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1 s, during normal aging, and after unilateral ureteral obstruction).
2 ry angiogenesis in the cornea and unilateral ureteral obstruction).
3 nce of prominent leukocyte infiltrates after ureteral obstruction.
4 d sterile inflammation induced by unilateral ureteral obstruction.
5 ion on kidney fibrosis induced by unilateral ureteral obstruction.
6 sis, cisplatin nephrotoxicity, and bilateral ureteral obstruction.
7 d levels of active TGF-beta after unilateral ureteral obstruction.
8 ed renal tubular epithelium after unilateral ureteral obstruction.
9 ding to tubular atrophy following unilateral ureteral obstruction.
10 elial cell (TEC) apoptosis during unilateral ureteral obstruction.
11 ent of fibrosis in a rat model of unilateral ureteral obstruction.
12 odel of renal fibrosis induced by unilateral ureteral obstruction.
13 the upper urinary tract following unilateral ureteral obstruction.
14 ntly found in patients with renal disease or ureteral obstruction.
15 was also increased in p27-/- mice following ureteral obstruction.
16 ve other common causes for cholecystitis and ureteral obstruction.
17 hemia/reperfusion injury (IRI) or unilateral ureteral obstruction.
18 ce had less renal fibrosis during unilateral ureteral obstruction.
19 otected against renal fibrosis in unilateral ureteral obstruction.
20 enal fibrosis in a mouse model of unilateral ureteral obstruction.
21 ontralateral kidneys of rats with unilateral ureteral obstruction.
22 nterstitial fibrosis in mice with unilateral ureteral obstruction.
23 ated gene expression in mice with unilateral ureteral obstruction.
24 s after subjecting the animals to unilateral ureteral obstruction.
25 ice with an MMP13 inhibitor after unilateral ureteral obstruction.
26 ofibroblasts in a murine model of unilateral ureteral obstruction.
27 enuated collagen deposition after unilateral ureteral obstruction.
28 exacerbated inflammation and fibrosis after ureteral obstruction.
29 beta-catenin, and expression of Snail after ureteral obstruction.
30 and macrophage infiltration after unilateral ureteral obstruction.
31 eys significantly increased after unilateral ureteral obstruction.
32 er in kidneys from CLOCK-deficient mice with ureteral obstruction.
33 to ischemia-reperfusion injury or unilateral ureteral obstruction.
34 chymal damage were significantly worse after ureteral obstruction.
35 ently available for the cancer patients with ureteral obstruction.
36 kidneys closely parallels that observed with ureteral obstruction.
37 ey injury induced by ischemia reperfusion or ureteral obstruction.
38 c cystinosis, in a mouse model of unilateral ureteral obstruction.
42 shared several clinical features, including ureteral obstruction (5/7 patients), lymphocele (3/7), b
43 on also occurred in kidneys after unilateral ureteral obstruction, a model of tubulointerstitial fibr
44 f a single dose of suramin immediately after ureteral obstruction abolished the expression of fibrone
47 lary atrophy in mice subjected to unilateral ureteral obstruction and a complete reversal of obesity
48 n1alpha1-eGFPL10a mice subject to unilateral ureteral obstruction and analyzed and validated the resu
49 nterstitial fibrosis in models of unilateral ureteral obstruction and aristolochic acid fibrosis asso
50 in renal fibrotic mice induced by unilateral ureteral obstruction and aristolochic acid nephropathy.
51 The area under the curve diminished during ureteral obstruction and correlated well with mean corti
52 These changes occurred in the unilateral ureteral obstruction and folic acid models of fibrosis a
53 Patients were clinically stable with known ureteral obstruction and had been referred for antegrade
55 18 induces TLR4 expression during unilateral ureteral obstruction and induces TLR4 expression in HK-2
56 reatment of idiopathic RPF aims at relieving ureteral obstruction and inducing disease regression, an
57 d kidney inflammation in both the unilateral ureteral obstruction and ischemic-reperfusion injury-ind
58 ow that renal fibrosis induced by unilateral ureteral obstruction and metastasis of human cancer xeno
59 onic kidney injury (cisplatin and unilateral ureteral obstruction and reanalyzed previously published
61 en-induced mice were subjected to unilateral ureteral obstruction and thymidine analogue labeling and
63 s and renal fibrosis in mice with unilateral ureteral obstruction, and also attenuates ER stress, pro
64 rile renal inflammation following unilateral ureteral obstruction, and in experimental pyelonephritis
66 dney of renal fibrosis induced by unilateral ureteral obstruction, and primarily located in interstit
67 ificantly at 14 and 21 days after unilateral ureteral obstruction, and renal oxidized protein levels
68 endoureterotomy is useful for other types of ureteral obstruction, and we aimed to assess its long-te
69 inflammation in murine models of unilateral ureteral obstruction, antimembrane basal GN, and infusio
70 aradigm for immune mediated inflammation and ureteral obstruction as a model for non-immune mediated
71 interstitial fibrosis in mouse kidney after ureteral obstruction, as demonstrated by a reduced inter
72 nt macrophages limited kidney fibrosis after ureteral obstruction by driving extracellular matrix deg
74 cantly more fibrosis after 7 d of unilateral ureteral obstruction compared with wild-type mice, despi
76 n in a mouse kidney injury model (unilateral ureteral obstruction), consisting of an initial increase
77 in the contralateral kidney after unilateral ureteral obstruction could promote lymphangiogenesis.
