ライフサイエンスコーパス: lipase

1 is Rv3775 (LipE) was annotated as a putative lipase.

2 r cholesterol esters are cleaved off by acid lipase.

3 ion of the oral phase and the use of gastric lipase.

4 tion of endocannabinoids by monoacylglycerol lipase.

5 cterial genera and the activity of exoenzyme lipase.

6 Candida antartica lipase B, and Mucor miehei lipase.

7 ene PLIP1, which encodes a plastid-localized lipase.

8 g than quinoa, especially against pancreatic lipase.

9 ch as Streptomyces chromofuscus PLD or serum lipase.

10 hanase with a conserved domain of family I.3 lipase.

11 se in structural dynamics of the immobilized lipase.

12 enerated the same kind of inhibitors against lipase.

13 s and glycerol through the action of neutral lipases.

14 ere studied using exogenous or overexpressed lipases.

15 modifications by kinases, phosphatases, and lipases.

16 n enol ester link and tested against several lipases.

17 for NAPE-PLD versus other tissue-associated lipases.

18 Worms deficient in lysosomal lipase 2 (lipl-2), a lysosomal enzyme that is transcript

19 ive Hnf4 signaling leads to up-regulation of lipase 3 and enzymes for mitochondrial beta-oxidation.

20 a (4%), thrombocytopenia (3%), and increased lipase (3%).

21 ivolumab and ipilimumab group were increased lipase (57 [10%] of 547), increased amylase (31 [6%]), a

22 e more effective at inhibiting of pancreatic lipase (74.5%) and of alpha-glucosidase (98.2%).

23 ition tests of alpha-glucosidase, pancreatic lipase, acetylcholinesterase and 15-lipoxygenase were pe

24 and ABHD5 ligands, demonstrating that ABHD5 lipase activation could be dissociated from its other fu

25 ctivity for Nape-pld compared with nontarget lipase activities such as Streptomyces chromofuscus PLD

26 anced protease and alpha-amylase and reduced lipase activities were observed in sprouted oat powder,

27 sorder that is caused by loss of lipoprotein lipase activity and characterized by chylomicronemia and

28 The fungal infection significantly reduced lipase activity and lipid mobilization, thus impairing t

29 shows that water molecules essential for the lipase activity can be replaced by the hydroxyl groups a

30 free fatty acids and attenuated lipoprotein lipase activity consistent with hallmarks of dyslipidemi

31 However, its lipase activity has never been characterized, and its pr

32 pression of the identified lipases and their lipase activity in a time-dependent manner.

33 ated with increased postprandial lipoprotein lipase activity in adipose tissue.

34 97, Gly342, and His363 are essential for the lipase activity of rLipE.

35 Bacterial lipase activity on mammalian lipids and phospholipids ca

36 It is concluded that polyurethanase with lipase activity represents a potential enzyme for the de

37 ongenital ichthyoses; and (v) lipoxygenases, lipase activity, and LIPN co-localize within putative la

38 h suppressed Gbeta expression exhibit higher lipase activity, and show phenotypes similar to plants o

39 ike protein 3 (ANGPTL3) inhibits lipoprotein lipase activity, increasing triglycerides and other lipi

40 olesterol micellar solubility and pancreatic lipase activity, was recorded.

41 showed the highest cellulase and the lowest lipase activity, while C. noveboracense had the highest

42 ctive than conventional roasting in reducing lipase activity.

43 antioxidant activity and PLE for inhibitory lipase activity.

44 a/alpha topology of members of the GDSL-like lipase/acylhydrolase family.

45 No activity was observed for lipase AK Amano 20, Candida antartica lipase B, and Muco

46 of the hydrolytic enzymes alpha-amylase and lipase along with stored food reserves (lipids, carbohyd

47 -specific phospholipase C and diacylglycerol lipase alpha is known, alternative pathways remain unset

48 the 2-AG-synthesizing enzyme diacylglycerol lipase alpha.

