A murine model of DenysDrash syndrome reveals novel transcriptional targets of WT1 in podocytes

By Ratelade Julien   Arrondel Christelle   Hamard Ghislaine   Garbay Serge   Harvey Scott   Biebuyck Nathalie   Schulz Herbert   Hastie Nick   Pontoglio Marco   Gubler Marie-Claire   Antignac Corinne   Heidet Laurence  

Human Molecular Genetics, Vol. 19, Iss. 1, 2010-01 ,pp. : 1-15

Oxford University Press

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Gonadal Effects of a Mouse Denys-Drash Syndrome Mutation

By Patek C.E.  

Transgenic Research, Vol. 14, Iss. 5, 2005-10 ,pp. : 691-702

Springer Publishing Company

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Murine Denys–Drash syndrome: evidence of podocyte de-differentiation and systemic mediation of glomerulosclerosis

By Patek C.E.  

Human Molecular Genetics, Vol. 12, Iss. 18, 2003-09 ,pp. : 2379-2394

Oxford University Press

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Large genomic fibrillin-1 (FBN1) gene deletions provide evidence for true haploinsufficiency in Marfan syndrome

By Mátyás Gábor   Alonso Sira   Patrignani Andrea   Marti Myriam   Arnold Eliane   Magyar István   Henggeler Caroline   Carrel Thierry   Steinmann Beat   Berger Wolfgang  

Human Genetics, Vol. 122, Iss. 1, 2007-08 ,pp. : 23-32

Springer Publishing Company

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Frasier syndrome is caused by defective alternative splicing of WT1 leading to an altered ratio of WT1 +/–KTS splice isoforms

By Klamt B.  

Human Molecular Genetics, Vol. 7, Iss. 4, 1998-04 ,pp. : 709-714

Oxford University Press

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