Found: 18
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Disruption of the TP53 locus in osteosarcoma leads to TP53 promoter gene fusions and restoration of parts of the TP53 signalling pathway.
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- Journal of Pathology, 2024, v. 262, n. 2, p. 147, doi. 10.1002/path.6219
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- Article
Loss of the tumour suppressor gene AIP mediates the browning of human brown fat tumours.
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- Journal of Pathology, 2017, v. 243, n. 2, p. 160, doi. 10.1002/path.4945
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- Article
A novel SERPINE1-FOSB fusion gene results in transcriptional up-regulation of FOSB in pseudomyogenic haemangioendothelioma.
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- Journal of Pathology, 2014, v. 232, n. 5, p. 534, doi. 10.1002/path.4322
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- Article
GRM1 is upregulated through gene fusion and promoter swapping in chondromyxoid fibroma.
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- Nature Genetics, 2014, v. 46, n. 5, p. 474, doi. 10.1038/ng.2927
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- Article
Somatic mosaic IDH1 and IDH2 mutations are associated with enchondroma and spindle cell hemangioma in Ollier disease and Maffucci syndrome.
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- Nature Genetics, 2011, v. 43, n. 12, p. 1256, doi. 10.1038/ng.1004
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- Article
Inactivation of RB1, CDKN2A, and TP53 have distinct effects on genomic stability at side‐by‐side comparison in karyotypically normal cells.
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- Genes, Chromosomes & Cancer, 2023, v. 62, n. 2, p. 93, doi. 10.1002/gcc.23096
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- Article
Genetic profiling of a chondroblastoma‐like osteosarcoma/malignant phosphaturic mesenchymal tumor of bone reveals a homozygous deletion of CDKN2A, intragenic deletion of DMD, and a targetable FN1‐FGFR1 gene fusion.
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- Genes, Chromosomes & Cancer, 2019, v. 58, n. 10, p. 731, doi. 10.1002/gcc.22764
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- Article
Recurrent Chromosome 22 Deletions in Osteoblastoma Affect Inhibitors of the Wnt/Beta-Catenin Signaling Pathway.
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- PLoS ONE, 2013, v. 8, n. 11, p. 1, doi. 10.1371/journal.pone.0080725
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- Article
Clonal Evolution through Loss of Chromosomes and Subsequent Polyploidization in Chondrosarcoma.
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- PLoS ONE, 2011, v. 6, n. 9, p. 1, doi. 10.1371/journal.pone.0024977
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- Article
Integrative genome and transcriptome analyses reveal two distinct types of ring chromosome in soft tissue sarcomas.
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- Human Molecular Genetics, 2014, v. 23, n. 4, p. 878, doi. 10.1093/hmg/ddt479
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- Article
Ring chromosomes, breakpoint clusters, and neocentromeres in sarcomas.
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- Genes, Chromosomes & Cancer, 2015, v. 54, n. 3, p. 156, doi. 10.1002/gcc.22228
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- Article
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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- Genes, Chromosomes & Cancer, 2013, v. 52, n. 10, p. 873, doi. 10.1002/gcc.22083
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- Article
A novel GTF2I/NCOA2 fusion gene emphasizes the role of NCOA2 in soft tissue angiofibroma development.
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- Genes, Chromosomes & Cancer, 2013, v. 52, n. 3, p. 330, doi. 10.1002/gcc.22033
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- Article
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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- Genes, Chromosomes & Cancer, 2012, v. 51, n. 5, p. 510, doi. 10.1002/gcc.21939
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- Article
Gene expression and single nucleotide polymorphism array analyses of spindle cell lipomas and conventional lipomas with 13q14 deletion.
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- Genes, Chromosomes & Cancer, 2011, v. 50, n. 8, p. 619, doi. 10.1002/gcc.20884
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- Article
Loss of NF2 defines a genetic subgroup of non‐FOS‐rearranged osteoblastoma.
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- Journal of Pathology: Clinical Research, 2020, v. 6, n. 4, p. 231, doi. 10.1002/cjp2.172
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- Article
NTRK fusions in osteosarcoma are rare and non‐functional events.
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- Journal of Pathology: Clinical Research, 2020, v. 6, n. 2, p. 107, doi. 10.1002/cjp2.158
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- Article
CDK4 is co-amplified with either TP53 promoter gene fusions or MDM2 through distinct mechanisms in osteosarcoma.
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- NPJ Genomic Medicine, 2024, v. 9, n. 1, p. 1, doi. 10.1038/s41525-024-00430-y
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- Article