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- 2024
-
Mark
Gene amplification in neoplasia : A cytogenetic survey of 80 131 cases
(
- Contribution to journal › Article
- 2023
-
Mark
Giemsa-negative chromosome bands preferentially recombine in cancer-associated translocations and gene fusions
(
- Contribution to journal › Article
-
Mark
Transcriptomic subtyping of malignant peripheral nerve sheath tumours highlights immune signatures, genomic profiles, patient survival and therapeutic targets
(
- Contribution to journal › Article
- 2020
-
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
- 2019
-
Mark
Cancer chromosome breakpoints cluster in gene-rich genomic regions
(
- Contribution to journal › Article
-
Mark
Most gene fusions in cancer are stochastic events
(
- Contribution to journal › Article
- 2018
-
Mark
Different patterns of clonal evolution among different sarcoma subtypes followed for up to 25 years
(
- Contribution to journal › Article
-
Mark
Inferior survival for patients with malignant peripheral nerve sheath tumors defined by aberrant TP53
(
- Contribution to journal › Article
- 2017
-
Mark
Scattered genomic amplification in dedifferentiated liposarcoma
(
- Contribution to journal › Article
- 2016
-
Mark
Genetic heterogeneity in rhabdomyosarcoma revealed by SNP array analysis.
(
- Contribution to journal › Article
- 2015
-
Mark
Soft tissue tumors
2015) p.583-614(
- Chapter in Book/Report/Conference proceeding › Book chapter
-
Mark
Tumors of bone
2015) p.566-582(
- Chapter in Book/Report/Conference proceeding › Book chapter
-
Mark
RNA sequencing of sarcomas with simple karyotypes: identification and enrichment of fusion transcripts.
(
- Contribution to journal › Article
-
Mark
Recurrent PRDM10 Gene Fusions in Undifferentiated Pleomorphic Sarcoma.
(
- Contribution to journal › Article
-
Mark
Protein expression of BIRC5, TK1, and TOP2A in malignant peripheral nerve sheath tumours - A prognostic test after surgical resection.
(
- Contribution to journal › Article
- 2014
-
Mark
Rearrangements of chromosome bands 15q12-q21 are secondary to HMGA2 deregulation in conventional lipoma.
(
- Contribution to journal › Article
-
Mark
Integrative Genome and Transcriptome Analyses Reveal Two Distinct Types of Ring Chromosome in Soft Tissue Sarcomas.
(
- Contribution to journal › Article
-
Mark
Fusions involving protein kinase C and membrane-associated proteins in benign fibrous histiocytoma.
(
- Contribution to journal › Article
-
Mark
Exomic analysis of myxoid liposarcomas, synovial sarcomas, and osteosarcomas
(
- Contribution to journal › Article
- 2013
-
Mark
Cytogenetic and single nucleotide polymorphism array findings in soft tissue tumors in infants
(
- Contribution to journal › Article
-
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
TERT promoter mutations occur frequently in gliomas and a subset of tumors derived from cells with low rates of self-renewal
(
- Contribution to journal › Article
- 2012
-
Mark
Disease-associated patterns of disomic chromosomes in hyperhaploid neoplasms.
(
- Contribution to journal › Article
-
Mark
Molecular genetic characterization of the 11q13 breakpoint in a desmoplastic fibroma of bone
(
- Contribution to journal › Article
-
Mark
The MDM2 SNP309 G allele is not preferentially amplified in bone and soft tissue tumors.
(
- Contribution to journal › Article
-
Mark
Retained heterodisomy is associated with high gene expression in hyperhaploid inflammatory leiomyosarcoma.
(
- Contribution to journal › Article
-
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
Recurrent Rearrangement of the PHF1 Gene in Ossifying Fibromyxoid Tumors.
(
- Contribution to journal › Article
- 2011
-
Mark
Chromosome banding analysis of cells from fine-needle aspiration biopsy samples from soft tissue and bone tumors: is it clinically meaningful?
(
- Contribution to journal › Article
-
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
Gene expression and single nucleotide polymorphism array analyses of spindle cell lipomas and conventional lipomas with 13q14 deletion.
