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- 2024
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Mark
MDM2 amplification in rod-shaped chromosomes provides clues to early stages of circularized gene amplification in liposarcoma
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- Contribution to journal › Article
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Mark
Osteosarcomas With Few Chromosomal Alterations or Adult Onset Are Genetically Heterogeneous
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- Contribution to journal › Article
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Mark
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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- Contribution to journal › Article
- 2023
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Mark
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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- Contribution to journal › Article
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Mark
Insertion of the CXXC domain of KMT2A into YAP1 : An unusual mechanism behind the formation of a chimeric oncogenic protein
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- Contribution to journal › Article
- 2022
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Mark
Overlapping morphological, immunohistochemical and genetic features of superficial CD34-positive fibroblastic tumor and PRDM10-rearranged soft tissue tumor
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- Contribution to journal › Article
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Mark
The diagnostic utility of DNA copy number analysis of core needle biopsies from soft tissue and bone tumors
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- Contribution to journal › Article
- 2020
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Mark
PHF1 fusions cause distinct gene expression and chromatin accessibility profiles in ossifying fibromyxoid tumors and mesenchymal cells
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- Contribution to journal › Article
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Mark
Loss of NF2 defines a genetic subgroup of non-FOS-rearranged osteoblastoma
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- Contribution to journal › Article
- 2019
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Mark
PRDM10 -rearranged Soft Tissue Tumor : A Clinicopathologic Study of 9 Cases
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- Contribution to journal › Article
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Mark
Gene fusion involving the insulin-like growth factor 1 receptor in an ALK-negative inflammatory myofibroblastic tumour
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- Contribution to journal › Article
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Mark
Aberrant receptor tyrosine kinase signaling in lipofibromatosis : a clinicopathological and molecular genetic study of 20 cases
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- Contribution to journal › Article
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Mark
Undifferentiated pleomorphic sarcomas with PRDM10 fusions have a distinct gene expression profile
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- Contribution to journal › Article
- 2017
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Mark
Frequent low-level mutations of Protein Kinase D2 in angiolipoma
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- Contribution to journal › Article
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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
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Mark
Loss of the tumor suppressor gene AIP mediates the browning of human brown fat tumors
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- Contribution to journal › Article
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Mark
Scattered genomic amplification in dedifferentiated liposarcoma
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- Contribution to journal › Article
- 2016
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Mark
FN1-EGF gene fusions are recurrent in calcifying aponeurotic fibroma.
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- Contribution to journal › Article
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Mark
High resolution digital autoradiographic and dosimetric analysis of heterogeneous radioactivity distribution in xenografted prostate tumors
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- Contribution to journal › Article
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Mark
Genetic heterogeneity in rhabdomyosarcoma revealed by SNP array analysis.
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- Contribution to journal › Article
- 2015
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Mark
RNA sequencing of sarcomas with simple karyotypes: identification and enrichment of fusion transcripts.
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- Contribution to journal › Article
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Mark
Gene fusion detection in formalin-fixed paraffin-embedded benign fibrous histiocytomas using fluorescence in situ hybridization and RNA sequencing.
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- Contribution to journal › Article
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Mark
Recurrent PRDM10 Gene Fusions in Undifferentiated Pleomorphic Sarcoma.
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- Contribution to journal › Article
- 2014
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Mark
Rearrangements of chromosome bands 15q12-q21 are secondary to HMGA2 deregulation in conventional lipoma.
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- Contribution to journal › Article
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Mark
Fusions involving protein kinase C and membrane-associated proteins in benign fibrous histiocytoma.
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- Contribution to journal › Article
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Mark
Integrative Genome and Transcriptome Analyses Reveal Two Distinct Types of Ring Chromosome in Soft Tissue Sarcomas.
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- Contribution to journal › Article
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Mark
A novel SERPINE1-FOSB fusion gene results in transcriptional up-regulation of FOSB in pseudomyogenic haemangioendothelioma.
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- Contribution to journal › Article
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Mark
GRM1 is upregulated through gene fusion and promoter swapping in chondromyxoid fibroma.
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- Contribution to journal › Article
- 2013
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Mark
Recurrent chromosome 22 deletions in osteoblastoma affect inhibitors of the wnt/beta-catenin signaling pathway.
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- Contribution to journal › Article
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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
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Mark
Cytogenetic and single nucleotide polymorphism array findings in soft tissue tumors in infants
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- Contribution to journal › Article
- 2012
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Mark
SNP array and FISH findings in two pleomorphic hyalinizing angiectatic tumors.
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- Contribution to journal › Article
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Mark
Recurrent Rearrangement of the PHF1 Gene in Ossifying Fibromyxoid Tumors.
(
- 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.
(
- Contribution to journal › Article
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Mark
Biphasic, Hyperdiploid Breast Tumors in Children: A Distinct Entity?
2012) In Journal of Pediatric Hematology/Oncology(
- Contribution to journal › Article
- 2011
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Mark
Gene expression and single nucleotide polymorphism array analyses of spindle cell lipomas and conventional lipomas with 13q14 deletion.
(
- Contribution to journal › Article
- 2010
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Mark
Concomitant deletions of tumor suppressor genes MEN1 and AIP are essential for the pathogenesis of the brown fat tumor hibernoma.
(
- Contribution to journal › Article