Determination of globotriaosylceramide analogs in the organs of a mouse model of Fabry disease
Author:
Publisher
Elsevier BV
Subject
Cell Biology,Molecular Biology,Biochemistry
Reference38 articles.
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3. Anderson-Fabry disease: clinical manifestations and impact of disease in a cohort of 98 hemizygous males;MacDermot;J. Med. Genet,2001
4. α-galactosidase A deficient mice: a model of Fabry disease;Ohshima;Proc. Natl. Acad. Sci. U.S.A,1997
5. Correction of enzymatic and lysosomal storage defects in Fabry mice by adenovirus-mediated gene transfer;Ziegler;Hum. Gene Ther,1999
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1. Distinctive accumulation of globotriaosylceramide and globotriaosylsphingosine in a mouse model of classic Fabry disease;Molecular Genetics and Metabolism Reports;2023-03
2. A universal GlycoDesign for lysosomal replacement enzymes to improve circulation time and biodistribution;Frontiers in Bioengineering and Biotechnology;2023-02-24
3. Efficient Delivery of Globotriaosylceramide Synthase siRNA using Polyhistidine‐Incorporated Lipid Nanoparticles;Macromolecular Bioscience;2023-02-10
4. Mass Spectrometric Comparison of the Cardiac Globotriaosylceramide Profile in 5 Patients With Fabry’s Disease;Circulation Journal;2022-12-23
5. Fabry disease pain: patient and preclinical parallels;Pain;2020-11-30
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