(
- Contribution to journal › Article
-
Mark
The t(X;6) in subungual exostosis results in transcriptional deregulation of the gene for insulin receptor substrate 4.
(
- Contribution to journal › Article
- 2010
-
Mark
Genomic characteristics of soft tissue sarcomas.
(
- Contribution to journal › Article
-
Mark
Fusion of the FUS and CREB3L2 genes in a supernumerary ring chromosome in low-grade fibromyxoid sarcoma.
(
- Contribution to journal › Article
-
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
-
Mark
Generation of trisomies in cancer cells by multipolar mitosis and incomplete cytokinesis.
(
- Contribution to journal › Article
-
Mark
Genomic Changes in Chromosomes 10, 16, and X in Malignant Peripheral Nerve Sheath Tumors Identify a High-Risk Patient Group.
(
- Contribution to journal › Article
- 2009
-
Mark
Bidirectionality and transcriptional activity of the EWSR1 promoter region
(
- Contribution to journal › Article
-
Mark
Expression levels of HMGA2 in adipocytic tumors correlate with morphologic and cytogenetic subgroups.
(
- Contribution to journal › Article
-
Mark
Characterization of a Hotspot Region on Chromosome 12 for Amplification in Ring Chromosomes in Atypical Lipomatous Tumors
(
- Contribution to journal › Article
-
Mark
Cytogenetic Analysis of 101 Giant Cell Tumors of Bone: Nonrandom Patterns of Telomeric Associations and Other Structural Aberrations
(
- Contribution to journal › Article
-
Mark
Telomeric associations correlate with telomere length reduction and clonal chromosome aberrations in giant cell tumor of bone.
(
- Contribution to journal › Article
-
Mark
Two genetic pathways, t(1;10) and amplification of 3p11-12, in myxoinflammatory fibroblastic sarcoma, haemosiderotic fibrolipomatous tumour, and morphologically similar lesions.
(
- Contribution to journal › Article
-
Mark
Identification of p53 as a strong predictor of survival for patients with malignant peripheral nerve sheath tumors
(
- Contribution to journal › Article
-
Mark
ISCN (2009): Important revisions and new additions to molecular methods for copy number detection for cytogenetic analysis
(
- Contribution to journal › Published meeting abstract
-
Mark
Genomic profiling of chondrosarcoma: chromosomal patterns in central and peripheral tumors.
(
- Contribution to journal › Article
- 2008
-
Mark
Molecular identification of COL6A3-CSF1 fusion transcripts in tenosynovial giant cell tumors
(
- Contribution to journal › Article
-
Mark
Fusion of the COL1A1 and USP6 genes in a benign bone tumor.
(
- Contribution to journal › Article
-
Mark
Cytogenetic and molecular cytogenetic findings in lipoblastoma.
(
- Contribution to journal › Article
-
Mark
POU5F1, encoding a key regulator of stem cell pluripotency, is fused to EWSR1 in hidradenoma of the skin and mucoepidermoid carcinoma of the salivary glands.
(
- Contribution to journal › Article
-
Mark
Heterogeneous genetic profiles in soft tissue myoepitheliomas
(
- Contribution to journal › Article
-
Mark
Frequent deletion of the CDKN2A locus in chordoma: analysis of chromosomal imbalances using array comparative genomic hybridisation.
(
- Contribution to journal › Article
- 2007
-
Mark
Comparison of the proximal promoter regions of the PAX3 and PAX7 genes
(
- Contribution to journal › Article
-
Mark
Successful treatment of a child with t(15;19)-positive tumor.
(
- Contribution to journal › Article
-
Mark
Tiling resolution array comparative genomic hybridization analysis of a fibrosarcoma of bone.
(
- Contribution to journal › Article
-
Mark
Unstable translocation (8;22) in a case of giant cell reparative granuloma.
(
- Contribution to journal › Article
-
Mark
Characterization of the native CREB3L2 transcription factor and the FUS/CREB3L2 chimera
(
- Contribution to journal › Article
-
Mark
Generation of human cortical neurons from a new immortal fetal neural stem cell line.
