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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.
18                                              Stearic acid (0%, 1.5%, and 5%) was added to HAMS, and t
19 9-1.22], palmitic acid 1.26 [1.15-1.37], and stearic acid 1.06 [1.00-1.13]).
20 33.35%), followed by palmitic acid (26.16%), stearic acid (10.07%), palmitelaidic acid (9.56%) and my
21  and consequently accumulates high levels of stearic acid (18:0) and low levels of 18:1.
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
24                                              Stearic acid (18:0) appears to be neutral in its LDL-C-r
25 nsaturated fat relative to saturated fat and stearic acid (18:0) consumption were significant predict
26      By contrast, oleic acid (18:1, n-9) and stearic acid (18:0) had no effect on scd1 mRNA levels.
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
31                                              Stearic acid (18:0), monounsaturates, and polyunsaturate
32                        Palmitic acid (16:0), stearic acid (18:0), palmitoleic acid (16:1n-7), and ole
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
40 ic acid (14.78%), palmitic acid (9.74%), and stearic acid (7.37%).
41 xy fatty acid (e.g., palmitic-acid-9-hydroxy-stearic-acid, 9-PAHSA).
42                                 In contrast, stearic acid, a free fatty acid that does not activate p
43 olecules reside in a layer between Al2O3 and stearic acid, a result that was verified by water contac
44 y 10-15% of total palmitic acid and 6-20% of stearic acid acylated in the secondary position.
45        Small amounts of a polar hydrocarbon, stearic acid, added to the ambient decane synergisticall
46                                              Stearic acid addition followed by irradiation creates me
47       Use of spin labels (Mn(2+) and 5-DOXYL-stearic acid) allowed for the determination of the posit
48 c acid, or the nonessential FAs, palmitic or stearic acids) allows normal repair, further acceleratio
49 peptide was required for the inhibition, but stearic acid alone was not inhibitory.
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
53                               The effects of stearic acid and gamma irradiation on pasting properties
54               SAD6-OE plants contained lower stearic acid and higher oleic acid levels, which upon re
55                      13C-NMR spectroscopy of stearic acid and oleic acid as well as fluorescence spec
56 ration of (45)Ca(2+) into the cells, whereas stearic acid and oleic acid did not (P < 0.05).
57                        A distinction between stearic acid and other saturated fats does not appear to
58 part because of the high correlation between stearic acid and other saturated fatty acids in typical
59                            The saturated FFA stearic acid and palmitic acid were less efficacious tha
60                                The saturated stearic acid and the monounsaturated oleic acid had no e
61      We found an inverse association between stearic acid and the risk of total, localized, and low-g
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
66                  Visceral fat mass and brain stearic acid, arachidonic acid, and DHA were higher in m
67 fatty acid-binding proteins interacting with stearic acid are described.
68                                        Using stearic acid as a model compound, we examine the influen
69 oils from pea samples contained palmitic and stearic acids as major saturated fatty acids.
70 event linking palmitic acid, oleic acid, and stearic acid at C78 of the 17.125 kDa ASV.
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
74              Here we identify the metabolite stearic acid (C18:0) and human transferrin receptor 1 (T
75                             Even 5 microM of stearic acid (C18:0) or palmitic acid (C16:0) also signi
76 nts showed that despite E2 co-administration stearic acid (C18:0), a fatty acid elevated in plasma fr
77 s are formed from some substrates, including stearic acid (C18:0).
78 hmic effects including saturated fatty acid (stearic acid, C18:0), monounsaturated fatty acid (oleic
79 -water interface, whereas the density of the stearic acid chain is higher in the bilayer center.
80 ncreased the proportion wherein ADRP and NBD-stearic acid colocalized by 3-fold.
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
83 ied in order to obtain procyanidin B4 3-O-di-stearic acid conjugate.
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
86                                          The stearic acid content in the surface free-fat of P3 incre
87 ysis allows for the achievement of high seed stearic acid content with no associated negative agronom
88 at nonconserved residues show an increase in stearic acid content yet retain healthy nodules.
89 ons at conserved residues showed the highest stearic acid content, and these mutations were found to
90 o have high levels of seed, nodule, and leaf stearic acid content.
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.
96                                SDPC with SA (stearic acid) for the sn-1 chain and DHA (docosahexaenoi
97 uric acid from coconut oil, and palmitic and stearic acids from cocoa butter.
