Sizing up sialic acid in glomerular disease
Author:
Publisher
American Society for Clinical Investigation
Subject
General Medicine
Reference23 articles.
1. Mutation in the key enzyme of sialic acid biosynthesis causes severe glomerular proteinuria and is rescued by N-acetylmannosamine
2. A Bifunctional Enzyme Catalyzes the First Two Steps in N-Acetylneuraminic Acid Biosynthesis of Rat Liver
3. UDP-GlcNAc 2-Epimerase: A Regulator of Cell Surface Sialylation
4. The UDP-N-acetylglucosamine 2-epimerase/N-acetylmannosamine kinase gene is mutated in recessive hereditary inclusion body myopathy
5. Mutations spectrum ofGNE in hereditary inclusion body myopathy sparing the quadriceps
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2. Explorations in a galaxy of sialic acids: a review of sensing horizons, motivated by emerging biomedical and nutritional relevance;Sensors & Diagnostics;2022
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4. Insulin resistance in glomerular podocytes: Potential mechanisms of induction;Archives of Biochemistry and Biophysics;2021-10
5. Elevated Plasma Free Sialic Acid Levels in Individuals with Reduced Glomerular Filtration Rates;Kidney360;2020-07-09
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