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Acatalasia

Known as: Acatalasemia, CATALASE DEFICIENCY, Takahara's Disease 
A rare autosomal recessive disorder resulting from the absence of CATALASE activity. Though usually asymptomatic, a syndrome of oral ulcerations and… Expand
National Institutes of Health

Papers overview

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Review
2019
Review
2019
Reactive species produced in the cell during normal cellular metabolism can chemically react with cellular biomolecules such as… Expand
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Review
2017
Review
2017
Abstract This review is centered on the antioxidant enzyme catalase and will present different aspects of this particular protein… Expand
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Review
2012
Review
2012
Enzyme catalase seems to be the main regulator of hydrogen peroxide metabolism. Hydrogen peroxide at high concentrations is a… Expand
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Highly Cited
2004
Highly Cited
2004
Studies using the nematode Caenorhabditis elegans as a model system to investigate the aging process have implicated the insulin… Expand
Highly Cited
2000
Highly Cited
2000
Partial or near-total lack of erythrocyte catalase activity is a rare condition, generally thought to be benign. However, little… Expand
Highly Cited
1990
Highly Cited
1990
To search for the molecular defect of Japanese-type acatalasemia, we cloned the mutant catalase gene from a person with this… Expand
Highly Cited
1980
Highly Cited
1980
To investigate the importance of catalase as a protecting enzyme against oxidative damage in phagocytic leukocytes, we have… Expand
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Highly Cited
1978
Highly Cited
1978
Abstract In human red blood cells the slow rate of production of hydrogen peroxide limits the rate of oxidation of mercury vapor… Expand
Highly Cited
1960
Highly Cited
1960
A clinical, biochemical and genetic study has been made of a rare hereditary disease, acatalasemia, characterized by the absence… Expand
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