Search Results - "Winand, M"
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SDHA Immunohistochemistry Detects Germline SDHA Gene Mutations in Apparently Sporadic Paragangliomas and Pheochromocytomas
Published in The journal of clinical endocrinology and metabolism (01-09-2011)“…Context: Pheochromocytoma-paraganglioma syndrome is caused by mutations in SDHB, SDHC, and SDHD, encoding subunits of succinate dehydrogenase (SDH), and in…”
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The impact of surgery in molecularly defined low-grade glioma: an integrated clinical, radiological, and molecular analysis
Published in Neuro-oncology (Charlottesville, Va.) (10-01-2018)“…Extensive resections in low-grade glioma (LGG) are associated with improved overall survival (OS). However, World Health Organization (WHO) classification of…”
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Adjuvant Procarbazine, Lomustine, and Vincristine Chemotherapy in Newly Diagnosed Anaplastic Oligodendroglioma: Long-Term Follow-Up of EORTC Brain Tumor Group Study 26951
Published in Journal of clinical oncology (20-01-2013)“…Anaplastic oligodendroglioma are chemotherapy-sensitive tumors. We now present the long-term follow-up findings of a randomized phase III study on the addition…”
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IL-7 Receptor Mutations and Steroid Resistance in Pediatric T cell Acute Lymphoblastic Leukemia: A Genome Sequencing Study
Published in PLoS medicine (20-12-2016)“…Pediatric acute lymphoblastic leukemia (ALL) is the most common childhood cancer and the leading cause of cancer-related mortality in children. T cell ALL…”
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IDH1 and IDH2 Mutations Are Prognostic but not Predictive for Outcome in Anaplastic Oligodendroglial Tumors: A Report of the European Organization for Research and Treatment of Cancer Brain Tumor Group
Published in Clinical cancer research (01-03-2010)“…Recent studies have shown the prognostic significance of IDH1 mutations in glioma. It is yet unclear if IDH1 mutations are predictive for outcome to…”
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Health Promoting Sports Federations: theoretical foundations and guidelines
Published in European journal of public health (24-10-2023)“…Abstract The potential for organised sports to promote health has been underexploited so far, according to researchers and policy-makers. Sports clubs have…”
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Defects in succinate dehydrogenase in gastrointestinal stromal tumors lacking KIT and PDGFRA mutations
Published in Proceedings of the National Academy of Sciences - PNAS (04-01-2011)“…Carney-Stratakis syndrome, an inherited condition predisposing affected individuals to gastrointestinal stromal tumor (GIST) and paraganglioma, is caused by…”
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Molecular classification of anaplastic oligodendroglioma using next-generation sequencing: a report of the prospective randomized EORTC Brain Tumor Group 26951 phase III trial
Published in Neuro-oncology (Charlottesville, Va.) (01-03-2016)“…Histopathological diagnosis of diffuse gliomas is subject to interobserver variation and correlates modestly with major prognostic and predictive molecular…”
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Somatic aberrations of mismatch repair genes as a cause of microsatellite-unstable cancers
Published in The Journal of pathology (01-12-2014)“…Lynch syndrome (LS) is caused by germline mutations in mismatch repair (MMR) genes, resulting in microsatellite‐unstable tumours. Approximately 35% of…”
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Impact of panel design and cut-off on tumour mutational burden assessment in metastatic solid tumour samples
Published in British journal of cancer (01-03-2020)“…Tumour mutational burden (TMB) has emerged as a promising biomarker to predict immune checkpoint inhibitors (ICIs) response in advanced solid cancers. However,…”
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Distinct gene mutation profiles among luminal-type and basal-type breast cancer cell lines
Published in Breast cancer research and treatment (01-05-2010)“…Breast cancer has for long been recognized as a highly diverse tumor group, but the underlying genetic basis has been elusive. Here, we report an extensive…”
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Succinate Dehydrogenase (SDH)-Deficient Pancreatic Neuroendocrine Tumor Expands the SDH-Related Tumor Spectrum
Published in The journal of clinical endocrinology and metabolism (01-10-2015)“…Context: Mutations in genes encoding the subunits of succinate dehydrogenase (SDH) can lead to pheochromocytoma/paraganglioma formation. However, SDH mutations…”
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SDHB immunohistochemistry: a useful tool in the diagnosis of Carney-Stratakis and Carney triad gastrointestinal stromal tumors
Published in Modern pathology (01-01-2011)“…Mutations in the tumor suppressor genes SDHB , SDHC , and SDHD (or collectively SDHx ) cause the inherited paraganglioma syndromes, characterized by…”
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Detection of spontaneous tumorigenic transformation during culture expansion of human mesenchymal stromal cells
Published in Experimental biology and medicine (Maywood, N.J.) (01-01-2014)“…Human mesenchymal stem/stromal cells (MSCs) have been explored in a number of clinical trials as a possible method of treating various diseases. However, the…”
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Personalised selection of experimental treatment in patients with advanced solid cancer is feasible using whole-genome sequencing
Published in British journal of cancer (01-09-2022)“…Background Biomarker-guided therapy in an experimental setting has been suggested to improve patient outcomes. However, trial-specific pre-screening tests are…”
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Reclassification of two germline DICER1 splicing variants leads to DICER1 syndrome diagnosis
Published in Familial cancer (01-10-2023)“…DICER1 syndrome is an inherited condition associated with an increased risk of developing hamartomatous and neoplastic lesions in diverse organs, mainly at…”
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Verification and Unmasking of Widely Used Human Esophageal Adenocarcinoma Cell Lines
Published in JNCI : Journal of the National Cancer Institute (24-02-2010)“…For decades, hundreds of different human tumor type–specific cell lines have been used in experimental cancer research as models for their respective tumors…”
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Non-pheochromocytoma (PCC)/paraganglioma (PGL) tumors in patients with succinate dehydrogenase-related PCC–PGL syndromes: a clinicopathological and molecular analysis
Published in European journal of endocrinology (01-01-2014)“…ObjectiveAlthough the succinate dehydrogenase (SDH)-related tumor spectrum has been recently expanded, there are only rare reports of…”
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Three-Gene Immunohistochemical Panel Adds to Clinical Staging Algorithms to Predict Prognosis for Patients With Esophageal Adenocarcinoma
Published in Journal of clinical oncology (20-04-2013)“…Esophageal adenocarcinoma (EAC) is a highly aggressive disease with poor long-term survival. Despite growing knowledge of its biology, no molecular biomarkers…”
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