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A multi-omic analysis of optineurin proteinopathy in a yeast model suggests the involvement of lipid metabolism in Amyotrophic Lateral Sclerosis
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/yea.1502openalex-snapshot
A suite of Gateway® cloning vectors for high‐throughput genetic analysis in Saccharomyces cerevisiae
inferredcites →https://doi.org/10.1007/s00216-013-7271-9openalex-snapshot
Optimised protocols for the metabolic profiling of S. cerevisiae by 1H-NMR and HRMAS spectroscopy
inferredcites →https://doi.org/10.1007/s12035-015-9165-7openalex-snapshot
Metabolomic Analysis Reveals Increased Aerobic Glycolysis and Amino Acid Deficit in a Cellular Model of Amyotrophic Lateral Sclerosis
inferredcites →https://doi.org/10.1016/0014-5793(96)00044-0openalex-snapshot
Role of mitochondria and C‐terminal membrane anchor of Bcl‐2 in Bax induced growth arrest and mortality in Saccharomyces cerevisiae
inferredcites →https://doi.org/10.1016/j.bbadis.2017.10.008openalex-snapshot
Effect of genetic variants of OPTN in the pathophysiology of Paget's disease of bone
inferredcites →https://doi.org/10.1016/j.bbamcr.2011.11.018openalex-snapshot
The ER–mitochondria interface: The social network of cell death
inferredcites →https://doi.org/10.1016/j.bone.2012.06.028openalex-snapshot
Genetic association study of UCMA/GRP and OPTN genes (PDB6 locus) with Paget's disease of bone
inferredcites →https://doi.org/10.1016/j.cub.2007.07.041openalex-snapshot
Optineurin Negatively Regulates TNFα- Induced NF-κB Activation by Competing with NEMO for Ubiquitinated RIP
inferredcites →https://doi.org/10.1016/j.exer.2015.08.020openalex-snapshot
Defects in autophagy caused by glaucoma-associated mutations in optineurin
inferredcites →https://doi.org/10.1016/j.neurobiolaging.2010.10.001openalex-snapshot
Analysis of OPTN as a causative gene for amyotrophic lateral sclerosis
inferredcites →https://doi.org/10.1016/j.neurobiolaging.2010.11.005openalex-snapshot
Screening of OPTN in French familial amyotrophic lateral sclerosis
inferredcites →https://doi.org/10.1016/j.neurobiolaging.2011.12.037openalex-snapshot
Novel deletion mutations of OPTN in amyotrophic lateral sclerosis in Japanese
inferredcites →https://doi.org/10.1016/j.neurobiolaging.2012.06.023openalex-snapshot
Screening for OPTN mutations in a cohort of British amyotrophic lateral sclerosis patients
inferredcites →https://doi.org/10.1016/j.neuron.2011.09.010openalex-snapshot
A Hexanucleotide Repeat Expansion in C9ORF72 Is the Cause of Chromosome 9p21-Linked ALS-FTD
inferredcites →https://doi.org/10.1016/j.neuron.2011.09.011openalex-snapshot
Expanded GGGGCC Hexanucleotide Repeat in Noncoding Region of C9ORF72 Causes Chromosome 9p-Linked FTD and ALS
inferredcites →https://doi.org/10.1016/s0014-5793(97)01087-9openalex-snapshot
Release of cytochrome c and decrease of cytochrome c oxidase in Bax‐expressing yeast cells, and prevention of these effects by coexpression of Bcl‐xL
inferredcites →https://doi.org/10.1016/s0076-6879(10)70007-0openalex-snapshot
Synthetic Genetic Array (SGA) Analysis in Saccharomyces cerevisiae and Schizosaccharomyces pombe
inferredcites →https://doi.org/10.1016/s0092-8674(03)01079-1openalex-snapshot
The Mechanisms of Vesicle Budding and Fusion
inferredcites →https://doi.org/10.1016/s1097-2765(00)80034-9openalex-snapshot
Bax Inhibitor-1, a Mammalian Apoptosis Suppressor Identified by Functional Screening in Yeast
inferredcites →https://doi.org/10.1021/acs.jproteome.5b00354openalex-snapshot
Analysis of the Human Adult Urinary Metabolome Variations with Age, Body Mass Index, and Gender by Implementing a Comprehensive Workflow for Univariate and OPLS Statistical Analyses
