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Blood Cells, Molecules & Diseases|January 11, 2002
A study of genes that may modulate the expression of hereditary hemochromatosis: transferrin receptor-1, ferroportin, ceruloplasmin, ferritin light and heavy chains, iron regulatory proteins (IRP)-1 and -2, and hepcidinP L Lee, T Gelbart, C West, et al.The Journal of Clinical Investigation|August 1, 1983
Metabolic compensation for profound erythrocyte adenylate kinase deficiency. A hereditary enzyme defect without hemolytic anemiaE Beutler, D Carson, H Dannawi, et al.Proceedings of the National Academy of Sciences of the United States of America|June 15, 1993
Gaucher disease as a paradigm of current issues regarding single gene mutations of humansE BeutlerAmerican Journal of Hematology|January 1, 1993
Study of glucose-6-phosphate dehydrogenase: history and molecular biologyE BeutlerProceedings of the National Academy of Sciences of the United States of America|June 1, 1983
Selectivity of proteases as a basis for tissue distribution of enzymes in hereditary deficienciesE BeutlerAnnual Review of Medicine|January 1, 1992
The molecular biology of G6PD variants and other red cell enzyme defectsE BeutlerThe Western Journal of Medicine|February 1, 1994
Bone marrow transplantation beyond treatment of aplasia and neoplasiaE BeutlerBailliere'S Clinical Haematology|March 14, 1998
Enzyme replacement therapy for Gaucher's diseaseE BeutlerPageof 195