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The Journal of Pathology|February 10, 2009
Two genetic pathways, t(1;10) and amplification of 3p11-12, in myxoinflammatory fibroblastic sarcoma, haemosiderotic fibrolipomatous tumour, and morphologically similar lesionsKarolin H Hallor, Raf Sciot, Johan Staaf, et al.Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology|December 16, 2003
Topoisomerase-II alpha is upregulated in malignant peripheral nerve sheath tumors and associated with clinical outcomeRolf I Skotheim, Anne Kallioniemi, Bodil Bjerkhagen, et al.The American Journal of Pathology|April 28, 2004
Activation of the GLI oncogene through fusion with the beta-actin gene (ACTB) in a group of distinctive pericytic neoplasms: pericytoma with t(7;12)Anna Dahlén, Christopher D M Fletcher, Fredrik Mertens, et al.Neuro-Oncology|February 3, 2009
Identification of p53 as a strong predictor of survival for patients with malignant peripheral nerve sheath tumorsHelge R Brekke, Matthias Kolberg, Rolf I Skotheim, et al.Clinical Sarcoma Research|May 17, 2012
Reclassification and subtyping of so-called malignant fibrous histiocytoma of bone: comparison with cytogenetic featuresFredrik Mertens, Salvatore Romeo, Judith Vmg Bovée, et al.Modern Pathology : an Official Journal of the United States and Canadian Academy of Pathology, Inc|June 28, 2018
Inferior survival for patients with malignant peripheral nerve sheath tumors defined by aberrant TP53Maren Høland, Matthias Kolberg, Stine Aske Danielsen, et al.Genes, Chromosomes & Cancer|February 17, 2012
Fusion of the AHRR and NCOA2 genes through a recurrent translocation t(5;8)(p15;q13) in soft tissue angiofibroma results in upregulation of aryl hydrocarbon receptor target genesYuesheng Jin, Emely Möller, Karolin H Nord, et al.Cancer Research|July 19, 2002
Prognostically important chromosomal aberrations in soft tissue sarcomas: a report of the Chromosomes and Morphology (CHAMP) Study GroupFredrik Mertens, Ulf Strömberg, Nils Mandahl, et al.Genes, Chromosomes & Cancer|June 14, 2013
Comprehensive genetic analysis identifies a pathognomonic NAB2/STAT6 fusion gene, nonrandom secondary genomic imbalances, and a characteristic gene expression profile in solitary fibrous tumorArezoo Mohajeri, Johnbosco Tayebwa, Anna Collin, et al.Genes, Chromosomes & Cancer|November 6, 2013
Exomic analysis of myxoid liposarcomas, synovial sarcomas, and osteosarcomasChristine G Joseph, Heejung Hwang, Yuchen Jiao, et al.Pageof 10