78 3 hours after reperfusion; after unilateral ureteral obstruction (day 7) in mice; and after gentamic
79 er ischemia-reperfusion injury or unilateral ureteral obstruction demonstrates that amphiregulin was
80 ys of diabetic rats and mice with unilateral ureteral obstruction depicted significant loss of SCAI e
81 diagnosis was established, and the degree of ureteral obstruction determined on urograms was compared
83 scriptomics (lithium-induced NDI, unilateral ureteral obstruction, endotoxin-induced NDI) or proteomi
84 ed to 3 models of renal fibrosis (unilateral ureteral obstruction, folic acid nephropathy [FAN], and
87 enges, namely, fistulae, abscesses, bowel or ureteral obstruction, hemorrhage, cancer and thickened m
90 allowed accurate prediction of the degree of ureteral obstruction in 44 (94%) of 47 patients with acu
91 nowledge, this is the first reported case of ureteral obstruction in a transplant kidney caused by an
93 ed ischemia-reperfusion injury or unilateral ureteral obstruction in mice with proximal tubule cell-s
94 in the fibrotic kidney induced by unilateral ureteral obstruction in mice, whereas renal Smad abundan
96 voluted tubule cells and those of unilateral ureteral obstruction in the afflicted mouse kidney sugge
97 n highly selected children with intraluminal ureteral obstruction in the hands of a very experienced
99 ed inflammation and fibrosis associated with ureteral obstruction in vivo Therefore, domain 4 of CTGF
106 ysyl oxidase inhibitor alleviated unilateral ureteral obstruction-induced tubular dilatation and prol
107 tubulointerstitial region of the unilateral ureteral obstruction-injured kidney in mice correlating
110 ession in the afflicted kidney by unilateral ureteral obstruction is accompanied by changes in Usf1 a
112 we report that renal nerve stimulation after ureteral obstruction is the primary profibrotic signal a
114 els of kidney fibrosis induced by unilateral ureteral obstruction, ischemia-reperfusion injury, or hi
116 ependent murine fibrosis model of unilateral ureteral obstruction, kidney fibrosis was unexpectedly m
117 rmethylation of 94 genes in mouse unilateral ureteral obstruction kidneys, which was markedly reduced
118 ul division of the isthmus, and avoidance of ureteral obstruction, long-term data revealed good graft
119 hen subjected to the normotensive unilateral ureteral obstruction model of endogenous RAS activation,
125 ers of disease progression in the unilateral ureteral obstruction model of renal interstitial fibrosi
128 placement were performed in 45 patients with ureteral obstruction (n = 40), leak (n = 3), or both (n
129 he normal and injured kidneys, we found that ureteral obstruction not just blocked the NP elimination
131 , compound 8, starting the day of unilateral ureteral obstruction operation, inhibited collagen depos
133 +) C57BL/6 mice were subjected to unilateral ureteral obstruction or sham surgery (n = 8/group; sham,
134 5 expression in fibrotic mouse kidneys after ureteral obstruction or unilateral ischemia-reperfusion
135 ed to 5/6 subtotal nephrectomy or unilateral ureteral obstruction, plasma levels of angiopoietin-2 al
138 elayed administration of MC1568 at 3 d after ureteral obstruction reversed the expression of alpha-SM
139 abetic rat and mouse kidneys with unilateral ureteral obstruction showed SMA expression, as evidenced
140 in treatment of mice subjected to unilateral ureteral obstruction similarly reduced YAP/TAZ levels an
141 injecting oleic acid followed by unilateral ureteral obstruction surgery in mice resulted in enhance
144 tion of folic acid nephropathy or unilateral ureteral obstruction, TbetaRII(endo+/-) mice exhibited l
148 s of ischemia/reperfusion AKI and unilateral ureteral obstruction to investigate the role of IL-33 (i
151 renal fibrosis disease induced by unilateral ureteral obstruction, transforming growth factor-beta ty
152 ts or wild-type mice subjected to unilateral ureteral obstruction, TRPC3 expression increased in the
