MeSH Review:
Acatalasia
- Molecular defect in human acatalasia fibroblasts. Crawford, D.R., Mirault, M.E., Moret, R., Zbinden, I., Cerutti, P.A. Biochem. Biophys. Res. Commun. (1988)
- A metabolic disorder similar to Zellweger syndrome with hepatic acatalasia and absence of peroxisomes, altered content and redox state of cytochromes, and infantile cirrhosis with hemosiderosis. Versmold, H.T., Bremer, H.J., Herzog, V., Siegel, G., Bassewitz, D.B., Irle, U., Voss, H., Lombeck, I., Brauser, B. Eur. J. Pediatr. (1977)
- Lack of peroxisomal catalase causes a progeric phenotype in Caenorhabditis elegans. Petriv, O.I., Rachubinski, R.A. J. Biol. Chem. (2004)
- Isolation of a cDNA clone for murine catalase and analysis of an acatalasemic mutant. Shaffer, J.B., Sutton, R.B., Bewley, G.C. J. Biol. Chem. (1987)
- Molecular analysis of human acatalasemia. Identification of a splicing mutation. Wen, J.K., Osumi, T., Hashimoto, T., Ogata, M. J. Mol. Biol. (1990)
- Properties of residual catalase in the erythrocytes of Japanese-type acatalasemia. Ogata, M., Mizugaki, J. Hum. Genet. (1979)
- Catalase and dehydroascorbate reductase in human polymorphonuclear leukocytes (PMN): possible functional relationship. Stankova, L., Bigley, R., Wyss, S.R., Aebi, H. Experientia (1979)
- Recovery of catalase activity after inhibition with aminotriazole in acatalasemia mice. Ogata, M., Mizugaki, J., Takahara, S. Tohoku J. Exp. Med. (1975)
- Activities of catalase in leucocytes and glucose-6-phosphate dehydrogenase in erythrocytes of hypocatalasemia and acatalasemia. Ogata, M., Mizugaki, J., Taketa, K., Takahara, S. Tohoku J. Exp. Med. (1977)
- Polyacrylamide gradient gel electrophoretic studies of residual catalase in acatalasemia. Ogata, M., Mizugaki, J., Izumi, M., Taketa, K. Physiological chemistry and physics and medical NMR. (1983)
- Factors involved in heavy metal poisoning. Clarkson, T.W. Fed. Proc. (1977)
- Activities of superoxide dismutase and glutathione peroxidase in the red cells of Japanese acatalasemia blood. Ogata, M., Mizugaki, J., Ueda, K., Ikeda, M. Tohoku J. Exp. Med. (1977)
- A novel catalase mutation detected by polymerase chain reaction-single strand conformation polymorphism, nucleotide sequencing, and western blot analyses is responsible for the type C of Hungarian acatalasemia. Góth, L., Rass, P., Madarasi, I. Electrophoresis (2001)
- Immunological properties of erythrocyte catalase in Japanese type acatalasemia. Ogata, M., Mizugaki, J. Acta Med. Okayama (1982)