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1 t not of estradiol 17beta-d-glucuronide or p-aminohippurate.
2 RPF was measured by clearance of para-aminohippurate.
3 ohippurate (18F-PFH) is similar to that of p-aminohippurate, a gold standard for the measurement of e
6 nd 69 age-matched healthy subjects with para-aminohippurate and inulin clearances and their response
7 h pharmacokinetic properties comparable to p-aminohippurate and superior to those of both (99m)Tc-mer
10 retion of the prototypic organic anion, para-aminohippurate, as well as of a large number of commonly
11 sport of the shared OAT1/OAT3 substrate, rho-aminohippurate, behaved similarly, except that stimulati
12 d loss of organic anion transport (e.g. para-aminohippurate) both ex vivo (in isolated renal slices)
13 (inulin), effective renal plasma flow (para-aminohippurate), BP, and hemodynamic responses to an inf
15 red pre- and post-CPAP using inulin and para-aminohippurate clearance techniques at baseline and in r
17 d part of the study, renal plasma flow (para-aminohippurate clearance) and glomerular filtration rate
18 nd renal vascular responses (inulin and para-aminohippurate clearance) to graded doses of an angioten
21 teral GFR, renal plasma flow (RPF), and para-aminohippurate extraction was measured 1 h before and 1
22 for taurocholate, estrone sulfate, and para-aminohippurate in renal slices from wild-type mice, wher
24 orted probenecid-sensitive uptake of [(3)H]p-aminohippurate (K(m) = 4 microM), which was trans-stimul
25 necid-sensitive and pH-dependent uptake of p-aminohippurate (Km = 15.4 FtM, V,,, ..ax = 20.6 pmol/106
27 xtracellular alphaKG on the kinetics of para-aminohippurate (PAH) and cidofovir transport was examine
29 es the transport of organic anions such as p-aminohippurate (PAH) and estrone sulfate as well as the
32 teral GFR, renal plasma flow (RPF), and para-aminohippurate (PAH) extraction were measured 1 h before
33 he prototypical organic anion substrate para-aminohippurate (PAH) reduced ochratoxin A secretion by a
36 rototypical substrates for Oat1, including p-aminohippurate (PAH), and was trans-stimulated when oocy
38 tes was inhibited by sulfate, oxalate, and p-aminohippurate (PAH), indicating affinity for these anio
39 ds and by renal clearance of inulin and para-aminohippurate (PAH), simultaneous cardiorenal hemodynam
45 OAT1, and the uptake of model substrate para-aminohippurate was studied in COS-7 cells expressing the
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