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Proceedings of the National Academy of Sciences of the United States of America|June 1, 1985
6-Phosphogluconolactonase deficiency, a hereditary erythrocyte enzyme deficiency: possible interaction with glucose-6-phosphate dehydrogenase deficiencyE Beutler, W Kuhl, T GelbartGenomics|April 1, 1992
Polymorphisms in the human glucocerebrosidase geneE Beutler, C West, T GelbartMolecular Medicine (Cambridge, Mass.)|November 1, 1994
Glucocerebrosidase mutations in Gaucher diseaseE Beutler, A Demina, T GelbartBlood 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 PegelowGene|December 20, 1988
Differential expression of the human glucocerebrosidase-coding geneO Reiner, M HorowitzPageof 234