49 r pharmacologic inhibition of diacylglycerol lipase-alpha (DAGL-alpha) impairs hippocampal CA1 LTP, d

50 Diacylglycerol lipase-alpha (DAGL-alpha), the principal biosynthetic en

51 l the extracts showed inhibitory activity of lipase, although those from T. molitor and extracted by

52 Their inhibitory activity on pancreatic lipase and alpha-amylase was assessed by traditional in

53 inistered a control diet with restored serum lipase and amylase levels (p < 0.05).

54 Serum lipase and amylase levels were analyzed at the end of th

55 g multibioactive products against pancreatic lipase and cholesterol absorption simultaneously.

56 fied that the mutant strain lost most of its lipase and esterase activities and displayed reduced vir

57 thers without DM (n = 18), were analysed for lipase and fatty acid transport proteins and fatty acid

58 ibition of both TG hydrolysis by lipoprotein lipase and hepatic uptake of remnant lipoproteins.

59 ere assessed on the inhibition of pancreatic lipase and interference on the bioaccessibility of chole

60 Our data suggest that LipE functions as a lipase and is important for M. tuberculosis intracellula

61 ignaling mediated by a LIPL-4 lysosomal acid lipase and its lipid chaperone LBP-8 increases mitochond

62 The faba bean exhibited high lipase and lipoxygenase (LOX) activities, with pH optima

63 However, the remaining activities of lipase and lipoxygenase after 30 min steam autoclaving w

64 gas to nitrogen, the residual activities of lipase and lipoxygenase after the same time of atmospher

65 rgon as plasma gas, the residual activity of lipase and lipoxygenase decreased to 42.50% and 87.72%,

66 on in activity of fat destabilizing enzymes (lipase and lipoxygenase), contaminants heavy metals (As,

67 ited along with the lipid degrading enzymes, lipase and lipoxygenase, resulting in a relatively short

68 FCS); a deficiency in the enzyme lipoprotein lipase and some associated proteins, termed familial chy

69 iocatalytic approaches based on the use of a lipase and transaminase, respectively, the combination o

70 sters were positive for the exocrine enzymes lipase and trypsinogen.

71 The effects of different lipases and galloyl donors/acceptors on the transesterif

72 ydrolyze host lipid substrates with secreted lipases and phospholipases for nutrient acquisition, col

73 elated with the expression of the identified lipases and their lipase activity in a time-dependent ma

74 pha-amylase, -alpha-glucosidase, -pancreatic lipase) and antioxidant potential (FRAP, ORAC), phenolic

75 was one (3%) grade 4 adverse event (elevated lipase) and no treatment-related deaths occurred.

76 sociated perilipins 2/3/5, hormone-sensitive lipase, and 1-acylglycerol-3-phosphate O-acyltransferase

77 atty acids were hydrolyzed by Candida rugosa lipase, and more selectivity is observed with Porcine Pa

78 three different classes of enzymes (amylase, lipase, and sulfatase), relying on two distinct mechanis

79 gically assessed amylase, insulin, glucagon, lipase, and/or trypsinogen in 78 organ donor pancreata f

80 ous downstream molecules, including kinases, lipases, and linkers, is crucial for B cell selection, s

81 rt and metabolism-related genes (lipoprotein lipase, apolipoprotein A1, apolipoprotein A4, apolipopro

82 zation of gas cell interfaces in dough since lipase application did not change GSB LVs.

83 y responsible for loaf volume increases upon lipase application.

84 Lipases are associated with food spoilage and are also u

85 Lipases are enzymes necessary for the proper distributio

86 Immobilized lipases are excellent biocatalysts for the enzymatic syn

87 in and hederacoside C slightly inhibited the lipase (around 10%) and protodioscin reduced the bioacce

88 g fatty acid uptake and identify lipoprotein lipase as a potential therapeutic target in melanoma.

