TP53 Gene Mutations and 17p Deletions in Human Astrocytomas
- 1 September 1991
- journal article
- research article
- Published by Wiley in Genes, Chromosomes and Cancer
- Vol. 3 (5) , 323-331
- https://doi.org/10.1002/gcc.2870030502
Abstract
No abstract availableKeywords
This publication has 33 references indexed in Scilit:
- Inactivation of the cellular p53 gene is a common feature of Friend virus-induced erythroleukemia: relationship of inactivation to dominant transforming alleles.Molecular and Cellular Biology, 1990
- DETECTION OF p53 PROTEIN IN GLIOMASJournal of Neuropathology and Experimental Neurology, 1990
- Loss of distinct regions on the short arm of chromosome 17 associated with tumorigenesis of human astrocytomas.Proceedings of the National Academy of Sciences, 1989
- The p53 proto-oncogene can act as a suppressor of transformationCell, 1989
- SV40 large tumor antigen forms a specific complex with the product of the retinoblastoma susceptibility geneCell, 1988
- Patient age, histologic features, and length of survival in patients with glioblastoma multiformeCancer, 1987
- Isolation of human‐p53‐specific monoclonal antibodies and their use in the studies of human p53 expressionEuropean Journal of Biochemistry, 1986
- Characterization of the human p53 gene.Molecular and Cellular Biology, 1986
- Brain TumorsPublished by Springer Nature ,1986
- Participation of p53 cellular tumour antigen in transformation of normal embryonic cellsNature, 1984