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Molecular Cell|September 12, 1998
Somatic mutation in individual liver cysts supports a two-hit model of cystogenesis in autosomal dominant polycystic kidney diseaseT J Watnick, V E Torres, M A Gandolph, et al.
The Journal of Biological Chemistry|September 25, 1999
Identification and characterization of polycystin-2, the PKD2 gene productY Cai, Y Maeda, A Cedzich, et al.
Clinical Nephrology|February 1, 1991
Oxalate, silicon and vanadium in acquired cystic kidney diseaseJ E Marco-Franco, V E Torres, D E Nixon, et al.
American Journal of Human Genetics|May 1, 1994
Evidence of linkage disequilibrium in the Spanish polycystic kidney disease I populationB Peral, C J Ward, J L San Millán, et al.
American Journal of Human Genetics|January 1, 1996
Screening the 3' region of the polycystic kidney disease 1 (PKD1) gene reveals six novel mutationsB Peral, J L San Millán, A C Ong, et al.
Kidney International|March 1, 1988
Idiopathic membranous nephropathy: the natural history of untreated patientsJ V Donadio, V E Torres, J A Velosa, et al.
Medicine|May 1, 1987
Renal involvement in relapsing polychondritisA Chang-Miller, M Okamura, V E Torres, et al.
The American Journal of Physiology|September 1, 1995
Continuous epithelial cell lines from ADPKD liver cysts exhibit characteristics of intrahepatic biliary epitheliumR D Perrone, S A Grubman, L C Rogers, et al.
Kidney International|June 1, 1988
Mechanisms affecting the development of renal cystic disease induced by diphenylthiazoleV E Torres, T J Berndt, M Okamura, et al.
Human Molecular Genetics|September 25, 1997
The GAP-related domain of tuberin, the product of the TSC2 gene, is a target for missense mutations in tuberous sclerosisM M Maheshwar, J P Cheadle, A C Jones, et al.
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