Understanding cerebral L-lysine metabolism: the role of L-pipecolate metabolism in Gcdh-deficient mice as a model for glutaric aciduria type I-Reference-Cited by-同舟云学术

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Understanding cerebral L-lysine metabolism: the role of L-pipecolate metabolism in Gcdh-deficient mice as a model for glutaric aciduria type I

Published:2014-09-12 Issue:2 Volume:38 Page:265-272
ISSN:0141-8955
Container-title:Journal of Inherited Metabolic Disease
language:en
Short-container-title:J Inherit Metab Dis

Author:

Posset Roland,Opp Silvana,Struys Eduard A.,Völkl Alfred,Mohr Heribert,Hoffmann Georg F.,Kölker Stefan,Sauer Sven W.,Okun Jürgen G.

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Link

http://link.springer.com/content/pdf/10.1007/s10545-014-9762-z

Reference27 articles.

1. Blemings KP, Crenshaw TD, Swick RW, Benevenga NJ (1994) Lysine-alpha-ketoglutarate reductase and saccharopine dehydrogenase are located only in the mitochondrial matrix in rat liver. J Nutr 124:1215–1221

2. Chang YF (1976) Pipecolic acid pathway: the major lysine metabolic route in the rat brain. Biochem Biophys Res Commun 69:174–180

3. Cimini AM, Moreno S, Giorgi M, Serafini B, Cerú MP (1993) Purification of peroxisomal fraction from rat brain. Neurochem Int 23:249–260

4. Danhauser K, Sauer SW, Haack TB et al (2012) DHTKD1 mutations cause 2-aminoadipic and 2-oxoadipic aciduria. Am J Hum Genet 91:1082–1087

5. Goodman SI, Markey SP, Moe PG, Miles BS, Teng CC (1975) Glutaric aciduria; a “new” disorder of amino acid metabolism. Biochem Med 12:12–21

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