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Steroid-resistant nephrotic syndrome and congenital anomalies of kidneys: Evidence of locus on chromosome 13q

Abhay Vats, Chandra Ishwad, Kalyani Vats, Michael L. Moritz, Demetrius Ellis, Christine M. Mueller, Urvashi Surti, Maria Parizhskaya, Manuel P. Meza, Leah W. Burke,

Kidney International · 2003 · 20 citations · 30 references

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30

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

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Mutations in ACTN4, encoding α-actinin-4, cause familial focal segmental glomerulosclerosis

Joshua M. Kaplan, Sung Hyun Kim, Kathryn N. North et al. · Nature Genetics · 2000 · 1.2K citations

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A principle for counting tissue structures on random sections

Ewald R. Weibel, Domingo M. Gómez · Journal of Applied Physiology · 1962 · 836 citations

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A human homologue of the Drosophila eyes absent gene underlies Branchio-Oto-Renal (BOR) syndrome and identifies a novel gene family

Sonia Abdelhak, Vasiliki Kalatzis, Roland Heilig et al. · Nature Genetics · 1997 · 679 citations

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GATA3 haplo-insufficiency causes human HDR syndrome

Hilde Van Esch, Peter Groenen, M. Andrew Nesbit et al. · Nature · 2000 · 654 citations

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