Synergistic heterozygosity in mice with inherited enzyme deficiencies of mitochondrial fatty acid β-oxidation

Molecular Genetics and Metabolism

Volumn 85, Issue 1, 2005, Pages 7-11

  Schuler, A Michele ^a   Gower, Barbara A ^b   Matern, Dietrich ^c   Rinaldo, Piero ^c   Vockley, Jerry ^c,d   Wood, Philip A ^a,b  

^a UNIVERSITY OF ALABAMA AT BIRMINGHAM   (United States)

^b UNIVERSITY OF ALABAMA AT BIRMINGHAM   (United States)

^c MAYO CLINIC   (United States)

^d CHILDREN S HOSPITAL OF PITTSBURGH   (United States)

Author keywords

Acyl CoA dehydrogenase; Acylcarnitine; Cold challenge; Fat oxidation; Heterozygous; Hypothermia; Inborn error of metabolism; Metabolic challenge; Mitochondrial; Mouse model

Indexed keywords

BUTYRYL COENZYME A DEHYDROGENASE; LONG CHAIN ACYL COENZYME A DEHYDROGENASE;

ANIMAL MODEL; ARTICLE; BODY TEMPERATURE; COLD TOLERANCE; COLD TREATMENT; CONTROLLED STUDY; ENZYME DEFICIENCY; FATTY ACID METABOLISM; FATTY ACID OXIDATION; FEMALE; GENE MUTATION; GENOTYPE; GLUCOSE BLOOD LEVEL; HETEROZYGOSITY; HYPOTHERMIA; INBORN ERROR OF METABOLISM; MALE; MITOCHONDRION; MOUSE; MUTATION; NONHUMAN; PRIORITY JOURNAL;

EID: 18044397840     PISSN: 10967192     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.ymgme.2004.09.006     Document Type: Article

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