Quantitation of acyl-CoA and acylcarnitine esters accumulated during abnormal mitochondrial fatty acid oxidation.-Reference-Cited by-同舟云学术

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Quantitation of acyl-CoA and acylcarnitine esters accumulated during abnormal mitochondrial fatty acid oxidation.

Published:1991-12 Issue:34 Volume:266 Page:22932-22938
ISSN:0021-9258
Container-title:Journal of Biological Chemistry
language:en
Short-container-title:Journal of Biological Chemistry

Author:

Kler R.S.,Jackson S.,Bartlett K.,Bindoff L.A.,Eaton S.,Pourfarzam M.,Frerman F.E.,Goodman S.I.,Watmough N.J.,Turnbull D.M.

Publisher

Elsevier BV

Subject

Cell Biology,Molecular Biology,Biochemistry

Reference33 articles.

1. Reverse-phase high-performance liquid chromatographic analysis of short-, medium- and long-chain acylcarnitines in urine and plasma

2. Neonatal glutaric aciduria type II: An X-linked recessive inherited disorder

3. Fluorometric assay of acyl-CoA dehydrogenases in normal and mutant human fibroblasts

4. Substrate Channeling of NADH and Binding of Dehydrogenases to Complex I

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