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1 % of dihydrosterculate was esterified to the sn-1 position.
2 lation of glycerol 3-phosphate (GPAT) at the sn-1 position.
3 n intermediate involved in remodeling at the sn-1 position.
4 and 1-20% of the total acyl groups from the sn-1 position.
5 rs, with the fatty acid predominately at the sn-1 position.
6 ion of a second arachidonate moiety into the sn-1 position.
7 euterated, saturated acyl chain (n:0) at the sn-1 position, adjacent to docosahexaenoic acid (DHA, 22
8 lcholine had about 21% less palmitate in the sn-1 position and 36 and 40%, respectively, more arachid
9 ly labile (Z)-vinyl ether substituent at the sn-1 position and a base-labile sn-2 acyl substituent th
10 log with a BODIPY-labeled alkyl ether at the sn-1 position and a N-(DNP)-8-amino-octanoyl group at th
11 tidylcholines containing stearic acid in the sn-1 position and an unsaturated fatty acid (either olei
12 plasmanylcholine containing palmitate at the sn-1 position and arachidonate at the sn-2 position were
13 have either 18:0 or 18:1 fatty acids in the sn-1 position and either 22:6 or 20:2 fatty acids in the
14 perdeuterated stearic acid, 18:0d35, in the sn-1 position and the fatty acid 18:0, 18:1 omega 9, 18:
15 ntained saturated stearic acid (18:0) in the sn-1 position and the monounsaturated oleic acid (18:1)
16 ated stearic acid (SA), respectively, at the sn-1 position and were synthesized with perdeuterated SA
17 cond myristate is then incorporated into the sn-1 position, but the mechanism has been unclear due to
18 osphate and dihydroxyacetonephosphate at the sn-1 position by glycerol-3-phosphate and dihydroxyaceto
20 ro-3-phospho-(1'-myo-inositol), in which the sn-1 position contains an ether-linked C16:0 chain; they
21 acyl chains at the stereospecific numbering (sn)-1 position from PC and likely a channeling of lysoph
22 e highly purified fraction hydrolyzed at the sn-1 position, implying that this PLA2 also has some int
23 PagP transfers a palmitate residue from the sn-1 position of a phospholipid to the N-linked hydroxym
24 orated into the sn-2 position of PC, but the sn-1 position of de novo DAG and indicated similar rates
25 ing VLC-PUFAs, specifically contained in the sn-1 position of glycerophosphatidylcholine, implicating
26 yzing the transfer of an acyl group from the sn-1 position of lecithin to vitamin A to generate all-t
27 lyzes the transfer of an acyl group from the sn-1 position of lecithin to vitamin A to generate retin
28 yzes the transfer of an acyl moiety from the sn-1 position of lecithin to vitamin A, generating all-t
31 in planta, E. coli CPS acts primarily on the sn-1 position of PC; coexpression of SfLPAT results in t
33 lyzes the transfer of an acyl group from the sn-1 position of phosphatidylcholine to all-trans-retino
36 positioning of saturated fatty acids at the sn-1 position of phospholipids, and nutritional, hormona
38 th the higher number of DBs are preferred in sn-1 position of TG enantiomers in hazelnut oil unlike t
39 g OxPCs with palmitic acid esterified to the sn-1 position of the glycerol backbone yielded a NL of 2
42 Circulating [3H]PAM is incorporated into sn-1 positions of brain phospholipids, mainly phosphatid
45 hospholipids containing palmitic acid at the sn-1 position that could be exploited for the design of
46 tic G3P acyltransferases (GPATs) acylate the sn-1 position to produce lysophosphatidic acid (1-acyl-L
48 gnificant percentage of acyl groups from the sn-1 position, when sn-2 is occupied by 18:0, 20:4, or 2
49 nt CPS prefers the stereospecific numbering (sn)-1 position whereas E. coli CPS acts on sn-2 of phosp
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