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Proceedings of the National Academy of Sciences of the United States of America|May 1, 1993
Analysis of pyruvate kinase-deficiency mutations that produce nonspherocytic hemolytic anemiaL Baronciani, E BeutlerAmerican Journal of Human Genetics|December 1, 1990
The NT 1311 polymorphism of G6PD: G6PD Mediterranean mutation may have originated independently in Europe and AsiaE Beutler, W KuhlThe Journal of Clinical Investigation|April 1, 1995
Molecular study of pyruvate kinase deficient patients with hereditary nonspherocytic hemolytic anemiaL Baronciani, E BeutlerBlood|October 1, 1983
Phosphoglycolate phosphatase and 2,3-diphosphoglycerate in red cells of normal and anemic subjectsR Somoza, E BeutlerTransfusion|March 1, 1984
Measurement of the viability of stored red cells by the single-isotope technique using 51Cr. Analysis of validityE Beutler, C WestAnnals of Human Genetics|October 1, 1977
The tissue distribution of hexosaminidase S and hexosaminidase CE Beutler, W KuhlBiochimica Et Biophysica Acta|September 18, 1980
Guanosine triphosphatase activity in human erythrocyte membranesE Beutler, W KuhlAmerican Journal of Hematology|April 1, 1987
Two new variants of glucose-6-phosphate dehydrogenase associated with hereditary non-spherocytic hemolytic anemia: G6PD Wayne and G6PD HuronY Ravindranath, E BeutlerProceedings of the National Academy of Sciences of the United States of America|March 1, 1985
High glucose concentrations partially release hexokinase from inhibition by glucose 6-phosphateS Fujii, E BeutlerPageof 42