89 sing four commercially available immobilized lipases as catalysts and two acyl donors: ferulic acid (

90 via activation of the conserved triglyceride lipase ATGL-1, triggers a feedback transcriptional loop

91 through repressing the adipose triglyceride lipase (ATGL) activity in neutrophils in prostaglandin E

92 Silencing adipose triglyceride lipase (ATGL) in human pseudoislets (shATGL) increased t

93 Silencing adipose triglyceride lipase (ATGL) in human pseudoislets with shRNA targeting

94 red lipolysis in global adipose triglyceride lipase (ATGL) knockout mice reduced free PAHSA levels an

95 of the lipolysis enzyme adipose triglyceride lipase (ATGL) resulted in large cytoplasmic LDs, whereas

96 ehydrogenase (POX), and adipose triglyceride lipase (ATGL), as well as markedly reduced lipid droplet

97 ride (TG) hydrolysis by adipose triglyceride lipase (ATGL), the major lipase in the liver.

98 a specific inhibitor of adipose triglyceride lipase (ATGL), the rate-limiting enzyme for intracellula

99 conserved regulator of adipose triglyceride lipase (ATGL)-mediated lipolysis that plays important ro

100 sis in the absence of adipocyte triglyceride lipase (ATGL).

101 y metabolic regulators, adipose triglyceride lipase (ATGL/bmm) and transcriptional cofactor PGC-1.

102 pharmacologic inhibition of monoacylglycerol lipase attenuates GBM proliferation.

103 By employing Candida antarctica lipase B (CALB) as the model enzyme with the Ser-His-Asp

104 d using tert-butanol as a solvent, 20 g/L of lipase B from Candida Antarctica, and vinyl cinnamate as

105 ed for lipase AK Amano 20, Candida antartica lipase B, and Mucor miehei lipase.

106 ally available food-grade Candida antarctica lipase B, Lipozyme(R) 435, was used as the biocatalyst.

107 Candida antarctica lipase B-catalysed synthesis of lipophilic esters of pol

108 ty acid conjugate using a Candida antarctica lipase B-rich extract, without further purification and

109 with octanoic acid using Candida antarctica lipase B.

110 oth sexes identified a role for triglyceride lipase brummer (bmm) in the regulation of sex difference

111 vation of insulin receptor (InR) and adipose lipase brummer (bmm).

112 They all regulate key intracellular lipases but do so to significantly different extents.

113 We found that the Geh lipase, but not other S. aureus lipases, prevents activa

114 stinal conditions worsened the inhibition of lipase, but slightly catalyzed the alpha-amylase.

115 y extension Ras, allosterically activate the lipase by promoting and stabilizing interactions between

116 increased HDL levels (P = 7.7 x 10(-7)), but lipase C risk variants (rs2043085, rs2070895) were assoc

117 The formation of NVOFAs was related to lipase catalysed lipid hydrolysis and the formation of v

118 into egg-yolk phosphatidylcholine (PC) in a lipase-catalyzed acidolysis and interesterification proc

119 Using lipase-catalyzed hydrolysis of tributyrin as a model rea

120 e 4-carboxyindanone followed by a subsequent lipase-catalyzed resolution turned out to be the most ef

121 ted protein 2 (PNLIPRP2), and carboxyl ester lipase (CEL), which may leak into the visceral fat or sy

122 Encapsulation of the lipase-coated lipid/PDMS droplets into a model protocell

123 Herein, we prepare aqueous suspensions of lipase-coated oil globules comprising a mixture of a tri

124 ibition of alpha-glucosidase, alpha-amylase, lipase, cyclooxygenases-1 and -2 (COX-1/COX-2), and lipo

125 triazole urea derivatives as diacylglycerol lipase (DAGL)-alpha inhibitors.

126 vity of the enzyme, the specific activity of lipase decreased.

127 Monoacylglycerol lipase deficiency affects diet-induced obesity, fat abso

128 Besides cytoplasmic lipase-dependent adipocyte fat mobilization, the metabol

129 d extracted chia seed oil and with different lipase derivatives to compare the omega-3 FAEE yield and

130 Furthermore, reutilization of lipase derivatives was studied to evaluate the stability

131 This occurs through its lipase domain.

132 e functions that extends from the N-terminal lipase domains to the C-terminal EDS1-PAD4 domains and m

133 brans suggesting their inhibitory effect on lipase during bran storage.

