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1 cid and linoleic acid) relative to saturated stearic acid.
2 ), both of which contained approximately 50% stearic acid.
3 are labeled on C5, C8, C10, C12, and C16 of stearic acid.
4 -soluble fluorescent probe, 6-(9-anthroyloxy)stearic acid.
5 , or a structured triacylglycerol containing stearic acid.
6 elongation system that converts palmitic to stearic acid.
7 acid analog, 5-doxylstearic acid, as well as stearic acid.
8 observed during MD simulations in oleic than stearic acid.
9 ose on the mineral surface is lower than for stearic acid.
10 nstead, it was acylated by palmitic acid and stearic acid.
11 caveolin-1 was acylated by palmitic acid and stearic acid.
12 ic acid, yielding the inactive product nitro-stearic acid.
13 idonic acid, linolenic acid, oleic acid, and stearic acid.
14 hase HPLC, and subsequently transformed into stearic acids.
15 ; cis,cis linoleic; trans elaidic; oleic; or stearic acids.
16 t fatty acid followed by oleic, palmitic and stearic acids.
17 EO against oxidation than both palmitic and stearic acids.
20 33.35%), followed by palmitic acid (26.16%), stearic acid (10.07%), palmitelaidic acid (9.56%) and my
22 n of the major dietary saturated fatty acids stearic acid (18:0) and palmitic acid (16:0) to monounsa
23 olipid linoleic acid (18:2) and phospholipid stearic acid (18:0) and the serum polyunsaturated fat: s
25 nsaturated fat relative to saturated fat and stearic acid (18:0) consumption were significant predict
27 ixed-chain phospholipids contained saturated stearic acid (18:0) in the sn-1 position and the monouns
28 docannabinoids, whereas emulsions containing stearic acid (18:0) or linolenic acid (18:3) had no such
29 er-protein-desaturase-mediated conversion of stearic acid (18:0) to oleic acid (18:1) is a key step,
30 ckbone of both GM2 and GA2 was identified as stearic acid (18:0) versus nervonic acid (24:1) for ST b
33 r circulating SFAs [palmitic acid (16:0) and stearic acid (18:0)] and MUFA [oleic acid (18:1n-9)] in
34 n healthy adult humans over 6 d using [U-13C]stearic acid (18:0*) and [U-13C]palmitic acid (16:0*) an
35 a-6), but high levels of palmitic (16:0) and stearic acids (18:0) as well as eicosadienoic acid (20:2
36 e order of cholesterol partitioning was 18:0(stearic acid),18:1n-9(oleic acid) PC > di18:1n-9PC > di1
37 hatidylcholines (PCs) having a perdeuterated stearic acid, 18:0d35, in the sn-1 position and the fatt
38 onseed oil determined palmitic acid (23.6%), stearic acid (2.3%), oleic acid (15.6%) and linoleic aci
39 ange fatty acids (C12:0 and C14:0) and epoxy stearic acid, 4-8-fold lower activity against C16:0, C18
43 olecules reside in a layer between Al2O3 and stearic acid, a result that was verified by water contac
48 c acid, or the nonessential FAs, palmitic or stearic acids) allows normal repair, further acceleratio
50 cids, 0.48 microg palmitic acid, 0.61 microg stearic acid and 0.83 microg oleic acid/caveolae prepara
51 s, the relatively strong association between stearic acid and apo-alpha-LA was also confirmed by mean
52 PAHs containing added model lipid compounds (stearic acid and cholesterol) were then subjected to SFE
58 part because of the high correlation between stearic acid and other saturated fatty acids in typical
62 3-diazol-4-yl) amino]-octadecanoic acid (NBD-stearic acid) and antisera to ADRP showed that 70, 24, a
63 re environmental contaminants from surfaces (stearic acid) and from air (geranyl acetate) than groome
64 fins of different melting point, cow tallow, stearic acid, and carnauba wax were determined by HTGC-F
65 ; appropriate labeling of trans fatty acids, stearic acid, and other non-cholesterol-raising fatty ac
71 0 related fragments containing an N-terminal stearic acid attachment and an amidated C terminus were
72 (9-trans-octadecenoic acid), oleic acid, and stearic acid by rat mitochondria was studied to determin
73 cl1) exhibited a delayed growth phenotype in stearic acid (C18 fatty acid) media and we isolated resc
76 nts showed that despite E2 co-administration stearic acid (C18:0), a fatty acid elevated in plasma fr
78 hmic effects including saturated fatty acid (stearic acid, C18:0), monounsaturated fatty acid (oleic
81 8:2 FTOH production, an associated trend in stearic acid concentrations was not clear because of com
82 n-PA or physiological and diabetic oleic and stearic acid concentrations, impaired EPC migration and
84 msacpd-c mutations cause an increase in leaf stearic acid content and an alteration of leaf structure
85 previously reported its involvement in leaf stearic acid content and impact on leaf structure and mo
87 ysis allows for the achievement of high seed stearic acid content with no associated negative agronom
89 ons at conserved residues showed the highest stearic acid content, and these mutations were found to
91 d D31-16:0 (palmitic) acid yielded D31-18:0 (stearic) acid, D29-18:1 (oleic and cis-vaccenic) acids,
92 EPR studies with a spin-labeled analogue of stearic acid detected a high-affinity binding site for t
93 A structurally similar compound, 5-doxyl stearic acid dissolved in a series of solvents, was used
94 prepared the corresponding palmitic acid and stearic acid esters, mayolene-16 (1) and mayolene-18 (2)
95 tively, than in the cellulose group, whereas stearic acid excretion was not significantly altered.
