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Fredrik Vult von Steyern

Researcher at Lund University

Publications -  43
Citations -  1669

Fredrik Vult von Steyern is an academic researcher from Lund University. The author has contributed to research in topics: Fluorescence in situ hybridization & Population. The author has an hindex of 19, co-authored 42 publications receiving 1412 citations.

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Comprehensive genetic analysis identifies a pathognomonic NAB2/STAT6 fusion gene, nonrandom secondary genomic imbalances, and a characteristic gene expression profile in solitary fibrous tumor

TL;DR: The hypothesis that the NAB2/STAT6 fusions will result in altered properties of the transcriptional co‐repressor NAB 2 ‐ a key regulator of the early growth response 1 (EGR1) transcription factor – was corroborated by global gene expression analysis; SFTs showed deregulated expression of EGR1 target genes, as well as of other, developmentally important genes.
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A novel SERPINE1-FOSB fusion gene results in transcriptional up-regulation of FOSB in pseudomyogenic haemangioendothelioma.

TL;DR: In this paper, the authors used chromosome banding analysis, fluorescence in situ hybridization (FISH), mRNA sequencing, RT-PCR and quantitative real-time PCR on a series of morphologically well-characterized pseudomyogenic haemangioendothelioma (PHE) to show that a balanced translocation, t(7;19)(q22;q13), detected as the sole cytogenetic aberration in two cases, results in fusion of the SERPINE1 and FOSB genes.
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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

TL;DR: The results suggest that this tumor constitutes an interesting model for evaluating the cellular effects of AHR signaling, and global gene expression analysis showed upregulation of CYP1A1 as well as other typical target genes of this pathway, such as those encoding toll‐like receptors.
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Recurrent Rearrangement of the PHF1 Gene in Ossifying Fibromyxoid Tumors

TL;DR: In this paper, the authors identified different structural rearrangements of chromosome band 6p21 in tumor cells from three cases of osteogenesis fibromyxoid tumor (OFMT), including one with typical, one with atypical, and one with malignant morphological features.