134 were used to monitor the clearance of these lipases during biologics process development.

135 it is a lipase, which we name TleV1 (type VI lipase effector Vibrio).

136 Endothelial lipase (EL) hydrolyzes phospholipids in high-density lip

137 ter adverse events related to treatment were lipase elevation (n = 7 [10.8%]), fatigue (n = 4 [6.2%])

138 s occurred in 12 (29%) patients and included lipase elevation, atrial fibrillation, hypophosphataemia

139 e D (PLD), a ubiquitously expressed membrane lipase enzyme activity in modulating phagocyte functions

140 pE) protein and demonstrated that LipE has a lipase/esterase activity.

141 nce shares similarities with other bacterial lipase/esterases and we demonstrated that it has esteras

142 e active sites of 43 active SHs encompassing lipases/esterases, GDSL lipases, proteases, Ser carboxyp

143 This lipase exhibited high efficiency for omega-3 (n-3), and

144 Adipose triglyceride lipase expression was decreased and insulin-mediated per

145 identified a gene encoding a novel class III lipase family member, Sl-LIP8, that is associated with a

146 2 interactions has important implications on lipases for screening of stilbenoid.

147 d population in BM was studied by applying a lipase from Fusarium oxysporum in the process.

148 ught to purify, identify, and characterize a lipase from S. liquefaciens isolated from cold raw cow's

149 Lipase from Thermomyces lanuginosus (TLL) was immobilize

150 0.4-25 muM) and glycerol ester hydrolase or lipase (gehB, IC(50) 1.5-25 muM).

151 through specific repression of ATGL/Brummer lipase gene expression in adipose (fat body).

152 is encoded by a member of the GDSL esterase/lipase gene family.

153 RNA level of hexokinase-2, hormone sensitive lipase, glutathione peroxidase-1, and myosin heavy chain

154 Purified lipase had Michaelis-Menten constant (Km) and catalytic

155 sp catalytic triad, a highly active cysteine-lipase having a Cys-His-Asp catalytic triad and addition

156 Inhibition of human Monoacylglycerol Lipase (hMGL) offers a novel approach for treating neuro

157 ymatic studies showed that hormone sensitive lipase (HSL) hydrolyzes luteal cholesterol esters.

158 ance of lipid droplets and hormone-sensitive lipase (HSL) in regulating the aggressive nature of panc

159 atty acid synthase (FASN), hormone-sensitive lipase (HSL), and acyl dehydrogenases was analyzed in vi

160 f LD through regulation of hormone-sensitive lipase (HSL), which was downregulated in human PDAC.

161 All extracts inhibited pancreatic lipase (IC(50) between 1.15 and 0.59 mg/mL), although th

162 Lipase immobilized in the GO aerogel exhibits a 5 to 10-

163 This allowed concluding that lipase impact on LV is exclusively related to stabilizat

164 That lipase impact on LV strongly depended on the flour used

165 Further studies on lipase in food models are needed.

166 of LDs indicating that ATGL is the principal lipase in human beta cells.

167 f LDs, indicating that ATGL is the principal lipase in human beta-cells.

168 of ATGL, the rate-limiting triglyceride (TG) lipase in many cell types.

169 hepatic flare in two patients, and increased lipase in one patient.

170 reatment-related adverse event was increased lipase in the durvalumab group (seven [2%] of 345 patien

171 dipose triglyceride lipase (ATGL), the major lipase in the liver.

172 ng alveoli, albumin in liver parenchyma, and lipase in the stomach lining.

173 on PIN-lipid interactions and the impact of lipases in bread making.

174 focus on specific functions of intracellular lipases in lipid partitioning, covering basic and transl

175 orophosphonate-binding serine hydrolases and lipases in S. aureus and synthesized target-selective ac

176 of 126 patients) and asymptomatic increased lipase (in 10 [8%]).

