Nov 6, 2014 · Glycogen storage disease type I (GSD I) is a rare disease of variable clinical severity that primarily affects the liver and kidney.

Glycogen storage disease type I (GSD I) is an inherited disease that prevents the liver from properly breaking down stored glycogen, which is necessary to maintain adequate blood sugar levels. GSD I is divided into two main types, GSD Ia and GSD Ib, which differ in cause, presentation, and treatment.

Purpose: Glycogen storage disease type I (GSD I) is a rare disease of variable clinical severity that primarily affects the liver and kidney.

Glycogen storage disease type III (GSD III), also known as Cori disease or Forbes disease, causes glycogen to build up in the liver and muscles. Symptoms typically appear within the first year of life. Children with this type of GSD may have …

Glutathione disulfide (GSSG) is a disulfide derived from two glutathione molecules. [1] In living cells, glutathione disulfide is reduced into two molecules of glutathione with reducing equivalents from the coenzyme NADPH. This reaction is catalyzed by the enzyme glutathione reductase. [2]

Oct 26, 2010 · Glycogen storage disease type I (GSD-I) consists of two subtypes: GSD-Ia, a deficiency in glucose-6-phosphatase-α (G6Pase-α) and GSD-Ib, which is characterized by an absence of a...

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Mar 29, 2021 · Glycogen storage diseases (GSDs) are known as complex disorders with overlapping manifestations. These features also preclude a specific clinical diagnosis, requiring more accurate...

GSDS 2.0 is designed for the visualization of annotated features for genes, and the generation of high-quality figures for publication. Besides the main features (i.e., coordinates of exons/CDS), other annotated features such as conserved elements and binding sites can also be displayed.

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