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Fine-tuned protein-lipid interactions in biological membranes: exploration and implications of the ORMDL-ceramide negative feedback loop in the endoplasmic reticulum.
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- Frontiers in Cell & Developmental Biology, 2024, p. 1, doi. 10.3389/fcell.2024.1457209
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- Article
Author Correction: Q-RAI data-independent acquisition for lipidomic quantitative profiling.
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- 2024
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- Correction Notice
Large-scale proteomics analysis of five brain regions from Parkinson's disease patients with a GBA1 mutation.
- Published in:
- NPJ Parkinson's Disease, 2024, v. 10, n. 1, p. 1, doi. 10.1038/s41531-024-00645-x
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- Article
Large-scale proteomics analysis of five brain regions from Parkinson's disease patients with a GBA1 mutation.
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- NPJ Parkinson's Disease, 2024, v. 10, n. 1, p. 1, doi. 10.1038/s41531-024-00645-x
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- Publication type:
- Article
Proteomics analysis of the brain from a Gaucher disease mouse identifies pathological pathways including a possible role for transglutaminase 1.
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- Journal of Neurochemistry, 2024, v. 168, n. 1, p. 52, doi. 10.1111/jnc.16024
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- Article
Q-RAI data-independent acquisition for lipidomic quantitative profiling.
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- Scientific Reports, 2023, v. 13, n. 1, p. 1, doi. 10.1038/s41598-023-46312-8
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- Article
Design of a stable human acid‐β‐glucosidase: towards improved Gaucher disease therapy and mutation classification.
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- FEBS Journal, 2023, v. 290, n. 13, p. 3383, doi. 10.1111/febs.16758
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- Article
Computational design and molecular dynamics simulations suggest the mode of substrate binding in ceramide synthases.
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- Nature Communications, 2023, v. 14, n. 1, p. 1, doi. 10.1038/s41467-023-38047-x
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- Article
The sphingolipid anteome: implications for evolution of the sphingolipid metabolic pathway.
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- FEBS Letters, 2022, v. 596, n. 18, p. 2345, doi. 10.1002/1873-3468.14457
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- Article
Elevation of gangliosides in four brain regions from Parkinson's disease patients with a GBA mutation.
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- NPJ Parkinson's Disease, 2022, v. 8, n. 1, p. 1, doi. 10.1038/s41531-022-00363-2
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- Article
Generation of a ceramide synthase 6 mouse lacking the DDRSDIE C-terminal motif.
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- PLoS ONE, 2022, v. 17, n. 7, p. 1, doi. 10.1371/journal.pone.0271675
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- Article
The fine‐tuning of cell membrane lipid bilayers accentuates their compositional complexity.
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- BioEssays, 2021, v. 43, n. 5, p. 1, doi. 10.1002/bies.202100021
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- Article
Ceramide Synthase 2 Null Mice Are Protected from Ovalbumin-Induced Asthma with Higher T Cell Receptor Signal Strength in CD4+ T Cells.
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- International Journal of Molecular Sciences, 2021, v. 22, n. 5, p. 2713, doi. 10.3390/ijms22052713
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- Article
Substrate reduction therapy using Genz‐667161 reduces levels of pathogenic components in a mouse model of neuronopathic forms of Gaucher disease.
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- Journal of Neurochemistry, 2021, v. 156, n. 5, p. 692, doi. 10.1111/jnc.15136
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- Article
Integrin Alpha E (CD103) Limits Virus-Induced IFN-I Production in Conventional Dendritic Cells.
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- Frontiers in Immunology, 2021, v. 11, p. N.PAG, doi. 10.3389/fimmu.2020.607889
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- Article
Proteomics analysis of a human brain sample from a mucolipidosis type IV patient reveals pathophysiological pathways.
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- 2021
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- journal article
The Lysosome and Nonmotor Symptoms: Linking Parkinson's Disease and Lysosomal Storage Disorders.
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- Movement Disorders, 2020, v. 35, n. 12, p. 2150, doi. 10.1002/mds.28232
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- Publication type:
- Article
NPC1 silent variant induces skipping of exon 11 (p.V562V) and unfolded protein response was found in a specific Niemann‐Pick type C patient.