98 state cancer; men in the highest quintile of stearic acid had a relative risk of 0.77 (95% CI: 0.56,
99 ic as other fatty acids such as linoleic and stearic acids had no such effect.
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.
103 acids was synthesized and then conjugated to stearic acid in 14 h.
104                            The proportion of stearic acid in CEs decreased in the intervention group
105 ith both protein and water suggests that the stearic acid in the adipocyte fatty acid-binding protein
106                           The consumption of stearic acid in the form of a structured triacylglycerol
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.
109                                          The stearic acid in the muscle fatty acid-binding protein is
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
113                                              Stearic acid increased the paste viscosity of un-irradia
114 PIP2, while at the same time arachidonic and stearic acids increased in FFA in saline-treated TBI rat
115 Huh-7 cells, the saturated FFA, palmitic and stearic acid, increased Bim mRNA 16-fold.
116 and eicosapentaenoic acid, but not saturated stearic acid, increased SU by 30% over control levels.
117                                              Stearic acid infusion only increased C17:0.
118 ndogenous production was assessed through: a stearic acid infusion, phytol supplementation, and a Hac
119                Of the saturated fatty acids, stearic acid is uniquely different in that it appears to
120                                              Stearic acid is used as an internal standard to calibrat
121  phenotypes were rescued, including the high stearic acid level.
122 tent in each fraction based on the number of stearic acid losses observed.
123 s required for the elongation of palmitic to stearic acid may be induced.
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
126 vation reagent (ocadecanol) or an inhibitor (stearic acid) might be added prior to heating.
127                                     Although stearic acid minimally affects LDL cholesterol, it does
128                               Importantly, a stearic acid-modified form of this peptide was required
129    Comparison of PO diets with diets rich in stearic acid, monounsaturated fatty acids (MUFAs), and p
130 t not membrane, diffusional component of NBD-stearic acid movement 2-fold.
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
135  oleic acid), but not saturated LCFAs (e.g., stearic acid) of corresponding lengths.
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).
139       Upon the addition of a small amount of stearic acid or phosphonic acid, immediate partial disso
140 nd 13% of lipid droplets contained ADRP, NBD-stearic acid, or both, respectively.
141              Palmitic acid esters of hydroxy-stearic acids (PAHSAs) are among the most upregulated FA
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
144                             Furthermore, the stearic acid paired with the DHA in mixed-chain lipids h
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
147 patients with RYGB, we found higher baseline stearic acid/palmitic acid (S/P) ratio.
148 id/stearic acid (OA/SA), and lower levels of stearic acid/palmitic acid (SA/PA) and arachidonic acid/
149                                        Serum stearic acid/palmitic acid ratio as a potential predicto
150 containing no PUFA (defined medium with 18:0/stearic acid) produced 6.5 M1dG/10(7) deoxynucleotides a
151                  Diets were designed to have stearic acid replaced with the following TFA isomers (pe
152 420 mPas to 557 and 652 mPas for 1.5% and 5% stearic acid, respectively.
153                 The titration of alpha-LA by stearic acid results in a fluorescence emission red shif
154 ive was to test whether the consumption of a stearic acid-rich structured triacylglycerol has adverse
155                                              Stearic acid-rich triacylglycerol in both unrandomized a
156 aturated fatty acids (palmitic acid (PA) and stearic acid (SA)) and unsaturated fatty acid (oleic aci
157                         Functional groups in stearic acid (SA), oleic acid (OA), and octadecylphospho
158  containing a cis double bond, and saturated stearic acid (SA), respectively, at the sn-1 position an
159           In contrast, in cells treated with stearic acid (SA, C18:0) as well as cells not treated wi
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
163            Available experimental values for stearic acid show a spread of 68 kJ mol(-1).
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
166                                         High stearic acid (STA) soybean oil is a trans-free, oxidativ
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
169                                            A stearic acid surface monolayer acted as the template, wh
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
177 scription of genes governing desaturation of stearic acid to oleic acid.
178 ultivariate RR for a 1% energy increase from stearic acid was 1.19 (95% CI: 1.02, 1.37).
179        Linoleic acid was epoxidized, whereas stearic acid was not metabolized.
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
184                         Palmitic, oleic, and stearic acids were associated with nBla g 1 from cockroa
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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