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1 s in humans, we propose C15:0 as a potential essential fatty acid.
2 und to be rich in linoleic acid, which is an essential fatty acid.
3 bnormalities of mice fed a diet deficient in essential fatty acids.
4 a significant intracellular accumulation of essential fatty acids.
5 lies the pool and growth recovery induced by essential fatty acids.
6 livery systems for the controlled release of essential fatty acids.
7 ave focused on foods rich in antioxidants or essential fatty acids.
8 ation or unwarranted oxidative metabolism of essential fatty acids.
9 SQ-LNS products contained micronutrients and essential fatty acids.
10 rovide energy (24% of total), protein (48%), essential fatty acids (23-100%), and essential amino aci
11 n choline pathways, vitamins B-12 and A, and essential fatty acids.A randomized controlled trial, the
12 infants have the capacity to convert dietary essential fatty acids administered enterally as 2H-label
13 ass spectrometry method employing 2H-labeled essential fatty acids allowed assessment of this in vivo
14 acid, glycolipids and phospholipids rich in essential fatty acids (alpha-linoleic and alpha-linoleni
15 level of linoleic acid (LA, 18:2omega-6), an essential fatty acid and key component of the human diet
17 -origin carbohydrates for energy and sparing essential fatty acids and amino acids for somatic growth
19 lcoholics who also have a marginal intake of essential fatty acids and antioxidants in their diets ma
21 for total parenteral nutrition (TPN) provide essential fatty acids and dense calories, they also prom
22 metabolic pathways belonging to the class of essential fatty acids and lipid oxidation were also obse
23 ill address recent research in metabolism of essential fatty acids and their long chain derivatives.
25 meet energy needs, 3) the adequate supply of essential fatty acids, and 4) the supply of sufficient f
26 nt source of bioavailable micronutrients and essential fatty acids, and capture fisheries have potent
28 good correlation of antecedent diet with the essential fatty acids, and there is reflection of the di
30 MF-2 cells are exactly mimicked by the three essential fatty acids, arachidonic, linoleic, and alpha-
32 an important role in membrane viscosity when essential fatty acids are available in the growth medium
33 ay have adverse consequences because natural essential fatty acids are destroyed and the new artifici
40 Keratinocytes were grown in medium with no essential fatty acids as well as in media with specially
45 cannot be bypassed in many bacteria because essential fatty acids cannot be obtained from the host.
47 nd in hindsight suggest re-evaluation of the essential fatty acid concept in light of the totality of
50 ell fatty acids may serve as a marker of the essential fatty acid content, especially of DHA and arac
51 sets, we determined whether insufficiency of essential fatty acids could result from geographic, intr
54 ent during early gestation, the influence of essential fatty acid deficiency during gestation and pos
55 , the diagnosis of zinc, biotin, protein, or essential fatty acid deficiency should be considered, es
63 emodeling in liver and peritoneal cells from essential fatty acid deficient mice was qualitatively si
64 idermal and dermal components, in a defined, essential-fatty-acid-deficient, serum-free culture mediu
66 alized proresolving mediators (SPM) includes essential fatty acid-derived lipoxins, resolvins, protec
67 d diiron enzymes function, whereas Ole1, the essential fatty acid desaturase, was resistant to iron d
68 Importance: Higher dietary intake of the essential fatty acid docosahexaenoic (DHA) has been asso
69 ammatory and proresolving mediators from the essential fatty acid docosahexaenoic acid (DHA) by macro
70 na contains the highest concentration of the essential fatty acid docosahexaenoic acid (DHA) in the b
72 rom animal and in vitro studies suggest that essential fatty acid (EFA) deficiency enhances cell-medi
73 in ADHD are similar to symptoms observed in essential fatty acid (EFA) deficiency in animals and hum
74 2 forms of oral long-chain omega-3 (omega-3) essential fatty acid (EFA) supplements, phospholipid (kr
75 -trans retinoic acid on the proliferation of essential fatty acid (EFA)-deficient and of EFA-suppleme
77 in that decrease when diets deficient in the essential fatty acids (EFA) alpha-linolenic acid and lin
78 ; the effect of serum can be mimicked by the essential fatty acids (EFA), arachidonic, linoleic, and
80 urified p-FABP(pm) preferentially bound with essential fatty acids (EFAs) and LCPUFAs over nonessenti
81 the 1950s established that a deficit of n-6 essential fatty acids (EFAs) leads to an inflammatory sk
83 on (PN)-associated liver disease and provide essential fatty acids (EFAs) needed to sustain growth an
86 discovered that are biosynthesized from the essential fatty acids eicosapentaenoic acid and docosahe
87 and cholesterol and increasing the intake of essential fatty acids, especially n - 3 fatty acids, red
