Related references
Note: Only part of the references are listed.The STRING database in 2021: customizable protein-protein networks, and functional characterization of user-uploaded gene/measurement sets
Damian Szklarczyk et al.
NUCLEIC ACIDS RESEARCH (2021)
Turning the spotlight on the oligosaccharide chain of GM1 ganglioside
Elena Chiricozzi et al.
GLYCOCONJUGATE JOURNAL (2021)
TRIP12 ubiquitination of glucocerebrosidase contributes to neurodegeneration in Parkinson's disease
Bo Am Seo et al.
NEURON (2021)
The structure of gangliosides hides a code for determining neuronal functions
Giulia Lunghi et al.
FEBS OPEN BIO (2021)
α-Synuclein fibrils subvert lysosome structure and function for the propagation of protein misfolding between cells through tunneling nanotubes
Aysegul Dilsizoglu Senol et al.
PLOS BIOLOGY (2021)
GBA1 mutations: Prospects for exosomal biomarkers in α-synuclein pathologies
Parker H. Johnson et al.
MOLECULAR GENETICS AND METABOLISM (2020)
Gangliosides in the differentiation process of primary neurons: the specific role of GM1-oligosaccharide
Erika Di Biase et al.
GLYCOCONJUGATE JOURNAL (2020)
Enforced C-Src Activation Causes Compartmental Dysregulation of PI3K and PTEN Molecules in Lipid Rafts of Tongue Squamous Carcinoma Cells by Attenuating Rac1-Akt-GLUT-1-Mediated Sphingolipid Synthesis
Chien-Wei Wu et al.
INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES (2020)
The SPID-GBA study: Sex distribution, Penetrance, Incidence, and Dementia in GBA-PD
Letizia Straniero et al.
NEUROLOGY-GENETICS (2020)
Modulation of calcium signaling depends on the oligosaccharide of GM1 in Neuro2a mouse neuroblastoma cells
Giulia Lunghi et al.
GLYCOCONJUGATE JOURNAL (2020)
GBA, Gaucher Disease, and Parkinson's Disease: From Genetic to Clinic to New Therapeutic Approaches
Giulietta M. Riboldi et al.
CELLS (2019)
A lysosome-plasma membrane-sphingolipid axis linking lysosomal storage to cell growth arrest
Maura Samarani et al.
FASEB JOURNAL (2018)
GBA1 deficiency negatively affects physiological alpha-synuclein tetramers and related multimers
Sangjune Kim et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2018)
Alterations in the properties of the cell membrane due to glycosphingolipid accumulation in a model of Gaucher disease
Gyula Batta et al.
SCIENTIFIC REPORTS (2018)
A Review of Gaucher Disease Pathophysiology, Clinical Presentation and Treatments
Jerome Stirnemann et al.
INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES (2017)
Evidence for the Involvement of Lipid Rafts and Plasma Membrane Sphingolipid Hydrolases in Pseudomonas aeruginosa Infection of Cystic Fibrosis Bronchial Epithelial Cells
Domitilla Schiumarini et al.
MEDIATORS OF INFLAMMATION (2017)
Survival and dementia in GBA-associated Parkinson's disease: The mutation matters
Roberto Cilia et al.
ANNALS OF NEUROLOGY (2016)
Src protein-tyrosine kinase structure, mechanism, and small molecule inhibitors
Robert Roskoski
PHARMACOLOGICAL RESEARCH (2015)
c-Src-induced activation of ceramide metabolism impairs membrane microdomains and promotes malignant progression by facilitating the translocation of c-Src to focal adhesions
Kentaro Kajiwara et al.
BIOCHEMICAL JOURNAL (2014)
Reduced glucocerebrosidase is associated with increased α-synuclein in sporadic Parkinson's disease
Karen E. Murphy et al.
BRAIN (2014)
Lipid Rafts in Neurodegeneration and Neuroprotection
Sandro Sonnino et al.
MOLECULAR NEUROBIOLOGY (2014)
A GCase Chaperone Improves Motor Function in a Mouse Model of Synucleinopathy
Franziska Richter et al.
NEUROTHERAPEUTICS (2014)
iPSC-derived neurons from GBA1-associated Parkinson's disease patients show autophagic defects and impaired calcium homeostasis
David C. Schoendorf et al.