177 ein profiling approach to unravel the active lipases, including other Serine hydrolases (SHs), expres

178 ents in the ripretinib group (n=85) included lipase increase (four [5%]), hypertension (three [4%]),

179 Three DLTs were reported: grade 3 lipase increase (n = 2; 100 mg and 200 mg twice a day) a

180 or worse treatment-related adverse event was lipase increase, which occurred in 14 (4%) of 353 patien

181 otransferase increased (33.9% vs 22.8%), and lipase increased (32.2% vs 27.4%); 13% of patients in th

182 Notably, as the thermal stability of lipase increased, as indicated by the temperature optimu

183 We studied the genotypic diversity of lipase induced hydrolytic rancidity (HR) level in the br

184 esulted in protein extracts with the highest lipase inhibition (~ 70%) in a dose-dependent way.

185 Lipase inhibition by all smoothies was over 50%.

186 Adding rabbit gastric lipase, lipase inhibitor (orlistat) and tocopherols to cod liver

187 eir functional roles and substrates, the pan-lipase inhibitor isopropyl dodecylfluorophosphonate was

188 overed the repeated loss of the triglyceride lipase inhibitor PNLIPRP1, suggesting enhanced triglycer

189 tat measurements in presence of a pancreatic lipase inhibitor proved to be an efficient way to widen

190 administration of JZL184, a monoacylglycerol lipase inhibitor, blocked SI deficits associated with in

191 ts potently with a covalent monoacylglycerol lipase inhibitor.

192 erine hydrolases by using a panel of neutral lipase inhibitors to identify an enzyme that reacts pote

193 xidant activity whereas a negative impact on lipase inhibitory activity was observed (p<.0001).

194 , antioxidant activity (DPPH) and pancreatic lipase inhibitory capacity were assayed.

195 Pancreatic lipase injected into mouse visceral adipose tissue hydro

196 We have examined the trans-resveratrol/lipase interaction by quantitative and qualitative analy

197 investigated the possibility that S. aureus lipases interface with the host immune system to blunt i

198 the activity of hepatic adipose triglyceride lipase, intrahepatic lipolysis, hepatic acetyl-CoA conte

199 We show that this lipase is located in the intermembrane space of the mito

200 st by immobilization of Candida antarctica B lipase is reported, coating single-core magnetic nanopar

201 ound that VPA0226, a constitutively secreted lipase, is required for escape of V. parahaemolyticus fr

202 been reported to allosterically activate the lipase, it is not known whether Rap1A has the same abili

203 ular dichroism measurement confirms that the lipase keeps its native conformation in the aerogel, and

204 Because dual pancreatic lipase knockouts are lethal, exocrine parotid acini lack

205 y that simultaneously monitors two high risk lipases known to impact biologics product quality, Phosp

206 e and day 3 compliance with triglyceride and lipase laboratory monitoring per protocol and time to di

207 Lysosomal acid lipase (LAL) hydrolyzes cholesteryl ester (CE) and retin

208 Lysosomal acid lipase (LAL) is a critical lipid hydrolase that generate

209 zation, the metabolic role of lysosomal acid lipase (LAL), highly expressed in adipocytes, is unclear

210 tream transcriptional target, lysosomal acid lipase (LAL).

211 ce protocol compliance with triglyceride and lipase level monitoring and mitigate propofol-related ha

212 ormal range, 30-130 U/L [0.5-2.2 ukat/L]), a lipase level of 172 U/L (2.9 ukat/L) (normal range, 0-60

213 opofol in the setting of triglyceride and/or lipase levels exceeding protocol cutoffs.

