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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 osolic aconitase, an iron-sulfur protein, in liver extracts.
4 rders of magnitude more abundant than CTP in liver extracts.
5 mplex, synthetic mixtures of metabolites and liver extracts.
6  in untargeted substrate searches with human liver extracts.
7 known product, 7alpha-hydroxycholesterol, in liver extracts.
8  molecular mass of myeloperoxidase, in human liver extracts.
9  in the lens and not in the brain, heart, or liver extracts.
10 homogeneity from the soluble fraction of pig liver extracts.
11 el comparable with that found in crude human liver extracts.
12 apoB RNA substrate with the transgenic mouse 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 es the cholesterol signal yield in a complex liver extract by a factor of 49.
30 Two of the protein-DNA complexes formed with liver extracts (C4 and C5) are due to the zinc finger pr
31            Homocarnitine production by human liver extracts depends upon the required BBOX cofactors,
32                             In contrast, rat liver extracts did not form AhR/DNA complexes after in v
33                                          The liver extract from an alcohol-fed rat was subjected to 2
34 mide in Hnf-1alpha(-/-) animals, we analyzed liver extracts from [(3)H]glibenclamide-injected animals
35 ese data, together with the observation that liver extracts from Abcb6-deficient mice suppress P450 e
36 analysis based on LC-HRMS was carried out on liver extracts from bulls experimentally treated with cl
37 enzyme, a property that was also observed in liver extracts from mice with streptozotocin-induced dia
38 ion as a negative regulator of GH signaling, liver extracts from motheaten mice deficient in SHP-1 or
39       We collected 700-MHz proton spectra of liver extracts from rats treated with a 4-day binge etha
40                                  Analysis of liver extracts from transgenic mice indicated a deficien
41 e stable in the liver, kidney and colon, and liver extracts have only 2-3% of the CBS enzyme activity
42 Full-length reelin protein was detectable in liver extracts in situ; acutely isolated liver cells als
43 C-MS based untargeted metabolic profiling of liver extracts in terms of reproducibility and number of
44 gh-resolution mass spectrometry screening of liver extracts incubated with TFM and was targeted for e
45 to the heme-bound form by mixing it with pig liver extract, indicating that mPGES2 is capable of form
46                            The HBOC-perfused livers extracted more oxygen than those perfused with RB
47                                     In human liver extracts, most of the glycogenin-2 was only detect
48 n and gel filtration chromatography of mouse liver extracts obtained at different circadian times to
49  2D NMR spectra of endogenous metabolites in liver extracts obtained from four inbred mouse strains i
50 inctive bands (48, 45, 40, and 38 kd) in the liver extracts of alcohol-fed rats.
51 on DEAE-5PW following fractionation of a rat liver extract on cation, anion and gel filtration resins
52                                              Liver extracts prepared from the mutants at multiple tim
53 mpositions were found in eluates of lung and liver extracts processed in a like manner.
54  from 60 human urine samples and 120 aqueous liver extracts, reaching a successful identification of
55 precipitation assays with regenerating mouse liver extracts reveal an association between HNF6 and Fo
56                     Biochemical assays using liver extract revealed up-regulated malate dehydrogenase
57 erformance liquid chromatography analysis on liver extracts revealed that taurine tetrahydroxy bile a
58 fined standard to assess mass accuracy and a liver extract to assess peak count and dynamic range.
59 ed to complex mixtures of lipids from bovine liver extract to confidently identify 35 unique structur
60 nsylated 7alpha-hydroxycholesterol) in human liver extracts using an LC-MS metabolomics/isotopic labe
61 d to the characterization of PCs in a bovine liver extract via a shotgun strategy.
62        Quantitation of testosterone in human liver extracts was also done as an example of the applic
63  not C/EBPalpha, and that insulin binding to liver extracts was increased compared to wild-type contr
64 [3-13C], and [4-13C]glutamate isotopomers in liver extracts was used to indirectly calculate the anap
65 utamate fractional enrichments determined in liver extracts were 23.0 +/- 1.1, 17.2 +/- 1.5, and 7.7
66                                         When liver extracts were examined by Western blot analysis, t
67 indicated that the changes observed in whole-liver extracts were localized to sinusoidal endothelial
68 cing/oxidizing equilibrium of glutathione in liver extracts, which has been implicated in diseases an
69                       Treatment of crude rat liver extracts with EDTA or heat decreased the specific