88 colostrum is potentially valuable source of essential fatty acids (FAs), but so far only few studies
94 t with regard to the biological functions of essential fatty acids, for example, involving neural tis
98 ntify changes in the apparent consumption of essential fatty acids in the United States from 1909 to
99 nsumption of omega-3 (n-3) and omega-6 (n-6) essential fatty acids in Western diets is thought to hav
100 mical mechanisms are not (as with folate and essential fatty acids); in other cases (such as the amin
101 Supplementation of animals and humans with essential fatty acids, in particular omega-3 fatty acids
102 wed EO's uniqueness for the 93 % presence of essential fatty acids, including linoleic n-6 (41 %), al
103 are produced via the enzymatic conversion of essential fatty acids, including the omega-3 fatty acids
104 e blood is a suitable biomarker of long-term essential fatty acid intake, and its performance is comp
105 s considered the best indicator of long-term essential fatty acid intake, but other tissues may prove
106 on of fatty acids the transport of exogenous essential fatty acids into the epidermis is an absolute
107 limitation of zooplankton production by this essential fatty acid is of central importance at the pel
108 the mammalian skin barrier requires both the essential fatty acid linoleate and the two lipoxygenases
109 the lipoxygenase-catalyzed oxidation of the essential fatty acid linoleate, which is esterified to t
110 a lipid metabolic pathway that converts the essential fatty acids linoleate and alpha-linolenate int
111 Soybean oil is a major dietary source of the essential fatty acids linoleic acid (LA) and alpha-linol
112 duced ability to elongate and desaturate the essential fatty acids linoleic acid and alpha-linolenic
113 .5 vs 47.3 +/- 0.1), while the percentage of essential fatty acid, linoleic acid, does not undergo si
114 ratio of ceramides, CHOL, and FA (either the essential fatty acid, linoleic acid, or the nonessential
116 These studies demonstrate a pivotal role of essential fatty acid metabolism in myocardial phospholip
117 choline, betaine, dimethylglycine, retinol, essential fatty acids, methionine, dimethylamine (DMA),
119 D11 removes glutaryl adducts from lipoate-an essential fatty acid modification required for the TCA c
121 s of docosahexaenoic acid/omega-3 long-chain essential fatty acid on externalizing behavior are more
122 well as the effects of supplementation with essential fatty acids or their derivatives on a number o
123 d mainly on the longer-chain products of the essential fatty acids, particularly docosahexaenoic acid
124 cialized pro-resolving mediators and omega-3 essential fatty acid pathways that could help us to unde
126 e structured lipids (SL1 and SL2) containing essential fatty acids, prepared by lipase catalysed inte
127 exing the liver function, bile acid release, essential fatty acid production, nucleoside release, and
128 ant foods, thus it is important find out how essential fatty acid requirements are met by vegetarians
130 r main focus will be the association between essential fatty acid status and various disease states,
132 human and mouse obesity models and show that essential fatty acid status is a factor influencing humo
135 atty acids to the diet, not only in terms of essential fatty acids such as linoleic (C18:2n-6) and al
136 ally depends on the uptake of the so-called "essential" fatty acids such as omega-3 (n-3) and omega-6
137 d proresolving mediators biosynthesized from essential fatty acids, such as docosahexaenoic acid, hav
138 er tissue and resident peritoneal cells from essential fatty acid sufficient and deficient mice.
140 es not recommend any CAM therapies for ADHD, essential fatty acid supplementation is likely well tole
141 prescribed non-topical medications included essential fatty acid supplements (72/104, 69 %), low-dos
143 base that also provides energy, protein, and essential fatty acids, targeted towards preventing malnu
144 vide energy for protein synthesis and supply essential fatty acids that are necessary for central ner
145 the leaves provides natural antioxidant and essential fatty acids that could fight cardiovascular re
146 is low in saturated fat and a source of both essential fatty acids, the omega-6 fatty acid linoleic a
147 ewer benefits are seen with ingestion of the essential fatty acids themselves, likely related to limi
149 sed maternal diets are an adequate source of essential fatty acids to support normal accumulation of
150 pacity of human infants to convert 18-carbon essential fatty acids to their elongated and desaturated
151 rtance of breast milk as a source of fat and essential fatty acids up until the end of the second yea
152 molecules or by supplementing the diet with essential fatty acids, vitamins and methyl group donors
154 holipid dihomogammalinolenic acid (20:3), an essential fatty acid, were inversely associated with the
155 g-chain fatty acids, including the n3 and n6 essential fatty acids, were significantly reduced, mediu
157 y status, supporting the view that DHA is an essential fatty acid with an important role in keeping i