(
- Contribution to journal › Article
-
Mark
Fusion genes in angiomatoid fibrous histiocytoma
(
- Contribution to journal › Article
-
Mark
Microarray analysis of gliomas reveals chromosomal position-associated gene expression patterns and identifies potential immunotherapy targets.
(
- Contribution to journal › Article
-
Mark
Genetic intratumour heterogeneity in high-grade brain tumours is associated with telomere-dependent mitotic instability.
(
- Contribution to journal › Article
-
Mark
Assessment of the clinical and molecular impact of different cytogenetic subgroups in a series of 272 lipomas with abnormal karyotype
(
- Contribution to journal › Article
- 2006
-
Mark
Truncation and fusion of HMGA2 in lipomas with rearrangements of 5q32-->q33 and 12q14-->q15.
(
- Contribution to journal › Article
-
Mark
Gene copy number changes in dermatofibrosarcoma protuberans - a fine-resolution study using array comparative genomic hybridization
(
- Contribution to journal › Article
-
Mark
Fusion of the SEC31L1 and ALK genes in an inflammatory myofibroblastic tumor.
(
- Contribution to journal › Article
-
Mark
Rearrangement of the COL12A1 and COL4A5 genes in subungual exostosis: molecular cytogenetic delineation of the tumor-specific translocation t(X;6)(q13-14;q22)
(
- Contribution to journal › Article
-
Mark
Prognostic significance of chromosome aberrations in high-grade soft tissue sarcomas
(
- Contribution to journal › Article
-
Mark
Identification of a novel amplicon at distal 17q containing the BIRC5/SURVIVIN gene in malignant peripheral nerve sheath tumours
(
- Contribution to journal › Article
-
Mark
Genomic profiling of bone and soft tissue tumors with supernumerary ring chromosomes using tiling resolution bacterial artificial chromosome microarrays.
(
- Contribution to journal › Article
-
Mark
Gene expression profiles relate to SS18/SSX fusion type in synovial sarcoma
(
- Contribution to journal › Article
- 2005
-
Mark
Absence of mutations of the BRAF gene in malignant melanoma of soft parts (clear cell sarcoma of tendons and aponeuroses)
(
- Contribution to journal › Article
-
Mark
Ewing tumours and synovial sarcomas have critical features of karyotype evolution in common with epithelial tumours.
(
- Contribution to journal › Article
-
Mark
Atypical lipomatous tumor with rare structural rearrangements involving chromosomes 8 and 12
(
- Contribution to journal › Article
-
Mark
Biallelic somatic inactivation of the NF1 gene through chromosomal translocations in a sporadic neurofibroma
(
- Contribution to journal › Article
-
Mark
Structural and numerical chromosome changes in colon cancer develop through telomere-mediated anaphase bridges, not through mitotic multipolarity.
(
- Contribution to journal › Article
-
Mark
Molecular cytogenetic characterization of an ins(4;X) occurring as the sole abnormality in an aggressive, poorly differentiated soft tissue sarcoma.
(
- Contribution to journal › Article
-
Mark
Fusion of the EWSR1 and ATF1 genes without expression of the MITF-M transcript in angiomatoid fibrous histiocytoma
(
- Contribution to journal › Article
-
Mark
Culturing of human tumor cells for use in immune gene tumor therapy
2005) World Federation of Neuro-Oncology Second Quadrennial Meeting and the Sixth Meeting of the European Association for Neuro-Oncology In Neuro-Oncology 7(3). p.371-371(
- Contribution to journal › Published meeting abstract
-
Mark
Clinicopathologic and molecular genetic characterization of low-grade fibromyxoid sarcoma, and cloning of a novel FUS/CREB3L1 fusion gene
(
- Contribution to journal › Article
- 2004
-
Mark
Molecular genetic characterization of the genomic ACTB-GLI fusion in pericytoma with t(7;12).
