Glucose-6-phosphate dehydrogenase deficiency: a historical perspective von Beutler, Ernest

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The definition of anemia: what is the lower limit of normal of the blood hemoglobin concentration? von Beutler, Ernest, Waalen, Jill

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PGK deficiency von Beutler, Ernest

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Lysosomal storage diseases: Natural history and ethical and economic aspects von Beutler, Ernest

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Hemochromatosis: genetics and pathophysiology von Beutler, Ernest

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Bone Morphogenetic Proteins 2, 4, and 9 Stimulate Murine Hepcidin 1 Expression Independently of Hfe, Transferrin Receptor 2 (Tfr2), and IL-6 von Truksa, Jaroslav, Peng, Hongfan, Lee, Pauline, Beutler, Ernest

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Serine Protease TMPRSS6 Is Required to Sense Iron Deficiency von Du, Xin, She, Ellen, Gelbart, Terri, Truksa, Jaroslav, Lee, Pauline, Xia, Yu, Khovananth, Kevin, Mudd, Suzanne, Mann, Navjiwan, Moresco, Eva Marie Y, Beutler, Ernest, Beutler, Bruce

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The global prevalence of glucose-6-phosphate dehydrogenase deficiency: A systematic review and meta-analysis von Nkhoma, Ella T., Poole, Charles, Vannappagari, Vani, Hall, Susan A., Beutler, Ernest

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Regulation of hepcidin and iron-overload disease von Lee, Pauline L, Beutler, Ernest

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Regulation of Hepcidin Transcription by Interleukin-1 and Interleukin-6 von Lee, Pauline, Peng, Hongfan, Gelbart, Terri, Wang, Lei, Beutler, Ernest

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Two BMP responsive elements, STAT, and bZIP/HNF4/COUP motifs of the hepcidin promoter are critical for BMP, SMAD1, and HJV responsiveness von Truksa, Jaroslav, Lee, Pauline, Beutler, Ernest

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The IL-6- and Lipopolysaccharide-Induced Transcription of Hepcidin in HFE-, Transferrin Receptor 2-, and β2-Microglobulin-Deficient Hepatocytes von Lee, Pauline, Peng, Hongfan, Gelbart, Terri, Beutler, Ernest

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Enzyme replacement in Gaucher disease von Beutler, Ernest

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Racial Variability in the UDP-Glucuronosyltransferase 1 (UGT1A1) Promoter: A Balanced Polymorphism for Regulation of Bilirubin Metabolism? von Beutler, Ernest, Gelbart, Terri, Demina, Anna

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Glucose-6-Phosphate Dehydrogenase Deficiency and Antimalarial Drug Development von Beutler, Ernest, Duparc, Stephan, G6PD Deficiency Working Group

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Penetrance of 845G→A (C282Y) HFE hereditary haemochromatosis mutation in the USA von Beutler, Ernest, Felitti, Vincent J, Koziol, James A, Ho, Ngoc J, Gelbart, Terri

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Chemical Chaperones Increase the Cellular Activity of N370S β-Glucosidase: A Therapeutic Strategy for Gaucher Disease von Sawkar, Anu R., Cheng, Wei-Chieh, Beutler, Ernest, Wong, Chi-Huey, Balch, William E., Kelly, Jeffery W.

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Gaucher disease: multiple lessons from a single gene disorder von Beutler, Ernest

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Hematologically important mutations: Gaucher disease von Beutler, Ernest, Gelbart, Terri, Scott, C. Ronald

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A Missense Mutation in Human Fatty Acid Amide Hydrolase Associated with Problem Drug Use von Sipe, Jack C., Chiang, Kyle, Gerber, Alexandra L., Beutler, Ernest, Cravatt, Benjamin F.

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