Physical Interaction between Wilms Tumor 1 and p73 Proteins Modulates Their Functions
Open Access
- 1 April 2000
- journal article
- Published by Elsevier in Journal of Biological Chemistry
- Vol. 275 (14) , 10202-10211
- https://doi.org/10.1074/jbc.275.14.10202
Abstract
No abstract availableKeywords
This publication has 59 references indexed in Scilit:
- The Wilms tumor suppressor gene wt1 is required for development of the spleenCurrent Biology, 1999
- Frasier syndrome is caused by defective alternative splicing of WT1 leading to an altered ratio of WT1 +/-KTS splice isoformsHuman Molecular Genetics, 1998
- Donor splice-site mutations in WT1 are responsible for Frasier syndromeNature Genetics, 1997
- WT-1 is required for early kidney developmentCell, 1993
- The expression of the Wilms' tumour gene, WT1, in the developing mammalian embryoMechanisms of Development, 1993
- Cytogenetics and molecular genetics of Wilms' Tumor of childhoodCancer Genetics and Cytogenetics, 1992
- Germline mutations in the Wilms' tumor suppressor gene are associated with abnormal urogenital development in Denys-Drash syndromeCell, 1991
- Role for the Wilms tumor gene in genital development?Proceedings of the National Academy of Sciences, 1990
- The candidate Wilms' tumour gene is involved in genitourinary developmentNature, 1990
- Isolation and characterization of a zinc finger polypeptide gene at the human chromosome 11 Wilms' tumor locusCell, 1990