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1 ll differentiation, alkaline phosphatase and intestinal fatty acid binding protein.
2 lline concentration and its correlation with intestinal fatty acid-binding protein.
3 failed to express the differentiation marker intestinal fatty acid-binding protein.
5 e of conformational fluctuations of unfolded intestinal fatty acid binding protein (131 aa, 15 kDa) b
6 rved mucosal abnormalities, plasma levels of intestinal fatty acid binding protein, a marker of enter
7 s a set of molecular dynamics simulations of intestinal fatty acid binding protein addressing the pro
8 port new measurements, using the acrylodated intestinal fatty acid binding protein (ADIFAB) method, o
10 ma gut epithelial barrier integrity markers (intestinal fatty acid binding protein and zonulin-1 leve
12 was no correlation between plasma levels of intestinal fatty acid-binding protein and citrulline.
13 ifferentiation defects such as expression of intestinal fatty acid-binding protein and pancreatic try
15 lyzed plasma levels of soluble CD14 (sCD14), intestinal fatty acid binding protein, and interleukin-6
16 ling constants in ubiquitin (alphabeta-fold) intestinal fatty acid binding protein (beta-barrel) and
17 c epithelial markers, the intestinal markers intestinal fatty acid binding protein, CDX1 and CDX2 wer
18 plasma citrulline</=12.2 mumol/L, and plasma intestinal fatty acid-binding protein concentration>/=35
22 ansgenic mice were studied that contained an intestinal fatty acid binding protein gene promoter (Fab
23 The equilibrium unfolding behavior of the intestinal fatty acid-binding protein has been investiga
24 nts were made on PA bound to recombinant rat intestinal fatty acid binding protein (I-FABP) at pH 5.5
27 6, and a gut microbial translocation marker (intestinal fatty acid binding protein (I-FABP)) were mea
34 three-dimensional solution structure of rat intestinal fatty acid-binding protein (I-FABP) complexed
35 he structure of Escherichia coli-derived rat intestinal fatty acid-binding protein (I-FABP) exhibits
36 iganded form of Escherichia coli-derived rat intestinal fatty acid-binding protein (I-FABP) has been
37 (apo) forms of Escherichia coli-derived rat intestinal fatty acid-binding protein (I-FABP) have been
38 ver fatty acid-binding protein (L-FABP), and intestinal fatty acid-binding protein (I-FABP) in order
39 ated on the day of the initial rise in serum intestinal fatty acid-binding protein (I-FABP) would res
40 acid-binding protein (A-FABP) and 17 of the intestinal fatty acid-binding protein (I-FABP), at locat
41 lysaccharide (LPS), endotoxin core antibody, intestinal fatty acid-binding protein (I-FABP), soluble
42 man genetic determinants of plasma levels of intestinal fatty acid-binding protein (I-FABP/FABP2), a
43 necrosis factor [TNF]), enterocyte turnover (intestinal fatty acid binding protein [I-FABP]), lipopol
45 ccur during the folding and unfolding of rat intestinal fatty acid binding protein (IFABP) are descri
54 ta is a functional all-beta sheet variant of intestinal fatty acid binding protein (IFABP) that was g
55 S) measurements have been carried out on the intestinal fatty acid binding protein (IFABP) to study m
56 a pancreas-specific transcription factor and intestinal fatty acid binding protein (IFABP), a marker
57 orporation of 4-(19)F-phenylalanine into the intestinal fatty acid binding protein (IFABP), a protein
58 , including alpha-lactalbumin, cytochrome c, intestinal fatty acid binding protein (IFABP), and myogl
59 eins, ileal lipid binding protein (ILBP) and intestinal fatty acid binding protein (IFABP), were exam
60 regulator (pCFTR) cDNA under control of the intestinal fatty acid-binding protein (iFABP) promoter w
61 acrophage migration inhibitory factor (MIF), intestinal fatty acid-binding protein (IFABP), and proin
62 his study evaluated the usefulness of plasma intestinal fatty-acid binding protein (IFABP) levels in
63 location markers (LPS, soluble CD14 [sCD14], intestinal fatty acid-binding protein [iFABP], and endot
64 s of four beta-sheet proteins, namely IFABP (intestinal fatty acid-binding protein), ILBP (ileal fatt
65 tive was to identify factors associated with intestinal fatty acid-binding protein in critically ill
66 individuals had higher plasma levels of LPS, intestinal fatty acid binding protein (indicating entero
70 troscopy, the bands contained both liver and intestinal fatty acid-binding proteins (L- and I-FABP) a
72 e isomaltase, cdx-2 homeodomain protein, and intestinal fatty acid binding protein promoter regions.
73 nsgenic mice, generated by utilizing the rat intestinal fatty acid-binding protein promoter (Fabpi),
74 by labeling site-specific mutants of the rat intestinal fatty acid binding protein (rI-FABP) with acr
75 d, there was a marked delay in expression of intestinal fatty acid binding protein, suggesting a role
78 icator of FFA, ADIFAB (acrylodan-labeled rat intestinal fatty acid-binding protein), was microinjecte
82 te directly activity of the promoter for the intestinal fatty acid-binding protein (xIFABP) gene, whi
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