Mouse model of encephalopathy and novel treatment strategies with substrate competition in glutaric aciduria type I

Molecular Genetics and Metabolism

Volumn 100, Issue SUPPL., 2010, Pages

  Zinnanti, William J ^a   Lazovic, Jelena ^b  

^a SUNY Downstate Medical Center   (United States)

^b CALIFORNIA INSTITUTE OF TECHNOLOGY   (United States)

Author keywords

Glutaric aciduria; Metabolic encephalopathy; Mouse model

Indexed keywords

GLUCOSE; GLUTARIC ACID; HYDROXYLYSINE; LYSINE; NEUROTRANSMITTER; TRYPTOPHAN;

AGE; AMINO ACID METABOLISM; AMINO ACID TRANSPORT; ANIMAL EXPERIMENT; ANIMAL MODEL; ARTICLE; BIOACCUMULATION; BLOOD BRAIN BARRIER; BRAIN INJURY; CITRIC ACID CYCLE; CORPUS STRIATUM; DISEASE PREDISPOSITION; GLUTARIC ACIDURIA TYPE I; HUNTINGTON CHOREA; INBORN ERROR OF METABOLISM; METABOLIC ENCEPHALOPATHY; MOUSE; NERVE CELL LESION; NONHUMAN; PRIORITY JOURNAL; UREA CYCLE DISORDER;

ANIMALS; BIOLOGICAL TRANSPORT; BRAIN DISEASES, METABOLIC; DISEASE MODELS, ANIMAL; DISEASE SUSCEPTIBILITY; GLUCOSE; HUMANS; MICE; MULTIPLE ACYL COENZYME A DEHYDROGENASE DEFICIENCY; SUBSTRATE SPECIFICITY;

ANIMALIA; MUS;

EID: 77950324112     PISSN: 10967192     EISSN: 10967206     Source Type: Journal    
DOI: 10.1016/j.ymgme.2010.02.022     Document Type: Article

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