ライフサイエンスコーパス: stearate

1 l that determines preferential attachment of stearate.

2 location virtually eliminated attachment of stearate.

3 modified with the fatty acids palmitate and stearate.

4 ihydroxy-palmitate and 18-hydroxy-9,10-epoxy-stearate.

5 stearates or a combination of palmitate and stearate.

6 ic transport of a fluorescent fatty acid NBD-stearate.

7 for laurate to a low of 13% of the dose for stearate.

8 activity was greatly stimulated by ascorbyl stearate.

9 activity but were less potent than ascorbyl stearate.

10 rporation into the fatty acids palmitate and stearate.

11 erase might be involved in the production of stearate.

12 d to form ethoxylated glucam (PEO(n)-glucam) stearates.

13 orescent fatty acid analogue, 12-anthroyloxy stearate (12-AS), between model membrane vesicles.

14 m Garcinia mangostana, generates an elevated stearate (18:0) phenotype in transgenic Brassica plants.

15 In addition, stearate (18:0) was reduced by 50% in leaves and by 30%

16 ificity for palmitate (16:0)-ACP rather than stearate (18:0)-ACP.

17 of spinach ACP with decanoate (10:0-ACP) and stearate (18:0-ACP) attached to the 4'-phosphopantethein

18 le reduction of oleate contributed little to stearate (2%).

19 s through the chemical reaction between zinc stearate and an excess amount of alcohols in hydrocarbon

20 Thermal decomposition of zinc stearate and gallium nitrate after hot injection of the

21 atty acid R(a) under all conditions, whereas stearate and myristate tracers consistently underestimat

22 B and desT in cells grown in the presence of stearate and their repression when oleate was present.

23 le mutant was unable to desaturate exogenous stearate and was an UFA auxotroph.

24 esized novel iodinated analogs of oleate and stearate, and we showed that heterogeneous S-acylation c

25 Chain elongation of palmitate to stearate appeared to occur in a different compartment.

26 Furthermore, ascorbyl stearate appears to be a general pleckstrin domain ligan

27 We identified ascorbyl stearate as a compound that binds to the pleckstrin doma

28 In addition, this paper introduces ascorbyl stearate as a pleckstrin domain ligand that can modulate

29 Ascorbyl palmitate (AP) and ascorbyl stearate (AS) are examples of food additives, which have

30 of vitamin A, retinyl palmitate and retinyl stearate, as well as several minor retinyl esters, in a

31 the carboxylate group of SCP-2 bound [1-13C]stearate at neutral pH; lack of electrostatic interactio

32 parate binding loci if alpha-LA indeed binds stearate at these concentrations.

33 he transmembrane span is the main signal for stearate attachment, but the sequence context and the ce

34 in hepatocytes in response to palmitate and stearate by a proteasome-dependent pathway.

35 t the desaturation of saturated fats such as stearate by SCD is an essential step mediating their ind

36 Stearate (C:18) completely inhibited the EGF-induced cel

37 The tsetse vector form requires synthesis of stearate (C18), whereas the bloodstream form needs myris

38 omal beta-oxidation of uniformly 13C-labeled stearate (C18:0) and oleate (C18:1) resulted in chain sh

39 18:1 cis), 9.4; palmitate (C16:0), 16.2; and stearate (C18:0), 21.0.

40 : pH titratability of the SCP-2 bound [1-13C]stearate carboxylate group.

41 ely 35% (P < 0.05) with weight loss, whereas stearate CoA (18:0; -17%; 0.65 +/- 0.05 vs. 0.54 +/- 0.0

42 rtially responsible for determining the high stearate composition of mangosteen seed oil and that Fat

43 nctionalized with lysine and polyoxyethylene stearate conjugate (LPS) to interact with ATB(0,+), an a

44 acylation site had a moderate effect on the stearate content.

45 Desaturation of stearate contributed 67% of the oleate, while reduction

46 The increase in stearate correlated with the presence of the ribozyme ge

47 organic excipients such as sucrose, lactose, stearate, dextrin, and starch were also detected.

48 urface: the chemical shift of bound [18-13C]-stearate; dicarboxylic/monocarboxylic acid cis-parinaric

49 However, in Scd1-/- mice, stearate does not induce lipogenesis, and Srebp-1c and P

50 we compared the activity of estradiol-17beta-stearate (E(2)-17beta-S) with that of estradiol-17beta (

51 lene terephthalate, polyisoprene, poly(vinyl stearate), ethylene-vinyl acetate, polyepoxide, paraffin

52 and hepatic glycogen stores are depleted in stearate-fed Scd1-/- mice.

53 -activated protein kinase is also induced by stearate feeding in Scd1-/- mice.

54 e increased FABP levels, the fraction of NBD-stearate found in cytosol, and the observed cytoplasmic

55 Pretreatment of cells with 0.15 mmol/L stearate from 0 to 6 hours inhibits, in parallel, both t

56 d salt, it could force the newly formed zinc stearate gradually but completely back onto the existing

57 In contrast, stearate had little effect on insulin-like growth factor

58 Cells treated with 0.1 mm [U-(13)C(18)]stearate had markedly disparate acetyl-CoA enrichments (

59 fatty acid spin-label, [15N,2H12]-5-nitroxyl stearate, have been obtained at the two sample orientati

60 chidonate, linoleate, oleate, palmitate, and stearate in equilibrium with bovine serum albumin (BSA).

