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Anne Forus

Researcher at University of Oslo

Publications -  50
Citations -  2588

Anne Forus is an academic researcher from University of Oslo. The author has contributed to research in topics: Comparative genomic hybridization & Chromosome 12. The author has an hindex of 27, co-authored 49 publications receiving 2533 citations. Previous affiliations of Anne Forus include Radboud University Nijmegen & Oslo University Hospital.

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Structure of the Supernumerary Ring and Giant Rod Chromosomes in Adipose Tissue Tumors

TL;DR: This work extensively investigated the structure and composition of rings and giant rods in a series of 17 WDLPS‐ALP samples and three intra‐ or intermuscular lipomas (IMLP), revealing a unique combination of particular features strikingly related to these tumors.
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MDM2 Gene Amplification and Transcript Levels in Human Sarcomas: Relationship to TP53 Gene Status

TL;DR: Signs are provided that increased MDM2 expression level, caused by gene amplification or altered regulation of transcription, is involved in tumor progression of some, but not all, sarcoma subtypes.
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Complex composition and co-amplification of SAS and MDM2 in ring and giant rod marker chromosomes in well-differentiated liposarcoma.

TL;DR: To begin to fathom the function of the extra abnormal chromosomes, the amplification of genes, including SAS, MDM2, and GADDI53/CHOP, known to be in the region 12q 13–14 were examined and SAS andMDM2 demonstrated constant co‐amplification.
Journal Article

Mapping of amplification units in the q13-14 region of chromosome 12 in human sarcomas: some amplica do not include MDM2

TL;DR: A panel of 98 human sarcomas of different subtypes was analyzed to characterize the 12q13-14 amplica and determine which of the genes GLI, A2MR, SAS, MDM2, and GADD153 (CHOP) in this region was most consistently amplified.
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Comparative genomic hybridization analysis of human sarcomas: II. Identification of novel amplicons at 6p and 17p in osteosarcomas

TL;DR: Using comparative genomic hybridization (CGH), regions of DNA amplification in primary and metastatic osteosarcomas are identified and mapped, indicating that these regions may harbor genes relevant for the development of these tumors.