Hypermethylation in the retinoblastoma gene is associated with unilateral, sporadic retinoblastoma
- 1 October 1997
- journal article
- Published by Elsevier BV in Cancer Genetics and Cytogenetics
- Vol. 98 (1), 43-49
- https://doi.org/10.1016/s0165-4608(96)00395-0
Abstract
No abstract availableKeywords
This publication has 12 references indexed in Scilit:
- 5′ CpG island methylation is associated with transcriptional silencing of the tumour suppressor p16/CDKN2/MTS1 in human cancersNature Medicine, 1995
- p53 activates expression of HIC-1, a new candidate tumour suppressor gene on 17p13.3Nature Medicine, 1995
- Frequency and parental origin of hypermethylated RB1 alleles in retinoblastomaHuman Genetics, 1994
- Complete Genomic Sequence of the Human Retinoblastoma Susceptibility GeneGenomics, 1993
- Oncogenic germ-line mutations in Sp1 and ATF sites in the human retinoblastoma geneNature, 1991
- Oncogenic Point Mutations in the Human Retinoblastoma Gene: Their Application to Genetic CounselingNew England Journal of Medicine, 1989
- Preferential germline mutation of the paternal allele in retinoblastomaNature, 1989
- Parental origin of mutations of the retinoblastoma geneNature, 1989
- Preferential mutation of paternally derived RB gene as the initial event in sporadic osteosarcomaNature, 1989
- DNA methylation and gene activityCell, 1988