Cowden Syndrome–Affected Patients with PTEN Promoter Mutations Demonstrate Abnormal Protein Translation
- 1 October 2007
- journal article
- research article
- Published by Elsevier in American Journal of Human Genetics
- Vol. 81 (4), 756-767
- https://doi.org/10.1086/521051
Abstract
No abstract availableKeywords
This publication has 39 references indexed in Scilit:
- Comparative genomic and functional analyses reveal a novel cis-acting PTEN regulatory element as a highly conserved functional E-box motif deleted in Cowden syndromeHuman Molecular Genetics, 2007
- Unopposed c-MYC expression in benign prostatic epithelium causes a cancer phenotypeThe Prostate, 2005
- Subset of individuals with autism spectrum disorders and extreme macrocephaly associated with germline PTEN tumour suppressor gene mutationsJournal of Medical Genetics, 2005
- Aberrant Regulation of Survivin by the RB/E2F Family of ProteinsJournal of Biological Chemistry, 2004
- PTEN Mutation Spectrum and Genotype-Phenotype Correlations in Bannayan-Riley-Ruvalcaba Syndrome Suggest a Single Entity With Cowden SyndromeHuman Molecular Genetics, 1999
- Databases on transcriptional regulation: TRANSFAC, TRRD and COMPELNucleic Acids Research, 1998
- Germline mutations of the PTEN gene in Cowden disease, an inherited breast and thyroid cancer syndromeNature Genetics, 1997
- Bannayan‐Riley‐Ruvalcaba syndromeAmerican Journal of Medical Genetics, 1992
- On Finding All Suboptimal Foldings of an RNA MoleculeScience, 1989
- Point mutations define a sequence flanking the AUG initiator codon that modulates translation by eukaryotic ribosomesCell, 1986