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1 with a decreased urine volume and increased urine osmolality.
2 ot accompanied by a proportional increase in urine osmolality.
3 er intake and urine volume, alongside higher urine osmolality.
5 , despite better renal free water excretion (urine osmolality 343+/-101 mOsm/kg versus 475+/-136; P<0
7 more fluid than wild-type mice and had lower urine osmolality (505 +/- 40 vs. 1081 +/- 68 milliosmola
9 ed therapeutic concentrations in the kidney, urine osmolality after administration of 1-deamino-8-D-a
11 izygous male pups showed a decrease in basal urine osmolalities and were unable to concentrate their
13 n a significant increase in water retention, urine osmolality and aquaporin-2 expression and phosphor
14 P levels, water and sodium reabsorption, and urine osmolality and decreased urine output (P </= 0.04,
15 otensin II (Ang II), aldosterone levels, and urine osmolality and electrolytes were measured in healt
17 ne cAMP levels, free water reabsorption, and urine osmolality and increased urine output (P </= 0.03
18 P levels, water and sodium reabsorption, and urine osmolality and increased urine output, while raxib
22 gents augment free water clearance, decrease urine osmolality, and correct serum [Na+] and serum osmo
23 and observed marked antidiuresis, increased urine osmolality, and increased solute-free water reabso
25 cantly greater urine flow rate and decreased urine osmolality as compared with control rats at compar
26 ral abnormalities, mutant mice exhibited low urine osmolality at baseline and after water restriction
27 , and [-/-] 2,616+/-229 (P < 0.025), whereas urine osmolalities before water deprivation did not diff
28 beta=0.11; 95% CI, 0.01 to 0.20; P=0.03) and urine osmolality (beta=0.08; 95% CI, 0.05 to 0.10; P<0.0
30 creased urine output by 3-5-fold and reduced urine osmolality by approximately 2-fold compared to veh
31 had a reduced urine flow and two-fold higher urine osmolality during the first 12 hours of treatment
32 ine specific gravity (USG), urine color, and urine osmolality have been widely advocated for screenin
35 )-14 also increased urine output and reduced urine osmolality in mice given free access to water.
36 y, caused increased urine output and reduced urine osmolality in mice that was associated with decrea
41 evated corticosterone, hypokalaemia, reduced urine osmolality, increased pulse pressure and cardiomyo
42 restriction of rats or mice led to increased urine osmolality, increased Sgk1 expression, increased e
43 urine outflow with concomitant reduction of urine osmolality, indicating a purely aquaretic effect a
45 ter than that in wild-type litter mates, and urine osmolality (<275 milliosmol) was much lower than i
46 mistry profiles, spleen function biomarkers, urine osmolality, neurodevelopment, transcranial Doppler
47 ion of the VR agonist dDAVP did not increase urine osmolality of AC6-deficient mice to the levels of
48 ots of plasma AVP concentration ([AVP]P) vs. urine osmolality (OsmU) were fitted to a sigmoidal curve
50 0.03) and polyuria (P < 0.04), with a lower urine osmolality (P < 0.003) as compared to Nhe3+/+ mice
53 is phenotype is the consequence of decreased urine osmolality secondary to renal vasopressin resistan
54 output, solute and urea excretion, serum and urine osmolality, serum creatinine, 24-h creatinine clea
55 ective OPCML variants had markedly increased urine osmolality suggesting greater ability to defend ag
56 ume, but there was a significant increase of urine osmolality, suggesting that DI may be caused by a
57 (GW3965) in WT mice elicited an increase in urine osmolality, suggesting that LXRbeta is a key recep
59 (cKO) of Wnk1 caused polyuria with decreased urine osmolality that persisted in water restriction and
60 ng defect with serum hyperosmolality and low urine osmolality that was not increased by a V2 vasopres
61 ater in UT-B- deficient mice (p < 0.01), and urine osmolality (U(osm)) was lower (1532 +/- 71 versus
63 , and index tests included USG, urine color, urine osmolality, urine cloudiness, additional dipstick
64 urine output and fluid intake, and increases urine osmolality, urine sodium concentration, and plasma
65 ia is further differentiated on the basis of urine osmolality, urine sodium level, and volume status.
67 ing capacity: Urine flow rate was higher and urine osmolality was lower than control rats despite an
68 water-deprived knockout mice was <10 mM, and urine osmolality was not increased by the V2 agonist DDA
69 In rats injected with lipopolysaccharide, urine osmolality was reduced by ~40%, along with medulla
71 3 have impairment in their water balance and urine osmolality, which correlates with the downregulati
72 how the association between water intake and urine osmolality, which is a hydration biomarker, varied
73 vasopressin and sodium, as well as elevated urine osmolality - with an increased risk of new-onset c