Search Results - "Forss, Sonja"
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From peroxisomal disorders to common neurodegenerative diseases – the role of ether phospholipids in the nervous system
Published in FEBS letters (01-09-2017)“…The emerging diverse roles of ether (phospho)lipids in nervous system development and function in health and disease are currently attracting growing interest…”
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Plasmalogens, platelet-activating factor and beyond – Ether lipids in signaling and neurodegeneration
Published in Neurobiology of disease (01-11-2020)“…Glycerol-based ether lipids including ether phospholipids form a specialized branch of lipids that in mammals require peroxisomes for their biosynthesis. They…”
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Reduced muscle strength in ether lipid‐deficient mice is accompanied by altered development and function of the neuromuscular junction
Published in Journal of neurochemistry (01-12-2017)“…Inherited deficiency in ether lipids, a subgroup of phospholipids whose biosynthesis needs peroxisomes, causes the fatal human disorder rhizomelic…”
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Peroxisomes in brain development and function
Published in Biochimica et biophysica acta (01-05-2016)“…Peroxisomes contain numerous enzymatic activities that are important for mammalian physiology. Patients lacking either all peroxisomal functions or a single…”
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Current and Future Pharmacological Treatment Strategies in X-Linked Adrenoleukodystrophy
Published in Brain pathology (Zurich, Switzerland) (01-07-2010)“…Mutations in the ABCD1 gene cause the clinical spectrum of the neurometabolic disorder X‐linked adrenoleukodystrophy/adrenomyeloneuropathy (X‐ALD/AMN)…”
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Targeting foam cell formation in inflammatory brain diseases by the histone modifier MS‐275
Published in Annals of clinical and translational neurology (01-11-2020)“…Objective To assess class I‐histone deacetylase (HDAC) inhibition on formation of lipid‐accumulating, disease‐promoting phagocytes upon myelin load in vitro,…”
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Neurofilament light chain as a potential biomarker for monitoring neurodegeneration in X-linked adrenoleukodystrophy
Published in Nature communications (22-03-2021)“…X-linked adrenoleukodystrophy (X-ALD), the most frequent monogenetic disorder of brain white matter, is highly variable, ranging from slowly progressive…”
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Vorinostat in the acute neuroinflammatory form of X‐linked adrenoleukodystrophy
Published in Annals of clinical and translational neurology (01-05-2020)“…Objective To identify a pharmacological compound targeting macrophages, the most affected immune cells in inflammatory X‐linked adrenoleukodystrophy (cerebral…”
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Impaired plasticity of macrophages in X-linked adrenoleukodystrophy
Published in Brain (London, England : 1878) (01-08-2018)“…Weinhofer et al. reveal impaired plasticity of macrophages, with intrinsic pro-inflammatory skewing and a decreased ability to establish proper…”
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Peroxisomal alterations in Alzheimer’s disease
Published in Acta neuropathologica (01-09-2011)“…In Alzheimer’s disease (AD), lipid alterations are present early during disease progression. As some of these alterations point towards a peroxisomal…”
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Homeostasis of phospholipids — The level of phosphatidylethanolamine tightly adapts to changes in ethanolamine plasmalogens
Published in Biochimica et biophysica acta (01-02-2015)“…Ethanolamine plasmalogens constitute a group of ether glycerophospholipids that, due to their unique biophysical and biochemical properties, are essential…”
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Metabolic rerouting via SCD1 induction impacts X-linked adrenoleukodystrophy
Published in The Journal of clinical investigation (15-04-2021)“…X-linked adrenoleukodystrophy (ALD) is a progressive neurodegenerative disease caused by mutations in ABCD1, the peroxisomal very long-chain fatty acid (VLCFA)…”
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Saturated very long-chain fatty acids regulate macrophage plasticity and invasiveness
Published in Journal of neuroinflammation (17-12-2022)“…Saturated very long-chain fatty acids (VLCFA, ≥ C22), enriched in brain myelin and innate immune cells, accumulate in X-linked adrenoleukodystrophy (X-ALD) due…”
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Abcd1 deficiency accelerates cuprizone-induced oligodendrocyte loss and axonopathy in a demyelinating mouse model of X-linked adrenoleukodystrophy
Published in Acta neuropathologica communications (18-06-2023)“…X-linked adrenoleukodystrophy (X-ALD), the most frequent, inherited peroxisomal disease, is caused by mutations in the ABCD1 gene encoding a peroxisomal lipid…”
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Overlapping and Distinct Features of Cardiac Pathology in Inherited Human and Murine Ether Lipid Deficiency
Published in International journal of molecular sciences (18-01-2023)“…Inherited deficiency in ether lipids, a subgroup of glycerophospholipids with unique biochemical and biophysical properties, evokes severe symptoms in humans…”
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ABCD1 Transporter Deficiency Results in Altered Cholesterol Homeostasis
Published in Biomolecules (Basel, Switzerland) (31-08-2023)“…X-linked adrenoleukodystrophy (X-ALD), the most common peroxisomal disorder, is caused by mutations in the peroxisomal transporter ABCD1, resulting in the…”
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Efficacy of HDAC Inhibitors in Driving Peroxisomal β-Oxidation and Immune Responses in Human Macrophages: Implications for Neuroinflammatory Disorders
Published in Biomolecules (Basel, Switzerland) (23-11-2023)“…Elevated levels of saturated very long-chain fatty acids (VLCFAs) in cell membranes and secreted lipoparticles have been associated with neurotoxicity and,…”
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Abcd2 is a strong modifier of the metabolic impairments in peritoneal macrophages of ABCD1-deficient mice
Published in PloS one (25-09-2014)“…The inherited peroxisomal disorder X-linked adrenoleukodystrophy (X-ALD), associated with neurodegeneration and inflammatory cerebral demyelination, is caused…”
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Very long-chain acyl-CoA synthetase 3: overexpression and growth dependence in lung cancer
Published in PloS one (23-07-2013)“…Lung cancer is the leading cause of cancer deaths worldwide. In the United States, only one in six lung cancer patients survives five years after diagnosis…”
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Disturbed neurotransmitter homeostasis in ether lipid deficiency
Published in Human molecular genetics (15-06-2019)Get full text
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