Mutations in the Wilms' tumour gene, WT1. What do they mean?
- 31 December 1995
- journal article
- editorial
- Published by Elsevier in European Journal Of Cancer
- Vol. 31 (13-14) , 2138-2140
- https://doi.org/10.1016/0959-8049(95)00558-7
Abstract
No abstract availableThis publication has 14 references indexed in Scilit:
- Splicing of exon 5 in the WT1 gene is disrupted in Wilms' tumourEuropean Journal Of Cancer, 1995
- P-element repressor autoregulation involves germ-line transcriptional repression and reduction of third intron splicing.Genes & Development, 1995
- A critical mutation in both WT1 alleles is not sufficient to cause Wilms' tumorFEBS Letters, 1995
- Expression of the wilms' tumor gene WT1 in human malignant mesothelioma cell lines and relationship to platelet‐derived growth factor A and insulin‐like growth factor 2 expressionGenes, Chromosomes and Cancer, 1995
- Infrequent mutation of theWT1 gene in 77 Wilms' tumorsHuman Mutation, 1994
- WT1 -Mediated Growth Suppression of Wilms Tumor Cells Expressing a WT1 Splicing VariantScience, 1993
- Low frequency of mutations in theWT1 coding region in Wilms' tumorGenes, Chromosomes and Cancer, 1993
- WT-1 is required for early kidney developmentCell, 1993
- The protein Sex-lethal antagonizes the splicing factor U2AF to regulate alternative splicing of transformer pre-mRNANature, 1993
- Isolation and characterization of a zinc finger polypeptide gene at the human chromosome 11 Wilms' tumor locusCell, 1990