Atgl) catalyzes the initiating step
38  step in triacylglycerol hydrolysis, adipose triglyceride lipase (ATGL) has been proposed to influenc
39                   Mice deficient for adipose triglyceride lipase (Atgl) in AT (atATGL-KO) were challe
40 aboratory and others have shown that adipose triglyceride lipase (ATGL) increases the activity of the
41                                      Adipose triglyceride lipase (ATGL) initiates intracellular trigl
42        Present results indicate that adipose triglyceride lipase (Atgl) interacts with perilipin-5 (P
43 sent investigation demonstrates that adipose triglyceride lipase (Atgl) is one of the enzymes involve
44                                      Adipose triglyceride lipase (ATGL) is rate-limiting for the init
45                                      Adipose triglyceride lipase (ATGL) is the predominant triacylgly
46            Neither protein levels of adipose triglyceride lipase (ATGL) nor phosphorylations of hormo
47 at (VF) was attributable to elevated adipose triglyceride lipase (Atgl) protein expression localized
48                            In liver, adipose triglyceride lipase (ATGL) serves as a major triacylglyc
49 porter 4 (GLUT4) was unaffected, and adipose triglyceride lipase (ATGL) was suppressed.
50 creases the colocalization of adipose tissue triglyceride lipase (Atgl) with its coactivator, Abhd5.
51 ctions as an endogenous inhibitor of adipose triglyceride lipase (ATGL), a key enzyme in intracellula
52 ipin proteins control lipolysis by adipocyte triglyceride lipase (ATGL), a key lipase in adipocytes a
53 tch gene 2 (G0S2) as an inhibitor of adipose triglyceride lipase (ATGL), a key mediator of intracellu
54 found that hepatic levels of SRA and adipose triglyceride lipase (ATGL), a major hepatic triacylglyce
55 ation and proteasomal degradation of adipose triglyceride lipase (ATGL), a rate limiting enzyme of TA
56 a lipid droplet scaffold, and adipose tissue triglyceride lipase (Atgl), a triglyceride-specific lipa
57 gulate fat metabolism by attenuating adipose triglyceride lipase (ATGL), but repression of oncogene-i
58  the rate-limiting lipolytic enzyme, adipose triglyceride lipase (ATGL), has two FoxO1-binding sites,
59 gnaling pathway on the expression of adipose triglyceride lipase (ATGL), hormone-sensitive lipase (HS
60  inhibit the principal TAG hydrolase adipose triglyceride lipase (ATGL), in the regulation of cardiac
61           Because the TAG hydrolase, adipose triglyceride lipase (ATGL), regulates baseline cardiac m
62 fectors hormone-sensitive lipase and adipose triglyceride lipase (ATGL), suggesting a link between ad
63 -modulates LD catabolism mediated by adipose triglyceride lipase (ATGL), the key enzyme for intracell
64  LDs interferes with the activity of adipose triglyceride lipase (ATGL), the key lipolytic enzyme in
65 e cell models, which express neither adipose triglyceride lipase (ATGL), the rate-limiting enzyme for
66 D size by inhibiting the activity of adipose triglyceride lipase (ATGL), the rate-limiting enzyme in
67 t hormone-sensitive lipase (HSL) and adipose triglyceride lipase (ATGL), two enzymes critical for lip
68 stimulates the enzymatic activity of adipose triglyceride lipase (ATGL), which catalyzes the hydrolys
69 , is a highly conserved regulator of adipose triglyceride lipase (ATGL)-mediated lipolysis that plays
70  was concomitant to an increase in adipocyte triglyceride lipase (ATGL)-mediated triglyceride breakdo
71  that paralleled a prolonged drop in adipose triglyceride lipase (ATGL).
72 quires the TG hydrolytic activity of adipose triglyceride lipase (ATGL).
