Recent development and gene therapy for glycogen storage disease type Ia-Reference-Cited by-同舟云学术

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Recent development and gene therapy for glycogen storage disease type Ia

Published:2017-09 Issue:3 Volume:1 Page:174-180
ISSN:2542-5684
Container-title:Liver Research
language:en
Short-container-title:Liver Research

Author:

Chou Janice Y.,Kim Goo-Young,Cho Jun-Ho

Funder

National Institutes of Health

Eunice Kennedy Shriver National Institute of Child Health and Human Development

Publisher

Elsevier BV

Subject

Gastroenterology,Hepatology

Reference52 articles.

1. Type I glycogen storage diseases: disorders of the glucose-6-phosphatase complex;Chou;Curr Mol Med,2002

2. Glycogen storage disease type I and G6Pase-β deficiency: etiology and therapy;Chou;Nat Rev Endocrinol,2010

3. Type I glycogen storage diseases: disorders of the glucose-6-phosphatase/glucose-6-phosphate transporter complexes;Chou;J Inherit Metab Dis,2015

4. The catalytic center of glucose-6-phosphatase: His176 is the nucleophile forming the phosphohistidine-enzyme intermediate during catalysis;Ghosh;J Biol Chem,2002

5. Continuous nocturnal intragastric feeding for management of type 1 glycogen-storage disease;Greene;N Engl J Med,1976

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1. A case study of a liver transplant-treated patient with glycogen storage disease type Ia presenting with multiple inflammatory hepatic adenomas: an analysis of clinicopathologic and genetic data;BMC Medical Genomics;2024-05-06

2. Medium-Chain Triglyceride Oil and Dietary Intervention Improved Body Composition and Metabolic Parameters in Children with Glycogen Storage Disease Type 1 in Jordan: A Clinical Trial;Foods;2024-04-02

3. Efficient and reproducible generation of human induced pluripotent stem cell-derived expandable liver organoids for disease modeling;Scientific Reports;2023-12-22

4. Glycogen storage disease type I: Genetic etiology, clinical manifestations, and conventional and gene therapies;Pediatric Discovery;2023-07-24

5. Gene therapy and genome editing for type I glycogen storage diseases;Frontiers in Molecular Medicine;2023-03-31

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