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- Molecular Genetics & Genomic Medicine, 2020, v. 8, n. 11, p. 1, doi. 10.1002/mgg3.1451
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- Article
Mice defective in interferon signaling help distinguish between primary and secondary pathological pathways in a mouse model of neuronal forms of Gaucher disease.
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- 2020
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- journal article
Innate immune response in neuronopathic forms of Gaucher disease confers resistance against viral-induced encephalitis.
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- Acta Neuropathologica Communications, 2020, v. 8, n. 1, p. N.PAG, doi. 10.1186/s40478-020-01020-6
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- Article
Lysosomal Storage Disorders Shed Light on Lysosomal Dysfunction in Parkinson's Disease.
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- International Journal of Molecular Sciences, 2020, v. 21, n. 14, p. 4966, doi. 10.3390/ijms21144966
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- Article
Hepatic triglyceride accumulation via endoplasmic reticulum stress-induced SREBP-1 activation is regulated by ceramide synthases.
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- Experimental & Molecular Medicine EMM, 2019, v. 51, n. 11, p. N.PAG, doi. 10.1038/s12276-019-0340-1
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- Article
Absence of infiltrating peripheral myeloid cells in the brains of mouse models of lysosomal storage disorders.
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- Journal of Neurochemistry, 2019, v. 148, n. 5, p. 625, doi. 10.1111/jnc.14483
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- Article
TLR9-mediated dendritic cell activation uncovers mammalian ganglioside species with specific ceramide backbones that activate invariant natural killer T cells.
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- PLoS Biology, 2019, v. 17, n. 3, p. 1, doi. 10.1371/journal.pbio.3000169
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- Article
In vivo inactivation of glycosidases by conduritol B epoxide and cyclophellitol as revealed by activity‐based protein profiling.
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- FEBS Journal, 2019, v. 286, n. 3, p. 584, doi. 10.1111/febs.14744
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- Article
Sphingolipid regulation of lung epithelial cell mitophagy and necroptosis during cigarette smoke exposure.
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- FASEB Journal, 2018, v. 32, n. 4, p. 1880, doi. 10.1096/fj.201700571R
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- Article
Ablation of ceramide synthase 2 exacerbates dextran sodium sulphate-induced colitis in mice due to increased intestinal permeability.
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- Journal of Cellular & Molecular Medicine, 2017, v. 21, n. 12, p. 3565, doi. 10.1111/jcmm.13267
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- Article
Critical Role for Very-Long Chain Sphingolipids in Invariant Natural Killer T Cell Development and Homeostasis.
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- Frontiers in Immunology, 2017, p. 1, doi. 10.3389/fimmu.2017.01386
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- Article
Altered lysosome distribution is an early neuropathological event in neurological forms of Gaucher disease.
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- FEBS Letters, 2017, v. 591, n. 5, p. 774, doi. 10.1002/1873-3468.12591
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- Article
K<sub>Ca</sub>3.1 upregulation preserves endothelium-dependent vasorelaxation during aging and oxidative stress.
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- Aging Cell, 2016, v. 15, n. 5, p. 801, doi. 10.1111/acel.12502
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- Article
Delineating pathological pathways in a chemically induced mouse model of Gaucher disease.
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- Journal of Pathology, 2016, v. 239, n. 4, p. 496, doi. 10.1002/path.4751
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- Article
Induction of the type I interferon response in neurological forms of Gaucher disease.
- Published in:
- 2016
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- Publication type:
- journal article
Altering sphingolipid composition with aging induces contractile dysfunction of gastric smooth muscle via K<sub>Ca</sub> 1.1 upregulation.
- Published in:
- Aging Cell, 2015, v. 14, n. 6, p. 982, doi. 10.1111/acel.12388
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- Article
LPS-mediated septic shock is augmented in ceramide synthase 2 null mice due to elevated activity of TNFα-converting enzyme.
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- FEBS Letters, 2015, v. 589, n. 17, p. 2213, doi. 10.1016/j.febslet.2015.06.045
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- Article
Virus-Induced Type I Interferon Deteriorates Control of Systemic Pseudomonas Aeruginosa Infection.
