Core Programs

Publications

Familial Focal Segmental Glomerulosclerosis (FSGS)

Winn MP, Conlon PJ, Lynn KL, Farrington MK, Creazzo T, Hawkins AF, Daskalakis N, Kwan SY, Ebersviller S, Burchette JL, Pericak-Vance MA, Howell DN, Vance JM, Rosenberg PB. A Mutation in the TRPC6 Cation Channel Causes Familial Focal Segmental Glomerulosclerosis. Science 2005 0: 1106215

Winn MP. Not all in the family: mutations of podocin in sporadic steroid-resistant nephrotic syndrome. J Am Soc Neophrology 13(2):577-579, 2002.

Neary JJ, Conlon PJ, Croke D, Dorman A, Keogan M, Zhang F, Vance JM, Pericak-Vance MA, Scott WK, Winn MP.Linkage of a gene causing familial membranoproliferative glomerulonephritis type III to chromosome 1. J Am Soc Nephrology 13(30:2025-2057, 2002.

Hsu SI, Ramirez SB, Winn MP, Bonventre JV, Owen WF. Evidence for genetic factors in the development and progression IgA nephropathy. Kidney International 57(5):1818-1835, 2000.

Winn MP, Conlon PJ, Lynn KL, Howell DN, Gross DA, Rogala AR, Smith AH, Graham FL, Bembe M, Quarles LD, Pericak-Vance MA, Vance JM. Clinical and genetic heterogeneity in familial focal segmental glomerulosclerosis. International Collaborative Group for the Study of Familial Focal Segmental Glomerulosclerosis. Kidney International 55(4):1241-6, 1999.

Winn MP, Conlon PJ, Lynn KL, Howell DN, Slotterbeck BD, Smith AH, Graham FL, Bembe M, Quarles LD, Pericak-Vance MA, Vance JM. Linkage of a gene causing familial focal segmental glomerulosclerosis to chromosome 11 and further evidence of genetic heterogeneity. Genomics 58(2):113-20, 1999.

Conlon PJ, Lynn K, Winn MP, Quarles LD, Bembe ML, Pericak-Vance M, Speer M, Howell DN. Spectrum of disease in familial focal and segmental glomerulosclerosis. Kidney International 56(5):1863-71, 1999.

Conlon PJ et al. Clinical And Pathological Features of Familial Focal Segmental Glomerulosclerosis. American Journal of Kidney Diseases 26(1):34-40, 1995.

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