Genomic variation in myeloperoxidase gene in the Japanese population

Japanese Journal of Infectious Diseases

Volumn 57, Issue 5, 2004, Pages

  Kameoka, Yosuke ^a   Persad, Amanda S ^b   Suzuki, Kazuo ^a  

^a NATIONAL INSTITUTE OF INFECTIOUS DISEASES   (Japan)

^b Burdock Group   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ARGININE; CYSTEINE; GENOMIC DNA; GLYCINE; HEMOPROTEIN; HISTIDINE; MYELOPEROXIDASE; SERINE; PEROXIDASE;

AMINO ACID SUBSTITUTION; CLINICAL EXAMINATION; CONFERENCE PAPER; DNA DETERMINATION; ENZYME DEFICIENCY; EXON; GENE MUTATION; GENETIC CODE; GENETIC VARIABILITY; HETEROZYGOSITY; HOMOZYGOSITY; HOST RESISTANCE; HUMAN; HUMAN CELL; INCIDENCE; INFECTION RESISTANCE; JAPAN; LEUKOCYTE DISORDER; MAJOR CLINICAL STUDY; NUCLEIC ACID BASE SUBSTITUTION; POPULATION GENETICS; PREVALENCE; ARTICLE; ENZYMOLOGY; GENETICS; MUTATION; NEUTROPHIL;

HUMANS; JAPAN; MUTATION; NEUTROPHILS; PEROXIDASE; VARIATION (GENETICS);

EID: 9144242497     PISSN: 13446304     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Conference Paper

References (8)

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2. Davey, C. A,. and Fenna, R. E (1996): A resolution X-ray crystal structure of the bisubstrate analogue inhibitors salicylhydroxamic acid bound to human myeloperoxidase: A model for prereaction complex with hydrogren peroxide. Biochemistry, 35, 10967-10973.
3. DeLeo, F.R., Goedken, M., McCormick, S. J. and Nauseef, W. M. (1998): A novel from hereditary myeloperoxidase deficiency linked to endoplasmic reticulum/proteasome degradation. J. Clin. Invest., 101, 2900-2909.
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5. Nauseef, W. M., Coley, M. McCormick, S. (1996): Effect of the R569W missense mutation on the biosynthesis of myeloperoxidase. J. Biol. Chem., 271, 9546-9549.
6. Ohashi, Y. Y., Kameoka, Y., Persad, A. S., Koi, F., Yamagoe, S., Hashimoto, K., and Suzuki, K. (2004): Novel missense mutation found in a Japanese patient with myeloperoxidase deficiency. Gene, 327, 195-200.
7. Romano, M., Dri, P. Dadalt, L., Patriarca, P. and Baralle, F. E (1997): Biochemical and molecular characterization of hereditary myeloproliferative deficiency. Blood, 90, 4126-4134.
8. Nunoi, H., Kohi, F., Kajiwara, H. and Suzuki, K. (2003): Prevalence inherited myeloperoxidase deficiency in Japan. Microbiol. Immunol., 47, 527-531.