Splicing of exon 5 in the WT1 gene is disrupted in Wilms' tumour
- 31 December 1995
- journal article
- Published by Elsevier in European Journal Of Cancer
- Vol. 31 (13-14), 2270-2276
- https://doi.org/10.1016/0959-8049(95)00474-2
Abstract
No abstract availableKeywords
This publication has 12 references indexed in Scilit:
- Regulation of Alternative Splicing in Vivo by Overexpression of Antagonistic Splicing FactorsScience, 1994
- Multiple aberrant splicing of the p53 transcript without genomic mutations around exon‐intron junctions in a case of chronic myelogenous leukaemia in blast crisis: a possible novel mechanism of p53 inactivationBritish Journal of Haematology, 1994
- WT1 Mutations Associated with Incomplete Denys-Drash Syndrome Define a Domain Predicted to Behave in a Dominant-Negative FashionGenomics, 1994
- RNA editing in the Wilms' tumor susceptibility gene, WT1.Genes & Development, 1994
- Mechanisms for selecting 5′ splice sites in mammalian pre-mRNA splicingTrends in Genetics, 1994
- WT1 -Mediated Growth Suppression of Wilms Tumor Cells Expressing a WT1 Splicing VariantScience, 1993
- Genomic Organization of the Human WT1 GeneJapanese Journal of Cancer Research, 1992
- Modulation of DNA Binding Specificity by Alternative Splicing of the Wilms Tumor wt1 Gene TranscriptScience, 1992
- Germline intronic and exonic mutations in the Wilms' tumour gene (WT1) affecting urogenital developmentNature Genetics, 1992
- Control of Alternative Splicing by the Differential Binding of U1 Small Nuclear Ribonucleoprotein ParticleScience, 1991