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1 , often exhibit little to no dissolution and excretion.
2 bolism, particularly in the mode of nitrogen excretion.
3 d positively correlated with urinary albumin excretion.
4 ion from nontargeted organs, through urinary excretion.
5 s that were associated with diminished virus excretion.
6 e-dependent increase in fractional phosphate excretion.
7 on rate, glycolytic metabolites, and lactate excretion.
8 racrine and circadian control of electrolyte excretion.
9 ransporter critical for whole-body manganese excretion.
10 ogens, promoting pathogen clearance by urine excretion.
11  applies to the control of renal electrolyte excretion.
12 anism of secretin-induced urinary HCO(3) (-) excretion.
13 ormation, renal excretion, and hepatobiliary excretion.
14 r molecules tending toward passive or active excretion.
15 GFR and glomerular protein filtration affect excretion.
16 irectly contribute to reduced urinary sodium excretion.
17 senical species (DMAs), facilitating urinary excretion.
18  excess and impaired systemic and biliary Mn excretion.
19 ning decline and change in duration of aMT6s excretion.
20 plasma protein binding and extensive biliary excretion.
21  absorption and hepatobiliary and intestinal excretion.
22 mainly due to a reduction in urinary albumin excretion.
23 positively correlated with fecal coprostanol excretion.
24 inimal Mn excess despite impaired biliary Mn excretion.
25 r (LDH5) stiripentol reduces urinary oxalate excretion.
26 etabolite concentrations as well as temporal excretion.
27 ry hyperoxaluria reduced the urinary oxalate excretion.
28  study compliance via para-aminobenzoic acid excretion.
29 SMX and its metabolites, likely due to plant excretion.
30 ne acrophase, morning offset and duration of excretion.
31 hepatic oxalate production and urine oxalate excretion.
32 acutely activates NCC to modulate renal NaCl excretion.
33 rimary and reduced secondary fecal bile acid excretion.
34 ficant evidence of reduced extra-renal urate excretion.
35 ecules with fast blood clearance and urinary excretion.
36 h well-established neuroendocrine control of excretion.
37  biotin inhibited organ uptake and increased excretion.
38 nary angiotensinogen and beta2-microglobulin excretion.
39 L) plays a key role in urinary acid and NaCl excretion.
40 randial PG through increased urinary glucose excretion.
41 ion, lipid droplet content, and triglyceride excretion.
42 charide (GB1107 surrogate) showed no sign of excretion.
43  liver and thereby to decrease biliary lipid excretion.
44 ermeability changes produce large changes in excretion.
45 n of [(11)C]13 and hepatobiliary and urinary excretions.
46 24HDR) with intake derived from 24-h urinary excretion (24HUE).
47 5.6]), living in Lome (2.8 [1.1-7.1]), HSV-2 excretion (26.7 [2.9-244.3]), C. trachomatis (11.7 [2.3-
48 o associated with increasing urinary protein excretion-a strong prognosticator of adverse renal outco
49 he absorption, distribution, metabolism, and excretion (ADME) data showed relatively poor aqueous sol
50 the absorption, distribution, metabolism and excretion (ADME) of metabolites.
51 he absorption, distribution, metabolism, and excretion (ADME) profile of the series were optimized re
52 ng absorption, distribution, metabolism, and excretion (ADME) profile while being devoid of a peptido
53 ro absorption, distribution, metabolism, and excretion (ADME) profiles were subjected to in vivo proo
54 NA absorption, distribution, metabolism, and excretion (ADME) properties are lacking.
55 vo absorption, distribution, metabolism, and excretion (ADME) properties of 24 yielded a preclinical
56 nd absorption, distribution, metabolism, and excretion (ADME) properties, further reflected in the en
57 ro absorption, distribution, metabolism, and excretion (ADME) properties, which was progressed into p
58 nd absorption, distribution, metabolism, and excretion (ADME) properties.
59 ot respond with increased urinary HCO(3) (-) excretion after stimulation with secretin and often pres
60 , but only subtle alterations of renal urate excretion and ABCG2 abundance.
61 ctance regulator (CFTR) in urinary HCO(3) (-)excretion and applied it in the patients before and afte
62 nvoluted tubule (DCT) regulates urinary NaCl excretion and BP.
