Frequent Abnormalities of the P15 and P16 Genes in Mycosis Fungoides and Sezary Syndrome
- 1 March 2002
- journal article
- Published by Elsevier in Journal of Investigative Dermatology
- Vol. 118 (3) , 493-499
- https://doi.org/10.1046/j.0022-202x.2001.01682.x
Abstract
No abstract availableKeywords
This publication has 46 references indexed in Scilit:
- CDKN2A/p16 inactivation in the prognosis of oligodendrogliomasInternational Journal of Cancer, 2000
- Detection of a Peripheral Blood T Cell Clone is an Independent Prognostic Marker in Mycosis FungoidesJournal of Investigative Dermatology, 2000
- Frequent Methylation Silencing of p15INK4b(MTS2) and p16INK4a (MTS1) in B-Cell and T-Cell LymphomasBlood, 1999
- Chromosome 9p21 Loss and p16 Inactivation in Primary Sclerosing Cholangitis-Associated CholangiocarcinomaJournal of Surgical Research, 1999
- Homozygous Deletions at Chromosome 9p21 Involving p16 and p15 Are Associated With Histologic Progression in Follicle Center LymphomaBlood, 1998
- Review of alterations of the cyclin-dependent kinase inhibitor INK4 family genes p15, p16, p18 and p19 in human leukemia–lymphoma cellsLeukemia, 1998
- Frequency of homozygous deletion at p16/CDKN2 in primary human tumoursNature Genetics, 1995
- Deletions of the cyclin-dependent kinase inhibitor genes p16INK4A and p15INK4B in non-Hodgkin's lymphomasBlood, 1995
- Cytogenetics of T-cell malignant lymphomaCancer Genetics and Cytogenetics, 1988
- Cutaneous T cell lymphoma: Mycosis fungoides, Sézary syndrome, and other variantsJournal of the American Academy of Dermatology, 1980