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- Cellular Physiology & Biochemistry (Karger AG), 2015, v. 36, n. 6, p. 2379, doi. 10.1159/000430200
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- Article
Innate immune responses in the brain of sphingolipid lysosomal storage diseases.
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- Biological Chemistry, 2015, v. 396, n. 6/7, p. 659, doi. 10.1515/hsz-2014-0301
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- Article
Identification of a Biomarker in Cerebrospinal Fluid for Neuronopathic Forms of Gaucher Disease.
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- PLoS ONE, 2015, v. 10, n. 3, p. 1, doi. 10.1371/journal.pone.0120194
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- Article
Sphingoid long chain bases prevent lung infection by Pseudomonas aeruginosa.
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- EMBO Molecular Medicine, 2014, v. 6, n. 9, p. 1205, doi. 10.15252/emmm.201404075
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- Article
The HIV-1 Envelope Transmembrane Domain Binds TLR2 through a Distinct Dimerization Motif and Inhibits TLR2-Mediated Responses.
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- PLoS Pathogens, 2014, v. 10, n. 8, p. 1, doi. 10.1371/journal.ppat.1004248
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- Article
Neuronal accumulation of glucosylceramide in a mouse model of neuronopathic Gaucher disease leads to neurodegeneration.
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- Human Molecular Genetics, 2014, v. 23, n. 4, p. 843, doi. 10.1093/hmg/ddt468
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- Article
RIPK3 as a potential therapeutic target for Gaucher's disease.
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- Nature Medicine, 2014, v. 20, n. 2, p. 204, doi. 10.1038/nm.3449
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- Article
The Yeast P5 Type ATPase, Spf1, Regulates Manganese Transport into the Endoplasmic Reticulum.
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- PLoS ONE, 2013, v. 8, n. 12, p. 1, doi. 10.1371/journal.pone.0085519
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- Publication type:
- Article
Impaired Epidermal Ceramide Synthesis Causes Autosomal Recessive Congenital Ichthyosis and Reveals the Importance of Ceramide Acyl Chain Length.
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- Journal of Investigative Dermatology, 2013, v. 133, n. 9, p. 2202, doi. 10.1038/jid.2013.153
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- Publication type:
- Article
Oxidized Phospholipids Induce Ceramide Accumulation in RAW 264.7 Macrophages: Role of Ceramide Synthases.
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- PLoS ONE, 2013, v. 8, n. 7, p. 1, doi. 10.1371/journal.pone.0070002
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- Publication type:
- Article
Ceramide Synthases Expression and Role of Ceramide Synthase-2 in the Lung: Insight from Human Lung Cells and Mouse Models
- Published in:
- PLoS ONE, 2013, v. 8, n. 5, p. 1, doi. 10.1371/journal.pone.0062968
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- Publication type:
- Article
Identification of N-acyl-fumonisin B1 as new cytotoxic metabolites of fumonisin mycotoxins.
- Published in:
- Molecular Nutrition & Food Research, 2013, v. 57, n. 3, p. 516, doi. 10.1002/mnfr.201200465
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- Article
Contribution of brain inflammation to neuronal cell death in neuronopathic forms of Gaucher's disease.
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- Brain: A Journal of Neurology, 2012, v. 135, n. 6, p. 1724, doi. 10.1093/brain/aws095
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- Article
Methylation of glycosylated sphingolipid modulates membrane lipid topography and pathogenicity of Cryptococcus neoformans.
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- Cellular Microbiology, 2012, v. 14, n. 4, p. 500, doi. 10.1111/j.1462-5822.2011.01735.x
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- Publication type:
- Article
Comparison of a molecular dynamics model with the X-ray structure of the N370S acid-β-glucosidase mutant that causes Gaucher disease.
- Published in:
- PEDS: Protein Engineering, Design & Selection, 2011, v. 24, n. 10, p. 773, doi. 10.1093/protein/gzr032
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- Article
Lysosomal storage disorders and Parkinson's disease: Gaucher disease and beyond.
- Published in:
- Movement Disorders, 2011, v. 26, n. 9, p. 1593, doi. 10.1002/mds.23774
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- Publication type:
- Article