63 tary phosphorus intake or urinary phosphorus excretion and BP.
64  shared between urinary sodium and potassium excretion and cardiovascular traits.
65                             Fractional Na(+) excretion and cortical oxygen tension were lower and ren
66                                       Oocyst excretion and diarrhea severity were observed daily, and
67 icant associations were detected between ENL excretion and fecal microbiome measured at baseline and
68 uation to high protein, yielding higher urea excretion and increased phenylalanine oxidation rates (P
69     The higher dose lowered urinary ammonium excretion and increased serum bicarbonate more than the
70 s and the hindgut perform essential roles in excretion and ionic and osmotic homeostasis.
71 ssociated with lower urinary nitrite/nitrate excretion and markedly increased urinary PGE(2) excretio
72 ss the association between usual 24-h sodium excretion and measures of adiposity among US adults.
73 riant in Exon-14 that was associated with DA excretion and multiple other renal traits indicating ple
74  takes into consideration changes in albumin excretion and other risk factors in addition to HbA(1c)
75 rious physiological processes including acid excretion and pH regulation.
76 t on Npt2a-null mice, but promoted phosphate excretion and reduced phosphate levels in normophophatem
77 osphate levels by increasing renal phosphate excretion and reducing 1,25-dihydroxyvitamin D3 [1,25(OH
78 ected to grazers, sloppy feeding (as well as excretion and respiration), viruses and viral lysate res
79 tegy to enhance the analysis of radionuclide excretion and retention kinetics.
80            This interplay between metabolite excretion and their chemotaxis-dependent reutilization i
81 romotes osmotic diuresis via urinary glucose excretion and therefore, might offer a novel treatment o
82  day 1 identified 24-hour urinary creatinine excretion and TIMP-2/mOsm as significant predictors of f
83 f drug absorption, distribution, metabolism, excretion and toxicity through fluidically coupled organ
84 ies, namely, metabolic transformation, renal excretion, and hepatobiliary excretion.
85  However, changes in SNGFR can alter protein excretion, and hyperfiltration with glomerular leak can
86 1) R from the brush border, decreased sodium excretion, and increased oxidative stress and BP in C57B
87 rallel, it suppressed urinary norepinephrine excretion, and induced c-Fos expressions in the area pos
88 ular filtration rate (GFR) and urine albumin excretion, and kidney injury was evaluated by histopatho
89 or models were used to estimate usual sodium excretion, and multiple linear and logistic regression m
90   Unfortunately, liver accumulation, biliary excretion, and no tumor uptake were observed on planar s
91 inal 0-2 scale: hepatic enhancement, biliary excretion, and the signal intensity in the portal vein.
92 ess is associated with increased free proton excretion, and thus with a decline in the kidney's acid
93 ood, low hepatobiliary excretion, fast renal excretion, and very low uptake of (18)F activity in bone
94                 Urinary sodium and potassium excretion are associated with blood pressure (BP) and ca
95                       Dynamic simulations of excretion are generally consistent with the results of t
96 ts absorption, distribution, metabolism, and excretion are poorly understood.
97 erular filtration rate and urinary potassium excretion associated with hyperkaliemia at day 3.
98 timulates ammoniagenesis that increases acid excretion but also leads to ammonia-induced complement a
99 nclude adaptive responses that increase acid excretion but lead to a decline in kidney function.
100 eved by a combination of managing intake and excretion but sometimes both drinking and urination are
101 k appears also to raise E2, E3, and 16ketoE2 excretion, but future studies need to confirm these asso
102 e immediate benefit of increased kidney acid excretion, but their chronic upregulation promotes infla
103 ced by a 27-fold increase in urinary glucose excretion by 3 hours (P<0.0001).
104            Vasopressin regulates renal water excretion by binding to a G(alpha) s-coupled receptor (V
105 racellular phosphate regulates its own renal excretion by eliciting concentration-dependent secretion
106                                        Water excretion by the kidney is regulated by the neurohypophy
107                 Inadequate urinary phosphate excretion can lead to severe hyperphosphatemia as in tum
108 -fold increase in efficiency of urinary iron excretion compared to intravenous injection.
109 advantages of (18)F labeling and low urinary excretion compared with (68)Ga-PSMA-11.
