Beutler, Ernest

Penetrance of 845G→A (C282Y) HFE hereditary haemochromatosis mutation in the USA

Beutler, E., Felitti, V. J., Koziol, J. A., Ho, N. J., & Gelbart, T. (2002) · The Lancet

Iron Metabolism and DisordersNeurological diseases and metabolism

Cited by 823

The serine protease TMPRSS6 is required to sense iron deficiency

Du, X., She, E., Gelbart, T., Truksa, J., Lee, P., Xia, Y., Khovananth, K., Mudd, S., Mann, N., Moresco, E. M. Y., et al. (2008) · Science

Iron Metabolism and DisordersFerroptosis and cancer prognosis

Cited by 578

Bone morphogenetic proteins 2, 4, and 9 stimulate murine hepcidin 1 expression independently of Hfe, transferrin receptor 2 (Tfr2), and IL-6

Truksa, J., Peng, H., Lee, P., & Beutler, E. (2006) · Proceedings of the National Academy of Sciences

Iron Metabolism and DisordersTGF-β signaling in diseases

Cited by 309

The IL-6- and lipopolysaccharide-induced transcription of hepcidin in HFE- , transferrin receptor 2-, and β 2 -microglobulin-deficient hepatocytes

Lee, P., Peng, H., Gelbart, T., & Beutler, E. (2004) · Proceedings of the National Academy of Sciences

Iron Metabolism and DisordersNeurological diseases and metabolism

Cited by 221

Evolution of the genome and the genetic code: selection at the dinucleotide level by methylation and polyribonucleotide cleavage

Beutler, E., Gelbart, T., Han, J. H., Koziol, J. A., & Beutler, B. (1989) · Proceedings of the National Academy of Sciences

RNA and protein synthesis mechanismsDNA and Nucleic Acid Chemistry

Cited by 189

Autosomal dominant hereditary hemochromatosis associated with a novel ferroportin mutation and unique clinical features

Sham, R. L., Phatak, P. D., West, C., Lee, P., Andrews, C., & Beutler, E. (2005) · Blood Cells, Molecules, and Diseases

Iron Metabolism and DisordersNeurological diseases and metabolism

Cited by 146

Iron storage disease: Facts, fiction and progress

Beutler, E. (2007) · Blood Cells, Molecules, and Diseases

Iron Metabolism and DisordersNeurological diseases and metabolism

Cited by 101

Prevalence of hemochromatosis-related symptoms among individuals with mutations in the HFE gene

Waalen, J., Felitti, V., Gelbart, T., Ho, N. J., & Beutler, E. (2002) · Mayo Clinic Proceedings

Iron Metabolism and DisordersNeurological diseases and metabolism

Cited by 71