ライフサイエンスコーパス: liver extract

1 of 0.18 ppm and detected over 3000 peaks in liver extract.

2 extract was 4-fold greater than that in the liver extract.

3 rders of magnitude more abundant than CTP in liver extracts.

4 mplex, synthetic mixtures of metabolites and liver extracts.

5 in untargeted substrate searches with human liver extracts.

6 known product, 7alpha-hydroxycholesterol, in liver extracts.

7 molecular mass of myeloperoxidase, in human liver extracts.

8 in the lens and not in the brain, heart, or liver extracts.

9 homogeneity from the soluble fraction of pig liver extracts.

10 el comparable with that found in crude human liver extracts.

11 apoB RNA substrate with the transgenic mouse liver extracts.

12 osolic aconitase, an iron-sulfur protein, in liver extracts.

13 Immunodepletion of ACF from rat liver extracts abolished editing activity.

14 e is demonstrated by the analysis of a crude liver extract and that of fingermarks.

15 characterized the cleavage activity in mouse liver extracts and found that the proteolytic cleavage a

16 on compared with pCol9GFP mice in both whole liver extracts and isolated HSCs.

17 Human KGF was detectable in liver extracts and serum prepared from e17.5-e19.5 embry

18 appearance of inducible NO synthase mRNA in liver extracts, and (3) immunohistochemical localization

19 ins are found in the cytoplasmic fraction of liver extracts, and a subset of them are also found in a

20 Bile, liver extracts, and bile salts were found to rapidly ina

21 ver, higher rates of fatty acid oxidation in liver extracts, and higher plasma beta-ketone levels com

22 Liver extracts are incubated with [U-(13)C(3)]malonyl-Co

23 esults on human plasma, egg yolk and porcine liver extracts are presented and discussed.

24 s increased with progressive injury in whole liver extracts, as well as in isolated stellate and endo

25 The activity of eEF-2K in mouse liver extracts, as well as the activity of purified reco

26 Endogenous PGC-1 from mouse liver extracts bound to PXR, and recombinant PGC-1 direc

27 iplet, 1.24 ppm) appeared in ethanol-treated liver extracts but not in control samples; based on chem

28 onsequently, removal of cisplatin adducts in liver extracts, but not in testis extracts, exhibits a c

29 Two of the protein-DNA complexes formed with liver extracts (C4 and C5) are due to the zinc finger pr

30 In contrast, rat liver extracts did not form AhR/DNA complexes after in v

31 The liver extract from an alcohol-fed rat was subjected to 2

32 mide in Hnf-1alpha(-/-) animals, we analyzed liver extracts from [(3)H]glibenclamide-injected animals

33 ese data, together with the observation that liver extracts from Abcb6-deficient mice suppress P450 e

34 enzyme, a property that was also observed in liver extracts from mice with streptozotocin-induced dia

35 ion as a negative regulator of GH signaling, liver extracts from motheaten mice deficient in SHP-1 or

36 We collected 700-MHz proton spectra of liver extracts from rats treated with a 4-day binge etha

37 Analysis of liver extracts from transgenic mice indicated a deficien

38 e stable in the liver, kidney and colon, and liver extracts have only 2-3% of the CBS enzyme activity

39 Full-length reelin protein was detectable in liver extracts in situ; acutely isolated liver cells als

40 C-MS based untargeted metabolic profiling of liver extracts in terms of reproducibility and number of

41 gh-resolution mass spectrometry screening of liver extracts incubated with TFM and was targeted for e

42 to the heme-bound form by mixing it with pig liver extract, indicating that mPGES2 is capable of form

43 The HBOC-perfused livers extracted more oxygen than those perfused with RB

44 In human liver extracts, most of the glycogenin-2 was only detect

45 2D NMR spectra of endogenous metabolites in liver extracts obtained from four inbred mouse strains i

46 inctive bands (48, 45, 40, and 38 kd) in the liver extracts of alcohol-fed rats.

47 on DEAE-5PW following fractionation of a rat liver extract on cation, anion and gel filtration resins

48 Liver extracts prepared from the mutants at multiple tim

49 mpositions were found in eluates of lung and liver extracts processed in a like manner.

50 from 60 human urine samples and 120 aqueous liver extracts, reaching a successful identification of

51 precipitation assays with regenerating mouse liver extracts reveal an association between HNF6 and Fo

52 Biochemical assays using liver extract revealed up-regulated malate dehydrogenase

53 erformance liquid chromatography analysis on liver extracts revealed that taurine tetrahydroxy bile a

54 fined standard to assess mass accuracy and a liver extract to assess peak count and dynamic range.

55 nsylated 7alpha-hydroxycholesterol) in human liver extracts using an LC-MS metabolomics/isotopic labe

56 d to the characterization of PCs in a bovine liver extract via a shotgun strategy.

57 Quantitation of testosterone in human liver extracts was also done as an example of the applic

58 not C/EBPalpha, and that insulin binding to liver extracts was increased compared to wild-type contr

59 [3-13C], and [4-13C]glutamate isotopomers in liver extracts was used to indirectly calculate the anap

60 utamate fractional enrichments determined in liver extracts were 23.0 +/- 1.1, 17.2 +/- 1.5, and 7.7

61 When liver extracts were examined by Western blot analysis, t

62 indicated that the changes observed in whole-liver extracts were localized to sinusoidal endothelial

63 Treatment of crude rat liver extracts with EDTA or heat decreased the specific