2,8-dihydroxyadenine

Known as: 6-amino-1H-purine-2,8(3H,7H)-dione, 6-amino-2,8-dihydroxypurine 
 
National Institutes of Health

Papers overview

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2014
2014
Adenine phosphoribosyltransferase (APRT) deficiency is a rare autosomal recessive enzyme defect of purine metabolism that usually… (More)
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2007
2007
The electrochemical behaviour of 2,8-dihydroxyadenine (2,8-DHA)- the main adenine oxidation product- has been investigated over a… (More)
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Review
2007
Review
2007
Adenine phosphoribosyltransferase (APRT, EC 2.4.2.7) deficiency is an enzymopathy of purine metabolism, which is inherited as an… (More)
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2000
2000
BACKGROUND We have developed a knockout mouse model for adenine phosphoribosyltransferase (APRT) deficiency, a condition that… (More)
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1996
1996
Adenine phosphoribosyltransferase (APRT) deficiency in humans is an autosomal recessive syndrome characterized by the urinary… (More)
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1996
1996
Deficiencies in different steps of purine metabolism give rise to a number of human inherited disorders. Lesch-Nyhan syndrome is… (More)
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1994
1994
Adenine phosphoribosyltransferase (APRT) catalyzes the synthesis of AMP from adenine and 5-phosphoribosyl-lpyrophosphate… (More)
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1993
1993
Homozygous adenine phosphoribosyltransferase deficiency is a genetic defect that is associated with 2,8-dihydroxyadenine… (More)
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1984
1984
Levels of sodium, potassium, calcium, and phosphate were examined in rats fed on an adenine diet. Among the electrolytes in the… (More)
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1980
1980
A new method of high performance liquid chromatography (HPLC) which makes it possible to analyse 2,8-dihydroxyadenine (DOA) in… (More)
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