Infrequent SMARCB1/INI1 gene alteration in epithelioid sarcoma: a useful tool in distinguishing epithelioid sarcoma from malignant rhabdoid tumor
- 1 March 2009
- journal article
- Published by Elsevier BV in Human Pathology
- Vol. 40 (3), 349-355
- https://doi.org/10.1016/j.humpath.2008.08.007
Abstract
No abstract availableKeywords
This publication has 18 references indexed in Scilit:
- Highly aggressive behavior of malignant rhabdoid tumor: a special reference to SMARCB1/INI1 gene alterations using molecular genetic analysis including quantitative real-time PCRZeitschrift für Krebsforschung und Klinische Onkologie, 2007
- hSNF5/INI1‐deficient tumours and rhabdoid tumours are convergent but not fully overlapping entitiesThe Journal of Pathology, 2006
- Extrarenal rhabdoid tumors of soft tissue: Clinicopathological and molecular genetic review and distinction from other soft‐tissue sarcomas with rhabdoid featuresPathology International, 2006
- Prognostic significance of dysadherin expression in epithelioid sarcoma and its diagnostic utility in distinguishing epithelioid sarcoma from malignant rhabdoid tumorLaboratory Investigation, 2006
- Snf5 tumor suppressor couples chromatin remodeling, checkpoint control, and chromosomal stabilityCancer Cell, 2005
- Cancer-associated mutations in chromatin remodeler hSNF5 promote chromosomal instability by compromising the mitotic checkpointGenes & Development, 2005
- Immunohistochemical Analysis of hSNF5/INI1 Distinguishes Renal and Extra-renal Malignant Rhabdoid Tumors From Other Pediatric Soft Tissue TumorsThe American Journal of Surgical Pathology, 2004
- Immunohistochemical Analysis of hSNF5/INI1 in Pediatric CNS NeoplasmsThe American Journal of Surgical Pathology, 2004
- Aberrations of the hSNF5/INI1 gene are restricted to malignant rhabdoid tumors or atypical teratoid/rhabdoid tumors in pediatric solid tumorsGenes, Chromosomes and Cancer, 2002
- Repression and activation by multiprotein complexes that alter chromatin structure.Genes & Development, 1996