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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
4 hylammonium), decynium-22, carnitine, PHA (p-aminohippurate), alanine, or inosine.
5  OAT1 inhibitor) and partially reversed by p-aminohippurate (an OAT1 substrate).
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
8                               In addition, p-aminohippurate and the dicarboxylates adipate and glutar
9             Sodium, potassium, lithium, para-aminohippurate, and creatinine clearances were measured
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
14       Renal plasma flow was measured by para-aminohippurate clearance and was converted to blood flow
15 red pre- and post-CPAP using inulin and para-aminohippurate clearance techniques at baseline and in r
16                      Renal plasma flow (para-aminohippurate clearance) and glomerular filtration rate
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
19 , and renal plasma flow was measured by para-aminohippurate clearance.
20                                         Para-aminohippurate extraction was likewise reduced to simila
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
23 restoration of the inhibitory effect of para-aminohippurate (% inhibition 34 +/- 4%).
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
26 , digoxin, and prostaglandin E(2), but not p-aminohippurate or S-dinitrophenyl glutathione.
27 xtracellular alphaKG on the kinetics of para-aminohippurate (PAH) and cidofovir transport was examine
28               Effects of these residues on p-aminohippurate (PAH) and cidofovir transport were assess
29 es the transport of organic anions such as p-aminohippurate (PAH) and estrone sulfate as well as the
30                                         Para-aminohippurate (PAH) and estrone-3-sulfate transport acr
31                                First, 5 mM p-aminohippurate (PAH) cis-inhibited the uptake of 1 micro
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
34                        The maximal rate of p-aminohippurate (PAH) secretion, in micromol/min per 100
35                   The transporter-mediated p-aminohippurate (PAH) uptake was saturable, probenecid-se
36 rototypical substrates for Oat1, including p-aminohippurate (PAH), and was trans-stimulated when oocy
37                             The uptakes of p-aminohippurate (PAH), estrone sulfate, and ochratoxin A
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
40 ened for probenecid-sensitive transport of p-aminohippurate (PAH).
41  well as the prototypical OAT substrate para-aminohippurate (PAH).
42 flow were measured with iothalamate and para-aminohippurate, respectively.
43                                         Para-aminohippurate significantly inhibited uric acid uptake
44  (tissue/medium (T/M) approximately 8) and p-aminohippurate (T/M = 2) transport.
45 OAT1, and the uptake of model substrate para-aminohippurate was studied in COS-7 cells expressing the
46      The renal clearances of inulin and para-aminohippurate were used to measure GFR and renal plasma

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