(
- Contribution to journal › Article
-
Mark
Genetic characterization of bone and soft tissue tumors
(
- Contribution to journal › Article
-
Mark
Expression of DOL54 is not restricted to myxoid liposarcomas with the FUS-DDIT3 chimera but is found in various sarcomas.1
(
- Contribution to journal › Article
-
Mark
Molecular cytogenetic characterization of recurrent translocation breakpoints in bizarre parosteal osteochondromatous proliferation (Nora's lesion).
(
- Contribution to journal › Article
-
Mark
Combined binary ratio labeling fluorescence in situ hybridization analysis of chordoma
(
- Contribution to journal › Article
-
Mark
Telomere shortening and mitotic dysfunction generate cytogenetic heterogeneity in a subgroup of renal cell carcinomas.
(
- Contribution to journal › Article
-
Mark
Mitotic instability associated with late genomic changes in bone and soft tissue tumours.
(
- Contribution to journal › Article
-
Mark
A novel FISH assay for SS18-SSX fusion type in synovial sarcoma
(
- Contribution to journal › Article
-
Mark
Amplification of chromosome 1 sequences in lipomatous tumors and other sarcomas
(
- Contribution to journal › Article
-
Mark
Retained heterodisomy for chromosome 12 in atypical lipomatous tumors: implications for ring chromosome formation.
(
- Contribution to journal › Article
-
Mark
The chimeric FUS/CREB3l2 gene is specific for low-grade fibromyxoid sarcoma.
(
- Contribution to journal › Article
-
Mark
Activation of the GLI Oncogene through Fusion with the beta-Actin Gene (ACTB) in a Group of Distinctive Pericytic Neoplasms: Pericytoma with t(7;12).
(
- Contribution to journal › Article
-
Mark
Abstracts from the Ninth Annual Meeting of the Society for Neuro-Oncology
(
- Contribution to journal › Article
- 2003
-
Mark
Chromosomal abnormalities in inflammatory pseudotumor of the urinary bladder
(
- Contribution to journal › Article
-
Mark
Ring chromosomes and low-grade gene amplification in an atypical lipomatous tumor with minimal nuclear atypia
(
- Contribution to journal › Article
-
Mark
Fusion, disruption, and expression of HMGA2 in bone and soft tissue chondromas
(
- Contribution to journal › Article
-
Mark
Fusion of the FUS and BBF2H7 genes in low grade fibromyxoid sarcoma
(
- Contribution to journal › Article
-
Mark
A novel fusion gene, SS18L1/SSX1, in synovial sarcoma
(
- Contribution to journal › Article
-
Mark
Clustering of deletions on chromosome 13 in benign and low-malignant lipomatous tumors
(
- Contribution to journal › Article
- 2002
-
Mark
RNA splicing mediated by YB-1 is inhibited by TLS/CHOP in human myxoid liposarcoma cells
(
- Contribution to journal › Article
-
Mark
Establishment and characterisation of a human clear cell sarcoma model in nude mice
(
- Contribution to journal › Article
-
Mark
Co-existence of SYT-SSX1 and SYT-SSX2 fusions in synovial sarcomas
(
- Contribution to journal › Article
-
Mark
Fusion of RDC1 with HMGA2 in lipomas as the result of chromosome aberrations involving 2q35-37 and 12q13-15.
(
- Contribution to journal › Article
-
Mark
SYT-SSX is critical for cyclin D1 expression in synovial sarcoma cells: A gain of function of the t(X;18)(p11.2;q11.2) translocation
(
- Contribution to journal › Article
-
Mark
Molecular cytogenetic mapping of recurrent chromosomal breakpoints in tenosynovial giant cell tumors.
(
- Contribution to journal › Article
-
Mark
Chromosomal aberrations in benign and malignant Bilharzia-associated bladder lesions analyzed by comparative genomic hybridization.
(
- Contribution to journal › Article
-
Mark
Cytogenetic aberrations and their prognostic impact in chondrosarcoma
(
- Contribution to journal › Article
-
Mark
Differentially amplified chromosome 12 sequences in low- and high-grade osteosarcoma.
(
- Contribution to journal › Article
-
Mark
Molecular genetic characterization of the EWS/ATF1 fusion gene in clear cell sarcoma of tendons and aponeuroses.