153 mean age, 45 years; P = .54) with unilateral ureteral obstruction underwent contemporaneous urinalysi
154 s of renal interstitial fibrosis, unilateral ureteral obstruction, unilateral ischemia-reperfusion, C
155 nancy should not be interpreted as a sign of ureteral obstruction unless the finding persists in the
156 schemic kidney injury is afforded by 24 h of ureteral obstruction (UO) applied 6 or 8 days prior to t
157 is in aging mice and in mice with unilateral ureteral obstruction (UUO) a known model of progressive
158 s, we subjected the hypomorphs to unilateral ureteral obstruction (UUO) and again found significant p
159 mice over a time course following unilateral ureteral obstruction (UUO) and compared to sham controls
160 s increased in mouse kidneys with unilateral ureteral obstruction (UUO) and in cultured NRK-52E cells
161 , in two models of kidney injury: unilateral ureteral obstruction (UUO) and ischemia reperfusion.
163 thelial cells of a mouse model of unilateral ureteral obstruction (UUO) and related cell models using
164 beta1 transgenic mice, and in the unilateral ureteral obstruction (UUO) and subtotal nephrectomy (SNX
165 xamined renal fibrosis induced by unilateral ureteral obstruction (UUO) in diabetic mouse models.
166 ction in renal fibrosis following unilateral ureteral obstruction (UUO) in mice, a model of progressi
168 y polarization and migration into unilateral ureteral obstruction (UUO) kidneys and unilateral ischem
170 aling and renal fibrosis in a rat unilateral ureteral obstruction (UUO) model by transferring a doxyc
173 d JNK targets were activated in a unilateral ureteral obstruction (UUO) model of renal fibrosis in vi
180 renal fibrosis-mice subjected to unilateral ureteral obstruction (UUO) or fed an adenine-rich diet-a
181 9a-2 in renal fibrosis induced by unilateral ureteral obstruction (UUO) or renal ischemia/reperfusion
183 stigated between 3 and 14 d after unilateral ureteral obstruction (UUO) or sham surgery (n = 8 mice p
185 of impaired renal growth: chronic unilateral ureteral obstruction (UUO) results in greater injury to
186 ne expression in a mouse model of unilateral ureteral obstruction (UUO) revealed significant inductio
189 l tubules of kidneys subjected to unilateral ureteral obstruction (UUO) using Cre-loxP-mediated gene
192 g this type of injury, modeled by unilateral ureteral obstruction (UUO), cells undergo epithelial-to-
193 odel of renal fibrosis induced by unilateral ureteral obstruction (UUO), HDAC8 was primarily expresse
194 odel of renal fibrosis induced by unilateral ureteral obstruction (UUO), in cultured mouse proximal t
195 urine fibrotic kidneys, following unilateral ureteral obstruction (UUO), resulting in an increase in
196 interstitial fibrosis induced by unilateral ureteral obstruction (UUO), the levels of renal ATX prot
197 rteen days after the induction of unilateral ureteral obstruction (UUO), wild-type mice reconstituted
198 at target myofibroblasts in mouse unilateral ureteral obstruction (UUO)-induced fibrotic kidneys.
217 mia-reperfusion (I/R, days 1-56), unilateral ureteral obstruction (UUO, days 1-10), and Alport mice (
218 chemia-reperfusion injury-(IRI-), unilateral ureteral obstruction-(UUO-), and folic acid- (FA-) induc
222 ssue collagen in the kidneys after sustained ureteral obstruction, when compared with their wild-type
223 fibrogenesis in mice subjected to unilateral ureteral obstruction, whereas activation of Hif in myelo
224 monstrated no evidence of ureteral reflux or ureteral obstruction, whereas an immediate prior cohort
225 antly in injured epithelium after unilateral ureteral obstruction, whereas downstream signaling from
226 Kidney hydronephrosis in C2RD was caused by ureteral obstruction, which was, in turn, induced by SCF
227 men, 137 women; mean age, 59 years) without ureteral obstruction who underwent unenhanced scanning a
229 tion may present with acute cholecystitis or ureteral obstruction without its classical clinical symp