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1 ted lipocalin, kidney injury molecule 1, and liver fatty acid-binding protein.
2 sterin, cystatin-C, beta2-microglobulin, and liver fatty acid binding protein-1) to healthy volunteer
3 hen PA loaded mitochondria were treated with liver fatty acid binding protein, a fifth of the phospho
4  stress (e.g., major urinary proteins in the liver, fatty acid binding proteins, adipose differentiat
5        The entire amino acid sequence of rat liver fatty acid-binding protein along with an amino-ter
6 latinase-associated lipocalin, IL-18, KIM-1, liver fatty acid binding protein, and albumin associated
7 in, IL-18, kidney injury molecule-1 (KIM-1), liver fatty acid binding protein, and albumin.
8  In contrast, the basal cytochrome P450 4A1, liver fatty acid-binding protein, and apoA-I and apoC-II
9 utrophil gelatinase-associated lipocalin and liver fatty acid-binding protein associations with both
10  including those for the anticipated targets liver fatty acid binding protein (Fabp1) and lactase-phl
11              A 35-nucleotide sequence in the liver fatty acid-binding protein gene (Fabpl) has been i
12 y data, we show that the test protein, human liver fatty acid binding protein, interacts reversibly a
13                                              Liver fatty acid binding protein (L-FABP) has been propo
14                          Although native rat liver fatty acid binding protein (L-FABP) is composed of
15                                     Although liver fatty acid binding protein (L-FABP) is known to bi
16                                              Liver fatty acid binding protein (L-FABP), a cytosolic p
17 ions with proteins--including serum albumin, liver fatty acid binding proteins (L-FABP), and organic
18 ed differing patterns of mRNA expression for liver fatty acid-binding protein (L-FABP) and I-FABP.
19 pression of the two lipid transfer proteins, liver fatty acid-binding protein (L-FABP) and MTP, which
20 In contrast, there was a marked reduction of liver fatty acid-binding protein (l-FABP) gene expressio
21                          Whereas the role of liver fatty acid-binding protein (L-FABP) in the uptake,
22                                              Liver fatty acid-binding protein (L-Fabp) is an abundant
23                                     Although liver fatty acid-binding protein (L-FABP) is an importan
24                     The possibility that the liver fatty acid-binding protein (L-FABP) may function i
25                                              Liver fatty acid-binding protein (L-Fabp) regulates muri
26                            Here we show that liver fatty acid-binding protein (L-Fabp), an abundant c
27 ce or absence of bovine serum albumin (BSA), liver fatty acid-binding protein (L-FABP), and intestina
28 mmunofluorescence colocalization showed that liver fatty acid-binding protein (L-FABP; binds LCFA-CoA
29 ng oligonucleotide and induced expression of liver fatty-acid binding protein (L-FABP) and adipocyte
30 iated lipocalin [NGAL], interleukin [IL]-18, liver fatty acid-binding protein [L-FABP], and kidney in
31                                              Liver fatty acid-binding protein (LFABP) is a 14 kDa cyt
32                                          Rat liver fatty acid-binding protein (LFABP) is distinctive
33  of hepatic cathepsin B and lower amounts of liver fatty acid-binding protein (LFABP) than their wild
34 ids were used to probe ligand binding to rat liver fatty acid-binding protein (LFABP), an atypical me
35                                              Liver fatty acid-binding protein (LFABP; FABP1) is expre
36 press cyclin D1 under the control of the rat liver fatty acid binding protein promoter.
37           Nucleotides -596 to +21 of the rat liver fatty acid-binding protein promoter were used to d
38               Furthermore, expression of the liver fatty acid binding protein reduced the availabilit
39 n dynamics around a beta-barrel protein, rat liver fatty acid-binding protein (rLFABP), to reveal the
40 ase, hepatic lipase, endothelial lipase, the liver fatty acid-binding protein, the beta3-adrenergic r
41 -alpha(+/+) cells, and hepatic expression of liver fatty acid binding protein was lower in p110-alpha
42 tal structure of the recombinant form of rat liver fatty acid-binding protein was completed to 2.3 A
43 to the apical region, and the mRNA for human liver fatty acid-binding protein was distributed diffuse
44                                      Fourth, liver fatty acid-binding protein was limited in stimulat
45  lipid transport or storage (adipophilin and liver fatty acid-binding protein) were also activated by

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