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The Quarterly Journal of Medicine|January 1, 1993
DNA diagnosis of fatal fructose intolerance from archival tissueM Ali, U Rosien, T M CoxThe Journal of Biological Chemistry|January 8, 2000
Expression, purification, and characterization of natural mutants of human aldolase B. Role of quaternary structure in catalysisP Rellos, J Sygusch, T M CoxMolecular Biology & Medicine|November 1, 1983
Allelic heterogeneity in adult hereditary fructose intolerance. Detection of structural mutations in the aldolase B moleculeT M Cox, M W O'Donnell, M CamilleriJournal of Inherited Metabolic Disease|March 28, 2012
Lysosomal delivery of therapeutic enzymes in cell models of Fabry diseaseD Marchesan, T M Cox, P B DeeganCell|June 17, 1988
Catalytic deficiency of human aldolase B in hereditary fructose intolerance caused by a common missense mutationN C Cross, D R Tolan, T M CoxJournal of Anatomy|June 15, 2000
Widespread expression of tartrate-resistant acid phosphatase (Acp 5) in the mouse embryoA R Hayman, A J Bune, T M CoxClinical Chemistry|October 1, 1987
Antibodies to porcine uteroferrin used in measurement of human tartrate-resistant acid phosphataseZ O Echetebu, T M Cox, D W MossThe Journal of Biological Chemistry|November 15, 1991
Biosynthesis of delta-aminolevulinic acid and the regulation of heme formation by immature erythroid cells in manL C Gardner, S J Smith, T M CoxParasite Immunology|February 1, 1995
Anti-interleukin-4 treatment diminishes secretion of Th2 cytokines and inhibits hepatic fibrosis in murine schistosomiasis japonicaA W Cheever, F D Finkelman, T M CoxPageof 12