ライフサイエンスコーパス: catabolized

1 garding the mechanisms by which factor Xa is catabolized.

2 specifically by which and how nutrients are catabolized.

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

4 ocrine cycle, whereas the internalized Hb is catabolized.

5 s then deactivated by CYP24A1 and ultimately catabolized.

6 hich cytoplasmic proteins and organelles are catabolized.

7 even though the supplied EA was extensively catabolized.

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

9 lower growth yields relative to strains that catabolized acetate.

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

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

12 es and tumors, while hypoxanthine is rapidly catabolized and poorly salvaged in vivo.

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

14 is to internalize macromolecules that can be catabolized and used to support cell growth and prolifer

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

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

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

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

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

20 Brown adipocytes catabolized BCAA in the mitochondria as nitrogen donors

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

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

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

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

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

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

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

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

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

30 ylsulfoniopropionate (DMSP) is thought to be catabolized by bacteria via the DMSP demethylation pathw

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

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

33 In mammals, glucose is catabolized by glycolysis into circulating lactate, whic

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

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

36 mine has emerged as a metabolic fuel that is catabolized by mitochondrial glutaminase to support tumo

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

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

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

40 into glycolysis ending in pyruvate, which is catabolized by several enzymes.

41 enoic acids (EETs) synthesized by CYP450 and catabolized by soluble epoxide hydrolase (sEH) are invol

42 n D (1,25(OH)(2)D), by the 1-hydroxylase and catabolized by the 24-hydroxylase.

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

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

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

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

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

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

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

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

51 Glucose is catabolized by two major metabolic pathways, glycolysis

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

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

54 However, surplus cholesterol cannot be catabolized due to the lack of enzymes capable of degrad

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

56 the primary substrate for ATP synthesis, is catabolized during glycolysis to generate ATP and precur

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

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

59 In vitro, DC12 was catabolized even by adipose tissue and was not stored in

60 In the intestine, oral fructose was catabolized faster in the villus bottom than in the tips

61 controls, suggesting resynthesis of proteins catabolized for fuel during the exercise.

62 Immunosuppressive adenosine (ADO) is catabolized from adenosine monophosphate (AMP) by CD73 i

63 -CEHC) in urine, feces, and plasma that were catabolized from administered oral d3- and intravenous d

64 -CEHC) in urine, feces, and plasma that were catabolized from administered oral d3- and intravenous d

65 The bacterium catabolized genistein and daidzein and responded by prod

66 All strains catabolized glucose and excreted acetate into the cultur

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

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

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

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

71 acetate are hepatically produced metabolites catabolized in extrahepatic organs.

72 Pyrimidine bases are rapidly catabolized in growing plant tissues.

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

74 eased from lipid droplet triacylglycerol are catabolized in peroxisomes, lipid droplet coat proteins

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

76 the periplasm, releasing GlcNAc1A, which is catabolized in the cytoplasm.

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

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

79 ated that uridine-derived ribose is actively catabolized in tumours.

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

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

82 obilized plasma lipids towards the BAT to be catabolized, induced thermogenesis and reduced body weig

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

84 Their actions are terminated when they are catabolized into inactive fragments by at least three di

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

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

87 They suggest that poorly catabolized lipoproteins, enriched in both APOC3 and APO

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

89 The (poly)phenols in CPF were catabolized more slowly than in CPE, suggesting protecti

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

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

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

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

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

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

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

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

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

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

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

101 6390 confirmed that acetate was incompletely catabolized, suggesting that the ability to catabolize a

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

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

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

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

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

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

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

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

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

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

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

113 The product, l-lyxonate, is catabolized to alpha-ketoglutarate by a previously chara

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

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

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

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

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

119 diaminobutyric acid (DABA), which is further catabolized to l-aspartate.

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

121 Accumulated lipids are catabolized to meet energy requirements during dormancy

122 smooth ER inside hepatocytes, where LDs are catabolized to produce lipoproteins.

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

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

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

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

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

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

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

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

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

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

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

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

135 Triglyceride-rich lipid droplets (LDs) are catabolized with high efficiency in hepatocytes to suppl

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

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