Search Results - "Dunnen, Wilfred den"
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Mesenchymal Differentiation Mediated by NF-κB Promotes Radiation Resistance in Glioblastoma
Published in Cancer cell (09-09-2013)“…Despite extensive study, few therapeutic targets have been identified for glioblastoma (GBM). Here we show that patient-derived glioma sphere cultures (GSCs)…”
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Hypoxia enhances migration and invasion in glioblastoma by promoting a mesenchymal shift mediated by the HIF1α–ZEB1 axis
Published in Cancer letters (01-04-2015)“…Highlights • Hypoxia is a potent cell specific inducer of mesenchymal trans-differentiation in GBM cells in vitro and also appears to occur in patient…”
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Single-cell whole genome sequencing reveals no evidence for common aneuploidy in normal and Alzheimer's disease neurons
Published in Genome Biology (31-05-2016)“…Alzheimer's disease (AD) is a neurodegenerative disease of the brain and the most common form of dementia in the elderly. Aneuploidy, a state in which cells…”
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VISTA expression by microglia decreases during inflammation and is differentially regulated in CNS diseases
Published in Glia (01-12-2018)“…V‐type immunoglobulin domain‐containing suppressor of T‐cell activation (VISTA) is a negative checkpoint regulator (NCR) involved in inhibition of T…”
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COVID‐19: immunopathology, pathophysiological mechanisms, and treatment options
Published in The Journal of pathology (01-07-2021)“…Coronavirus disease 2019 (COVID‐19), caused by severe acute respiratory syndrome coronavirus 2 (SARS‐CoV‐2), continues to spread globally despite the worldwide…”
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Neurofibromatosis type 1 associated low grade gliomas: A comparison with sporadic low grade gliomas
Published in Critical reviews in oncology/hematology (01-08-2016)“…Abstract Neurofibromatosis type 1 (NF1) is an autosomal dominant disorder, associated with a variable clinical phenotype including café-au-lait spots,…”
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CD146 increases stemness and aggressiveness in glioblastoma and activates YAP signaling
Published in Cellular and molecular life sciences : CMLS (01-08-2022)“…Glioblastoma (GBM), a highly malignant and lethal brain tumor, is characterized by diffuse invasion into the brain and chemo-radiotherapy resistance resulting…”
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Mutations in potassium channel kcnd3 cause spinocerebellar ataxia type 19
Published in Annals of neurology (01-12-2012)“…Objective: To identify the causative gene for the neurodegenerative disorder spinocerebellar ataxia type 19 (SCA19) located on chromosomal region 1p21‐q21…”
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Frequency of nuclear mutant huntingtin inclusion formation in neurons and glia is cell‐type‐specific
Published in Glia (01-01-2017)“…Huntington's disease (HD) is an autosomal dominant inherited neurodegenerative disorder that is caused by a CAG expansion in the Huntingtin (HTT) gene, leading…”
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The Potential of Ferroptosis-Targeting Therapies for Alzheimer's Disease: From Mechanism to Transcriptomic Analysis
Published in Frontiers in aging neuroscience (20-12-2021)“…Alzheimer's disease (AD), the most common form of dementia, currently affects 40-50 million people worldwide. Despite the extensive research into amyloid β…”
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ER stress and UPR activation in glioblastoma: identification of a noncanonical PERK mechanism regulating GBM stem cells through SOX2 modulation
Published in Cell death & disease (18-09-2019)“…Patients with aggressive brain tumors, named glioblastoma multiforme (GBM), have a poor prognoses. Here we explored if the ER stress/unfolded protein response…”
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Genotype―phenotype correlations in spastic paraplegia type 7: a study in a large Dutch cohort
Published in Brain (London, England : 1878) (01-10-2012)“…Spastic paraplegia type 7 is an autosomal recessive neurodegenerative disorder mainly characterized by progressive bilateral lower limb spasticity and referred…”
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Distinct amyloid-β and tau-associated microglia profiles in Alzheimer’s disease
Published in Acta neuropathologica (01-05-2021)“…Alzheimer’s disease (AD) is the most prevalent form of dementia and is characterized by abnormal extracellular aggregates of amyloid-β and intraneuronal…”
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Glioblastoma and its treatment are associated with extensive accelerated brain aging
Published in Aging cell (01-03-2024)“…Progressive neurocognitive dysfunction is the leading cause of a reduced quality of life in patients with primary brain tumors. Understanding how the human…”
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MGMT-STP27 Methylation Status as Predictive Marker for Response to PCV in Anaplastic Oligodendrogliomas and Oligoastrocytomas. A Report from EORTC Study 26951
Published in Clinical cancer research (01-10-2013)“…The long-term follow-up results from the EORTC-26951 trial showed that the addition of procarbazine, CCNU, and vincristine (PCV) after radiotherapy increases…”
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Feasibility of bevacizumab-IRDye800CW as a tracer for fluorescence-guided meningioma surgery
Published in Journal of neurosurgery (01-05-2023)“…Meningiomas are frequently occurring, often benign intracranial tumors. Molecular fluorescence can be used to intraoperatively identify residual meningioma…”
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Possible Obesogenic Effects of Bisphenols Accumulation in the Human Brain
Published in Scientific reports (29-05-2018)“…Evidence of bisphenols’ obesogenic effects on humans is mixed and inconsistent. We aimed to explore the presence of bisphenol A (BPA), bisphenol F (BPF) and…”
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Intrinsic Molecular Subtypes of Glioma Are Prognostic and Predict Benefit From Adjuvant Procarbazine, Lomustine, and Vincristine Chemotherapy in Combination With Other Prognostic Factors in Anaplastic Oligodendroglial Brain Tumors: A Report From EORTC Study 26951
Published in Journal of clinical oncology (20-01-2013)“…Intrinsic glioma subtypes (IGSs) are molecularly similar tumors that can be identified based on unsupervised gene expression analysis. Here, we have evaluated…”
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Involvement of the cerebellum in Parkinson disease and dementia with Lewy bodies
Published in Annals of neurology (01-06-2017)“…Brains from patients with Parkinson disease or dementia with Lewy bodies show aggregation of alpha‐synuclein in precerebellar brainstem structures…”
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On the distribution of intranuclear and cytoplasmic aggregates in the brainstem of patients with spinocerebellar ataxia type 2 and 3
Published in Brain pathology (Zurich, Switzerland) (01-05-2017)“…The polyglutamine (polyQ) diseases are a group of genetically and clinically heterogeneous neurodegenerative diseases, characterized by the expansion of polyQ…”
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