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Nuclear lipidome is altered in amyotrophic lateral sclerosis: a preliminary study
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Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1001/jamaneurol.2014.1214openalex-snapshot
Dietary ω-3 Polyunsaturated Fatty Acid Intake and Risk for Amyotrophic Lateral Sclerosis
inferredcites →https://doi.org/10.1006/mcne.2002.1199openalex-snapshot
Disruption of PLC-$beta;1-Mediated Signal Transduction in Mutant Mice Causes Age-Dependent Hippocampal Mossy Fiber Sprouting and Neurodegeneration
inferredcites →https://doi.org/10.1007/s00401-011-0850-yopenalex-snapshot
Cell stress induces TDP-43 pathological changes associated with ERK1/2 dysfunction: implications in ALS
inferredcites →https://doi.org/10.1007/s00401-016-1586-5openalex-snapshot
Inside out: the role of nucleocytoplasmic transport in ALS and FTLD
inferredcites →https://doi.org/10.1007/s00401-018-1835-xopenalex-snapshot
Energy metabolism in ALS: an underappreciated opportunity?
inferredcites →https://doi.org/10.1007/s00401-018-1934-8openalex-snapshot
Mitochondria, ER, and nuclear membrane defects reveal early mechanisms for upper motor neuron vulnerability with respect to TDP-43 pathology
inferredcites →https://doi.org/10.1007/s00412-010-0289-2openalex-snapshot
Nuclear pore biogenesis into an intact nuclear envelope
inferredcites →https://doi.org/10.1007/s11064-017-2263-3openalex-snapshot
Ischemia/Reperfusion-Induced Translocation of PKCβII to Mitochondria as an Important Mediator of a Protective Signaling Mechanism in an Ischemia-Resistant Region of the Hippocampus
inferredcites →https://doi.org/10.1007/s12017-014-8317-7openalex-snapshot
Dietary Lipid Unsaturation Influences Survival and Oxidative Modifications of an Amyotrophic Lateral Sclerosis Model in a Gender-Specific Manner
inferredcites →https://doi.org/10.1016/j.bbalip.2010.02.002openalex-snapshot
Lipid mediators in the nucleus: Their potential contribution to Alzheimer's disease
inferredcites →https://doi.org/10.1016/j.cell.2014.12.019openalex-snapshot
Glial Lipid Droplets and ROS Induced by Mitochondrial Defects Promote Neurodegeneration
inferredcites →https://doi.org/10.1016/j.cell.2018.05.047openalex-snapshot
The Inner Nuclear Membrane Is a Metabolically Active Territory that Generates Nuclear Lipid Droplets
inferredcites →https://doi.org/10.1016/j.cell.2019.04.001openalex-snapshot
Neuron-Astrocyte Metabolic Coupling Protects against Activity-Induced Fatty Acid Toxicity
inferredcites →https://doi.org/10.1016/j.cmet.2018.03.003openalex-snapshot
Mitochondria Bound to Lipid Droplets Have Unique Bioenergetics, Composition, and Dynamics that Support Lipid Droplet Expansion
inferredcites →https://doi.org/10.1016/j.coph.2018.02.007openalex-snapshot
Metabotropic glutamate receptor involvement in the pathophysiology of amyotrophic lateral sclerosis: new potential drug targets for therapeutic applications
inferredcites →https://doi.org/10.1016/j.devcel.2015.02.017openalex-snapshot
Nuclear Pore Basket Proteins Are Tethered to the Nuclear Envelope and Can Regulate Membrane Curvature
inferredcites →https://doi.org/10.1016/j.nbd.2016.01.007openalex-snapshot
Interplay between TDP-43 and docosahexaenoic acid-related processes in amyotrophic lateral sclerosis
inferredcites →https://doi.org/10.1016/j.neuroscience.2004.12.023openalex-snapshot
Metabotropic glutamate receptor/phospholipase C pathway: A vulnerable target to Creutzfeldt-Jakob disease in the cerebral cortex
inferredcites →https://doi.org/10.1016/j.neuroscience.2012.06.039openalex-snapshot
Cellular neurochemical characterization and subcellular localization of phospholipase C β1 in rat brain
inferredcites →https://doi.org/10.1038/38508openalex-snapshot
Phospholipase C isozymes selectively couple to specific neurotransmitter receptors
inferredcites →https://doi.org/10.1038/ncomms7626openalex-snapshot
