Sulfite oxidase deficiency. Biochemical and clinical investigations of a hereditary metabolic disorder in sulfur metabolism.
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Structure-Based Alteration of Substrate Specificity and Catalytic Activity of Sulfite Oxidase from Sulfite Oxidation to Nitrate ReductionMagnetic resonance imaging and magnetic resonance spectroscopy in isolated sulfite oxidase deficiencySulfite Oxidase Activity of Cytochrome c: Role of Hydrogen PeroxideTheoretical and experimental studies of the spin trapping of inorganic radicals by 5,5-dimethyl-1-pyrroline N-oxide (DMPO). 3. Sulfur dioxide, sulfite, and sulfate radical anionsProtein Radical Formation Resulting from Eosinophil Peroxidase-catalyzed Oxidation of SulfiteDiagnosis of inherited metabolic disorders affecting the nervous systemStroke in children: genetic and metabolic issues.The clinical chemistry of inorganic sulfate.Molybdopterin synthase mutations in a mild case of molybdenum cofactor deficiency.Molybdenum: an essential trace element.Molybdenum cofactor biosynthesis in humans. Identification of two complementation groups of cofactor-deficient patients and preliminary characterization of a diffusible molybdopterin precursor.Toxicology of sulphiting agents. I: Animal studies.Transient Kinetic Analysis of Hydrogen Sulfide Oxidation Catalyzed by Human Sulfide Quinone OxidoreductaseInborn errors of molybdenum metabolism: combined deficiencies of sulfite oxidase and xanthine dehydrogenase in a patient lacking the molybdenum cofactor.Sulfite-mediated oxidation of myeloperoxidase to a free radical: immuno-spin trapping detection in human neutrophils.Human sulfite oxidase R160Q: identification of the mutation in a sulfite oxidase-deficient patient and expression and characterization of the mutant enzyme.What getting sick means.Sulfite hypersensitivity. A critical review.Absence of hepatic molybdenum cofactor. An inborn error of metabolism associated with lens dislocation.Impairment of glutathione biosynthetic pathway in uraemia and dialysis.Chemical Biology of H2S Signaling through Persulfidation.A child with Myhre syndrome presenting with corectopia and tetralogy of Fallot.Structural Insights into the Incorporation of the Mo Cofactor into Sulfite Oxidase from Site-Directed Spin Labeling.
P2860
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P2860
Sulfite oxidase deficiency. Biochemical and clinical investigations of a hereditary metabolic disorder in sulfur metabolism.
description
1977 nî lūn-bûn
@nan
1977年の論文
@ja
1977年論文
@yue
1977年論文
@zh-hant
1977年論文
@zh-hk
1977年論文
@zh-mo
1977年論文
@zh-tw
1977年论文
@wuu
1977年论文
@zh
1977年论文
@zh-cn
name
Sulfite oxidase deficiency. Bi ...... disorder in sulfur metabolism.
@en
type
label
Sulfite oxidase deficiency. Bi ...... disorder in sulfur metabolism.
@en
prefLabel
Sulfite oxidase deficiency. Bi ...... disorder in sulfur metabolism.
@en
P2093
P1476
Sulfite oxidase deficiency. Bi ...... disorder in sulfur metabolism.
@en
P2093
Cloherty JP
Johnson JL
Rajagopalan KV
P304
P356
10.1056/NEJM197711102971902
P407
P577
1977-11-01T00:00:00Z