61 d to measure the cytoplasmic movement of NBD-stearate in hepatocytes.

62 rse MnO nanocrystals by simple heating of Mn stearate in octadecene was studied systematically and qu

63 Chain shortening of stearate in peroxisomes generates acetyl-CoA, which is s

64 the relative concentrations of palmitate and stearate in phosphatidylethanolamine, phosphatidylinosit

65 able marker gene, was shown to increase leaf stearate in two of 13 maize lines.

66 a confirmed the presence of two disaccharide stearates in the surfactant, which were undetectable by

67 e (and very poorly with [3H]myristate or [3H]stearate) in digitonin-permeabilized cells.

68 angosteen (Garcinia mangostana) stores 18:0 (stearate) in its seed oil in amounts of up to 56% by wei

69 > 0.5), the relative amount of palmitate and stearate increased from 35+/-5 to 44+/-8% and 4+/-1 to 7

70 ediated trait was heritable, as evidenced by stearate increases in the leaves of the R1 plants derive

71 were immediately placed in Ringer's lactate; stearate indicator microelectrodes were placed in tempor

72 e microvoltammetry, used in combination with stearate indicator, Ag-AgCl reference and stainless stee

73 a show that the saturated FFAs palmitate and stearate induced cholangiocyte lipoapoptosis by way of c

74 Palmitate and stearate induced cholangiocyte lipoapoptosis in a concen

75 strate that the saturated FFAs palmitate and stearate induced robust and rapid cell death in cholangi

76 rget, PUMA, were critical for palmitate- and stearate-induced cholangiocyte lipoapoptosis.

77 w here that a diet high in the saturated fat stearate induces lipogenic genes in wild-type mice, with

78 toplasmic tail of HA contain only palmitate, stearate is exclusively attached to a cysteine positione

79 Surprisingly, this stearate labeled near the carboxyl end undergoes more lo

80 titanium vapor deposited onto a C18 cadmium stearate Langmuir-Blodgett monolayer supported on Au, Si

81 s, proved decisive for the formation of zinc stearate-like (ZnSt2) soaps.

82 leaves of the R1 plants derived from a high-stearate line.

83 rotein, in which addition of alpha-LA to the stearate-loaded indicator protein reverses the decrease

84 In addition, we found that stearate markedly promoted mineralization of CVCs as com

85 Therefore, a stearate metabolite derived from lipogenesis might be a

86 5-doxylstearic acid-loaded apo-alpha-LA with stearate (micelles) seem to suggest separate binding loc

87 tly used in the chain elongation of a second stearate molecule to form very long chain fatty acids.

88 n the biotransformation of 8:2 fluorotelomer stearate monoester (8:2 FTS) in aerobic soils was conduc

89 Cytoplasmic transport of NBD-stearate occurred by isotropic diffusion with no evidenc

90 ure of [(13)C]-labeled myristate, palmitate, stearate, oleate, and linoleate was infused in healthy m

91 fed in random order were laurate, palmitate, stearate, oleate, elaidate (the trans isomer of oleate),

92 f different fatty acids methyl esters (FAME: stearate, oleate, linoletate and linolenate) on a mixtur

93 The inhibitory effect of stearate on cell proliferation was dose and time depende

94 tides were also modified by palmitate and/or stearate on Cys residues.

95 e of multiple concentrations of [U-(13)C(18)]stearate or [U-(13)C(16)] palmitate.

96 azone in HepG2 cells in culture using [U-13C]stearate or [U-13C]oleate and mass isotopomer analysis.

97 own in the presence of 0.7 mmol/liter [U-13C]stearate or [U-13C]oleate, and in the presence and absen

98 Cys residues were acylated by palmitates or stearates or a combination of palmitate and stearate.

99 residues was acylated by either palmitate or stearate, or both Cys residues were acylated by palmitat

100 eate (20% by weight) but not with palmitate, stearate, or linoleate.

101 phatidylcholine molecular species containing stearate paired with a polyunsaturated fatty acid to Ptd

102 The stearated peptide blocked the binding of Lyn to the beta

103 (glutamate pool), and in chain elongation of stearate (peroxisomal pool).

104 The plants with the altered stearate phenotype were shown to express ribozyme RNA.

105 abundant with small amounts of palmitate and stearate, possibly because of the way the fused recombin

106 The biosynthesis of lupeol-3-(3'R-hydroxy)-stearate (procrim b, 1) was investigated in the Mexican

107 In the absence of SCD1, stearate promotes oxidation, leading to protection from

108 ssion by 38% (p = 0.01) and 53% (p = 0.006); stearate similarly decreased expression of PGC-1alpha an

109 The stearate spin-labeled at C5 has the highest affinity for

110 ransgenic plants that accumulate 55-68% more stearate than plants expressing the wild-type enzyme.

111 The peptide was N-stearated to enable cellular internalization.

112 omponents were observed on Teflon and ferric-stearate-treated surfaces.

113 in Brassica seeds led to the accumulation of stearate up to 22% in seed oil.

114 e a study of beta-oxidation of palmitate and stearate using HepG2 cells cultured in the presence of m

115 rences in the fatty acid pattern of HA: more stearate was attached if human viruses were grown in mam

116 Exogenous stearate was converted to 18:1Delta9 and supported the g

117 but the saturated fatty acids palmitate and stearate were not effective.