inferredcites →https://doi.org/10.1038/362059a0openalex-snapshot
Mutations in Cu/Zn superoxide dismutase gene are associated with familial amyotrophic lateral sclerosis
inferredcites →https://doi.org/10.1038/nature08971openalex-snapshot
Mutations of optineurin in amyotrophic lateral sclerosis
inferredcites →https://doi.org/10.1038/nature16148openalex-snapshot
Drosophila Ionotropic Receptor 25a mediates circadian clock resetting by temperature
inferredcites →https://doi.org/10.1038/ng.132openalex-snapshot
TARDBP mutations in individuals with sporadic and familial amyotrophic lateral sclerosis
inferredcites →https://doi.org/10.1038/ng.2434openalex-snapshot
Inhibition of RNA lariat debranching enzyme suppresses TDP-43 toxicity in ALS disease models
inferredcites →https://doi.org/10.1038/ng.562openalex-snapshot
Genome-wide association study identifies variants at CSF1, OPTN and TNFRSF11A as genetic risk factors for Paget's disease of bone
inferredcites →https://doi.org/10.1038/nmeth.2557openalex-snapshot
The CRAPome: a contaminant repository for affinity purification–mass spectrometry data
inferredcites →https://doi.org/10.1038/s41598-017-17389-9openalex-snapshot
Lipidomics Reveals Cerebrospinal-Fluid Signatures of ALS
inferredcites →https://doi.org/10.1039/c5mb00711aopenalex-snapshot
Multi-platform mass spectrometry analysis of the CSF and plasma metabolomes of rigorously matched amyotrophic lateral sclerosis, Parkinson's disease and control subjects
inferredcites →https://doi.org/10.1073/pnas.0802082105openalex-snapshot
A yeast TDP-43 proteinopathy model: Exploring the molecular determinants of TDP-43 aggregation and cellular toxicity
inferredcites →https://doi.org/10.1073/pnas.1109434108openalex-snapshot
A yeast functional screen predicts new candidate ALS disease genes
inferredcites →https://doi.org/10.1073/pnas.1405752111openalex-snapshot
Optineurin is an autophagy receptor for damaged mitochondria in parkin-mediated mitophagy that is disrupted by an ALS-linked mutation
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/jbc.m114.562827openalex-snapshot
Proline Biosynthesis Is Required for Endoplasmic Reticulum Stress Tolerance in Saccharomyces cerevisiae
inferredcites →https://doi.org/10.1089/omi.2016.0106openalex-snapshot
Metabolic Biomarkers and Neurodegeneration: A Pathway Enrichment Analysis of Alzheimer's Disease, Parkinson's Disease, and Amyotrophic Lateral Sclerosis
inferredcites →https://doi.org/10.1093/database/bar062openalex-snapshot
YeastMine—an integrated data warehouse for Saccharomyces cerevisiae data as a multipurpose tool-kit
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/10.1093/hmg/ddx096openalex-snapshot
A critical role of Hrd1 in the regulation of optineurin degradation and aggresome formation
inferredcites →https://doi.org/10.1093/nar/gkm324openalex-snapshot
LIPID MAPS online tools for lipid research
inferredcites →https://doi.org/10.1093/nar/gkt400openalex-snapshot
SGAtools: one-stop analysis and visualization of array-based genetic interaction screens
inferredcites →https://doi.org/10.1093/nar/gkv380openalex-snapshot
MetaboAnalyst 3.0—making metabolomics more meaningful
inferredcites →https://doi.org/10.1101/gr.1239303openalex-snapshot
Cytoscape: A Software Environment for Integrated Models of Biomolecular Interaction Networks
inferredcites →https://doi.org/10.1101/gr.211649.116openalex-snapshot
Yeast genetic interaction screen of human genes associated with amyotrophic lateral sclerosis: identification of MAP2K5 kinase as a potential drug target
inferredcites →https://doi.org/10.1111/ene.12956openalex-snapshot
Metabolomics in amyotrophic lateral sclerosis: how far can it take us?
