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| Content Provider | World Health Organization (WHO)-Global Index Medicus |
|---|---|
| Author | Salomoni, P. Dvorkina, M. Michod, D. |
| Description | Country affiliation: United kingdom Author Affiliation: Salomoni P ( Samantha Dickson Brain Cancer Unit, UCL Cancer Institute, 72 Huntley Street, London WC1E 6BT, UK. p.salomoni@cancer.ucl.ac.uk) |
| Abstract | The promyelocytic leukaemia gene PML was originally identified at the t(15;17) translocation of acute promyelocytic leukaemia, which generates the oncogene PML-retinoic acid receptor . PML epitomises a subnuclear structure called PML nuclear body. Current models propose that PML through its scaffold properties is able to control cell growth and survival at many different levels. Here we discuss the current literature and propose new avenues for investigation. |
| File Format | HTM / HTML |
| e-ISSN | 20414889 |
| DOI | 10.1038/cddis.2011.122 |
| Journal | Cell Death and Disease |
| Volume Number | 3 |
| Language | English |
| Publisher | Nature Publishing Group |
| Publisher Date | 2012-01-12 |
| Publisher Place | Great Britain (UK) |
| Access Restriction | Open |
| Subject Keyword | Translocation, Genetic Research Support, Non-u.s. Gov't Gene Expression Regulation, Neoplastic Oncogene Proteins, Fusion Leukemia, Promyelocytic, Acute Receptors, Retinoic Acid Cell Death Genetics Transcription, Genetic Cell Differentiation Tretinoin Signal Transduction Neoplastic Stem Cells Metabolism Nuclear Proteins Discipline Cell Biology Pathology Animals Cell Cycle Transcription Factors Mice Tumor Suppressor Proteins Cell Nucleus |
| Content Type | Text |
| Resource Type | Article |
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