ライフサイエンスコーパス: odd chain

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

2 ucing C(21:0)-C(29:0) fatty acids, including odd-chain and branched ones.

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

4 Odd-chain and stable isotope-labeled acyl-CoAs were used

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

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

7 nstrate that wild-type mice fed an 11-carbon odd-chain dicarboxylic acid (undecanedioic acid, DC(11))

8 Odd-chain dicarboxylic acids like DC(11) are not present

9 nsaturated FA, conjugated linoleic acids and odd chain FA, compared to feeding maize silage.

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

11 evels of lactate and several medium- to long/odd-chain FAs.

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

13 that the PAP strain had increased levels of odd chain fatty acids esterified into TAGs, suggesting t

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

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

16 nnected pathways that involve reduced plasma odd-chain fatty acid levels, decreased gamma and beta el

17 ting the synthesis of pentadecanoic acid, an odd-chain fatty acid, from Bacteroides acidifaciens.

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

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

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

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

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

23 oxidation of branched-chain amino acids and odd-chain fatty acids to the TCA cycle.

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

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

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

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

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

29 Supplementation with odd-chain fatty acids, cholesterol or vitamin B(12) rest

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

31 species, including TGs comprised of shorter, odd-chain fatty acids, which strongly suggests an increa

32 ential precursor for the biosynthesis of the odd-chain fatty acids.

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

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

35 porting mouse brain tissue by the diagnostic odd-chained fatty acids and reflected control bacterial

36 short-chain PFAS alternatives, H-PFCAs, and odd-chain FTCAs were found to increase over time.

37 leiotropic changes, including an increase in odd-chain glycerophospholipids, and perturbations in the

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

54 opionic acid facilitated the biosynthesis of odd-chain PUFAs without the need for genetically modifie

55 proach led to an increased yield of specific odd-chain PUFAs, including C17:2omega6, C17:3omega3, C17

56 and TWEEN 80 to stimulate the production of odd-chain PUFAs.

57 , which enables the controlled production of odd-chain PUFAs.

58 (1.4 kJ/mol) of interlamellae interfaces of odd-chain samples, possibly due to registration/packing.

59 Dietary odd-chain saturated fatty acids (OCFAs) are present in t

60 GAT1 KK was associated with higher levels of odd-chain saturated triacylglycerols than DGAT1 AA, and

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

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

63 ed variations in the milk lipidome with many odd chain triacylglycerides upregulated in hay milk.