NPHS2 mutation associated with recurrence of proteinuria after transplantation

NPHS2, encoding the glomerular protein podocin, is mutated in autosomal recessive steroid-resistant nephrotic syndrome

Nicolas Boute, Olivier Gribouval, Séverine Roselli et al. · Nature Genetics · 2000 · 1.4K citations

Medicine, Genetics, Nephrology +13

Novel Mutations in NPHS2 Detected in Both Familial and Sporadic Steroid-Resistant Nephrotic Syndrome

Stephanie M. Karle, Barbara Uetz, Vera Ronner et al. · Journal of the American Society of Nephrology · 2002 · 248 citations · Full text

Medicine, Genetics, Molecular Genetics +14

NPHS2 mutations in late-onset focal segmental glomerulosclerosis: R229Q is a common disease-associated allele

Hiroyasu Tsukaguchi, Akulapalli Sudhakar, Tu C. Le et al. · Journal of Clinical Investigation · 2002 · 235 citations · Full text

Medicine, Genetics, Molecular Genetics +17

NPHS2 mutations in late-onset focal segmental glomerulosclerosis: R229Q is a common disease-associated allele

Hiroyasu Tsukaguchi, Akulapalli Sudhakar, Tu C. Le et al. · Journal of Clinical Investigation · 2002 · 204 citations · Full text

Medicine, Genetics, Molecular Genetics +17

Co-Localization of Nephrin, Podocin, and the Actin Cytoskeleton

Moin A. Saleem, Lan Ni, Ian R. Witherden et al. · American Journal Of Pathology · 2002 · 180 citations · Full text

Life Sciences, Cell Biology, Molecular Biology +12