WT1 and PAX-2 Podocyte Expression in Denys-Drash Syndrome and Isolated Diffuse Mesangial Sclerosis

This publication has 59 references indexed in Scilit:

• Identification of Constitutional WT1 Mutations, in Patients with Isolated Diffuse Mesangial Sclerosis, and Analysis of Genotype/Phenotype Correlations by Use of a Computerized Mutation Database
  American Journal of Human Genetics, 1998
• Expression of the Wilms' tumour gene WT1 in the developing human and in paediatric renal tumours: an immunohistochemical study.
  Molecular Pathology, 1997
• Identification of nuclear localization signals within the zinc fingers of the WT1 tumor suppressor gene product
  FEBS Letters, 1996
• DNA binding capacity of the WT1 protein is abolished by Denys—Drash syndrome WT1 point mutations
  Human Molecular Genetics, 1995
• Microcephaly and congenital nephrotic syndrome owing to diffuse mesangial sclerosis: an autosomal recessive syndrome.
  Journal of Medical Genetics, 1994
• WT-1 is required for early kidney development
  Cell, 1993
• Evidence that WT1 mutations in Denys — Drash syndrome patients may act in a dominant-negative fashion
  Human Molecular Genetics, 1993
• Germline mutations in the Wilms' tumor suppressor gene are associated with abnormal urogenital development in Denys-Drash syndrome
  Cell, 1991
• FAMILIAL EARLY‐ONSET NEPHROTIC SYNDROME: DIFFUSE MESANGIAL SCLEROSIS
  Acta Paediatrica, 1982
• A syndrome of pseudohermaphroditism, Wilms' tumor, hypertension, and degenerative renal disease
  The Journal of Pediatrics, 1970