-
1
-
-
0036911337
-
Specific heterodimer formation is a prerequisite for uroplakins to exit from the endoplasmic reticulum
-
Tu L, Sun TT, Kreibich G. Specific heterodimer formation is a prerequisite for uroplakins to exit from the endoplasmic reticulum. Mol Biol Cell 2002; 13: 4221-4230
-
(2002)
Mol Biol Cell
, vol.13
, pp. 4221-4230
-
-
Tu, L.1
Sun, T.T.2
Kreibich, G.3
-
2
-
-
24344488394
-
Assembly of urothelial plaques: Tetraspanin function in membrane protein trafficking
-
Hu CC, Liang FX, Zhou G et al. Assembly of urothelial plaques: tetraspanin function in membrane protein trafficking. Mol Biol Cell 2005; 16: 3937-3950
-
(2005)
Mol Biol Cell
, vol.16
, pp. 3937-3950
-
-
Hu, C.C.1
Liang, F.X.2
Zhou, G.3
-
3
-
-
32644478044
-
Urothelial differentiation in chronically urine-deprived bladders of patients with end-stage renal disease
-
Stahlschmidt J, Varley CL, Toogood G, Selby PJ, Southgate J. Urothelial differentiation in chronically urine-deprived bladders of patients with end-stage renal disease. Kidney Int 2005; 68: 1032-1040
-
(2005)
Kidney Int
, vol.68
, pp. 1032-1040
-
-
Stahlschmidt, J.1
Varley, C.L.2
Toogood, G.3
Selby, P.J.4
Southgate, J.5
-
5
-
-
0037218908
-
Uroplakin gene expression in normal human tissues and locally advanced bladder cancer
-
Olsburgh J, Harnden P, Weeks R et al. Uroplakin gene expression in normal human tissues and locally advanced bladder cancer. J Pathol 2003; 199: 41-49
-
(2003)
J Pathol
, vol.199
, pp. 41-49
-
-
Olsburgh, J.1
Harnden, P.2
Weeks, R.3
-
6
-
-
20244376018
-
Molecular identification and characterization of Xenopus egg uroplakin III, an egg raft-associated transmembrane protein that is tyrosine-phosphorylated upon fertilization
-
Sakakibara K, Sato K, Yoshino K et al. Molecular identification and characterization of Xenopus egg uroplakin III, an egg raft-associated transmembrane protein that is tyrosine-phosphorylated upon fertilization. J Biol Chem 2005; 280: 15029-15037
-
(2005)
J Biol Chem
, vol.280
, pp. 15029-15037
-
-
Sakakibara, K.1
Sato, K.2
Yoshino, K.3
-
7
-
-
0036889493
-
Role of membrane proteins in permeability barrier function: Uroplakin ablation elevates urothelial permeability
-
Hu P, Meyers S, Liang FX et al. Role of membrane proteins in permeability barrier function: Uroplakin ablation elevates urothelial permeability. Am J Physiol Renal Physiol 2002; 283: F1200-F1207
-
(2002)
Am J Physiol Renal Physiol
, vol.283
-
-
Hu, P.1
Meyers, S.2
Liang, F.X.3
-
8
-
-
0034722328
-
Ablation of uroplakin III gene results in small urothelial plaques, urothelial leakage, and vesicoureteral reflux
-
Hu P, Deng FM, Liang FX et al. Ablation of uroplakin III gene results in small urothelial plaques, urothelial leakage, and vesicoureteral reflux. J Cell Biol 2000; 151: 961-972
-
(2000)
J Cell Biol
, vol.151
, pp. 961-972
-
-
Hu, P.1
Deng, F.M.2
Liang, F.X.3
-
9
-
-
27744557667
-
De novo uroplakin IIIa mutations cause renal adysplasia leading to severe kidney failure
-
Jenkins D, Bitner-Glindzicz M, Malcolm S et al. De novo uroplakin IIIa mutations cause renal adysplasia leading to severe kidney failure. J Am Soc Nephrol 2005; 16: 2141-2149
-
(2005)
J Am Soc Nephrol
, vol.16
, pp. 2141-2149
-
-
Jenkins, D.1
Bitner-Glindzicz, M.2
Malcolm, S.3
-
10
-
-
0036713958
-
Management of the infant with end-stage renal failure
-
Rees L. Management of the infant with end-stage renal failure. Nephrol Dial Transplant 2002; 17: 1564-1567
-
(2002)
Nephrol Dial Transplant
