ライフサイエンスコーパス: odd chain

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1 Waals gap is 0.3 A smaller for crystals with odd chains.

2 rmediates in the metabolism of valine and of odd-chain and branched-chain fatty acids.

3 g-chain ceramides using two nonphysiological odd chain ceramide (C17 and C25) internal standards was

4 ientry and multiexit biosynthesis of various odd-chain compounds at high efficiency.

5 the sum of even chain-saturated FA (ECSFA), odd chain-FA (OCFA), unsaturated FA (UFA), conjugated li

6 terification of propionate and catabolism of odd chain fatty acids and select amino acids.

7 ased methylmalonic acid, propionylcarnitine, odd chain fatty acids, and sphingoid bases, a new potent

8 trate lyases required for growth on even and odd chain fatty acids.

9 y acids (precursors of acetyl-CoA) by medium-odd-chain fatty acids (precursors of acetyl-CoA and anap

10 ely correlated with plasma concentrations of odd-chain fatty acids [OCFAs; pentadecanoic acid (15:0)

11 P. gingivalis, were also able to incorporate odd-chain fatty acids into lipid A when grown in the pre

12 Propionyl-CoA generated by beta-oxidation of odd-chain fatty acids is metabolized via the methylcitra

13 A product of beta-oxidation of odd-chain fatty acids is propionyl-CoA.

14 rmediate from the degradation of propionate, odd-chain fatty acids, and some amino acids.

15 sed by high concentrations of linoleic acid, odd-chain fatty acids, and very long-chain fatty acids,

16 ncentrations of linoleic acid, stearic acid, odd-chain fatty acids, and very-long-chain saturated fat

17 Increased concentrations of BCAAs and odd-chain fatty acids, both of which are metabolized to

18 one-carbon metabolism and the catabolism of odd-chain fatty acids, branched-chain amino acids, and c

19 ecursors of propionyl-CoA, i.e., propionate, odd-chain fatty acids, isoleucine, threonine, and valine

20 tissues and in bacteria grown in culture on odd-chain fatty acids.

21 e involved in the catabolism of amino acids, odd-chained fatty acids and other metabolites.

22 The lipid A contains odd-chain hydroxylated fatty acids, lacks phosphate, and

23 , in differentiating adipocytes, unsaturated odd chain length fatty acids in TAG molecular species co

24 sulting in the absence of Delta8 unsaturated odd chain length fatty acids.

25 pocytes, leading to a marked accumulation of odd chain length fatty acyl moieties.

26 , which is manifested in the accumulation of odd chain length unbranched fatty acids in all major lip

27 nerated by the peroxisomal beta-oxidation of odd chain-length dicarboxylic fatty acids.

28 In contrast, both even- and odd-chain-length alcohols (C3 to C7) were able to induce

29 pane oxidation and of the oxidation of other odd-chain-length alkanes following beta-oxidation, was a

30 (-1).mg protein(-1)) following growth on the odd-chain-length alkanes, propane and pentane.

31 es were observed in response to even- versus odd-chain-length alkanes.

32 Specifically, odd-chain-length films are oriented such that the last C

33 al production of the full range of even- and odd-chain-length MCFAs and found that MCFA production is

34 SAM films with odd chain lengths (n, m = 14 and 16) have a consistently

35 ol biosynthetic pathway for the synthesis of odd-chain molecules and the development of a complementa

36 mine sensor, with pronounced selectivity for odd chains of medium length.

37 Odd chain PFA (15:0, 17:0) concentrations were significa

38 (1.4 kJ/mol) of interlamellae interfaces of odd-chain samples, possibly due to registration/packing.

39 ngly, levels of pentadecylic acid (C15:0, an odd-chain SFA) and palmitoleic acid were inversely corre

40 By contrast, measured odd-chain SFAs (15:0 [pentadecanoic acid] and 17:0 [hept

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