Pompe disease: Shared and unshared features of lysosomal storage disorders-Reference-Cited by-同舟云学术

Pompe disease: Shared and unshared features of lysosomal storage disorders

Published:2015-01 Issue:1 Volume:3 Page:e1068978
ISSN:2167-5511
Container-title:Rare Diseases
language:en
Short-container-title:Rare Diseases

Author:

Lim Jeong-A¹,Kakhlon Or²,Li Lishu¹,Myerowitz Rachel¹³,Raben Nina¹

Affiliation:

1. Laboratory of Muscle Stem Cells and Gene Regulation; National Institute of Arthritis and Musculoskeletal and Skin Diseases; National Institutes of Health; Bethesda, MD USA

2. Department of Neurology; Hadassah-Hebrew University Medical Center; Ein Kerem, Jerusalem, Israel

3. St. Mary's College of Maryland; St. Mary's City, MD USA

Publisher

Informa UK Limited

Subject

General Medicine

Link

https://www.tandfonline.com/doi/pdf/10.1080/21675511.2015.1068978

Reference51 articles.

1. Lysosomal storage disorders: The cellular impact of lysosomal dysfunction

2. Hirschhorn R, Reuser AJ. Glycogen Storage Disease Type II: Acid alpha-Glucosidase (Acid Maltase) Deficiency. The Metabolic and Molecular Basis of Inherited Disease. New York, NY: McGraw-Hill, 2001:3389-420

3. Pompe disease: from pathophysiology to therapy and back again

4. Glycoengineered Acid α-Glucosidase With Improved Efficacy at Correcting the Metabolic Aberrations and Motor Function Deficits in a Mouse Model of Pompe Disease

5. Glycosylation-independent Lysosomal Targeting of Acid α-Glucosidase Enhances Muscle Glycogen Clearance in Pompe Mice

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3. Lysosomes as coordinators of cellular catabolism, metabolic signalling and organ physiology;Nature Reviews Molecular Cell Biology;2023-11-24

4. From Acid Alpha-Glucosidase Deficiency to Autophagy: Understanding the Bases of POMPE Disease;International Journal of Molecular Sciences;2023-08-05

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