(
- Contribution to journal › Article
-
Mark
Molecular genetic characterization of the EWS/CHN and RBP56/CHN fusion genes in extraskeletal myxoid chondrosarcoma.
(
- Contribution to journal › Article
-
Mark
Prognostically important chromosomal aberrations in soft tissue sarcomas: a report of the Chromosomes and Morphology (CHAMP) Study Group.
(
- Contribution to journal › Article
-
Mark
Correlation between clinicopathological features and karyotype in 100 cartilaginous and chordoid tumours. A report from the Chromosomes and Morphology (CHAMP) Collaborative Study Group
(
- Contribution to journal › Article
-
Mark
A full-coverage, high-resolution human chromosome 22 genomic microarray for clinical and research applications.
(
- Contribution to journal › Article
- 2001
-
Mark
DNA copy number amplifications in sarcomas with homogeneously staining regions and double minutes
(
- Contribution to journal › Article
-
Mark
Identification of cytogenetic subgroups and karyotypic pathways in transitional cell carcinoma
(
- Contribution to journal › Article
-
Mark
No EWS/FLI1 fusion transcripts in giant-cell tumors of bone
(
- Contribution to journal › Article
-
Mark
Multivariate analyses of genomic imbalances in solid tumors reveal distinct and converging pathways of karyotypic evolution
(
- Contribution to journal › Article
-
Mark
Biallelic inactivation of TP53 rarely contributes to the development of malignant peripheral nerve sheath tumors
(
- Contribution to journal › Article
-
Mark
Telomere dysfunction triggers extensive DNA fragmentation and evolution of complex chromosome abnormalities in human malignant tumors
(
- Contribution to journal › Article
-
Mark
Characterization of chromosomal abnormalities in uroepithelial carcinomas by G-banding, spectral karyotyping and fish analysis
(
- Contribution to journal › Article
-
Mark
Comparative genomic hybridization of postirradiation sarcomas
(
- Contribution to journal › Article
-
Mark
Cloning of the der(17)t(X;17)(p11;q25) alveolar soft part sarcoma identifies the ASPL-TFE3 gene fusion, a new molecular diagnostic marker
(
- Contribution to journal › Article
-
Mark
Cloning of the der(17)t(X;17)(p11;q25) of alveolar soft part sarcoma identifies the ASPL-TFE3 gene fusion, a new molecular diagnostic marker
(
- Contribution to journal › Article
-
Mark
The der(17)t(X;17)(p11;q25) of human alveolar soft part sarcoma fuses the TFE3 transcription factor gene to ASPL, a novel gene at 17q25
(
- Contribution to journal › Article
- 2000
-
Mark
Locus-specific multifluor FISH analysis allows physical characterization of complex chromosome abnormalities in neoplasia
(
- Contribution to journal › Article
-
Mark
Radiation-associated sarcomas are characterized by complex karyotypes with frequent rearrangements of chromosome arm 3p
(
- Contribution to journal › Article
-
Mark
Chromosomal breakage-fusion-bridge events cause genetic intratumor heterogeneity
(
- Contribution to journal › Article
- 1999
-
Mark
Variable stability of chromosomes containing amplified alpha-satellite sequences in human mesenchymal tumours
(
- Contribution to journal › Article
-
Mark
Hibernomas are characterized by homozygous deletions in the multiple endocrine neoplasia type I region. Metaphase fluorescence in situ hybridization reveals complex rearrangements not detected by conventional cytogenetics
(
- Contribution to journal › Article
-
Mark
Recurrent t(16;17)(q22;p13) in aneurysmal bone cysts
(
- Contribution to journal › Debate/Note/Editorial
-
Mark
Cytogenetic aberrations in Ewing sarcoma: are secondary changes associated with clinical outcome?
