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Charles R Roe

Showing results (11-20 of 24) with videos related to

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The Journal of Clinical Investigation|July 18, 2002
Treatment of cardiomyopathy and rhabdomyolysis in long-chain fat oxidation disorders using an anaplerotic odd-chain triglycerideCharles R Roe, Lawrence Sweetman, Diane S Roe, et al.
American Journal of Veterinary Research|March 2, 2010
Effect of dietary fats with odd or even numbers of carbon atoms on metabolic response and muscle damage with exercise in Quarter Horse-type horses with type 1 polysaccharide storage myopathyLisa A Borgia, Stephanie J Valberg, Molly E McCue, et al.
American Journal of Veterinary Research|August 4, 2009
Effect of triheptanoin on muscle metabolism during submaximal exercise in horsesMolly E McCue, Stephanie J Valberg, Joe D Pagan, et al.
Molecular Genetics and Metabolism|March 23, 2005
Pyruvate carboxylase deficiency: clinical and biochemical response to anaplerotic diet therapyFanny Mochel, Pascale DeLonlay, Guy Touati, et al.
American Journal of Physiology. Endocrinology and Metabolism|November 12, 2009
Parenteral and enteral metabolism of anaplerotic triheptanoin in normal rats. II. Effects on lipolysis, glucose production, and liver acyl-CoA profileLei Gu, Guo-Fang Zhang, Rajan S Kombu, et al.
Analytical Biochemistry|May 23, 2002
Assay of the concentration and (13)C isotopic enrichment of propionyl-CoA, methylmalonyl-CoA, and succinyl-CoA by gas chromatography-mass spectrometryTakhar Kasumov, Wenjun Z Martini, Aneta E Reszko, et al.
Plos One|October 10, 2014
Anaplerotic triheptanoin diet enhances mitochondrial substrate use to remodel the metabolome and improve lifespan, motor function, and sociability in MeCP2-null miceMin Jung Park, Susan Aja, Qun Li, et al.
Scientific Reports|March 1, 2023
Maximum dose, safety, tolerability and ketonemia after triheptanoin in glucose transporter type 1 deficiency (G1D)Ignacio Málaga, Adrian Avila, Sharon Primeaux, et al.
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.
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.
Pageof 3

Showing results (11-20 of 24) with videos related to

Sort By:
Pageof 3
The Journal of Clinical Investigation|July 18, 2002
Treatment of cardiomyopathy and rhabdomyolysis in long-chain fat oxidation disorders using an anaplerotic odd-chain triglycerideCharles R Roe, Lawrence Sweetman, Diane S Roe, et al.
American Journal of Veterinary Research|March 2, 2010
Effect of dietary fats with odd or even numbers of carbon atoms on metabolic response and muscle damage with exercise in Quarter Horse-type horses with type 1 polysaccharide storage myopathyLisa A Borgia, Stephanie J Valberg, Molly E McCue, et al.
American Journal of Veterinary Research|August 4, 2009
Effect of triheptanoin on muscle metabolism during submaximal exercise in horsesMolly E McCue, Stephanie J Valberg, Joe D Pagan, et al.
Molecular Genetics and Metabolism|March 23, 2005
Pyruvate carboxylase deficiency: clinical and biochemical response to anaplerotic diet therapyFanny Mochel, Pascale DeLonlay, Guy Touati, et al.
American Journal of Physiology. Endocrinology and Metabolism|November 12, 2009
Parenteral and enteral metabolism of anaplerotic triheptanoin in normal rats. II. Effects on lipolysis, glucose production, and liver acyl-CoA profileLei Gu, Guo-Fang Zhang, Rajan S Kombu, et al.
Analytical Biochemistry|May 23, 2002
Assay of the concentration and (13)C isotopic enrichment of propionyl-CoA, methylmalonyl-CoA, and succinyl-CoA by gas chromatography-mass spectrometryTakhar Kasumov, Wenjun Z Martini, Aneta E Reszko, et al.
Plos One|October 10, 2014
Anaplerotic triheptanoin diet enhances mitochondrial substrate use to remodel the metabolome and improve lifespan, motor function, and sociability in MeCP2-null miceMin Jung Park, Susan Aja, Qun Li, et al.
Scientific Reports|March 1, 2023
Maximum dose, safety, tolerability and ketonemia after triheptanoin in glucose transporter type 1 deficiency (G1D)Ignacio Málaga, Adrian Avila, Sharon Primeaux, et al.
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.
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.
Pageof 3