ライフサイエンスコーパス: catabolized

1 esterol homeostasis, and, finally, how it is catabolized.

2 ocrine cycle, whereas the internalized Hb is catabolized.

3 s then deactivated by CYP24A1 and ultimately catabolized.

4 hich cytoplasmic proteins and organelles are catabolized.

5 even though the supplied EA was extensively catabolized.

6 garding the mechanisms by which factor Xa is catabolized.

7 concentrations of complexes, Th-PN1(K7E) was catabolized 5- to 10-fold less efficiently than Th-PN1,

8 lower growth yields relative to strains that catabolized acetate.

9 Alternatively, glucose can be catabolized anaerobically via glycolysis to lactate, whi

10 hich, after endocytosis, were preferentially catabolized and excreted into the bile.

11 tend the previous evidence that BCAAs can be catabolized and serve as respiratory substrates at multi

12 GlcNAc must be phosphorylated by Hxk1 to be catabolized, and also for it to enter the anabolic pathw

13 ]-Tyr4-bombesin was rapidly internalized and catabolized at 37 degrees C with approximately 10% of th

14 en incubated at 37 degrees C, but it was not catabolized at 4 degrees C incubation.

15 molecules found in vivo have been partially catabolized at either the E(1480)-(1481)G or E(1667)-(16

16 g-deficient PN1 variant, PN1(K7E), should be catabolized at the same rate as complexes formed with na

17 ites taken up by proliferating cells are not catabolized, but instead are used as building blocks dur

18 Levulinate is catabolized by 3 parallel pathways to propionyl-CoA, ace

19 a highly toxic by-product of metabolism, is catabolized by a limited number of bacterial species uti

20 These nucleotides are catabolized by a number of distinct phosphodiesterase (P

21 ptide hormone released by adipocytes, can be catabolized by adipose angiotensin-converting enzyme 2 (

22 ese results demonstrate that 15d-PGJ2 can be catabolized by Aor, thereby attenuating subsequent Nrf2

23 torage organelles that in hepatocytes may be catabolized by autophagy for use as an energy source, bu

24 per year(1,2), an estimated 10% of which is catabolized by bacteria through the DMSP cleavage pathwa

25 structurally diverse aromatic compounds are catabolized by bacteria to form benzoyl-coenzyme A (benz

26 steine, indicating that cysteine is actively catabolized by cysteine desulfhydrases.

27 adenine nucleotides released from cells and catabolized by deamination to inosine.

28 al chelator and a peptide linker that can be catabolized by hepatic lysozymes.

29 val of aquatic ecosystems, chitin is rapidly catabolized by marine bacteria.

30 nose supplementation because >95% Man-6-P is catabolized by MPI.

31 Purine nucleotides can be fully catabolized by plants to recycle nutrients.

32 low-glucose and hypoxic conditions, proline catabolized by POX was used preferentially for ATP produ

33 Cysteinyl glycine (Cys-Gly) was also catabolized by the bacteria, yielding glycine, H(2)S, am

34 e the gut, HMOs are preferentially bound and catabolized by the beneficial bacteria.

35 o studies in mice showed that 90% of Tac was catabolized by the kidney with a t1/2 of 1 h and a filtr

36 l into soluble particles that are eventually catabolized by the liver.

37 line, and associated organic acids) were not catabolized by the the frdA::cat(+) strain, indicating t

38 d previously that all-trans retinoic acid is catabolized by these oxidative enzymes, and that an inhi

39 eins with a molecular mass of 23-30 kDa were catabolized by thioredoxin.

40 g, dictate whether lipids are synthesized or catabolized by tissues.

41 , tyrosine hydroxylase (TH), and tyrosine is catabolized by tyrosine aminotransferase (TAT).

42 Since (GlcNAc)2 is rapidly catabolized by V. furnissii, a non-hydrolyzable thioglyc

43 tial depletion of glycogen reserves which is catabolized during freezing to produce cryoprotective co

44 epatocytes reside on the sER, LDs can now be catabolized efficiently to provide triglyceride for lipo

45 ocess by which cytoplasmic organelles can be catabolized either to remove defective structures or as

46 All strains catabolized glucose and excreted acetate into the cultur

47 ete primarily lactate ( approximately 70% of catabolized glucose carbon).

48 L. donovani catabolized glucose to CO(2), succinate, acetate, and py

49 Indeed, A4V SOD catabolized GSNO more efficiently than WT SOD throughout

50 Heme released from catabolized host red blood cell hemoglobin is toxic, so

51 Pyrimidine bases are rapidly catabolized in growing plant tissues.

52 Unlike in mice, [(18)F]-FAC is rapidly catabolized in humans; thus, we used another dCK PET pro

53 and protein stores available in autumn were catabolized in proportion to their availability above a

54 increased 0.4 ppm for each gram of lean mass catabolized in the higher dose birds.