NATURE COMMUNICATIONS (2014)
Directed Dopaminergic Neuron Differentiation from Human Pluripotent Stem Cells
Pengbo Zhang et al.
JOVE-JOURNAL OF VISUALIZED EXPERIMENTS (2014)
A Multicenter Study of Glucocerebrosidase Mutations in Dementia With Lewy Bodies
Michael A. Nalls et al.
JAMA NEUROLOGY (2013)
Glucocerebrosidase deficiency in substantia nigra of parkinson disease brains
Matthew E. Gegg et al.
ANNALS OF NEUROLOGY (2012)
A clinical and family history study of Parkinson's disease in heterozygous glucocerebrosidase mutation carriers
Alisdair McNeill et al.
JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY (2012)
Gaucher disease gene GBA functions in immune regulation
Jun Liu et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2012)
Saturated Fatty Acids Induce c-Src Clustering within Membrane Subdomains, Leading to JNK Activation
Ryan G. Holzer et al.
CELL (2011)
Gaucher Disease Glucocerebrosidase and α-Synuclein Form a Bidirectional Pathogenic Loop in Synucleinopathies
Joseph R. Mazzulli et al.
CELL (2011)
Transcriptional Activation of Lysosomal Exocytosis Promotes Cellular Clearance
Diego L. Medina et al.
DEVELOPMENTAL CELL (2011)
Animal models for Gaucher disease research
Tamar Farfel-Becker et al.
DISEASE MODELS & MECHANISMS (2011)
Cell surface sphingolipid glycohydrolases in neuronal differentiation and aging in culture
Massimo Aureli et al.
JOURNAL OF NEUROCHEMISTRY (2011)
Photoactivable sphingosine as a tool to study membrane microenvironments in cultured cells
Massimo Aureli et al.
JOURNAL OF LIPID RESEARCH (2010)
Deregulated Sphingolipid Metabolism and Membrane Organization in Neurodegenerative Disorders
Marco Piccinini et al.
MOLECULAR NEUROBIOLOGY (2010)
Lipid Rafts As a Membrane-Organizing Principle
Daniel Lingwood et al.
SCIENCE (2010)
Secondary lipid accumulation in lysosomal disease
Steven U. Walkley et al.
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR CELL RESEARCH (2009)
Activity of plasma membrane β-galactosidase and β-glucosidase
Massimo Aureli et al.
FEBS LETTERS (2009)
Multicenter Analysis of Glucocerebrosidase Mutations in Parkinson's Disease
E. Sidransky et al.
NEW ENGLAND JOURNAL OF MEDICINE (2009)
A Gene Network Regulating Lysosomal Biogenesis and Function
Marco Sardiello et al.
SCIENCE (2009)
Lipid composition of microdomains is altered in a cell model of Gaucher disease
Leanne K. Hein et al.
JOURNAL OF LIPID RESEARCH (2008)
Secondary sphingolipid accumulation in a macrophage model of Gaucher disease
Leanne K. Hein et al.
MOLECULAR GENETICS AND METABOLISM (2007)
Murine models of acute neuronopathic Gaucher disease
Ida Berglin Enquist et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2007)
Heterozygosity for a Mendelian disorder as a risk factor for complex disease
E. Sidransky
CLINICAL GENETICS (2006)
Dynamic and structural properties of sphingolipids as driving forces for the formation of membrane domains
Sandro Sonnino et al.
CHEMICAL REVIEWS (2006)
Divergent phenotypes in Gaucher disease implicate the role of modifiers
O Goker-Alpan et al.
JOURNAL OF MEDICAL GENETICS (2005)
Parkinsonism among Gaucher disease carriers
O Goker-Alpan et al.
JOURNAL OF MEDICAL GENETICS (2004)
Glucocerebrosidase mutations in subjects with parkinsonism
A Lwin et al.
MOLECULAR GENETICS AND METABOLISM (2004)
Toxicity of glucosylsphingosine (glucopsychosine) to cultured neuronal cells: a model system for assessing neuronal damage in Gaucher disease type 2 and 3
UH Schueler et al.
NEUROBIOLOGY OF DISEASE (2003)
Glucosylceramide modulates membrane traffic along the endocytic pathway
DJ Sillence et al.
JOURNAL OF LIPID RESEARCH (2002)
JAK-STAT signaling mediates gangliosides-induced inflammatory responses in brain microglial cells
OS Kim et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2002)
Share Paper
