Altered hepatic sulfur metabolism in cystathionine β‐synthase‐deficient homocystinuria: regulatory role of taurine on competing cysteine oxidation pathways
Author:
Affiliation:
1. Department of PediatricsUniversity of Colorado Health Sciences CenterAuroraColoradoUSA
2. Department of MedicineUniversity of Colorado Health Sciences CenterAuroraColoradoUSA
Publisher
Wiley
Subject
Genetics,Molecular Biology,Biochemistry,Biotechnology
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1096/fj.14-253633
Reference36 articles.
1. Dealing with methionine/homocysteine sulfur: cysteine metabolism to taurine and inorganic sulfur
2. A rationale for cystine supplementation in severe homocystinuria
3. Dietary practices in pyridoxine non-responsive homocystinuria: A European survey
4. Treatment of Inherited Homocystinurias
5. High homocysteine and thrombosis without connective tissue disorders are associated with a novel class of cystathionine β-synthase (CBS) mutations
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