ライフサイエンスコーパス: monoglyceride

1 n PLRP2 hydrolyzed long-chain tri-, di-, and monoglycerides.

2 ides, and other minor ones, such as 1- and 2-monoglycerides, 1,2-diglycerides, vegetable stanols and

3 The monoglyceride 2-arachidonoylglycerol (2-AG) meets severa

4 ysis reactions that lead to a reduction in 1-monoglycerides and an increase in 1,2-diglycerides, espe

5 t was noticed, however, that in the thickest monoglyceride bilayer used in this study, both the SS- a

6 The low ratio in the monoglyceride bilayer was not reversed in GMO-ether bila

7 It is proposed that the thickness of monoglyceride bilayers modulates proton transfer in nati

8 The differential effects of relatively thick monoglyceride bilayers on proton transfer in both dioxol

9 onlinear and remained basically unaltered in monoglyceride bilayers with various thicknesses.

10 fluorinated Trp analogs in both lecithin and monoglyceride bilayers.

11 lated bilayers, or variable fatty acid chain monoglyceride bilayers.

12 Their long-chain aliphatic alcohols and monoglycerides compositions are reported for the first t

13 This study suggests that short chain monoglycerides could be used with Tween 80 to prepare tr

14 , ionization of ammonium adducts of diacetyl monoglyceride derivatives in positive-ion mode markedly

15 s include free fatty acids and their esters, monoglyceride, diglyceride, and triglyceride.

16 -/- animals is due to the presence of excess monoglyceride esters in the fur.

17 s of different natures, fatty acids, esters, monoglycerides, fatty amides, aldehydes, ketones, alcoho

18 hydrolysis products were 1,2-diglycerides, 2-monoglycerides, glycerol and fatty acids, although small

19 sis to identify and quantify regioisomers of monoglycerides in biological samples.

20 lication of this approach in the analysis of monoglycerides in multiple biologic tissues demonstrated

21 bserved in the modulation of diglyceride and monoglyceride levels in BAT.

22 Human monoglyceride lipase (MGL) is a recently identified lipa

23 Monoglyceride lipase (MGL) is required for efficient hyd

24 Here we tested the hypothesis that monoglyceride lipase (MGL), a serine hydrolase that conv

25 Monoglyceride lipase (MGLL) expression was analyzed by q

26 cid amide hydrolase paralogs (FAAH1, FAAH2), monoglyceride lipase, N-acylethanolamine acid amidase, N

27 eroxisomal genes, such as CD36, Ly-6D, Rbp7, monoglyceride lipase, pyruvate dehydrogenase kinase-4, a

28 nterneurons; and 4) is metabolized by either monoglyceride lipase, which is located in the inhibitory

29 hrough measures of diacylglycerol lipase and monoglyceride lipase, which synthesize and degrade 2-ara

30 rably attenuated in phospholipid relative to monoglyceride membranes.

31 This does not occur with monoglyceride membranes.

32 of magnitude larger in phospholipid than in monoglyceride membranes.

33 contrast with results previously obtained in monoglyceride membranes.

34 Some sn2 monoglyceride might ultimately serve as the backbone for

35 Quantitative analysis of monoglyceride molecular species has remained challenging

36 markably, the regiospecificity of individual monoglyceride molecular species is also diverse from tis

37 toxicity of microemulsions composed of a 30% monoglyceride oil, 20% Tween 80 and 50% aqueous buffer w

38 The influence of palm oil replacement with a monoglyceride-palm oil-water gel (hydrogel) on physical

39 The thickness of monoglyceride planar bilayers has significant effects on

40 Monoglycerides play a central role in lipid metabolism a

41 Facile isomerization of the monoglyceride product is observed and complicates the re

42 rofiling, identification and quantitation of monoglyceride regioisomers directly from tissue extracts

43 tion enables the differentiation of discrete monoglyceride regioisomers without chromatography throug

44 migration and preserves regiospecificity of monoglyceride structural isomers.

45 pase (MGL), a serine hydrolase that converts monoglycerides to fatty acid and glycerol, participates

46 ex endothelial cell glycerolipids, including monoglycerides, triglycerides, phosphatidylcholine, and

47 Monoglyceride was inactive while lysophosphatidate had p

48 ternary phase diagram containing short chain monoglycerides was larger than for di- and triglycerides

49 all proportions of 1,3-diglycerides and of 1-monoglycerides were also found.

50 tion can be absorbed intact, i.e. as the sn2 monoglyceride, whereas the sn1,3 fatty acids are absorbe

51 re formed from an appropriate combination of monoglyceride with various fatty acid lengths and solven