Drosophila model of human inherited triosephosphate isomerase deficiency glycolytic enzymopathy

Genetics

Volumn 174, Issue 3, 2006, Pages 1237-1246

  Celotto, Alicia M ^b   Frank, Adam C ^b   Seigle, Jacquelyn L ^b   Palladino, Michael J ^a  

^a UNIVERSITY OF PITTSBURGH SCHOOL OF MEDICINE   (United States)

^b NONE

Author keywords

[No Author keywords available]

Indexed keywords

TRIOSEPHOSPHATE ISOMERASE;

ANIMAL CELL; ANIMAL EXPERIMENT; ARTICLE; BIOENERGY; CONTROLLED STUDY; DROSOPHILA; FAMILIAL DISEASE; GENE MUTATION; GENETIC CODE; HEREDITY; INBORN ERROR OF METABOLISM; MISSENSE MUTATION; MOLECULAR CLONING; MOTOR DYSFUNCTION; NONHUMAN; PATHOPHYSIOLOGY; PHENOTYPE; PRIORITY JOURNAL;

AMINO ACID SEQUENCE; AMINO ACID SUBSTITUTION; ANIMALS; DISEASE MODELS, ANIMAL; DROSOPHILA; GENE EXPRESSION REGULATION, ENZYMOLOGIC; HUMANS; LONGEVITY; METABOLIC DISEASES; METABOLISM, INBORN ERRORS; MOLECULAR SEQUENCE DATA; MUTATION, MISSENSE; REVERSE TRANSCRIPTASE POLYMERASE CHAIN REACTION; SEQUENCE HOMOLOGY, AMINO ACID; THREONINE; TRANSGENES; TRIOSE-PHOSPHATE ISOMERASE;

EID: 33751316738     PISSN: 00166731     EISSN: 00166731     Source Type: Journal    
DOI: 10.1534/genetics.106.063206     Document Type: Article

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