Reduction of lysosome abundance and GAG accumulation after odiparcil treatment in MPS I and MPS VI models-Reference-Cited by-同舟云学术

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Reduction of lysosome abundance and GAG accumulation after odiparcil treatment in MPS I and MPS VI models

Published:2023-12 Issue: Volume:37 Page:101011
ISSN:2214-4269
Container-title:Molecular Genetics and Metabolism Reports
language:en
Short-container-title:Molecular Genetics and Metabolism Reports

Author:

Tuyaa-Boustugue Pascale,Jantzen Ingrid,Zhang Haoyue,Young Sarah P.,Broqua Pierre,Tallandier Mireille,Entchev Eugeni

Publisher

Elsevier BV

Subject

Endocrinology,Genetics,Molecular Biology

Reference43 articles.

1. The Mucopolysaccharidoses;Neufeld,2001

2. Lysosomal storage diseases;Alroy;J. Inborn Error. Metabol. Screen.,2014

3. Lysosomal storage diseases;Ferreira;Transl. Sci. Rare Dis.,2017

4. Pathogenesis of skeletal and connective tissue involvement in the mucopolysaccharidoses: glycosaminoglycan storage is merely the instigator;Clarke;Rheumatology.,2011

5. Mucopolysaccharidosis Type I;Kubaski;Diagnostics (Basel),2020

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