(
- Contribution to journal › Article
-
Mark
Unique cytological features and chromosome aberrations in chondroid lipoma: a case report based on fine-needle aspiration cytology, histopathology, electron microscopy, chromosome banding, and molecular cytogenetics
(
- Contribution to journal › Article
-
Mark
The structure and dynamics of ring chromosomes in human neoplastic and non-neoplastic cells
(
- Contribution to journal › Article
- 1998
-
Mark
A case of dermatofibrosarcoma protuberans with a ring chromosome 5 and a rearranged chromosome 22 containing amplified COL1A1 and PDGFB sequences
(
- Contribution to journal › Article
- 1996
-
Mark
Expression patterns of the human sarcoma-associated genes FUS and EWS and the genomic structure of FUS
(
- Contribution to journal › Article
- 1994
-
Mark
Fusion of the FUS gene with ERG in acute myeloid leukemia with t(16;21)(p11;q22)
(
- Contribution to journal › Article
- 1993
-
Mark
Comparative cytogenetic and DNA flow cytometric analysis of 150 bone and soft-tissue tumors
(
- Contribution to journal › Article
- 1992
-
Mark
Rearrangement of the transcription factor gene CHOP in myxoid liposarcomas with t(12;16)(q13;p11)
(
- Contribution to journal › Article
-
Mark
Chromosome aberrations in 35 primary ovarian carcinomas
(
- Contribution to journal › Article
- 1991
-
Mark
New chromosomal rearrangement, t(12;22)(p13;q12), in acute nonlymphocytic leukemia
(
- Contribution to journal › Article
- 1990
-
Mark
Deletion of 14q in non‐Hodgkin's lymphoma
(
- Contribution to journal › Article
-
Mark
Localization of the chromosomal breakpoints of the t(12;16) in liposarcoma to subbands 12q13.3 and 16p11.2
(
- Contribution to journal › Article
-
Mark
Bone marrow karyotypes in 94 children with acute leukemia
(
- Contribution to journal › Article
-
Mark
Complex karyotypic changes, including rearrangements of 12q13 and 14q24, in two leiomyosarcomas
(
- Contribution to journal › Article
-
Mark
Remarkably long survival of a patient with Ph1-positive chronic myeloid leukemia and 5' bcr rearrangement
(
- Contribution to journal › Article
- 1989
-
Mark
Complex karyotypic anomalies in a bizarre leiomyoma of the uterus.
(
- Contribution to journal › Article
-
Mark
No abnormal C‐band polymorphism in lung cancer patients
(
- Contribution to journal › Article
-
Mark
Characteristic karyotypic anomalies identify subtypes of malignant fibrous histiocytoma
(
- Contribution to journal › Article
- 1988
-
Mark
Do clonal chromosome abnormalities prognosticate early relapse in hodgkin's disease?
(
- Contribution to journal › Letter
-
Mark
Trisomy 5 and t(5;14)(q11;q32) as the sole abnormalities in two different clones from a centroblastic non-Hodgkin's lymphoma
(
- Contribution to journal › Article
-
Mark
Normal frequency of structural chromosome aberrations in fibroblasts from patients with non‐Hodgkin's lymphoma
(
- Contribution to journal › Article
-
Mark
Breakprone chromosome bands in fibroblasts from patients with non‐Hodgkin's lymphoma do not coincide with bands involved in primary rearrangements in non‐Hodgkin's lymphomas
(
- Contribution to journal › Article
- 1987
-
Mark
CYTOGENETIC STUDIES IN HODGKIN'S DISEASE
(
- Contribution to journal › Article
-
Mark
Prognostic implication of cytogenetic findings in 106 patients with non-Hodgkin lymphoma
(
- Contribution to journal › Article
-
Mark
New structural chromosomal rearrangements in congenital leukemia
(
- Contribution to journal › Article
-
Mark
A new specific chromosomal rearrangement, t(8;16) (p11;p13), in acute monocytic leukaemia
(
- Contribution to journal › Article
- 1986
-
Mark
High resolution banding analysis of the reciprocal translocation t(6;9) in acute nonlymphocytic leukemia
(
- Contribution to journal › Article
-
Mark
Reciprocal translocation (11;19)(q23;p13) in congenital acute lymphoblastic leukemia
(
- Contribution to journal › Article
- 1983
-
Mark
Effects of continuous Trichloroethylene inhalation on different strains of mice
(
- Contribution to journal › Article