Human heme oxygenase-1 deficiency: A lesson on serendipity in the discovery of the novel disease

Pediatrics International

Volumn 49, Issue 2, 2007, Pages 125-132

  Koizumi, Shoichi ^a,b  

^a KANAZAWA UNIVERSITY GRADUATE SCHOOL OF MEDICAL SCIENCE   (Japan)

^b KANAZAWA UNIVERSITY HOSPITAL   (Japan)

Author keywords

Bilirubin; Carbon monoxide; Heme; Heme oxygenase; Serendipity

Indexed keywords

HEME OXYGENASE 1;

ANAMNESIS; CARDIOVASCULAR DISEASE; CASE STUDY; CELL DAMAGE; CLINICAL FEATURE; ENDOTHELIUM CELL; ENZYME ACTIVITY; ENZYME DEFICIENCY; ENZYMOLOGY; GENETIC POLYMORPHISM; GENETIC TRANSFECTION; GROWTH RETARDATION; HEME OXYGENASE 1 DEFICIENCY; HUMAN; KIDNEY DISEASE; LUNG DISEASE; MACROPHAGE; MOLECULAR BIOLOGY; MONOCYTE; MOTOR DEVELOPMENT; NERVOUS SYSTEM; NONHUMAN; PATHOPHYSIOLOGY; PEDIATRICS; PRIORITY JOURNAL; PROMOTER REGION; RELIGION; REVIEW;

ANIMALS; BILIRUBIN; BIOMEDICAL RESEARCH; BIOSYNTHETIC PATHWAYS; HEME; HEME OXYGENASE-1; HUMANS; INFANT, NEWBORN; MALE; METABOLISM, INBORN ERRORS; MICE; MICE, KNOCKOUT;

EID: 34147164095     PISSN: 13288067     EISSN: 1442200X     Source Type: Journal    
DOI: 10.1111/j.1442-200X.2007.02353.x     Document Type: Review

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