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- 2020
-
Loss of NF2 defines a genetic subgroup of non-FOS-rearranged osteoblastoma
Saba, Karim H. LU
; Cornmark, Louise
LU
; Hofvander, Jakob
LU
; Magnusson, Linda
LU
; Nilsson, Jenny
LU
; van den Bos, Hilda
; Spierings, Diana C.J.
; Foijer, Floris
; Staaf, Johan
LU
and Brosjö, Otte
, et al.
(2020)
In Journal of Pathology: Clinical Research
6(4).
p.231-237
Mark
- 2019
-
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
Saba, Karim H LU
; Cornmark, Louise
LU
; Rissler, Marianne
LU
; Fioretos, Thoas
LU
; Åström, Kristina
; Haglund, Felix
; Rosenberg, Andrew E
; Brosjö, Otte
and Nord, Karolin H
LU
(2019)
In Genes, Chromosomes and Cancer
58(10).
p.731-736
Mark
- 2018
- Different patterns of clonal evolution among different sarcoma subtypes followed for up to 25 years
- EURO-B.O.S.S. : A European study on chemotherapy in bone-sarcoma patients aged over 40: Outcome in primary high-grade osteosarcoma
- 2015
- Prognostic factors and follow-up strategy for superficial soft-tissue sarcomas: Analysis of 622 surgically treated patients from the scandinavian sarcoma group register.
- RNA sequencing of sarcomas with simple karyotypes: identification and enrichment of fusion transcripts.
- Recurrent PRDM10 Gene Fusions in Undifferentiated Pleomorphic Sarcoma.
- 2014
- Fetthaltiga mjukdelstumörer i rörelseapparaten ofta godartade.
- Integrative Genome and Transcriptome Analyses Reveal Two Distinct Types of Ring Chromosome in Soft Tissue Sarcomas.
-
Fusions involving protein kinase C and membrane-associated proteins in benign fibrous histiocytoma.
Płaszczyca, Anna ; Nilsson, Jenny LU ; Magnusson, Linda LU ; Brosjö, Otte ; Larsson, Olle ; Vult von Steyern, Fredrik LU ; Domanski, Henryk LU ; Lilljebjörn, Henrik LU
; Fioretos, Thoas
LU
and Tayebwa, Johnbosco
LU
, et al.
(2014)
In International Journal of Biochemistry & Cell Biology
53(Apr 8).
p.475-481
Mark
- 2013
- A Benign Vascular Tumor With a New Fusion Gene: EWSR1-NFATC1 in Hemangioma of the Bone.
- Recurrent chromosome 22 deletions in osteoblastoma affect inhibitors of the wnt/beta-catenin signaling pathway.
- Comprehensive genetic analysis identifies a pathognomonic NAB2/STAT6 fusion gene, nonrandom secondary genomic imbalances, and a characteristic gene expression profile in solitary fibrous tumor.
- 2012
- The MDM2 SNP309 G allele is not preferentially amplified in bone and soft tissue tumors.
- Retained heterodisomy is associated with high gene expression in hyperhaploid inflammatory leiomyosarcoma.