214 Outcome measures included pancreatic lipase levels, the systemic inflammatory response (conce

215 Lipase lid domains cover the active site to control both

216 Heterodimeric complexes containing the lipase-like protein ENHANCED DISEASE SUSCEPTIBILITY1 (ED

217 The EDS1 family of structurally unique lipase-like proteins EDS1, SAG101, and PAD4 evolved in s

218 CED DISEASE SUSCEPTIBILITY1 (EDS1) family of lipase-like proteins for all resistance outputs.

219 Adding rabbit gastric lipase, lipase inhibitor (orlistat) and tocopherols to c

220 (allele frequency=0.36), mapping to hepatic lipase (LIPC), to be associated with a smaller increase

221 The endothelial lipase LIPG possesses serine phospholipase activity and

222 is of propyl gallate (PG) using a food-grade lipase (Lipozyme(R) 435).

223 des, markers of lipogenesis, and lipoprotein lipase (LPL) activity in adults participating in a doubl

224 anged in ppHF dams, but systemic lipoprotein lipase (LPL) activity was increased, suggesting that inc

225 or, capturing the soluble enzyme lipoprotein lipase (LPL) during export from the TGN.

226 Lipoprotein lipase (LPL) hydrolyzes fatty acids (FAs) from triglycer

227 Lipoprotein lipase (LPL) is active in capillaries, where it plays a

228 Lipoprotein lipase (LPL) is an enzyme responsible for clearing trigl

229 Lipoprotein lipase (LPL) is central to triglyceride metabolism.

230 The enzyme lipoprotein lipase (LPL) is responsible for breaking down triglyceri

231 Lipoprotein lipase (LPL) is responsible for the intravascular proces

232 We show that lipoprotein lipase (LPL) may more efficiently hydrolyze medium lengt

233 Lipoprotein lipase (LPL) plays a central role in triglyceride (TG) m

234 The binding of lipoprotein lipase (LPL) to GPIHBP1 focuses the intravascular hydrol

235 Using RNA in situ hybridization, lipoprotein lipase (LPL) was found to be expressed in endothelial ce

236 pillary endothelial cells, binds lipoprotein lipase (LPL) within the subendothelial spaces and shuttl

237 rexpression of the gene encoding lipoprotein lipase (LPL), which was upregulated in zebrafish melanoc

238 bition (DSI) was limited by monoacylglycerol lipase (MAGL) but not by fatty acid amide hydrolase.

239 ith regional differences in monoacylglycerol lipase (MAGL) expression in postmortem brain tissue, suc

240 Monoacylglycerol lipase (MAGL) is the enzyme degrading the endocannabinoi

241 ve focused on inhibition of monoacylglycerol lipase (MAGL) to enhance signaling of the most abundant

242 ies of tetrazine probes for monoacylglycerol lipase (MAGL) were synthesized and the most reactive one

243 Monoacylglycerol lipase (MAGL), a serine hydrolase extensively expressed

244 nt actions of inhibitors of monoacylglycerol lipase (MAGL), the major degradative enzyme of the endoc

245 ional target MGLL, encoding monoacylglycerol lipase (MAGL), to regulate the self-renewal and tumorige

246 y acid synthase (FASN), and monoacylglycerol lipase (MAGL).

247 n 1 (GPIHBP1) and with its chaperone protein lipase maturation factor 1 (LMF1), we obtained a stable

248 Rhizomucor miehei lipase mediated-hydrolysis of sardine oil was conducted

249 Monoacylglycerol lipase (MGL) is the last enzymatic step in triglyceride

250 t (HFD)-induced obesity for monoacylglycerol lipase (MGL), an enzyme that is also known to hydrolyze

251 Inhibitors of monoacylglycerol lipase (MGL), the enzyme that deactivates the endocannab

252 at are potent inhibitors of monoacylglycerol lipase (MGL), the primary degrading enzyme for the endoc

253 This lipase must be delivered into the host cytoplasm where i

254 al-specific knockout of adipose triglyceride lipase not only reduced fetal beta-cell area and blood i

255 determinants such as exoenzymes (proteases, lipases, nucleases) and downregulate the expression of s

256 nity were not due to direct functions of the lipase on mammalian cells, but rather a result of inacti

257 aminotranferases (one [2%] of 46), increased lipase or amylase (two [4%]), and pancreatitis (one [2%]

258 in different organic solvents without using lipase or other enzymes.

