Ernest Beutler, M.D.
Affiliations: | 1959-1979 | Hematology | City of Hope, Duarte, CA, United States |
Area:
Red Blood Cell Enzymes; Inherited hematological disease;Website:
www.cityofhope.orgGoogle:
"Ernest Beutler"Bio:
https://en.wikipedia.org/wiki/Ernest_Beutler
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Parents
Sign in to add mentor| Leon O. Jacobson | grad student | Chicago | ||
| (Beginning in 1944, Jacobson served as the Associate Director of the Health Division and the Section Chief of H-I, Clinical Medicine and Medical Research. He worked under Director of the Health Division, Robert S. Stone. During World War II, he was also a) | ||||
Children
Sign in to add trainee| Bruce Alan Beutler | research assistant | City of Hope National Medical Center (Cell Biology Tree) | |
| Satish K. Srivastava | post-doc | 1966-1973 | City of Hope |
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Publications
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| Beutler E, Geet CV, Loo DMWMt, et al. (2010) Polymorphisms and mutations of human TMPRSS6 in iron deficiency anemia Blood Cells Molecules and Diseases. 44: 16-21 |
| Truksa J, Gelbart T, Peng H, et al. (2009) Suppression of the hepcidin-encoding gene Hamp permits iron overload in mice lacking both hemojuvelin and matriptase-2/TMPRSS6 British Journal of Haematology. 147: 571-581 |
| Lee P, Rice L, McCarthy JJ, et al. (2009) Severe iron overload with a novel aminolevulinate synthase mutation and hepatitis C infection. A case report. Blood Cells, Molecules & Diseases. 42: 1-4 |
| Du X, She E, Gelbart T, et al. (2008) The serine protease TMPRSS6 is required to sense iron deficiency. Science (New York, N.Y.). 320: 1088-92 |
| Beutler E. (2008) Glucose-6-phosphate dehydrogenase deficiency: a historical perspective. Blood. 111: 16-24 |
| Waalen J, Felitti VJ, Gelbart T, et al. (2008) Screening for hemochromatosis by measuring ferritin levels: a more effective approach. Blood. 111: 3373-6 |
| Friedman J, Waalen J, Takeda A, et al. (2008) Evidence for Increased Red Cell Turnover in Unexplained Anemia in Patients Over 70 Years of Age Blood. 112: 3445-3445 |
| Aslan D, Crain K, Beutler E. (2007) A new case of human atransferrinemia with a previously undescribed mutation in the transferrin gene. Acta Haematologica. 118: 244-7 |
| Pereira MM, Gelbart T, Ristoff E, et al. (2007) Chronic non-spherocytic hemolytic anemia associated with severe neurological disease due to γ-glutamylcysteine synthetase deficiency in a patient of Moroccan origin Haematologica. 92 |
| Beutler E. (2007) Iron storage disease: facts, fiction and progress. Blood Cells, Molecules & Diseases. 39: 140-7 |