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Annual Review of Pathology|April 30, 2009
Regulation of hepcidin and iron-overload diseasePauline L Lee, Ernest BeutlerHaematologica|May 18, 2006
The genetic basis of human erythrocyte pyridoxal kinase activity variationJonathan M Flanagan, Ernest BeutlerScience (New York, N.Y.)|May 3, 2008
The serine protease TMPRSS6 is required to sense iron deficiencyXin Du, Ellen She, Terri Gelbart, et al.Acta Haematologica|December 22, 2007
A new case of human atransferrinemia with a previously undescribed mutation in the transferrin geneDeniz Aslan, Karen Crain, Ernest BeutlerBlood Cells, Molecules & Diseases|August 11, 2007
The role of STAT, AP-1, E-box and TIEG motifs in the regulation of hepcidin by IL-6 and BMP-9: lessons from human HAMP and murine Hamp1 and Hamp2 gene promotersJaroslav Truksa, Pauline Lee, Ernest BeutlerClinical Chemistry|November 26, 2002
Haptoglobin polymorphism and iron homeostasisErnest Beutler, Terri Gelbart, Pauline LeeThe Journal of Laboratory and Clinical Medicine|August 24, 2004
Mutations in the gene encoding cytosolic beta-glucosidase in Gaucher diseaseErnest Beutler, Lisa Beutler, Carol WestBlood Cells, Molecules & Diseases|June 18, 2002
Severe jaundice in a patient with a previously undescribed glucose-6-phosphate dehydrogenase (G6PD) mutation and Gilbert syndromeErnest Beutler, Terri Gelbart, William MillerBlood Cells, Molecules & Diseases|September 13, 2005
Chronic inflammation does not appear to modify the homozygous hereditary hemochromatosis phenotypeErnest Beutler, Jill Waalen, Terri GelbartBlood|November 11, 2008
Two BMP responsive elements, STAT, and bZIP/HNF4/COUP motifs of the hepcidin promoter are critical for BMP, SMAD1, and HJV responsivenessJaroslav Truksa, Pauline Lee, Ernest BeutlerPageof 33