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By Kurbegovic Almira   Ct Olivier   Couillard Martin   Ward Christopher J.   Harris Peter C.   Trudel Marie  

Human Molecular Genetics, Vol. 19, Iss. 7, 2010-04 ,pp. : 1174-1189

Oxford University Press

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Kidney-specific inactivation of Ofd1 leads to renal cystic disease associated with upregulation of the mTOR pathway

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Oxford University Press

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Downregulation of NCC and NKCC2 cotransporters by kidney-specific WNK1 revealed by gene disruption and transgenic mouse models

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Human Molecular Genetics, Vol. 20, Iss. 5, 2011-03 ,pp. : 855-866

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Comparative Analysis of the Polycystic Kidney Disease 1 (PKD1) Gene Reveals an Integral Membrane Glycoprotein with Multiple Evolutionary Conserved Domains

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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

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