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Journal of Chromatography|April 15, 1992
Rapid separation of creatine, phosphocreatine and adenosine metabolites by ion-pair reversed-phase high-performance liquid chromatography in plasma and cardiac tissueM D Scott, L J Baudendistel, T E Dahms
Biochimica Et Biophysica Acta|April 30, 1993
Decreased catalase activity is the underlying mechanism of oxidant susceptibility in glucose-6-phosphate dehydrogenase-deficient erythrocytesM D Scott, T C Wagner, D T Chiu
The Journal of Biological Chemistry|October 15, 1990
Entrapment of purified alpha-hemoglobin chains in normal erythrocytes. A model for beta thalassemiaM D Scott, P Rouyer-Fessard, B H Lubin, et al.
Blood|May 1, 1991
NADPH, not glutathione, status modulates oxidant sensitivity in normal and glucose-6-phosphate dehydrogenase-deficient erythrocytesM D Scott, L Zuo, B H Lubin, et al.
The Journal of Laboratory and Clinical Medicine|July 1, 1991
Erythrocyte defense against hydrogen peroxide: preeminent importance of catalaseM D Scott, B H Lubin, L Zuo, et al.
Modern Pathology : an Official Journal of the United States and Canadian Academy of Pathology, Inc|June 1, 1994
Intravascular (angiotropic) large cell lymphoma: determination of monoclonality by polymerase chain reaction on paraffin-embedded tissuesJ P Sleater, G H Segal, M D Scott, et al.
Free Radical Biology & Medicine|January 1, 1992
Activated oxygen generation by a primaquine metabolite: inhibition by antioxidants derived from Chinese herbal remediesY L Hong, H Z Pan, M D Scott, et al.
Infection and Immunity|June 1, 1995
Functional expression of falcipain, a Plasmodium falciparum cysteine proteinase, supports its role as a malarial hemoglobinaseF Salas, J Fichmann, G K Lee, et al.
Biochemical Pharmacology|July 15, 1990
Antimalarial activity of diethyldithiocarbamate. Potentiation by copperS R Meshnick, M D Scott, B Lubin, et al.
British Journal of Haematology|April 1, 1992
Alpha- and beta-haemoglobin chain induced changes in normal erythrocyte deformability: comparison to beta thalassaemia intermedia and Hb H diseaseM D Scott, P Rouyer-Fessard, M S Ba, et al.
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