Identification of a novel PTEN intronic deletion in Li-Fraumeni syndrome and its effect on RNA processing
- 1 November 2000
- journal article
- Published by Elsevier in Cancer Genetics and Cytogenetics
- Vol. 123 (1) , 65-68
- https://doi.org/10.1016/s0165-4608(00)00303-4
Abstract
No abstract availableKeywords
This publication has 21 references indexed in Scilit:
- Exclusion of a major role for the PTEN tumour-suppressor gene in breast carcinomasBritish Journal of Cancer, 1999
- Allelic loss of chromosome 10q23 is associated with tumor progression in breast carcinomasOncogene, 1998
- PTEN/MMAC1/TEP1 involvement in primary prostate cancersOncogene, 1998
- PTEN mutations in gliomas and glioneuronal tumorsOncogene, 1998
- Germline mutations in PTEN are present in Bannayan-Zonana syndromeNature Genetics, 1997
- Germline mutations of the PTEN gene in Cowden disease, an inherited breast and thyroid cancer syndromeNature Genetics, 1997
- Identification of a candidate tumour suppressor gene, MMAC1, at chromosome 10q23.3 that is mutated in multiple advanced cancersNature Genetics, 1997
- PTEN , a Putative Protein Tyrosine Phosphatase Gene Mutated in Human Brain, Breast, and Prostate CancerScience, 1997
- Germ-line transmission of a mutated p53 gene in a cancer-prone family with Li–Fraumeni syndromeNature, 1990
- Germ Line p53 Mutations in a Familial Syndrome of Breast Cancer, Sarcomas, and Other NeoplasmsScience, 1990