Alterations of the MMAC1/PTEN Gene in Lymphoid Malignancies
Open Access
- 1 June 1998
- journal article
- Published by American Society of Hematology in Blood
- Vol. 91 (11) , 4388-4390
- https://doi.org/10.1182/blood.v91.11.4388
Abstract
No abstract availableThis publication has 8 references indexed in Scilit:
- The Role of MMAC1 Mutations in Early-Onset Breast Cancer: Causative in Association with Cowden Syndrome and Excluded in BRCA1-Negative CasesAmerican Journal of Human Genetics, 1997
- P-TEN, the tumor suppressor from human chromosome 10q23, is a dual-specificity phosphataseProceedings of the National Academy of Sciences, 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
- Recurrent abnormalities of chromosome bands 10q23–25 in non-Hodgkin's lymphomaGenes, Chromosomes and Cancer, 1992
- The mutational spectrum of single base-pair substitutions in mRNA splice junctions of human genes: Causes and consequencesHuman Genetics, 1992
- SPLICING OF MESSENGER RNA PRECURSORSAnnual Review of Biochemistry, 1986