Frequent allelic imbalance suggests involvement of a tumor suppressor gene at 1p36 in the pathogenesis of human lung cancers
- 1 June 2000
- journal article
- Published by Wiley in Genes, Chromosomes and Cancer
- Vol. 28 (3) , 342-346
- https://doi.org/10.1002/1098-2264(200007)28:3<342::aid-gcc13>3.0.co;2-a
Abstract
No abstract availableKeywords
This publication has 18 references indexed in Scilit:
- Deletion mapping of chromosomal region 1p32-pter in primary breast cancerGenes, Chromosomes and Cancer, 1999
- Report of the fourth international workshop on human chromosome 1 mapping 1998Cytogenetic and Genome Research, 1998
- Is a p53-Regulated Inhibitor of G2/M ProgressionMolecular Cell, 1997
- Accumulation of genetic changes during development and progression of hepatocellular carcinoma: Loss of heterozygosity on chromosome arm Ip occurs at an early stage of hepatocarcinogenesisGenes, Chromosomes and Cancer, 1995
- Cytogenetic analysis of short term cultured squamous cell carcinomas of the lungCancer Genetics and Cytogenetics, 1995
- Allelic loss of chromosome 1p36 in neuroblastoma is of preferential maternal origin and correlates with N–myc amplificationNature Genetics, 1993
- The gene for the type II (p75) tumor necrosis factor receptor (TNF-RII) is localized on band 1p36.2?p36.3Human Genetics, 1991
- Loss of alleles from the distal short arm of chromosome 1 occurs late in melanoma tumor progression.Proceedings of the National Academy of Sciences, 1989
- Loss of heterozygosity for the short arm of chromosome 1 in human neuroblastomas: correlation with N-myc amplification.Proceedings of the National Academy of Sciences, 1989
- Mutation and Cancer: Statistical Study of RetinoblastomaProceedings of the National Academy of Sciences, 1971