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- 2017
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Mark
In-depth genetic analysis of sclerosing epithelioid fibrosarcoma reveals recurrent genomic alterations and potential treatment targets
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- Contribution to journal › Article
- 2013
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Mark
Comprehensive genetic analysis identifies a pathognomonic NAB2/STAT6 fusion gene, nonrandom secondary genomic imbalances, and a characteristic gene expression profile in solitary fibrous tumor.
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- Contribution to journal › Article
- 2012
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Mark
FOSL1 as a candidate target gene for 11q12 rearrangements in desmoplastic fibroblastoma.
(
- Contribution to journal › Article
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Mark
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 genes.
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- Contribution to journal › Article
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Mark
Malignant fibrous histiocytoma and fibrosarcoma of bone: a re-assessment in the light of currently employed morphological, immunohistochemical and molecular approaches
(
- Contribution to journal › Article
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Mark
Recurrent Rearrangement of the PHF1 Gene in Ossifying Fibromyxoid Tumors.
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- Contribution to journal › Article
- 2011
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Mark
The t(X;6) in subungual exostosis results in transcriptional deregulation of the gene for insulin receptor substrate 4.
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- Contribution to journal › Article
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Mark
Somatic mosaic IDH1 and IDH2 mutations are associated with enchondroma and spindle cell hemangioma in Ollier disease and Maffucci syndrome
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- Contribution to journal › Article
- 2010
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Mark
Heterogeneous and Complex Rearrangements of Chromosome Arm 6q in Chondromyxoid Fibroma. Delineation of Breakpoints and Analysis of Candidate Target Genes.
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- Contribution to journal › Article
- 2009
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Mark
Two genetic pathways, t(1;10) and amplification of 3p11-12, in myxoinflammatory fibroblastic sarcoma, haemosiderotic fibrolipomatous tumour, and morphologically similar lesions.
(
- Contribution to journal › Article