Abnormal Lipid Metabolism in Cystathionine β-Synthase-deficient Mice, an Animal Model for Hyperhomocysteinemia
Author:
Publisher
Elsevier BV
Subject
Cell Biology,Molecular Biology,Biochemistry
Reference41 articles.
1. Homocystinuria due to cystathionine synthase deficiency: Enzymatic and ultrastructural studies
2. Endothelial dysfunction in a murine model of mild hyperhomocyst(e)inemia
3. Homocysteine-induced endoplasmic reticulum stress causes dysregulation of the cholesterol and triglyceride biosynthetic pathways
4. Overexpression of cellular glutathione peroxidase rescues homocyst(e)ine-induced endothelial dysfunction
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