1 – 44 of 44
- show: 250
- |
- sort: year (new to old)
Close
Embed this list
<iframe src=" "
width=" "
height=" "
allowtransparency="true"
frameborder="0">
</iframe>
- 2024
-
Mark
MDM2 amplification in rod-shaped chromosomes provides clues to early stages of circularized gene amplification in liposarcoma
(
- Contribution to journal › Article
-
Mark
Disruption of the TP53 locus in osteosarcoma leads to TP53 promoter gene fusions and restoration of parts of the TP53 signalling pathway
(
- Contribution to journal › Article
-
Mark
Osteosarcomas With Few Chromosomal Alterations or Adult Onset Are Genetically Heterogeneous
(
- Contribution to journal › Article
- 2023
-
Mark
Inactivation of RB1, CDKN2A and TP53 have distinct effects on genomic stability at side-by-side comparison in karyotypically normal cells
(
- Contribution to journal › Article
-
Mark
Insertion of the CXXC domain of KMT2A into YAP1 : An unusual mechanism behind the formation of a chimeric oncogenic protein
(
- Contribution to journal › Article
- 2022
-
Mark
Overlapping morphological, immunohistochemical and genetic features of superficial CD34-positive fibroblastic tumor and PRDM10-rearranged soft tissue tumor
(
- Contribution to journal › Article
-
Mark
The diagnostic utility of DNA copy number analysis of core needle biopsies from soft tissue and bone tumors
(
- Contribution to journal › Article
-
Mark
Amplification of ERBB2 (HER2) in embryonal rhabdomyosarcoma : A potential treatment target in rare cases?
(
- Contribution to journal › Article
- 2020
-
Mark
NTRK fusions in osteosarcoma are rare and non-functional events
(
- Contribution to journal › Article
-
Mark
Loss of NF2 defines a genetic subgroup of non-FOS-rearranged osteoblastoma
(
- Contribution to journal › Article
-
Mark
Deep sequencing of myxoinflammatory fibroblastic sarcoma
(
- Contribution to journal › Article
-
Mark
Genomic and transcriptomic features of dermatofibrosarcoma protuberans : Unusual chromosomal origin of the COL1A1-PDGFB fusion gene and synergistic effects of amplified regions in tumor development
(
- Contribution to journal › Article
-
Mark
PHF1 fusions cause distinct gene expression and chromatin accessibility profiles in ossifying fibromyxoid tumors and mesenchymal cells
(
- Contribution to journal › Article
- 2019
-
Mark
PRDM10 -rearranged Soft Tissue Tumor : A Clinicopathologic Study of 9 Cases
(
- Contribution to journal › Article
-
Mark
Aberrant receptor tyrosine kinase signaling in lipofibromatosis : a clinicopathological and molecular genetic study of 20 cases
(
- Contribution to journal › Article
-
Mark
Undifferentiated pleomorphic sarcomas with PRDM10 fusions have a distinct gene expression profile
(
- Contribution to journal › Article
- 2017
-
Mark
Frequent low-level mutations of Protein Kinase D2 in angiolipoma
(
- Contribution to journal › Article
-
Mark
In-depth genetic analysis of sclerosing epithelioid fibrosarcoma reveals recurrent genomic alterations and potential treatment targets
(
- Contribution to journal › Article
-
Mark
Loss of the tumor suppressor gene AIP mediates the browning of human brown fat tumors
(
- Contribution to journal › Article
-
Mark
Scattered genomic amplification in dedifferentiated liposarcoma
(
- Contribution to journal › Article
- 2016
-
Mark
FN1-EGF gene fusions are recurrent in calcifying aponeurotic fibroma.
(
- Contribution to journal › Article
- 2015
-
Mark
RNA sequencing of sarcomas with simple karyotypes: identification and enrichment of fusion transcripts.
(
- Contribution to journal › Article
-
Mark
Gene fusion detection in formalin-fixed paraffin-embedded benign fibrous histiocytomas using fluorescence in situ hybridization and RNA sequencing.
(
- Contribution to journal › Article
-
Mark
Recurrent PRDM10 Gene Fusions in Undifferentiated Pleomorphic Sarcoma.
(
- Contribution to journal › Article
-
Mark
Non-fibrosing sclerosing epithelioid fibrosarcoma: An unusual variant.
2015) In Histopathology(
- Contribution to journal › Letter
- 2014
-
Mark
Myoepithelioma of bone with a novel FUS-POU5F1 fusion gene
(
- Contribution to journal › Article
-
Mark
Rearrangements of chromosome bands 15q12-q21 are secondary to HMGA2 deregulation in conventional lipoma.
(
- Contribution to journal › Article
-
Mark
Fusions involving protein kinase C and membrane-associated proteins in benign fibrous histiocytoma.
(
- Contribution to journal › Article
-
Mark
Recurrent EWSR1-CREB3L1 Gene Fusions in Sclerosing Epithelioid Fibrosarcoma.
(
- Contribution to journal › Article
-
Mark
A novel SERPINE1-FOSB fusion gene results in transcriptional up-regulation of FOSB in pseudomyogenic haemangioendothelioma.
(
- Contribution to journal › Article
-
Mark
GRM1 is upregulated through gene fusion and promoter swapping in chondromyxoid fibroma.
(
- Contribution to journal › Article
- 2013
-
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.
(
- Contribution to journal › Article
-
Mark
A Benign Vascular Tumor With a New Fusion Gene: EWSR1-NFATC1 in Hemangioma of the Bone.
(
- Contribution to journal › Article
- 2012
-
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
-
Mark
Biphasic, Hyperdiploid Breast Tumors in Children: A Distinct Entity?
2012) In Journal of Pediatric Hematology/Oncology(
- Contribution to journal › Article
-
Mark
A novel GTF2I/NCOA2 fusion gene emphasizes the role of NCOA2 in soft tissue angiofibroma development.
2012) In Genes, Chromosomes and Cancer(
- Contribution to journal › Letter
-
Mark
Recurrent Rearrangement of the PHF1 Gene in Ossifying Fibromyxoid Tumors.
(
- Contribution to journal › Article
-
Mark
SNP array and FISH findings in two pleomorphic hyalinizing angiectatic tumors.
(
- Contribution to journal › Article
-
Mark
The retinoblastoma gene undergoes rearrangements in BRCA1-deficient basal-like breast cancer.
(
- Contribution to journal › Article
-
Mark
Characterisation of amplification patterns and target genes at chromosome 11q13 in CCND1-amplified sporadic and familial breast tumours.
(
- Contribution to journal › Article
- 2011
-
Mark
HMGA2 and MDM2 expression in lipomatous tumors with partial, low-level amplification of sequences from the long arm of chromosome 12.
(
- Contribution to journal › Article
-
Mark
FUS-CREB3L2/L1-Positive Sarcomas Show a Specific Gene Expression Profile with Upregulation of CD24 and FOXL1.
(
- Contribution to journal › Article
-
Mark
Translocation t(7;19)(q22;q13)-a recurrent chromosome aberration in pseudomyogenic hemangioendothelioma?
(
- Contribution to journal › Article
- 2010
-
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