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Blood Cells, Molecules & Diseases|January 10, 2002
Synergy between TLR2 and TLR4: a safety mechanismE Beutler, T Gelbart, C WestBritish Journal of Haematology|March 1, 1986
Blood cell phosphogluconolactonase: assay and propertiesE Beutler, W Kuhl, T GelbartProceedings of the National Academy of Sciences of the United States of America|July 8, 1998
Racial variability in the UDP-glucuronosyltransferase 1 (UGT1A1) promoter: a balanced polymorphism for regulation of bilirubin metabolism?E Beutler, T Gelbart, A DeminaAmerican Journal of Human Genetics|May 1, 1990
Linkage of the PvuII polymorphism with the common Jewish mutation for Gaucher diseaseA Zimran, T Gelbart, E BeutlerGenomics|January 1, 1993
Identification of six new Gaucher disease mutationsE Beutler, T Gelbart, C WestThe Journal of Clinical Investigation|January 1, 1986
Erythrocyte glutathione synthetase deficiency leads not only to glutathione but also to glutathione-S-transferase deficiencyE Beutler, T Gelbart, C PegelowDrug 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.Pageof 42