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1 odistribution profiles with both hepatic and renal excretion.
2  injection followed by a decline, indicating renal excretion.
3 a protein binding, a necessary condition for renal excretion.
4 and ultimate elimination of the K(+) load by renal excretion.
5 ydrodynamic diameter by >15 nm and prevented renal excretion.
6             18F-FB-[Lys3]BBN had predominant renal excretion.
7 arance from tissue compartments primarily by renal excretion.
8 e injected dose per gram]) and predominantly renal excretion.
9 ncomitant rapid disappearance from blood and renal excretion.
10 e, unless the investigational agent involves renal excretion.
11 in very high for several days due to lack of renal excretion.
12 r, first-order process and that there was no renal excretion.
13  of the radiotracer from the blood and rapid renal excretion.
14 , DS exhibited a progressive increase in MBG renal excretion (66 +/-13 pmol/24 hours at week 4 versus
15            (68)Ga-NOTA-UBI-29-41 showed high renal excretion (83.2% +/- 7.3%) of injected dose and ra
16 ion and excrete from normal tissue/organ via renal excretion after complete targeting to the tumor si
17  function may have abnormal renal transit of renal excretion agents during exercise, although their b
18 bution in the abdomen and pelvis with little renal excretion and bladder activity-characteristics ben
19 efficacy of N-BPs is hampered by their rapid renal excretion and high affinity for bone.
20 above 15 mg kg(-1) : high dose expedited the renal excretion and shortened the blood retention.
21                                              Renal excretion and vasodilation did not account for the
22 .21 percentage injected dose per gram), fast renal excretion, and low background; tumor-to-blood and
23                       Diuresis, natriuresis, renal excretion, and tissue levels of MBG and OLC were m
24 ng and locally produced inhibitors; impaired renal excretion; and current therapies.
25                         Sulfoconjugation and renal excretion are important determinants of the wide i
26 ncreased efflux of bile acids into blood for renal excretion as well as hydroxylation of bile acids b
27 sing renal activity at 1-2 min (PETinitial), renal excretion at 2-10 min (PETearly), and, subsequentl
28 N) and (99m)Tc(CO)(3)(dd,ll-LAN) showed good renal excretion, averaging 85% and 77% that of (131)I-OI
29                              There is little renal excretion compared with (18)F-FDG.
30                                              Renal excretion fractions were measured from 10 to 14 di
31                                          The renal excretion fractions were measured from 12-24 discr
32                                    The 24-hr renal excretion fractions were measured from conjugate e
33 ac arrest and resuscitation, sepsis, reduced renal excretion, hypoxia induced cancer, decreased extra
34                                Moreover, the renal excretion kinetic and intrahepatic albumin binding
35 d in 5-25% of the human population, impaired renal excretion leads to hyperuricemia.
36                                              Renal excretion of 8-iso PGF(2alpha) was increased in An
37 ent relies on fluid resuscitation to promote renal excretion of active metabolite, withholding the do
38 titution at the cleavage site resulted in no renal excretion of AIM.
39 lasma bile salt levels predominantly through renal excretion of bile products.
40 e, we conclude that strategies to accelerate renal excretion of bile salt and other toxins should be
41 testinal calcium may increase absorption and renal excretion of both phosphate and oxalate.
42  wider range of values for serum calcium and renal excretion of calcium than we observe in control li
43 e kidney proximal tubule (PT) participate in renal excretion of drugs and endogenous compounds.
44                                              Renal excretion of imatinib was less than 10% of the tot
45 g for 1 wk decreased PMg++ 18%, TZR 25%, and renal excretion of magnesium (UMg) and calcium (UCa) mor
46 uction is explained partly by the absence of renal excretion of metabolizable organic anions, leaving
47                                     Impaired renal excretion of NOx is a contributor to the high plas
48 a volume by at least 3 mechanisms: increased renal excretion of salt and water, vasodilation, and inc
49 ium excretion by the kidney is essential for renal excretion of sufficient amounts of protons and to
50 lthough the plasma clearance and the rate of renal excretion of the (99m)Tc(CO)(3)(LAN) complexes wer
51 he renal proximal tubule is critical for the renal excretion of the prototypic organic anion, para-am
52           These reactions result in enhanced renal excretion of the sulfate-conjugated reaction produ
53                               Because of the renal excretion of the tracer, the absorbed dose was hig
54 aminoguanidine (AG) can improve turnover and renal excretion of these substances.
55 mplicates them as substantial players in the renal excretion of urate.
56  genes seem to be involved in regulating the renal excretion of uric acid which underscores the impor
57            These substances rapidly increase renal excretion or reduce renal tubular reabsorption and
58 ptake and urinary clearance, visualizing the renal excretion pathway from cortex to ureter.
59  from systemic blood circulation through the renal excretion route.
60                               This defect in renal excretion was associated with a severe, PTH-induce
61 inetic parameters (solubility, permeability, renal excretion) were substantially improved by a bioiso
62 ly low activity and small size lead to rapid renal excretion when applied in vivo, limiting its thera
63 t showed rapid blood clearance and exclusive renal excretion, which provides a clear abdominal field
64 PET imaging and biodistribution showed rapid renal excretion with low liver activity.
65  can be easily cleared from the body through renal excretion without causing accumulation/toxicity pr

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