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Authors: Karl Tryggvason
Journal Article
The podocyte protein nephrin is required for cardiac vessel formation Get access
Human Molecular Genetics, Volume 20, Issue 11, 1 June 2011, Pages 2182–2194, https://doi.org/10.1093/hmg/ddr106
Published: 14 March 2011
Journal Article
Genotype/phenotype correlations of NPHS1 and NPHS2 mutations in nephrotic syndrome advocate a functional inter-relationship in glomerular filtration Get access
Human Molecular Genetics, Volume 11, Issue 4, 15 February 2002, Pages 379–388, https://doi.org/10.1093/hmg/11.4.379
Published: 15 February 2002
Journal Article
Defective nephrin trafficking caused by missense mutations in the NPHS1 gene: insight into the mechanisms of congenital nephrotic syndrome Get access
Human Molecular Genetics, Volume 10, Issue 23, 1 November 2001, Pages 2637–2644, https://doi.org/10.1093/hmg/10.23.2637
Published: 01 November 2001
Journal Article
The murine nephrin gene is specifically expressed in kidney, brain and pancreas: inactivation of the gene leads to massive proteinuria and neonatal death Get access
Human Molecular Genetics, Volume 10, Issue 1, 1 January 2001, Pages 1–8, https://doi.org/10.1093/hmg/10.1.1
Published: 01 January 2001
Journal Article
Mild Congenital Muscular Dystrophy in Two Patients with an Internally Deleted Laminin α2-Chain Get access
Human Molecular Genetics, Volume 6, Issue 5, 1 May 1997, Pages 747–752, https://doi.org/10.1093/hmg/6.5.747
Published: 01 May 1997
Journal Article
Deletions of both α5(IV) and α6(IV) collagen genes in Alport syndrome and in Alport syndrome associated with smooth muscle tumours Get access
Human Molecular Genetics, Volume 4, Issue 1, January 1995, Pages 99–108, https://doi.org/10.1093/hmg/4.1.99
Published: 01 January 1995