259 High glucose levels did not alter placental lipase or transporter expression or the profile and abun

260 Specifically, catalase, lipase, or alkaline phosphatase-filled colloidosomes are

261 , CEE extracts being stronger (fenugreek for lipase -p = 0.009-, and quinoa for alpha-amylase -p < 0.

262 The lipase partially purified by ultrafiltration and gel fil

263 ity lipoprotein cholesterol, the lipoprotein lipase pathway or circulating lipoprotein(a) may be effi

264 itors for other serine hydrolases, including lipases, peptidases, and proteases.

265 Pancreatic triglyceride lipase (PNLIP) increased in adipose tissue during pancre

266 ancreas expresses pancreatic triacylglycerol lipase (PNLIP), pancreatic lipase-related protein 2 (PNL

267 se in apparent activity than the lyophilized lipase powder in transesterification of geraniol and vin

268 oteins, lactoferrin and bile salt-stimulated lipase, presented different kinetics of release during d

269 that the Geh lipase, but not other S. aureus lipases, prevents activation of innate cells in culture.

270 ive SHs encompassing lipases/esterases, GDSL lipases, proteases, Ser carboxypeptidases, ABHD protein,

271 mpathectomy and loss of adipose triglyceride lipase protect mice from GDF15-induced weight loss.

272 enzymatic resolution with immobilized Amano Lipase PS-30.

273 olvent-free glycerolysis of anchovy oil with lipase PS-DI from Burkholderia cepacia.

274 rol/triacylglycerol ratio of 3/1, 9.0% (w/w) Lipase PS-DI, a stirring rate of 200 rpm, and a reaction

275 nstrate the impact of HCP-mAb interaction on lipase quantification.

276 c triacylglycerol lipase (PNLIP), pancreatic lipase-related protein 2 (PNLIPRP2), and carboxyl ester

277 The corresponding acid lipase(s) catalyzing these reactions remains to be ident

278 We, thus, aimed to determine the pancreatic lipase(s) regulating lipotoxicity during AP.

279 Staphylococcus aureus secretes at least two lipases, Sal1 and glycerol ester hydrolase (Geh), with s

280 e promoter regions of genes encoding the TAG lipases SDP1 and DALL5 and acyl-thioesterase KAT5.

281 Addition of rabbit gastric lipase significantly increased the release of HNE during

282 yelin and a proteoglycan mediate lipoprotein lipase sorting in the TGN.

283 atidylethanolamines were the most accessible lipase substrates.

284 -18 followed by a physicochemical coating of lipase surface with a dense layer of PEG.

285 , with sequence similarity to plant esterase/lipase/thioesterase (ELT) proteins, is essential for tri

286 atment-related adverse events were increased lipase (three [7%]) and febrile neutropenia (three [7%])

287 ves and compared with commercial immobilized lipases to produce omega-3 rich FAEE.

288 A method involving extraction, lipase treatment, clean-up, and detection and quantifica

289 electivity is observed with Porcine Pancreas lipase type II.

290 Here, we showed that the stabilization of lipase upon MPCI to polymer brush surfaces resulted from

291 il catalysed by polyethylene glycol-modified lipases using a biocatalyst with higher stability than c

292 r shrimp fed diets 3 and 7, while intestinal lipase was significantly higher in shrimp fed diets 7 an

293 nzymes (alpha-amylase, alpha-glucosidase and lipase) was evaluated.

294 and the phosphorylation of hormone-sensitive lipase were attenuated in iWAT of Gcgr(-/-) mice.

295 upon enzymatic activity and are selective to lipases were developed under the name of shifting-nitrox

296 c wheat lines differing in PIN haplotype and lipases were used in bread making.

297 s are lethal, exocrine parotid acini lacking lipases were used to verify the results.

298 n of the putative effector indicates it is a lipase, which we name TleV1 (type VI lipase effector Vib

299 of pancreatic disease and normal amylase and lipase who underwent the examination with the same proto

300 of this method is demonstrated for two other lipases with different structures, promising unprecedent