Mutations associated with functional disorder of xanthine oxidoreductase and hereditary xanthinuria in humans

International Journal of Molecular Sciences

Volumn 13, Issue 11, 2012, Pages 15475-15495

  Ichida, Kimiyoshi ^a   Amaya, Yoshihiro ^b   Okamoto, Ken ^c   Nishino, Takeshi ^c,d  

^a TOKYO UNIVERSITY OF PHARMACY AND LIFE SCIENCES   (Japan)

^b NIIGATA UNIVERSITY GRADUATE SCHOOL OF MEDICAL AND DENTAL SCIENCES   (Japan)

^c NIPPON MEDICAL SCHOOL   (Japan)

^d UNIVERSITY OF TOKYO   (Japan)

Author keywords

Flavoproteins; Gout; Hereditary xanthinuria; Xanthine dehydrogenase; Xanthine oxidase; Xanthine oxidoreductase; Xanthine oxidoreductase deficiency; Xanthinuria

Indexed keywords

ALLOPURINOL; FLAVINE ADENINE NUCLEOTIDE; IRON; SULFUR; URIC ACID; XANTHINE OXIDASE; XANTHINE OXIDASE INHIBITOR; ALDEHYDE OXIDASE; XANTHINE; XANTHINE DEHYDROGENASE;

AMINO ACID SEQUENCE; AMINO TERMINAL SEQUENCE; CARBOXY TERMINAL SEQUENCE; CRYSTAL STRUCTURE; DIFFERENTIAL DIAGNOSIS; ENZYME ACTIVATION; ENZYME ACTIVITY; ENZYME MECHANISM; ENZYME SUBSTRATE; FUNCTIONAL DISEASE; GENE; HUMAN; HYDROXYLATION; HYPOURICEMIA; MOCO SULFURASE GENE; MUTATIONAL ANALYSIS; NONHUMAN; PHENOTYPIC VARIATION; PROTEIN DOMAIN; REACTION ANALYSIS; RESIDUE ANALYSIS; REVIEW; SEQUENCE ANALYSIS; STRUCTURE ACTIVITY RELATION; STRUCTURE ANALYSIS; URIC ACID BLOOD LEVEL; URINALYSIS; XANTHINE OXIDOREDUCTASE GENE; XANTHINURIA; ANIMAL; CHEMISTRY; DEFICIENCY; GENETIC ASSOCIATION; GENETICS; METABOLISM; METABOLISM, INBORN ERRORS; MUTATION; PROTEIN CONFORMATION; PURINE-PYRIMIDINE METABOLISM, INBORN ERRORS;

ALDEHYDE OXIDASE; ANIMALS; DIAGNOSIS, DIFFERENTIAL; ENZYME ACTIVATION; GENETIC ASSOCIATION STUDIES; HUMANS; METABOLISM, INBORN ERRORS; MUTATION; PROTEIN CONFORMATION; PROTEIN INTERACTION DOMAINS AND MOTIFS; PURINE-PYRIMIDINE METABOLISM, INBORN ERRORS; XANTHINE; XANTHINE DEHYDROGENASE;

EID: 84870688466     PISSN: 16616596     EISSN: 14220067     Source Type: Journal    
DOI: 10.3390/ijms131115475     Document Type: Review

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