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Dihydropyrimidine Dehydrogenase Deficiency

Known as: Pyrimidinemia, Familial, Hereditary Thymine-Uraciluria, Thymine-Uracilurias, Hereditary 
An autosomal recessive disorder affecting DIHYDROPYRIMIDINE DEHYDROGENASE and causing familial pyrimidinemia. It is characterized by thymine… 
National Institutes of Health

Papers overview

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2010
2010
Given a connected simple (p, q)-graph G = (V,E) and ∅ = M ⊆ V, we initiate a study of the set-valued function f : V → 2M… 
2007
2007
본 논문은 분산 보안 정책을 지정하기 위해 객체그룹을 사용하는 u-헬스케어 컴퓨팅 환경에서 응용 서비스를 위해 동적보안 서비스를 지원하는데 설계된 보안 객체에 대해 기술한다. 특히 u… 
2005
2005
Approval of 'race-based' drug is stimulating efforts to detect and predict true subgroups for drug response 
Review
2004
Review
2004
Abstract 5- fluorouracil (5-FU) is a chemotherapeutic agent widely used in the treatment of solid malignancies, especially in… 
2003
2003
Motivation. The interaction of alkali metal with thymine is an interesting target of studies in connection with bioinorganic… 
Review
1996
Review
1996
5-Fluorouracil (FU) is metabolized by dihydropyrimidine dehydrogenase (DPD). Patients with suspected or proven DPD deficiency… 
1986
1986
Inflammation and the release of potentially damaging substances, such as reactive oxygen intermediates (ROI) and lipid oxidation… 
1981
1981
Three types of experiments have been used to study the metabolism of thymine nucleotides by human cells. (1) Cells were labelled… 
1962
1962
IT is well known that X-irradiation of the pyrimidine bases in aqueous solutions in the presence of oxygen causes peroxidation at…