Generation and expansion of highly pure motor neuron progenitors from human pluripotent stem cells
inferredcites →https://doi.org/10.1038/s41593-017-0047-3openalex-snapshot
TDP-43 pathology disrupts nuclear pore complexes and nucleocytoplasmic transport in ALS/FTD
inferredcites →https://doi.org/10.1046/j.1471-4159.2003.01670.xopenalex-snapshot
Protein kinase and protein phosphatase expression in amyotrophic lateral sclerosis spinal cord
inferredcites →https://doi.org/10.1073/pnas.1508767112openalex-snapshot
Glycosphingolipids are modulators of disease pathogenesis in amyotrophic lateral sclerosis
inferredcites →https://doi.org/10.1074/mcp.m700407-mcp200openalex-snapshot
Discovering Novel Interactions at the Nuclear Pore Complex Using Bead Halo
inferredcites →https://doi.org/10.1080/15548627.2018.1474311openalex-snapshot
Cryptic exon splicing function of TARDBP interacts with autophagy in nervous tissue
inferredcites →https://doi.org/10.1083/jcb.200601002openalex-snapshot
Nuclear pore complex assembly and maintenance in POM121- and gp210-deficient cells
inferredcites →https://doi.org/10.1086/425287openalex-snapshot
A Mutation in the Vesicle-Trafficking Protein VAPB Causes Late-Onset Spinal Muscular Atrophy and Amyotrophic Lateral Sclerosis
inferredcites →https://doi.org/10.1091/mbc.e08-05-0517openalex-snapshot
Lipid Microdomains in Cell Nucleus
inferredcites →https://doi.org/10.1093/brain/awm190openalex-snapshot
Oxidative and endoplasmic reticulum stress interplay in sporadic amyotrophic lateral sclerosis
inferredcites →https://doi.org/10.1093/hmg/ddv439openalex-snapshot
Amyotrophic lateral sclerosis and denervation alter sphingolipids and up-regulate glucosylceramide synthase
inferredcites →https://doi.org/10.1096/fj.13-234419openalex-snapshot
Human omental and subcutaneous adipose tissue exhibit specific lipidomic signatures
inferredcites →https://doi.org/10.1097/01.jnen.0000171649.86718.f2openalex-snapshot
Abnormal Group I Metabotropic Glutamate Receptor Expression and Signaling in the Frontal Cortex in Pick Disease
inferredcites →https://doi.org/10.1111/j.1471-4159.2010.07070.xopenalex-snapshot
Plasmalogen synthesis is regulated via alkyl‐dihydroxyacetonephosphate‐synthase by amyloid precursor protein processing and is affected in Alzheimer’s disease
inferredcites →https://doi.org/10.1126/science.154.3757.1662openalex-snapshot
Nuclei from Rat Liver: Isolation Method That Combines Purity with High Yield
inferredcites →https://doi.org/10.1152/ajpcell.2000.279.4.c1259openalex-snapshot
Sterol carrier protein-2 localization in endoplasmic reticulum and role in phospholipid formation
inferredcites →https://doi.org/10.1242/jcs.158915openalex-snapshot
Nuclear pore targeting of the yeast Pom33 nucleoporin depends on karyopherin- and lipid-binding
inferredcites →https://doi.org/10.1248/bpb.31.719openalex-snapshot
Decreased Expression of Phospholipase C-.BETA.1 Protein in Endoplasmic Reticulum Stress-Loaded Neurons
inferredcites →https://doi.org/10.2174/092986709788682164openalex-snapshot
Plasmalogens in Biological Systems: Their Role in Oxidative Processes in Biological Membranes, their Contribution to Pathological Processes and Aging and Plasmalogen Analysis
inferredcites →https://doi.org/10.2741/2269openalex-snapshot
Myocardial Lipidomics. Developments in myocardial nuclear lipidomics
inferredcites →https://doi.org/10.4161/auto.25239openalex-snapshot
PRKCB/protein kinase C, beta and the mitochondrial axis as key regulators of autophagy
inferredcites →https://doi.org/10.4161/cc.8.8.8161openalex-snapshot
A new take on ceramide: Starving cells by cutting off the nutrient supply
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Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.1016/j.semcdb.2020.08.012openalex-snapshot
The role of lipids in the central nervous system and their pathological implications in amyotrophic lateral sclerosis
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