55 that the essential amino acid tryptophan is catabolized in the tumor tissue by the rate-limiting enz

56 Because a large amount of the IGF-I was catabolized in vivo, we also studied the catabolism of I

57 Glucose is catabolized in yeast via two fundamental routes, glycoly

58 ranscription microarray results, D-serine is catabolized into acetate via the phosphotransacetylase (

59 cidating the pathway by which cholesterol is catabolized is necessary to understand the molecular mec

60 propose that the excess PC thus generated is catabolized, leading to TG synthesis and steatosis by wa

61 a variety of additional S-nitrosothiols were catabolized more readily by A4V SOD than by WT SOD.

62 edlings revealed that seed storage lipid was catabolized more slowly, long-chain acyl-CoA substrates

63 lthough more than 95% of incoming mannose is catabolized, most of the mannose released by intracellul

64 e and repressed when readily transported and catabolized nitrogen sources are available in the enviro

65 constant (the fraction of the vascular pool catabolized per unit time), by external losses, and by r

66 ith large HDL, and perhaps medium HDL, being catabolized primarily by the liver.

67 well understood, the pathways by which SA is catabolized remain elusive.

68 ciated dFdC deamination but were efficiently catabolized (removed) by mycoplasma PyNP.

69 dividuals deposited reserves over winter and catabolized reserves over summer, mainly because regulat

70 ite observations that COMT is estrogenically catabolized, sex differences in its prefrontal repercuss

71 DL isolated from sPLA(2) transgenic mice was catabolized significantly faster than (131)I-HDL isolate

72 Glycerol is catabolized solely by glycerol kinase (encoded by glpK)

73 6390 confirmed that acetate was incompletely catabolized, suggesting that the ability to catabolize a

74 dipropyl triamines are clearly more actively catabolized than the corresponding methyl and ethyl syst

75 P. putida KT2440 catabolized the d-stereoisomers of lysine, phenylalanine

76 -hydroxyacid derived from 4-HNE) is primarly catabolized through a pathway that phosphorylates the C-

77 rizes it to a C-3 hydroxy compound, which is catabolized through beta-oxidation.

78 rts glutamine to glutamate, which is further catabolized through the tricarboxylic acid cycle for the

79 eviously we reported that 4-hydroxyacids are catabolized through two parallel pathways.

80 In vitro, fibroblasts from controls catabolized thymidine in medium; by contrast, MNGIE fibr

81 ate (epsilon-Ap(4)), respectively, which are catabolized to 1,N(6)-ethenoadenosine (epsilon-Ado) as t

82 or glycosylation, while the rest (86-93%) is catabolized to 3H2O via PMI.

83 In catabolic pathway A, 4,8-DHNA is catabolized to 4-phospho-8-hydroxynonanoyl-CoA, 3,8-dihy

84 vate or [(14)C]threonine, either of which is catabolized to [(14)C]acetyl-CoA in the mitochondrion.

85 lization, ADCs with noncleavable linkers are catabolized to amino acid-linker-warheads within the lys

86 act as proteinuria with the remaining 97-99% catabolized to amino acids.

87 preconditioned medium, the cellular MSH was catabolized to generate GlcN-Ins and AcCys.

88 H]GlcN, it was shown that these residues are catabolized to generate radiolabeled products that are u

89 rovide a better understanding of how DMSP is catabolized to generate the important climate-active gas

90 These molecules can be catabolized to manufacture many of the building blocks r

91 te, and acetoin, suggesting that glucose was catabolized to pyruvate that was then catabolized via th

92 n tissue samples, (3)H-DHT was predominantly catabolized to the 5alpha-androstane-3alpha,17beta-diol

93 de 2,4-dichlorophenoxybutyric acid, which is catabolized to the auxin 2,4-dichlorophenoxyacetic acid

94 chlorocatechol, respectively, which are then catabolized to tricarboxylic acid cycle intermediates vi

95 data showed that 125I-labeled des(1-3)IGF-I catabolized very fast, with a rapid appearance of nonpre

96 The 125I-labeled IGF-I catabolized very quickly when incubated at 37 degrees C

97 acids in pectin and xylan, respectively, are catabolized via committed metabolic pathways to supply c

98 bumin while allowing "altered" albumin to be catabolized via lysosomal pathways.

99 D-gluconate which is primarily catabolized via the Entner-Doudoroff (ED) pathway, has b

100 ballylate to cis-aconitate, which is further catabolized via the Krebs cycle.

101 se was catabolized to pyruvate that was then catabolized via the lactate dehydrogenase, pyruvate form

102 anoic acid (4,8-DHNA), which is subsequently catabolized via two parallel pathways we previously repo

103 r binding to the IGF receptor and is rapidly catabolized with release of breakdown products.

104 , as a branched-chain amino acid, Leu can be catabolized within muscle, thus posing the possibility t