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1 ers of the small bowel, ovaries, breast, and renal pelvis.
2 nary tract, such as the bladder, ureter, and renal pelvis.
3 adder, causing dilation of the ureter and/or renal pelvis.
4 16, 25, 30, or 35 cm above the level of the renal pelvis.
5 illae (2 vertical and 3 horizontal), and the renal pelvis.
6 e medulla, where they release urine into the renal pelvis.
7 rine attenuation was lower in the obstructed renal pelvis (7.4 HU) than in the bladder (11.4 HU) (P <
8 ly removed by peristaltic contraction of the renal pelvis, a smooth muscle structure unique to placen
9 mon disease characterized by dilation of the renal pelvis and calices, resulting in loss of kidney fu
11 ee transitional cell carcinomas (TCC) of the renal pelvis and five Wilms' tumors were compared with n
12 dynamic injection of a DNA solution into the renal pelvis and found that luciferase expression was st
13 inner and outer medulla, papillary tips, and renal pelvis and from glomeruli isolated by sieving.
14 a were observed in groups at the wall of the renal pelvis and in the angular space formed by the pole
18 included 76 renal cell, 24 transitional cell renal pelvis and ureter, and 22 other kidney cancers.
19 iferation causes abnormal development of the renal pelvis and ureter, leading to defective pyelourete
21 lionic fibers projected into the wall of the renal pelvis and/or to the interlobar arteries extending
22 er the induction of elevated pressure in the renal pelvis, and after the pressure was returned to nor
24 gauge needle was inserted into the opacified renal pelvis, and double-contrast pyelography was perfor
27 en with cancer (renal-cell cancer in 759 and renal-pelvis cancer in 136) were identified by cross-lin
31 n of alimentary tract, retention of urine in renal pelvis, distension of bladder, and the development
33 ient with transitional cell carcinoma of the renal pelvis, hydronephrosis proximal to the tumor may c
36 erase expression quickly decreased following renal pelvis injection, the use of the piggyBac transpos
37 To assess renal injury, we performed the renal pelvis injections on uninephrectomised mice and fo
39 cassette to drive human CAII cDNA, into the renal pelvis of CAII-deficient mice results in expressio
40 expressed in nascent urothelia in ureter and renal pelvis of human embryos, and it is suggested that
44 Formation of a lymphoid aggregate in the renal pelvis precedes the invasion of the kidney by infl
46 ensin type 1 receptor genes do not develop a renal pelvis, resulting in the buildup of urine and prog
47 s, but HB-EGF expression did not increase in renal pelvis smooth muscle cells under identical conditi
48 eter actively propels tubular fluid from the renal pelvis to the bladder, and this peristalsis, which
50 eteropelvic junction (UPJ) region, where the renal pelvis transitions to the ureter, is the most comm
51 cidence for all urothelial cancers combined (renal pelvis, ureter, and bladder cancers: adjusted IRR
52 n development affecting the renal parechyma, renal pelvis, ureter, bladder and urethra; they show evi
53 /=18 years) with urothelial carcinoma of the renal pelvis, ureter, bladder, or urethra at 16 sites in
54 urothelial cancer, including cancers of the renal pelvis, ureter, bladder, or urethra, from eight ho
55 d disease (OR, 1.6; 95% CI, 0.8-3.0) and for renal pelvis/ureter cancers (OR, 1.7; 95% CI, 0.5-5.4).
56 ptoms, the association of malrotation of the renal pelvis with calculus increases the risk of hematur
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