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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

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Acatalasemia Japanese typeHypocatalasemia
Catalase deficiencyIn BloodMicrobiologicalchemically induced
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Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
Review
2016
Review
2016
Transformation of Step-Growth Polymerization into Living Chain-Growth Polymerization.
 
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Review
2012
Review
2012
Catalase enzyme mutations and their association with diseases
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
Catalase deficiency renders remnant kidneys more susceptible to oxidant tissue injury and renal fibrosis in mice.
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
Lack of Peroxisomal Catalase Causes a Progeric Phenotype in Caenorhabditis elegans*
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
Hereditary catalase deficiencies and increased risk of diabetes
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
Stability of several biochemical markers of bone metabolism.
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
Molecular analysis of human acatalasemia. Identification of a splicing mutation.
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
Role of catalase in the oxidation of mercury vapor.
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 normal human female as a mosaic of X-chromosome activity: studies using the gene for C-6-PD-deficiency as a marker.
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
Hypocatalasemia: a new genetic carrier state.
A clinical, biochemical and genetic study has been made of a rare hereditary disease, acatalasemia, characterized by the absence… Expand
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