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

Access to resources Recommend Favorite

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

Access to resources Recommend Favorite

WT1 Haploinsufficiency Supports Milder Renal Manifestation in Two Patients with Denys-Drash Syndrome

By  

Sexual Development, Vol. 11, Iss. 1, 2017-01 ,pp. : 34-39

Karger

Access to resources Recommend Favorite

Sex-specific roles of -catenin in mouse gonadal development

By Liu Chia-Feng   Bingham Nathan   Parker Keith   Yao Humphrey H.-C.  

Human Molecular Genetics, Vol. 18, Iss. 3, 2009-02 ,pp. : 405-417

Oxford University Press

Access to resources Recommend Favorite

A mouse model of Waardenburg syndrome type 4 with a new spontaneous mutation of the endothelin-B receptor gene

By Matsushima Yoshibumi   Shinkai Yusuke   Kobayashi Yasuhito   Sakamoto Michihiro   Kunieda Tetsuo   Tachibana Masayoshi  

Mammalian Genome, Vol. 13, Iss. 1, 2002-01 ,pp. : 30-35

Springer Publishing Company

Access to resources Recommend Favorite