Aortopathies in mouse models of Pompe, Fabry and Mucopolysaccharidosis IIIB lysosomal storage diseases-Reference-Cited by-同舟云学术

Aortopathies in mouse models of Pompe, Fabry and Mucopolysaccharidosis IIIB lysosomal storage diseases

Published:2020-05-19 Issue:5 Volume:15 Page:e0233050
ISSN:1932-6203
Container-title:PLOS ONE
language:en
Short-container-title:PLoS ONE

Author:

Belfiore Maria Paola,Iacobellis Francesca,Acampora Emma,Caiazza Martina,Rubino Marta,Monda Emanuele,Magaldi Maria Rosaria,Tarallo Antonietta,Sasso Marcella,De Pasquale Valeria,Grassi Roberto,Cappabianca Salvatore,Calabrò Paolo,Fecarotta Simona,Esposito Salvatore,Esposito Giovanni,Pisani Antonio,Pavone Luigi Michele,Parenti Giancarlo,Limongelli Giuseppe^ORCID

Publisher

Public Library of Science (PLoS)

Subject

Multidisciplinary

Reference41 articles.

1. Lysosomal storage disease overview;A Sun;Ann Transl Med,2018

2. Lysosomal storage diseases;FM Platt;Nat Rev Dis Primers,2018

3. Lysosomal storage diseases: from pathophysiology to therapy;G Parenti;Annu Rev Med,2015

4. Lysosomal storage disorders affecting the heart: a review;V Nair;Cardiovasc Pathol,2019

5. Pompe Disease: From Basic Science to Therapy;L Kohler;Neurotherapeutics,2018

Cited by 13 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Metabolic rewiring and autophagy inhibition correct lysosomal storage disease in mucopolysaccharidosis IIIB;iScience;2024-03

2. Congenital Heart Malformations Masked by Infantile Gangliosidosis—Case Report and Growing Evidence for Metabolic Disease-Associated Aortopathies;Diagnostics;2024-02-24

3. Lentiviral Gene Therapy for Mucopolysaccharidosis II with Tagged Iduronate 2-Sulfatase Prevents Life-Threatening Pathology in Peripheral Tissues But Fails to Correct Cartilage;Human Gene Therapy;2024-02-02

4. An Overview of Molecular Mechanisms in Fabry Disease;Biomolecules;2022-10-12

5. Lysosomal positioning diseases: beyond substrate storage;Open Biology;2022-10