98 state cancer; men in the highest quintile of stearic acid had a relative risk of 0.77 (95% CI: 0.56,
100 reported to control the accumulation of seed stearic acid; however, no study has previously reported
101 amounts of oleic, arachidonic, palmitic, and stearic acids; however, basal fatty acid release from in
102 89; 95% CI: 1.27, 2.83; P-trend = 0.001) and stearic acid (HR: 1.62; 95% CI: 1.09, 2.41; P-trend = 0.
105 ith both protein and water suggests that the stearic acid in the adipocyte fatty acid-binding protein
107 ationalize the stronger binding affinity for stearic acid in the human muscle fatty acid-binding prot
108 and a 70% increase in the ratio of oleic to stearic acid in the liver versus Cyp27(+/+) controls.
110 of different phosphatidylcholines containing stearic acid in the sn-1 position and an unsaturated fat
111 well as saturated fatty acids (palmitic and stearic acids) in almond (Prunus dulcis) kernel oils wit
112 ytes with saturated fatty acids (palmitic or stearic acids) in the presence of ethanol increased secr
114 PIP2, while at the same time arachidonic and stearic acids increased in FFA in saline-treated TBI rat
116 and eicosapentaenoic acid, but not saturated stearic acid, increased SU by 30% over control levels.
118 ndogenous production was assessed through: a stearic acid infusion, phytol supplementation, and a Hac
124 acids, palmitic acid methyl ester (PAME) and stearic acid methyl ester (SAME), being released from th
125 ociation occurred at concentrations at which stearic acid micelles and aggregates begin to form in th
129 Comparison of PO diets with diets rich in stearic acid, monounsaturated fatty acids (MUFAs), and p
131 rfine interaction with D2O is determined for stearic acid, n-SASL, spin-labeled systematically at the
132 wed that higher baseline level of oleic acid/stearic acid (OA/SA), and lower levels of stearic acid/p
133 sed by high concentrations of linoleic acid, stearic acid, odd-chain fatty acids, and very-long-chain
134 ed by 2H NMR order parameter measurements on stearic acid of all individual types of phospholipids in
136 d from glutaric acid, glyoxal, malonic acid, stearic acid, oleic acid, squalene, monoethanol amine su
137 y investigating the case of SAM formation of stearic acid on a water droplet in hexadecane and of per
138 aracter, hydrophilic glucose and amphiphilic stearic acid, onto a soil mineral analogue (Al2O3).
142 ds, branched palmitic acid esters of hydroxy stearic acids (PAHSAs), with beneficial metabolic and an
143 as branched palmitic acid esters of hydroxy stearic acids (PAHSAs); each family consists of multiple
145 ns, fatty acids (FAs), including oleic acid, stearic acid, palmitic acid and myristic acid, were the
146 ic acid, palmitoleic acid, myristoleic acid, stearic acid, palmitic acid, and myristic acid had littl
148 id/stearic acid (OA/SA), and lower levels of stearic acid/palmitic acid (SA/PA) and arachidonic acid/
150 containing no PUFA (defined medium with 18:0/stearic acid) produced 6.5 M1dG/10(7) deoxynucleotides a
154 ive was to test whether the consumption of a stearic acid-rich structured triacylglycerol has adverse
156 aturated fatty acids (palmitic acid (PA) and stearic acid (SA)) and unsaturated fatty acid (oleic aci
158 containing a cis double bond, and saturated stearic acid (SA), respectively, at the sn-1 position an
160 A ethyl ester, oleic acid (OA, C18:n-9), and stearic acid (SA, C18:0) did not alter the membrane exci
161 derivatives of EGCG with other fatty acids (stearic acid, SA; eicosapentaenoic acid, EPA; and docosa
162 unsaturated fatty acids and lower values for stearic acid, saturated and polyunsaturated fatty acids
164 Measurements of the rotational dynamics of stearic acid spin labels (SASL) incorporated into cardia
165 n and cholesterol on interactions of 14N:15N stearic acid spin-label pairs in fluid-phase phosphatidy
167 terol, oleic acid, trans fatty acids (TFAs), stearic acid (STE), TFA+STE (4% of energy each), and 12:
168 unlike beta-lactoglobulin, TL binds 16-doxyl stearic acid, suggesting less steric hindrance and great
170 er after consumption of the diet enriched in stearic acid than after consumption of the carbohydrate
171 m-conjugated imidazole-substituted oleic and stearic acids that blocked peroxidase activity of cytoch
172 te tested was the monophosphate of dihydroxy stearic acid (threo-910-phosphonoxy-hydroxy-octadecanoic
173 ycerol 3-phosphate, malate, myo-inositol, or stearic acid tissue concentrations were found, suggestin
174 is the reversible attachment of palmitic or stearic acid to cysteine residues, catalysed by protein
175 branches that were partially esterified with stearic acid to form ethoxylated glucam (PEO(n)-glucam)
176 er protein desaturase-mediated conversion of stearic acid to oleic acid (18:1) is the key step that r
180 oating performance, glycerol, oleic acid and stearic acid were added; however, mandarin quality gener
181 ective cohort, circulating palmitic acid and stearic acid were associated with higher diabetes risk,
182 At baseline, circulating palmitic acid and stearic acid were positively associated with adiposity,
183 However, C(10)-sphingosine, octylamine, and stearic acid were unable to increase PDK1 autophosphoryl
185 istic acid], 16:0 [palmitic acid], and 18:0 [stearic acid]) were positively associated with incident
186 one-third of the saturated fat in cashews is stearic acid, which is relatively neutral on blood lipid
187 arinii of the rare fatty acid cis-9,10-epoxy stearic acid, which was not detected in the lipids of ra
188 of 8:2 fluorotelomer alcohol (8:2 FTOH) and stearic acid, which would be released by cleavage of the
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