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Archives of Internal Medicine|April 1, 1978
A rapid method for the diagnosis of acute uric acid nephropathyJ Kelton, W N Kelley, E W HolmesThe Journal of Biological Chemistry|September 25, 1976
Human adenosine deaminase. Distribution and propertiesM B Van der Weyden, W N KelleyFamily Process|May 31, 2021
Expanding the Traumatic Stress Framework to Incorporate a Socioecological Family Systems PerspectiveAmber N Kelley, Michael G Curtis, Elizabeth WielingThe Journal of Biological Chemistry|June 25, 1980
Human adenosine deaminase and its binding protein in normal and adenosine deaminase-deficient fibroblast cell strainsP E Daddona, M A Frohman, W N KelleyEnzyme|January 1, 1987
Genetic analysis of human hypoxanthine-guanine phosphoribosyltransferase deficiencyL J Silverman, W N Kelley, T D PalellaThe Journal of Clinical Investigation|September 1, 1979
Radioimmunochemical quantitation of human adenosine deaminaseP E Daddona, M A Frohman, W N KelleyThe Journal of Clinical Investigation|July 1, 1972
Hypoxanthine-guanine phosphoribosyltransferase: characteristics of the mutant enzyme in erythrocytes from patients with the Lesch-Nyhan syndromeW J Arnold, J C Meade, W N KelleyCryobiology|August 1, 1983
Permeability of intact and dechorionated zebra fish embryos to glycerol and dimethyl sulfoxideB Harvey, R N Kelley, M J Ashwood-SmithProceedings of the National Academy of Sciences of the United States of America|February 1, 1983
Human hypoxanthine (guanine) phosphoribosyltransferase: an amino acid substitution in a mutant form of the enzyme isolated from a patient with goutJ M Wilson, G E Tarr, W N KelleyThe Journal of Biological Chemistry|August 10, 1979
Human adenine phosphoribosyltransferase. Affinity purification, subunit structure, amino acid composition, and peptide mappingJ A Holden, G S Meredith, W N KelleyPageof 13