110                          24 hr urine albumin excretion correlated highly with decreasing podocyte den
111       During diuretic treatment, higher PGE2 excretion correlated with lower free water clearance, an
112 ting that early increases in urinary albumin excretion could be predictive of adolescents with T1DM w
113 roposed model was calibrated against urinary excretion data for 42 drugs, and the utility for DICN pr
114 ptake of each chemical and was compared with excretion data from a prior human subject study with the
115 Stiripentol for several weeks: urine oxalate excretion decreased by two-thirds.
116 l, both nanoparticles led to higher consumer excretion, despite contrasting particle stability and ph
117 e sampled for evidence of virus exposure and excretion during a prospective nine year serial cross-se
118 anism of secretin-induced urinary HCO(3) (-) excretion, explain metabolic alkalosis in patients with
119 rance kinetics from blood, low hepatobiliary excretion, fast renal excretion, and very low uptake of
120  Here, we dynamically profile the uptake and excretion fluxes of a liver cancer cell line (HepG2) and
121 red parasite strain totally prevented oocyst excretion following infection with wild-type T. gondii,
122 ight into the importance of intestinal urate excretion for serum urate homeostasis.
123  is important to correct 24-h urinary sodium excretion for within-person variance.
124  C-21 dose-dependently increased urine Na(+) excretion from 0.023+/-0.01 to 0.064+/-0.02, 0.087+/-0.0
125    Dietary sodium restriction reduced sodium excretion from 160 to 64 mmol per day.
126                        Transition of albumin excretion from normal to microalbuminuria, a 5-fold incr
127 and thus with a decline in the kidney's acid excretion function, which could potentiate the risk of r
128                  Urinary TX metabolite (TXM) excretion, gastrointestinal tolerance, and ET-related sy
129 ney-specific biodistribution and rapid renal excretion (&gt;80% injected dose in 4 h), compared to nativ
130 ology and function, BP, sodium and potassium excretion, gut microbiome, flow cytometry, catecholamine
131 atic manganese uptake for subsequent biliary excretion has been proposed as the underlying disease me
132 id in osmoregulation, acid-base balance, and excretion have been well documented.
133                    Increased urinary oxalate excretion (hyperoxaluria) promotes the formation of calc
134 tify 50 loci for sodium and 13 for potassium excretion in a large-scale genome-wide association study
135 t NTCP inhibition still promoted cholesterol excretion in Abcg8(-/-) mice.
136  predicted from data for 24-h urinary sodium excretion in adult kidney transplant recipients in 1992-
137 support an important role for ABCG2 in urate excretion in both the human kidney and intestinal tract,
138  thus links glutamine addiction to glutamate excretion in cancer and points toward potential drug tar
139 high AGE formation in diabetes and decreased excretion in CKD or by dietary modifications in these di
140 f first-pass drug absorption, metabolism and excretion in humans-using computationally scaled data fr
141 stration reduced significantly urine oxalate excretion in rats.
142 h fecal coprostanol and total neutral sterol excretion in recipient mice.
143 of the regulation and dysregulation of water excretion in the kidney.
144  such as bioconversion, bioaccumulation, and excretion in vivo.
145  cholesterol transport genes for its biliary excretion, including scavenger receptor class B member 1
146      These adaptations included decreased BA excretion, increased pool size, altered BA composition,
147 n humans and their elimination and potential excretion into human milk are not yet fully understood.
148 difficile infection because of their biliary excretion into the gastrointestinal tract and disruption
149               Twenty-four hour urine oxalate excretion is an inaccurate measure for endogenous oxalat
150                          Higher usual sodium excretion is associated with overweight/obesity and cent
151    This suggests that impaired hepatobiliary excretion is not the primary cause for manganese overloa
152 hosphate (ATP), but the reason for glutamate excretion is unclear.
