Lack of major involvement of human uroplakin genes in vesicoureteral reflux: Implications for disease heterogeneity

Lack of major involvement of human uroplakin genes in vesicoureteral reflux: Implications for disease heterogeneity. primary vesicoureteral reflux (vur) is a hereditary disorder characterized by the retrograde flow of urine into the ureters and kidneys. it affects about 1% of the young children and...

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Veröffentlicht in:	Kidney international 2004-07, Vol.66 (1), p.10-19
Hauptverfasser:	Jiang, Songshan, Gitlin, Jordan, Deng, Fang-Ming, Liang, Feng-Xia, Lee, Andy, Atala, Anthony, Bauer, Stuart B., Ehrlich, Garth D., Feather, Sally A., Goldberg, Judith D., Goodship, Judith A., Goodship, Timothy H.J., Hermanns, Monika, Hu, Fen Ze, Jones, Katrin E., Malcolm, Sue, Mendelsohn, Cathy, Preston, Robert A., Retik, Alan B., Schneck, Francis X., Wright, Victoria, Ye, Xiang Y., Woolf, Adrian S., Wu, Xue-Ru, Ostrer, Harry, Shapiro, Ellen, Yu, Jun, Sun, Tung-Tien
Format:	Artikel
Sprache:	eng
Schlagworte:	Alanine Amino Acid Substitution Animals Base Sequence Biological and medical sciences Case-Control Studies Chromosome Mapping Cytosine Embryo, Mammalian - metabolism Exons Gene Expression Genetic Predisposition to Disease Genotype Guanine Humans hydronephrosis Introns Medical sciences Membrane Glycoproteins - genetics Membrane Glycoproteins - metabolism Membrane Proteins - genetics Membrane Proteins - metabolism Mice Mice, Inbred BALB C Molecular Sequence Data Mutation, Missense Nephrology. Urinary tract diseases Polymerase Chain Reaction Polymorphism, Single Nucleotide Proline Thymine Urinary system involvement in other diseases. Miscellaneous Urinary tract. Prostate gland uroplakin Uroplakin Ia Uroplakin Ib Uroplakin II Uroplakin III urothelium Urothelium - embryology Vesico-Ureteral Reflux - genetics vesicoureteral reflux (VUR)
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