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American Journal of Physiology. Endocrinology and Metabolism|May 18, 2006
Parenteral and enteral metabolism of anaplerotic triheptanoin in normal ratsRenée P Kinman, Takhar Kasumov, Kathryn A Jobbins, et al.
Living Journal of Computational Molecular Science|April 2, 2026
Quantifying Spatially Resolved Hydration Thermodynamics Using Grid Inhomogeneous Solvation Theory [Article v1.0]Valentin J Egger-Hoerschinger, Franz Waibl, Vjay Molino, et al.
American Journal of Human Genetics|May 1, 1993
Medium-chain acyl-CoA dehydrogenase (MCAD) deficiency: diagnosis by acylcarnitine analysis in bloodJ L Van Hove, W Zhang, S G Kahler, et al.
Nucleic Acids Research|November 23, 2013
Saccharomyces genome database provides new regulation dataMaria C Costanzo, Stacia R Engel, Edith D Wong, et al.
Journal of the National Cancer Institute|January 22, 2004
Effects of reduced cigarette smoking on the uptake of a tobacco-specific lung carcinogenStephen S Hecht, Sharon E Murphy, Steven G Carmella, et al.
Molecular Genetics and Metabolism|January 20, 2007
REMOVED: Short-chain acyl-CoA dehydrogenase gene mutation (319 C>T) presents with clinical heterogeneity and is candidate founder mutation in Ashkenazi Jewish populationIngrid Tein, Orly Elpeleg, Bruria Ben-Zeev, et al.
Molecular Genetics and Metabolism|October 3, 2002
Identification of isobutyryl-CoA dehydrogenase and its deficiency in humansTien V Nguyen, Brage S Andresen, Thomas J Corydon, et al.
Human Molecular Genetics|April 1, 1996
Cloning and characterization of human very-long-chain acyl-CoA dehydrogenase cDNA, chromosomal assignment of the gene and identification in four patients of nine different mutations within the VLCAD geneB S Andresen, P Bross, C Vianey-Saban, et al.
Molecular Genetics and Metabolism|December 7, 2007
Short-chain acyl-CoA dehydrogenase gene mutation (c.319C>T) presents with clinical heterogeneity and is candidate founder mutation in individuals of Ashkenazi Jewish originIngrid Tein, Orly Elpeleg, Bruria Ben-Zeev, et al.
JAMA Neurology|August 12, 2014
Triheptanoin for glucose transporter type I deficiency (G1D): modulation of human ictogenesis, cerebral metabolic rate, and cognitive indices by a food supplementJuan M Pascual, Peiying Liu, Deng Mao, et al.
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