153 hyperfiltration restores sodium and chloride excretion it imposes added physical stress on the filtra
154 ysis shows that urinary sodium and potassium excretion loci are over-represented in behavioural respo
155 er, despite the continuously elevated solute excretion, long-term osmotic diuresis does not occur in
156 rphic mouse (kl/kl) with impaired urinary Pi excretion, low autophagy, and premature organ dysfunctio
157 se in the percentage of subjects with iodine excretion &lt;100 ug/24 h (P < 0.001) was observed, without
158     Persistently increased urinary phosphate excretion maintains serum phosphate levels within the no
159 systemic circulation and prevent its urinary excretion, making difficult its detection and quantitati
160 port into bile is a major route of manganese excretion, manganese levels in the brain, blood, and liv
161 tress and that they involve several distinct excretion mechanisms, including direct plasma membrane t
162                             Reduced net acid excretion (NAE) capacity indicates a decrease in renal f
163 iency uptake kinetics and fractional urinary excretion of 0.025%, whereas albumin and alpha(1) -micro
164 netics and 50-fold higher fractional urinary excretion of 1.15%.
165                                        Urine excretion of 6 AngII-regulated proteins was quantified u
166 n studies revealed significant hepatobiliary excretion of [(18)F]FGlc-FAPI; however, small-animal PET
167 tes insipidus is a syndrome characterized by excretion of abnormally large volumes of dilute urine.
168 , the absence of Gpr116 results in a primary excretion of acid in KO mouse urine, leading to mild met
169                                      Urinary excretion of all other analytes was unchanged between th
170 reversible leukoencephalopathy and a urinary excretion of alpha-ketoglutarate (alphaKG) that was mark
171                                        Urine excretion of AngII signature proteins correlated strongl
172 ncreases tissue exposure in mice and reduces excretion of ASO in urine, histological review of skelet
173 ng in increased hepatic production and fecal excretion of BAs, reduced hepatic cholesterol, and decre
174        Our results indicate that the urinary excretion of beta(2) -m and RBP4 differs from that of al
175 i compared with normal controls, and urinary excretion of both cathepsins was significantly greater i
176 d secondarily systemically followed by renal excretion of byproducts were the predominant elimination
177                      Total urinary and fecal excretion of catabolites accounted for <5% of each of th
178 of cell wall extensibility via the polarized excretion of cell wall-loosening compounds at the tip.
179 t of ADPKD patients, lower levels of urinary excretion of citrate, an endogenous inhibitor of calcium
180 higher (p < 0.001, p < 0.001), and the fecal excretion of deoxycholic (p < 0.03, p < 0.02) and chenod
181 thesis, production of queuine/queuosine, and excretion of dietary mercury.
182 2) are critically involved in absorption and excretion of diverse cationic drugs.
183       Cow milk consumption increases urinary excretion of E1 in humans.
184         The analysis also quantified urinary excretion of ECM proteins and peptides.
185                                      Urinary excretion of ECM-derived peptides was enhanced in cFSGS,
186               We have known for decades that excretion of electrolytes is dependent on time of day, w
187                                        Urine excretion of ferulic acid was higher (p < 0.001, p < 0.0
188 0.6 +/- 16.0%; P = 0.04), indicating partial excretion of inert gas across small pulmonary arteries.
189 ust ingestion estimates were made from fecal excretion of inert tracers with corrections for dietary
190 e, secretory pathway-mediated assemblage and excretion of infective particles represent appealing tar
191 e external calcite structure produced by the excretion of interlocking plates by the phytoplankton co
192 ferences in urine KP activity and fractional excretion of KP metabolites.
193 eability, measured by the urinary fractional excretion of lactulose-to-mannitol ratio (LMR) at recrui
194 nsipidus (DI) is a disorder characterized by excretion of large amounts of hypotonic urine.
195 per mille) during the day at high pH and the excretion of lighter Zn isotopes (-0.4 per mille < Delta
196 lunted this response and inhibited efficient excretion of lodged crystals.
197                                      Urinary excretion of LTE(4) was measured by ELISA.
198                                      Urinary excretion of mammalian-microbial co-metabolites hippurat
199  tubule epithelial cells, mediates the renal excretion of many clinically important drugs.
200  in adsorption, distribution, metabolism and excretion of metabolites and pharmaceuticals, as well as
201 concentration ability, and augmented urinary excretion of Na(+) and urea in both mutant mice.
202                                              Excretion of naphthalene-derived metabolites was also ac
203                                    Excessive excretion of oxalate in the urine results in the formati
204 ominant males differentially upregulated the excretion of particular MUPs, including the pheromone MU
205                             We found urinary excretion of pentosidine was increased ca. twofold in pa
206 in silico analysis did not identify enhanced excretion of peptides derived from cathepsin B or C.