, vol.17
, pp. 1564-1567
-
-
Rees, L.1
-
11
-
-
3042806874
-
Lack of major involvement of human uroplakin genes in vesicoureteral reflux: Implications for disease heterogeneity
-
Jiang S, Gitlin J, Deng F et al. Lack of major involvement of human uroplakin genes in vesicoureteral reflux: Implications for disease heterogeneity. Kidney Int 2004; 66: 10-19
-
(2004)
Kidney Int
, vol.66
, pp. 10-19
-
-
Jiang, S.1
Gitlin, J.2
Deng, F.3
-
12
-
-
2142655028
-
Functional obstruction: The renal pelvis rules
-
Mendelsohn C. Functional obstruction: The renal pelvis rules. J Clin Invest 2004; 113: 957-959
-
(2004)
J Clin Invest
, vol.113
, pp. 957-959
-
-
Mendelsohn, C.1
-
13
-
-
19944426308
-
Roles of uroplakins in plaque formation, umbrella cell enlargement, and urinary tract diseases
-
Kong XT, Deng FM, Hu P et al. Roles of uroplakins in plaque formation, umbrella cell enlargement, and urinary tract diseases. J Cell Biol 2004; 167: 1195-1204
-
(2004)
J Cell Biol
, vol.167
, pp. 1195-1204
-
-
Kong, X.T.1
Deng, F.M.2
Hu, P.3
-
14
-
-
0036144736
-
A family study and the natural history of prenatally detected unilateral multicystic dysplastic kidney
-
Belk RA, Thomas DF, Mueller RF, Godbole P, Markham AF, Weston MJ. A family study and the natural history of prenatally detected unilateral multicystic dysplastic kidney. J Urol 2002; 167: 666-669
-
(2002)
J Urol
, vol.167
, pp. 666-669
-
-
Belk, R.A.1
Thomas, D.F.2
Mueller, R.F.3
Godbole, P.4
Markham, A.F.5
Weston, M.J.6
-
15
-
-
84942922074
-
Chapter 21. Maldevelopment of the human kidney and lower urinary tract: An overview
-
In: Vize PD, Woolf AS, Bard JBL, eds. Elsevier Science/Academic Press
-
Woolf AS, Welham SJM, Hermann MM, Winyard PJD. Chapter 21. Maldevelopment of the human kidney and lower urinary tract: An overview. In: Vize PD, Woolf AS, Bard JBL, eds. The Kidney: From Normal Development to Congenital Disease. Elsevier Science/Academic Press 2003; 377-393
-
(2003)
The Kidney: From Normal Development to Congenital Disease
, pp. 377-393
-
-
Woolf, A.S.1
Welham, S.J.M.2
Hermann, M.M.3
Winyard, P.J.D.4
-
16
-
-
30744476739
-
Mutations in hepatocyte nuclear factor-1β and their related phenotypes
-
Edghill EL, Bingham C, Ellard S, Hattersley AT. Mutations in hepatocyte nuclear factor-1β and their related phenotypes. J Med Genet 2005; 43: 84-90
-
(2005)
J Med Genet
, vol.43
, pp. 84-90
-
-
Edghill, E.L.1
Bingham, C.2
Ellard, S.3
Hattersley, A.T.4
-
17
-
-
0035310999
-
Organization of uroplakin subunits: Transmembrane topology, pair formation and plaque composition
-
Liang FX, Riedel I, Deng FM et al. Organization of uroplakin subunits: transmembrane topology, pair formation and plaque composition. Biochem J 1994; 355: 13-18
-
(1994)
Biochem J
, vol.355
, pp. 13-18
-
-
Liang, F.X.1
Riedel, I.2
Deng, F.M.3
-
18
-
-
16944366271
-
Further delineation of renal-coloboma syndrome in patients with extreme variability of phenotype and identical PAX2 mutations
-
Schimmenti LA, Cunliffe HE, McNoe LA et al. Further delineation of renal-coloboma syndrome in patients with extreme variability of phenotype and identical PAX2 mutations. Am J Hum Genet 1997; 60: 869-878
-
(1997)
Am J Hum Genet
, vol.60
, pp. 869-878
-
-
Schimmenti, L.A.1
Cunliffe, H.E.2
McNoe, L.A.3
-
19
-
-
0028321382
-
Mammalian uroplakins. A group of highly conserved urothelial differentiation-related membrane proteins
-
Wu XR, Lin JH, Walz T et al. Mammalian uroplakins. A group of highly conserved urothelial differentiation-related membrane proteins. J Biol Chem 1994; 269: 13716-13724
