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1 paraoxonase-1 (PON1) was investigated, using peroxidized 1-palmitoyl-2-oleoyl phosphatidylcholine (PC
2        HLE B-3 cell membranes were prepared, peroxidized, and used to examine whether hGSTA1-1 and hG
3 re obtained from reaction of DNA with either peroxidizing arachidonic acid (20:4omega6) or peroxyl ra
4 resent study we have examined the ability of peroxidizing arachidonic acid (AA, 20:4omega6) to induce
5 -revealed positive fluorescence staining for peroxidized carbonyl products.
6         15-Lipoxygenase 2 (15-LOX2), a lipid-peroxidizing enzyme, is mainly expressed in the luminal
7  addition of a polar oxygen atom on numerous peroxidized fatty acids reorients the acyl chain, whereb
8                                       Mildly peroxidized ghost membranes transferred overall ChOOH an
9 in which approximately 4% of the Ch had been peroxidized, giving mainly 5alpha-OOH, transferred total
10  generality of this conformational motif for peroxidized glycerophospholipids within membranes.
11 was associated with partial tolerance to the peroxidizing herbicide paraquat.
12      Protox is the target of light-dependent peroxidizing herbicides and is inhibited at nanomolar le
13           Addition of *NO (0.5-20 microM) to peroxidizing lipid led to cessation of oxygen uptake, wh
14 ron-binding and iron-oxidizing protection of peroxidizing lipid membranes, were both significantly de
15 damage, generation of reactive oxidants that peroxidize lipids and damage other cellular components,
16 n also leads to preferential accumulation of peroxidized lipids and 4-hydroxynonenal (4-HNE) adducts
17 ize of LDs is a combination of enrichment in peroxidized lipids and a defect in their catabolism.
18                        Dietary oxidants like peroxidized lipids could perturb cellular redox status a
19 onstrated increased lipid droplets (LDs) and peroxidized lipids in both neurons and astrocytes, consi
20  very low abundance (20 pmol umol(-1) lipid) peroxidized lipids in subcellular compartments and their
21 found that iPLA2B-mediated detoxification of peroxidized lipids is sufficient to suppress p53-driven
22 direct antioxidant, prevents the increase of peroxidized lipids that alter both metabolic pathways an
23 ating conduits(3,4) for the replenishment of peroxidized lipids(5).
24 mation of damaged membrane components (i.e., peroxidized lipids) as well as a terminating condensatio
25                                              Peroxidized lipids, generated by reactive oxygen species
26 ipid vesicles containing a small fraction of peroxidized lipids, the N-terminal Met residues in alpha
27 tion of active oxidation products, including peroxidized lipids.
28  of cell death driven by the accumulation of peroxidized lipids.
29  but not PON1, catalyzes PLOOH hydrolysis in peroxidized low density lipoprotein.
30                 Decreased ability to replace peroxidized membrane fatty acid by this metabolic pathwa
31 cavenge peroxides but in addition can reduce peroxidized membrane phospholipids.
32 rols of various fatty acid compositions were peroxidized over time at 60 degrees C and the kinetic cu
33  reported for 12 selected in vivo native and peroxidized phosphatidylcholines and phosphatidylethanol
34    We found a severalfold increase in plasma peroxidized phosphatidylcholines, inflammatory and pro-a
35                                              Peroxidized phosphatidylethanolamine (PEox) species have
36          Ectopic GPx4 overcame this, reduced peroxidized phospholipid accumulation, blocked Az-PC acc
37  However, its molecular targets, identity of peroxidized phospholipid species, and their signaling ro
38 detect and quantify intactin vivo ROS-driven peroxidized phospholipids (LPOx-PLs) in bovine retina ex
39                                  Circulating peroxidized phospholipids also increased in humans with
40 or PNPLA9 gene) can preferentially hydrolyze peroxidized phospholipids, it may eliminate the ferropto
41 esulting from the unrestrained occurrence of peroxidized phospholipids, which are subject to iron-med
42 n process for the formation of aggregates of peroxidized plasma membrane lipids.
43 ion (IDA) spectra confirmed the structure of peroxidized PLs, revealing that peroxidized species (+O-
44 structure of peroxidized PLs, revealing that peroxidized species (+O-OH) dominated over single O-adde
45 t has been especially well characterized for peroxidized species of phosphatidylcholines (PC).
46        The ability of Lp-PLA(2) to hydrolyze peroxidized species of phosphatidylserine (PS), acting a