73 ulated lipolysis by interacting with adipose triglyceride lipase (ATGL, also called desnutrin or PNPL
74 gree, but it did not affect adipose or liver triglyceride lipase (ATGL, known also as Pnpla2) mRNA in
75                                Since adipose triglyceride lipase (ATGL/PNPLA2) is the key enzyme for
76  we hypothesized that the absence of adipose triglyceride lipase (ATGL/PNPLA2)-the main enzyme for in
77 verexpressing desnutrin (also called adipose triglyceride lipase [ATGL]) in adipocytes (aP2-desnutrin
78 t directly inhibits transcription of adipose triglyceride lipase, ATGL.
79 cated that CGI-58 may stimulate an epidermal triglyceride lipase beyond ATGL required for the adequat
80 t a level much lower than that of pancreatic triglyceride lipase, but close to that of carboxyl ester
81 -chain saturated fatty acids, but pancreatic triglyceride lipase did not appear to have a role in the
82 essions of hormone-sensitive lipase, adipose triglyceride lipase enzymes, leptin, adiponectin and glu
83                           Changes in adipose triglyceride lipase expression correlated with increased
84  ex vivo activity of 11beta-HSD1 and adipose triglyceride lipase expression in subcutaneous fat biops
85 antly with an increase in myocardial adipose triglyceride lipase expression.
86 e molecular cloning of a novel member of the triglyceride lipase family, a 2.4-kb cDNA encoding human
87  tightly regulated by several members of the triglyceride lipase family, including endothelial lipase
88                                          The triglyceride lipase gene family plays a central role in
89 ely related enzymes among the members of the triglyceride lipase gene family with regard to primary s
90  lipase, a relatively recent addition to the triglyceride lipase gene family, is a major determinant
91 dothelial lipase (EL) is a new member of the triglyceride lipase gene family, which includes lipoprot
92 ase (EL), a recently described member of the triglyceride lipase gene family.
93 in the C-terminal domain of human pancreatic triglyceride lipase (hPTL) makes a major contribution in
94 nges in lipoprotein lipase (LpL) and hepatic triglyceride lipase (HTGL) similar to those found in IDD
95 at endothelial lipase is distinct from other triglyceride lipases in showing the highest activity on
96 pin RNA-mediated silencing of adipose tissue triglyceride lipase inhibited both forskolin-stimulated
97  corticosterone-infused rats with an adipose triglyceride lipase inhibitor blocked corticosterone-ind
98 on during the newborn period when pancreatic triglyceride lipase is not expressed.
99  The amphipathic, helical lid found in other triglyceride lipases is truncated in the structure of ch
100       GPB was hydrolyzed by human pancreatic triglyceride lipase, pancreatic lipase-related protein 2
101                         Furthermore, adipose triglyceride lipase, plasma membrane-associated fatty ac
102                                   Pancreatic triglyceride lipase (PNLIP) is essential for dietary fat
103  Defective lipolysis in mice lacking adipose triglyceride lipase provokes severe cardiac steatosis an
104 op, the lid, controls activity of pancreatic triglyceride lipase (PTL) by moving from a position that
105 f carboxyl ester lipase (CEL) and pancreatic triglyceride lipase (PTL) in lipid nutrient absorption.
106                                   Pancreatic triglyceride lipase (PTL) requires colipase for activity
107                  Enzyme assays of pancreatic triglyceride lipase (PTL) showed that there was a colipa
108              This study generated pancreatic triglyceride lipase (PTL)-null mice to test the hypothes
109              The most abundant is pancreatic triglyceride lipase (PTL).
110                         In vitro, pancreatic triglyceride lipase requires colipase to restore activit
111 also named desnutrin, iPLA2zeta, and adipose triglyceride lipase), resulting in increased fatty acid
112                                          The triglyceride lipase (tlTGL) from Thermomyces (formerly H
113 ncoding hormone-sensitive lipase and adipose triglyceride lipase, two enzymes involved in lipolysis a
114 orage by decreasing transcription of adipose triglyceride lipase via the mTORC1-mediated pathway, alt
115 equence, have distinct lipolytic properties (triglyceride lipase vs. phospholipase) as well as differ

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