Characterization of a major modifier locus for polycystic kidney disease ( Modpkdr1 ) in the Han:SPRD( cy /+) rat in a region conserved with a mouse modifier locus for Alport syndrome

By Hoffman S.  

Human Molecular Genetics, Vol. 11, Iss. 18, 2002-06 ,pp. : 2165-2173

Oxford University Press

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Autosomal dominant polycystic kidney disease: clues to pathogenesis

By Harris Peter C.  

Human Molecular Genetics, Vol. 8, Iss. 10, 1999-10 ,pp. : 1861-1866

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Genetic interaction studies link autosomal dominant and recessive polycystic kidney disease in a common pathway

By Garcia-Gonzalez Miguel A.   Menezes Luis F.   Piontek Klaus B.   Kaimori Junya   Huso David L.   Watnick Terry   Onuchic Luiz F.   Guay-Woodford Lisa M.   Germino Gregory G.  

Human Molecular Genetics, Vol. 16, Iss. 16, 2007-08 ,pp. : 1940-1950

Oxford University Press

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Genetic evidence for a trans -heterozygous model for cystogenesis in autosomal dominant polycystic kidney disease

By Koptides Michael   Mean Richard   Demetriou Kyproula   Pierides Alkis   Deltas C. Constantinou  

Human Molecular Genetics, Vol. 9, Iss. 3, 2000-02 ,pp. : 447-452

Oxford University Press

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Strong homophilic interactions of the Ig-like domains of polycystin-1, the protein product of an autosomal dominant polycystic kidney disease gene, PKD1

By Ibraghimov-Beskrovnaya Oxana   Bukanov Nikolay O.   Donohue Lincoln C.   Dackowski William R.   Klinger Katherine W.   Landes Gregory M.  

Human Molecular Genetics, Vol. 9, Iss. 11, 2000-07 ,pp. : 1641-1649

Oxford University Press

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