207 ), imparting high biocompatibility and >90 % excretion of QDs within 2 weeks of intravenous administr
208 on is associated with an increase in urinary excretion of sex steroid hormones and their metabolites
209                                Reduced fecal excretion of short-chain fatty acids (including butyrate
210 used a nonsignificant increase in fractional excretion of sodium at day 3, which was absent at week 6
211 diabetic controls, this increased fractional excretion of sodium from ~1% to ~25% of the filtered loa
212                                   Fractional excretion of sodium increased significantly with empagli
213 lozin monotherapy versus placebo (fractional excretion of sodium, 1.2+/-0.7% versus 0.7+/-0.4%; P=0.0
214 t in combination with bumetanide (fractional excretion of sodium, 5.8+/-2.5% versus 3.9+/-1.9%; P=0.0
215 xalate stones) had a 40% decrease in urinary excretion of succinate, a 35% increase in serum succinat
216 ration of aromatic compounds to optimize the excretion of such products while keeping precursor molec
217 ansgenic biosensor to visualize the vascular excretion of the genetically tagged plasma protein DBP-E
218                     Herein we report urinary excretion of the latter analytes and related fractional
219 or serum neutralizing antibody) and/or stool excretion of the vaccine strain, stratified by HBGA stat
220 f 19 kidney transplant recipients, the urine excretion of these 6 proteins was significantly lower fo
221                    Our findings suggest that excretion of these biomarkers may be influenced by chang
222                               To monitor the excretion of these garlic metabolites in a larger cohort
223  the intensity of absorption, metabolism and excretion of these pigments.
224 odel yields segmental deliveries and urinary excretion of volume and key solutes that are consistent
225 ea transporter (UT) inhibition increases the excretion of water and urea, but the effect on uremic ca
226                       Remarkably, fractional excretions of 6 lysine and arginine-derived glycation fr
227           We conclude that higher fractional excretions of glycation adducts are potential biomarkers
228 trophic interactions, in which the metabolic excretions of one species are the primary resource for a
229 s estradiol (E2), estriol (E3), and 16ketoE2 excretion only increased after semiskimmed milk consumpt
230  contrast, C-21 did not increase urine Na(+) excretion or renal interstitial cGMP in SHR.
231 increases in urine volume (p < 0.01), sodium excretion (p < 0.01), and creatinine clearance (p < 0.00
232 e at delivery (p = 0.049), increased protein excretion (p = 0.01), more extreme laboratory derangemen
233 nd absorption, distribution, metabolism, and excretion parameters as well as mass spectrometry experi
234                                          The excretion pathomechanisms of SARS-CoV-2 are actually unk
235  at 1 h after injection), indicating a renal excretion pathway.
236  bariatric surgery can influence absorption, excretion, pharmacokinetics, and pharmacodynamics of var
237 .g. immunoglobulin G [IgG]), urinary nephrin excretion (podocyte injury) and serum levels of the solu
238                              Honeydew is the excretion product of phloem-feeding hemipteran insects s
239 educed PT length can account for the urinary excretion profile in LS.
240                             Whereas the fast excretion profile of the TD139 surrogate indicated that
241                              Altered PK, and excretion profiles of acetaminophen were observed in ant
242  with diabetes duration, most recent albumin excretion rate (AER), updated mean triglycerides, baseli
243 as accurate by comparing measured creatinine excretion rate (CER) to CER estimated using a 4-variable
244 ar filtration rate (GFR) and urinary albumin excretion rate (UAER) are used to diagnose and classify
245                     The mean urinary albumin excretion rate after washout was 40% (95% CI, 0 to 80) h
246 l-based GFR per year and the urinary albumin excretion rate after washout.
247 -density lipoprotein, triglycerides, albumin excretion rate, and DCCT/EDIC mean updated hemoglobin A1
248 oparticles increased nitrogen and phosphorus excretion rates more than copper nanoparticles, but over
249   We tested this hypothesis by measuring the excretion rates of nitrogen and phosphorus of Physella a
250 h nitrogen and phosphorus had overall higher excretion rates than ones in ambient (no nutrients added
251  each test beverage due to decreased urinary excretion rates, 2) glucose (glu)- and amino acid (AA)-b
252           Due to the increasing use and high excretion rates, high quantities of the antidiabetic dru
253 ate for older adults due to attenuated urine excretion rates.
