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Novel X-linked glomerulopathy is associated with a COL4A5 missense mutation in a non-collagenous interruptionBECKNELL, Brian; ZENDER, Gloria A; HOUSTON, Ronald et al.Kidney international. 2011, Vol 79, Num 1, pp 120-127, issn 0085-2538, 8 p.Article

A risk allele for focal segmental glomerulosclerosis in African Americans is located within a region containing APOL1 and MYH9GENOESE, Giulio; TONNA, Stephen J; KNOB, Andrea U et al.Kidney international. 2010, Vol 78, Num 7, pp 698-704, issn 0085-2538, 7 p.Article

A systems view of genetics in chronic kidney diseaseKELLER, Benjamin J; MARTINI, Sebastian; SEDOR, John R et al.Kidney international. 2012, Vol 81, Num 1, pp 14-21, issn 0085-2538, 8 p.Article

Renal outcomes of agalsidase beta treatment for Fabry disease: role of proteinuria and timing of treatment initiationWARNOCK, David G; ORTIZ, Alberto; LEMAY, Roberta et al.Nephrology, dialysis, transplantation (Print). 2012, Vol 27, Num 3, pp 1042-1049, issn 0931-0509, 8 p.Article

The retinitis pigmentosa GTPase regulator interacting protein 1 (RPGRIP1) links RPGR to the nephronophthisis protein networkGERNER, Martin; HARIBASKAR, Ramachandran; PÜTZ, Michael et al.Kidney international. 2010, Vol 77, Num 10, pp 891-896, issn 0085-2538, 6 p.Article

A novel renal carbonic anhydrase type III plays a role in proximal tubule dysfunctionGAILLY, P; JOURET, F; SCHEINMAN, S. J et al.Kidney international. 2008, Vol 74, Num 1, pp 52-61, issn 0085-2538, 10 p.Article

End-stage renal disease in patients with Fabry disease: natural history data from the Fabry RegistryORTIZ, Alberto; CIANCIARUSO, Bruno; WARNOCK, David G et al.Nephrology, dialysis, transplantation (Print). 2010, Vol 25, Num 3, pp 769-775, issn 0931-0509, 7 p.Article

Genotype―phenotype correlation in primary hyperoxaluria type 1: the p.Gly170Arg AGXT mutation is associated with a better outcomeHARAMBAT, Jérôme; FARGUE, Sonia; DURRBACH, Antoine et al.Kidney international. 2010, Vol 77, Num 5, pp 443-449, issn 0085-2538, 7 p.Article

Transcription factor HNF1β and novel partners affect nephrogenesis. CommentaryFISCHER, Evelyne; PONTOGLIO, Marco; RYFFEL, Gerhart U et al.Kidney international. 2008, Vol 74, Num 2, issn 0085-2538, 145-147, 210-217 [11 p.]Article

Evidence of angiogenesis and microvascular regression in autosomal-dominant polycystic kidney disease kidneys : A corrosion cast studyWEI, W; POPOV, V; WALOCHA, J. A et al.Kidney international. 2006, Vol 70, Num 7, pp 1261-1268, issn 0085-2538, 8 p.Article

Inverted formin 2 mutations with variable expression in patients with sporadic and hereditary focal and segmental glomerulosclerosisGBADEGESIN, Rasheed A; LAVIN, Peter J; OTTATI, Carolina et al.Kidney international. 2012, Vol 81, Num 1, pp 94-99, issn 0085-2538, 6 p.Article

Aberrant glycosylation of IgA1 is inherited in both pediatric IgA nephropathy and Henoch-Schönlein purpura nephritisKIRYLUK, Krzysztof; MOLDOVEANU, Zina; SANDERS, John T et al.Kidney international. 2011, Vol 80, Num 1, pp 79-87, issn 0085-2538, 9 p.Article

A missense mutation in podocin leads to early and severe renal disease in micePHILIPPE, A; WEBER, S; ESQUIVEL, E. L et al.Kidney international. 2008, Vol 73, Num 9, pp 1038-1047, issn 0085-2538, 10 p.Article

Genetics of hypercalciuric stone forming diseasesDEVUYST, O; PIRSON, Y.Kidney international. 2007, Vol 72, Num 9, pp 1065-1072, issn 0085-2538, 8 p.Article

Alterations of uromodulin biology : A common denominator of the genetically heterogeneous FJHN/MCKD syndromeVYLET'AL, P; KUBLOVA, M; SIMMONDS, A et al.Kidney international. 2006, Vol 70, Num 6, pp 1155-1169, issn 0085-2538, 15 p.Article

α- and β-Adducin polymorphisms affect podocyte proteins and proteinuria in rodents and decline of renal function in human IgA nephropathyFERRANDI, Mara; CUSI, Daniele; PETERS, Luanne L et al.Journal of molecular medicine (Berlin. Print). 2010, Vol 88, Num 2, pp 203-217, issn 0946-2716, 15 p.Article