Search Results - "de Graaff, Marieke A"
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Mediator complex subunit 12 exon 2 mutation analysis in different subtypes of smooth muscle tumors confirms genetic heterogeneity
Published in Human pathology (01-08-2013)“…Summary Recently, heterozygous mutations in exon 2 of the mediator complex subunit 12 gene have been described in 50% to 70% of uterine leiomyomas; the…”
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Molecular signatures of tumor progression in myxoid liposarcoma identified by N-glycan mass spectrometry imaging
Published in Laboratory investigation (01-09-2020)“…Myxoid liposarcoma (MLS) is the second most common subtype of liposarcoma, accounting for ~6% of all sarcomas. MLS is characterized by a pathognomonic…”
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High-Throughput Screening of Myxoid Liposarcoma Cell Lines: Survivin Is Essential for Tumor Growth
Published in Translational oncology (01-08-2017)“…Myxoid liposarcoma (MLS) is a soft tissue sarcoma characterized by a recurrent t(12;16) translocation. Although tumors are initially radio- and chemosensitive,…”
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4
NY-ESO-1 (CTAG1B) expression in mesenchymal tumors
Published in Modern pathology (01-04-2015)“…New York esophageal squamous cell carcinoma 1 (NY-ESO-1, CTAG1B) is a cancer-testis antigen and currently a focus of several targeted immunotherapeutic…”
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Inactivation of SDH and FH cause loss of 5hmC and increased H3K9me3 in paraganglioma/pheochromocytoma and smooth muscle tumors
Published in Oncotarget (17-11-2015)“…Succinate dehydrogenase (SDH) and fumarate hydratase (FH) are tricarboxylic acid (TCA) cycle enzymes and tumor suppressors. Loss-of-function mutations give…”
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High-grade sarcoma diagnosis and prognosis: Biomarker discovery by mass spectrometry imaging
Published in Proteomics (Weinheim) (01-06-2016)“…The combination of high heterogeneity, both intratumoral and intertumoral, with their rarity has made diagnosis, prognosis of high‐grade sarcomas difficult…”
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Inhibition of Bcl-2 family members sensitises soft tissue leiomyosarcomas to chemotherapy
Published in British journal of cancer (24-05-2016)“…Background: Leiomyosarcoma is an aggressive soft tissue sarcoma with a 5-year survival rate of 15 to 60%. Treatment options for inoperable or metastatic…”
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Establishment and characterization of a new human myxoid liposarcoma cell line (DL-221) with the FUS-DDIT3 translocation
Published in Laboratory investigation (01-08-2016)“…Myxoid liposarcoma has the pathognomonic fusion oncogene FUS-DDIT3 encoding a chimeric transcription factor. Metastatic risk is higher with an increased round…”
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A translocation t(6;14) in two cases of leiomyosarcoma: Molecular cytogenetic and array-based comparative genomic hybridization characterization
Published in Cancer genetics (01-11-2015)“…Leiomyosarcomas are malignant mesenchymal tumors that recapitulate smooth muscle cell differentiation. Tumors are characterized by a genetic heterogeneity with…”
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High-Throughput Screening of Myxoid Liposarcoma Cell Lines: Survivin Is Essential for Tumor Growth12
Published in Translational oncology (24-06-2017)“…Myxoid liposarcoma (MLS) is a soft tissue sarcoma characterized by a recurrent t(12;16) translocation. Although tumors are initially radio- and chemosensitive,…”
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Journal Article