inferredcites →https://doi.org/10.1111/mmi.12075openalex-snapshot
A yeast model of optineurin proteinopathy reveals a unique aggregation pattern associated with cellular toxicity
inferredcites →https://doi.org/10.1126/science.1066901openalex-snapshot
Adult-Onset Primary Open-Angle Glaucoma Caused by Mutations in Optineurin
inferredcites →https://doi.org/10.1126/science.1154584openalex-snapshot
TDP-43 Mutations in Familial and Sporadic Amyotrophic Lateral Sclerosis
inferredcites →https://doi.org/10.1126/science.1165942openalex-snapshot
Mutations in FUS, an RNA Processing Protein, Cause Familial Amyotrophic Lateral Sclerosis Type 6
inferredcites →https://doi.org/10.1126/science.1166066openalex-snapshot
Mutations in the FUS/TLS Gene on Chromosome 16 Cause Familial Amyotrophic Lateral Sclerosis
inferredcites →https://doi.org/10.1126/science.1205405openalex-snapshot
Phosphorylation of the Autophagy Receptor Optineurin Restricts Salmonella Growth
inferredcites →https://doi.org/10.1126/science.aaa0769openalex-snapshot
Systematic humanization of yeast genes reveals conserved functions and genetic modularity
inferredcites →https://doi.org/10.1136/jnnp-2013-305546openalex-snapshot
Genetic counselling in ALS: facts, uncertainties and clinical suggestions
inferredcites →https://doi.org/10.1136/jnnp.2010.234963openalex-snapshot
Optineurin mutations in Japanese amyotrophic lateral sclerosis: Table 1
inferredcites →https://doi.org/10.1136/jnnp.2011.242313openalex-snapshot
Novel optineurin mutations in patients with familial and sporadic amyotrophic lateral sclerosis
inferredcites →https://doi.org/10.1186/1471-2121-11-4openalex-snapshot
Regulation of endocytic trafficking of transferrin receptor by optineurin and its impairment by a glaucoma-associated mutant
inferredcites →https://doi.org/10.1371/journal.pbio.1000614openalex-snapshot
Molecular Determinants and Genetic Modifiers of Aggregation and Toxicity for the ALS Disease Protein FUS/TLS
inferredcites →https://doi.org/10.1371/journal.pbio.1001052openalex-snapshot
A Yeast Model of FUS/TLS-Dependent Cytotoxicity
inferredcites →https://doi.org/10.1371/journal.pone.0001078openalex-snapshot
Optimized Protein Extraction for Quantitative Proteomics of Yeasts
inferredcites →https://doi.org/10.1534/g3.113.009431openalex-snapshot
gitter: A Robust and Accurate Method for Quantification of Colony Sizes From Plate Images
inferredcites →https://doi.org/10.1534/genetics.112.140467openalex-snapshot
The Ubiquitin–Proteasome System of Saccharomyces cerevisiae
inferredcites →https://doi.org/10.3109/17482968.2012.684213openalex-snapshot
Mutational analysis of familial and sporadic amyotrophic lateral sclerosis withOPTNmutations in Japanese population
inferredcites →https://doi.org/10.3109/21678421.2015.1089909openalex-snapshot
Optineurin mutations in patients with sporadic amyotrophic lateral sclerosis in China
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Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.47749/t/unicamp.2022.1265921openalex-snapshot
Saccharomyces cerevisiae, a platform for drug discovery
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