Metabolism of lysine in α-aminoadipic semialdehyde dehydrogenase-deficient fibroblasts: Evidence for an alternative pathway of pipecolic acid formation
Author:
Publisher
Wiley
Subject
Cell Biology,Genetics,Molecular Biology,Biochemistry,Structural Biology,Biophysics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1016/j.febslet.2009.11.055/fullpdf
Reference16 articles.
1. Metabolism of lysine in rat liver;Higashino;Biochem. Biophys. Res. Commun.,1967
2. Familial hyperlysinemia with lysine-ketoglutarate reductase insufficiency;Dancis;J. Clin. Invest.,1969
3. Multiple enzyme defects in familial hyperlysinemia;Dancis;Pediatr. Res.,1976
4. Biosynthesis of saccharopine and pipecolic acid from l- and dl-14C-lysine by human and dog liver in vitro;Ghadimi;Biochem. Med.,1971
5. Lysine metabolism in the human and the monkey: demonstration of pipecolic acid formation in the brain and other organs;Chang;Neurochem. Res.,1982
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