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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
2016
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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2005
2005
BACKGROUND Catalase is one of the important antioxidant enzymes regulating the levels of intracellular hydrogen peroxide and… 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
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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
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2000
2000
The determination of bone metabolism markers is useful in monitoring pharmacological therapy for osteoporosis (1)(2)(3). During… Expand
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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
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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
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1962
1962
The question why human females do not synthesize twice as much of those enzymes controlled by a locus on the X-chromosome as do… Expand
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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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