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Literature DB >> 10989435

Mammalian branched-chain acyl-CoA dehydrogenases: molecular cloning and characterization of recombinant enzymes.

J Vockley¹, A Mohsen al-W, B Binzak, J Willard, A Fauq.

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Year: 2000 PMID： 10989435 DOI： 10.1016/s0076-6879(00)24236-5

Source DB: PubMed Journal: Methods Enzymol ISSN： 0076-6879 Impact factor: 1.600

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15 in total

1. Metabolic analysis reveals evidence for branched chain amino acid catabolism crosstalk and the potential for improved treatment of organic acidurias.

Authors: Stephen McCalley; David Pirman; Michelle Clasquin; Kendall Johnson; Shengfang Jin; Jerry Vockley
Journal: Mol Genet Metab Date: 2019-05-21 Impact factor: 4.797

Review 2. Newborn screening: After the thrill is gone.

Authors: Jerry Vockley
Journal: Mol Genet Metab Date: 2007-07-02 Impact factor: 4.797

3. Evidence for involvement of medium chain acyl-CoA dehydrogenase in the metabolism of phenylbutyrate.

Authors: Kaitlyn Kormanik; Heejung Kang; Dean Cuebas; Jerry Vockley; Al-Walid Mohsen
Journal: Mol Genet Metab Date: 2012-10-18 Impact factor: 4.797

4. Low expression of long-chain acyl-CoA dehydrogenase in human skeletal muscle.

Authors: Amy C Maher; Al-Walid Mohsen; Jerry Vockley; Mark A Tarnopolsky
Journal: Mol Genet Metab Date: 2010-03-19 Impact factor: 4.797

5. Characterization of new ACADSB gene sequence mutations and clinical implications in patients with 2-methylbutyrylglycinuria identified by newborn screening.

Authors: Jaffar Alfardan; Al-Walid Mohsen; Sara Copeland; Jay Ellison; Laura Keppen-Davis; Marianne Rohrbach; Berkley R Powell; Jane Gillis; Dietrich Matern; Jeffrey Kant; Jerry Vockley
Journal: Mol Genet Metab Date: 2010-05-23 Impact factor: 4.797

Mammalian branched-chain acyl-CoA dehydrogenases: molecular cloning and characterization of recombinant enzymes.

1. Metabolic analysis reveals evidence for branched chain amino acid catabolism crosstalk and the potential for improved treatment of organic acidurias.

Review 2. Newborn screening: After the thrill is gone.

3. Evidence for involvement of medium chain acyl-CoA dehydrogenase in the metabolism of phenylbutyrate.

4. Low expression of long-chain acyl-CoA dehydrogenase in human skeletal muscle.

5. Characterization of new ACADSB gene sequence mutations and clinical implications in patients with 2-methylbutyrylglycinuria identified by newborn screening.

6. Kinetic and spectral properties of isovaleryl-CoA dehydrogenase and interaction with ligands.

7. An acyl-CoA dehydrogenase microplate activity assay using recombinant porcine electron transfer flavoprotein.

8. Evidence for physical association of mitochondrial fatty acid oxidation and oxidative phosphorylation complexes.

9. c-Myc programs fatty acid metabolism and dictates acetyl-CoA abundance and fate.

10. Clinical and neurocognitive outcome in symptomatic isovaleric acidemia.