254 ynamics, substrate conversion and production excretion rates.
255 , raw bovine milk, and Ascaris suum nematode excretions), recovering size and stiffness distributions
256  drugs (e.g. distribution, circulation time, excretion, redox properties) is also mentioned.
257 entally that partial inhibition of glutamate excretion reduces cell growth.
258                The kidneys demonstrated high excretion-related retention, whereas all other tissue de
259 ve increased glucose consumption and lactate excretion relative to the same cells in the quiescent st
260 omparative metabolomics of plant tissues and excretions revealed that ascr#18 is converted into short
261 tro absorption, distribution, metabolism and excretion screening approach, analogues were synthesized
262 the single most abundant protein in T. muris excretions/secretions, is non-immunogenic during infecti
263 co absorption, distribution, metabolism, and excretion studies demonstrated that the incorporation of
264 nd absorption, distribution, metabolism, and excretion testing.
265 d with Stiripentol had a lower urine oxalate excretion than control patients.
266 ave been widely shown to benefit from diatom excretions that accumulate within the microenvironment s
267 articipants in the lowest quartile of sodium excretion, the adjusted prevalence ratios in the highest
268 mal level of creatinine in the serum and its excretion through urine in apparently healthy individual
269 h has found animal-mediated nutrient supply (excretion) to be highly predictable based on allometric
270                      The highly heritable DA excretion trait is substantially influenced by a previou
271 as calculated as the ratio of urinary iodine excretion (UIE) to total iodine intake.
272 sis of undiluted sweat immediately after its excretion using a flow-through glucose biosensor.
273 study (GWAS) on urinary sodium and potassium excretion using data from 446,237 individuals of Europea
274 ectrometry (LC-MS/MS) and deduced fractional excretion using reported plasma levels and urinary and p
275 f the latter analytes and related fractional excretion values, exploring the link to MA and early dec
276 le absorption, distribution, metabolism, and excretion values.
277                        Mean urinary ammonium excretion was 25% lower and serum bicarbonate concentrat
278          The ratio between urinary and fecal excretion was also altered in antibiotic treated animals
279 ed >=1 24-h urine sample, and urinary solute excretion was analyzed.
280                                Fecal oxalate excretion was enhanced in wild-type mice with CKD.
281                             Fractional Na(+) excretion was increased and oxygen consumption reduced i
282             Urinary pregnanediol glucuronide excretion was not significantly affected.
283             Cumulative urinary d3-alpha-CEHC excretion was not significantly changed by any intervent
284                    A 1000-mg/d higher sodium excretion was significantly associated with 3.8-units hi
285 ration and tubular uptake to urinary protein excretion, we developed a mathematical model of protein
286               Consistent with its role in Pi excretion, we found that dietary Pi induces MFS2 express
287  chloride, potassium, phosphate, and calcium excretion were assessed in response to the Npt2a inhibit
288 , and urinary prostacyclin metabolite (PGIM) excretion were measured at randomization and after 2 wee
289 enin concentration, and urinary endothelin-1 excretion were similar between knockout and control mice
290 ronic nanoparticle exposure doubled nutrient excretion when compared to the control.
291 ease in biliary cholesterol and phospholipid excretion whereas biliary bile salt output and bile salt
292 significant increase in urinary estrone (E1) excretion, whereas estradiol (E2), estriol (E3), and 16k
293 retion and markedly increased urinary PGE(2) excretion, whereas GFR, plasma renin concentration, and
294 re different between nitrogen and phosphorus excretion, which could have implications for the resulti
295 essin antagonists) predominantly cause water excretion, which increases the osmolality of the circula
296 -I [TSP1]) and hypothesized that their urine excretion will correlate with IFTA in kidney transplant
297 ic acid nephropathy, and elevated beta(2) -m excretion with increased single nephron glomerular filtr
298 functionalization layer facilitated 90% ErNP excretion within 2 weeks without detectable toxicity in
299 minated completely through hepatic and renal excretion within four weeks of injection with no evidenc
300 f the RNA nanoparticle were cleared by renal excretion within half hour after systemic injection.

 
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