Publications by authors named "J-M Ferraz"

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LIMP-2 deficiency-associated glycolipid abnormalities in mice.
Paulo Gaspar, André R A Marques, Maria J Ferraz, Markus Damme, Gertjan Kramer

Biochim Biophys Acta Mol Cell Biol Lipids· October 2025

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Glucosylated cholesterol accumulates in atherosclerotic lesions and impacts macrophage immune response.
André R A Marques, Inês S Ferreira, Quélia Ribeiro, Maria J Ferraz, Elizeth Lopes

J Lipid Res· June 2025

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Preclinical efficacy and safety of adeno-associated virus 5 alpha-galactosidase: A gene therapy for Fabry disease.
Jolanda M P Liefhebber, Giso Brasser, Elisabeth A Spronck, Roelof Ottenhoff, Lieke Paerels, Maria J Ferraz

Mol Ther Methods Clin Dev· December 2024

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6-O-alkyl 4-methylumbelliferyl-β-D-glucosides as selective substrates for GBA1 in the discovery of glycosylated sterols.
Stef Bannink, Kateryna O Bila, Joosje van Weperen, Nina A M Ligthart, Maria J Ferraz

J Lipid Res· November 2024

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Human glucocerebrosidase mediates formation of xylosyl-cholesterol by β-xylosidase and transxylosidase reactions.
Daphne E Boer, Mina Mirzaian, Maria J Ferraz, Kimberley C Zwiers, Merel V Baks

J Lipid Res· July 2024

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Consequences of excessive glucosylsphingosine in glucocerebrosidase-deficient zebrafish.
Lindsey T Lelieveld, Sophie Gerhardt, Saskia Maas, Kimberley C Zwiers, Claire de Wit, Maria J Ferraz

J Lipid Res· May 2022

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Glucosylated cholesterol in skin: Synthetic role of extracellular glucocerebrosidase.
Daphne E C Boer, Mina Mirzaian, Maria J Ferraz, Andreea Nadaban, Anne Schreuder

Clin Chim Acta· November 2020

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Role of β-glucosidase 2 in aberrant glycosphingolipid metabolism: model of glucocerebrosidase deficiency in zebrafish.
Lindsey T Lelieveld, Mina Mirzaian, Chi-Lin Kuo, Marta Artola, Maria J Ferraz

J Lipid Res· November 2019

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α-galactosidase A1.1 can functionally complement human α-galactosidase A deficiency associated with Fabry disease.
Kassiani Kytidou, Jules Beekwilder, Marta Artola, Eline van Meel, Ruud H P Wilbers, Maria J Ferraz

J Biol Chem· June 2018

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Simultaneous quantitation of sphingoid bases by UPLC-ESI-MS/MS with identical C-encoded internal standards.
M Mirzaian, P Wisse, M J Ferraz, A R A Marques, P Gaspar

Clin Chim Acta· March 2017

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Accurate quantification of sphingosine-1-phosphate in normal and Fabry disease plasma, cells and tissues by LC-MS/MS with (13)C-encoded natural S1P as internal standard.
Mina Mirzaian, Patrick Wisse, Maria J Ferraz, André R A Marques, Tanit L Gabriel

Clin Chim Acta· August 2016

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Glucosylated cholesterol in mammalian cells and tissues: formation and degradation by multiple cellular β-glucosidases.
André R A Marques, Mina Mirzaian, Hisako Akiyama, Patrick Wisse, Maria J Ferraz

J Lipid Res· March 2016

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Biochemical response to substrate reduction therapy versus enzyme replacement therapy in Gaucher disease type 1 patients.
Bouwien E Smid, Maria J Ferraz, Marri Verhoek, Mina Mirzaian, Patrick Wisse

Orphanet J Rare Dis· March 2016

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Lyso-glycosphingolipid abnormalities in different murine models of lysosomal storage disorders.
Maria J Ferraz, André R A Marques, Paulo Gaspar, Mina Mirzaian, Cindy van Roomen

Mol Genet Metab· February 2016

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Synthesis and Evaluation of Hybrid Structures Composed of Two Glucosylceramide Synthase Inhibitors.
Richard J B H N van den Berg, Erwin R van Rijssel, Maria Joao Ferraz, Judith Houben, Anneke Strijland

ChemMedChem· December 2015

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Development of an acid ceramidase activity-based probe.
Cécile M J Ouairy, Maria J Ferraz, Rolf G Boot, Marc P Baggelaar, Mario van der Stelt

Chem Commun (Camb)· April 2015

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Mass spectrometric quantification of glucosylsphingosine in plasma and urine of type 1 Gaucher patients using an isotope standard.
Mina Mirzaian, Patrick Wisse, Maria J Ferraz, Henrik Gold, Wilma E Donker-Koopman

Blood Cells Mol Dis· April 2015

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Gaucher disease and Fabry disease: new markers and insights in pathophysiology for two distinct glycosphingolipidoses.
Maria J Ferraz, Wouter W Kallemeijn, Mina Mirzaian, Daniela Herrera Moro, Andre Marques

Biochim Biophys Acta· May 2014

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