-
(1994)
J Biol Chem
, vol.269
, pp. 13716-13724
-
-
Wu, X.R.1
Lin, J.H.2
Walz, T.3
-
20
-
-
0028261374
-
Uroplakins Ia and Ib, two major differentiation products of bladder epithelium, belong to a family of four transmembrane domain (4TM) proteins
-
Yu J, Lin JH, Wu XR, Sun TT. Uroplakins Ia and Ib, two major differentiation products of bladder epithelium, belong to a family of four transmembrane domain (4TM) proteins. J Cell Biol 1994; 125: 171-182
-
(1994)
J Cell Biol
, vol.125
, pp. 171-182
-
-
Yu, J.1
Lin, J.H.2
Wu, X.R.3
Sun, T.T.4
-
21
-
-
33646791894
-
Mutations in Uroplakin IIIA are a rare cause of renal hypodysplasia in humans
-
Schonfelder EM, Knuppel T, Tasic V et al. Mutations in Uroplakin IIIA are a rare cause of renal hypodysplasia in humans. Am J Kidney Dis 2006; 47: 1004-1012
-
(2006)
Am J Kidney Dis
, vol.47
, pp. 1004-1012
-
-
Schonfelder, E.M.1
Knuppel, T.2
Tasic, V.3
-
22
-
-
7044231172
-
Understanding primary vesicoureteric reflux and associated nephropathies
-
Woolf AS, Wilcox DT. Understanding primary vesicoureteric reflux and associated nephropathies. Curr Paediatr 2004; 14: 563-567
-
(2004)
Curr Paediatr
, vol.14
, pp. 563-567
-
-
Woolf, A.S.1
Wilcox, D.T.2
-
23
-
-
0033875535
-
Uroplakin and androgen receptor expression in the human fetal genital tract: Insights into the development of the vagina
-
Shapiro E, Huang Y, Wu XR. Uroplakin and androgen receptor expression in the human fetal genital tract: Insights into the development of the vagina. J Urol 2000; 164: 1048-1051
-
(2000)
J Urol
, vol.164
, pp. 1048-1051
-
-
Shapiro, E.1
Huang, Y.2
Wu, X.R.3
-
24
-
-
0028107563
-
Precursor sequence, processing, and urothelium-specific expression of a major 15-kDa protein subunit of asymmetric unit membrane
-
Lin JH, Wu XR, Kreibich G, Sun TT. Precursor sequence, processing, and urothelium-specific expression of a major 15-kDa protein subunit of asymmetric unit membrane. J Biol Chem 1994; 269: 1775-1784
-
(1994)
J Biol Chem
, vol.269
, pp. 1775-1784
-
-
Lin, J.H.1
Wu, X.R.2
Kreibich, G.3
Sun, T.T.4
-
26
-
-
25144453720
-
Maternal diet programs embryonic kidney gene expression
-
Welham SJM, Riley PR, Wade A, Hubank M, Woolf AS. Maternal diet programs embryonic kidney gene expression. Physiol Genomics 2005; 22: 48-56
-
(2005)
Physiol Genomics
, vol.22
, pp. 48-56
-
-
Welham, S.J.M.1
Riley, P.R.2
Wade, A.3
Hubank, M.4
Woolf, A.S.5
-
27
-
-
17844387376
-
Implication of Wt1 in the pathogenesis of nephrogenic failure in a mouse model of retinoic acid-induced caudal regression syndrome
-
Tse HK, Leung MB, Woolf AS et al. Implication of Wt1 in the pathogenesis of nephrogenic failure in a mouse model of retinoic acid-induced caudal regression syndrome. Am J Pathol 2005; 166: 1295-1307
-
(2005)
Am J Pathol
, vol.166
, pp. 1295-1307
-
-
Tse, H.K.1
Leung, M.B.2
Woolf, A.S.3
-
28
-
-
2342642088
-
Genitourinary anomaly in congenital varicella syndrome: Case report and review
-
Fujita H, Yoshii A, Maeda J et al. Genitourinary anomaly in congenital varicella syndrome: Case report and review. Pediatr Nephrol 2004; 19: 554-557
-
(2004)
Pediatr Nephrol
, vol.19
, pp. 554-557
-
-
Fujita, H.1
Yoshii, A.2
Maeda, J.3
-
29
-
-
27644545340
-
Congenital varicella syndrome in the third trimester
-
Koren G. Congenital varicella syndrome in the third trimester. Lancet 2005; 366: 1591-1592
-
(2005)
Lancet
, vol.366
, pp. 1591-1592
-
-
Koren, G.1
|