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Drug Metabolism and Disposition: the Biological Fate of Chemicals|March 22, 2001
Genetics of iron storage and hemochromatosisE Beutler, V Felitti, T Gelbart, et al.
Biochemical Pharmacology|March 15, 1988
Mechanism of improved maintenance of 2,3-diphosphoglycerate in stored blood by the xanthone compound 2-(2-hydroxyethoxy)-6-(1-H-tetrazole-5-yl)xanthen-9-one (BW A440C)E Beutler, L Forman, C West, et al.
American Journal of Hematology|September 1, 1986
G-6-PD Walter Reed: possible insight into "structural" NADP in G-6-PDE Beutler, K Hartman, T Gelbart, et al.
Annals of Internal Medicine|September 9, 2000
The effect of HFE genotypes on measurements of iron overload in patients attending a health appraisal clinicE Beutler, V Felitti, T Gelbart, et al.
The Journal of Biological Chemistry|March 5, 1991
DNA sequence abnormalities of human glucose-6-phosphate dehydrogenase variantsE Beutler, W Kuhl, T Gelbart, et al.
Acta Haematologica|January 13, 2001
Three Gaucher-disease-producing mutations in a patient with Gaucher disease: mechanism and diagnostic implicationsE Beutler, H Liebman, T Gelbart, et al.
Clinical Genetics|March 21, 2002
A previously undescribed nonsense mutation of the HFE geneE Beutler, M J Griffin, T Gelbart, et al.
Blood|October 9, 1999
The molecular basis of a case of gamma-glutamylcysteine synthetase deficiencyE Beutler, T Gelbart, T Kondo, et al.
Acta Haematologica|February 29, 2000
Effect of ozone on red blood cell enzymes and intermediatesA Zimran, G Wasser, L Forman, et al.
Blood Cells, Molecules & Diseases|January 1, 1995
A strategy for cloning the hereditary hemochromatosis geneE Beutler, T Gelbart, C West, et al.
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