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E J Benz

Showing results (21-30 of 115) with videos related to

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Annual Review of Medicine|January 1, 1982
The thalassemia syndromes: models for the molecular analysis of human diseaseE J Benz, B G Forget
Proceedings of the National Academy of Sciences of the United States of America|April 11, 1992
Beta-globin nonsense mutation: deficient accumulation of mRNA occurs despite normal cytoplasmic stabilityS J Baserga, E J Benz
Pathobiology Annual|January 1, 1980
Pathogenesis of the thalassemia syndromesE J Benz, B G Forget
Hematologic Pathology|January 1, 1988
Antenatal diagnosis of the hemoglobinopathiesA I Radin, E J Benz
The New England Journal of Medicine|December 22, 1977
Regulation of hemoglobin synthesis during the development of the red cell. (Second of three parts)A W Nienhuis, E J Benz
The New England Journal of Medicine|December 15, 1977
Regulation of hemoglobin synthesis during the development of the red cell (first of three parts)A W Nienhuis, E J Benz
The Journal of Clinical Investigation|December 1, 1971
Defect in messenger RNA for human hemoglobin synthesis in beta thalassemiaE J Benz, B G Forget
The Journal of Biological Chemistry|November 15, 1992
Differential translation of the Na,K-ATPase subunit mRNAsP Devarajan, M Gilmore-Hebert, E J Benz
Annals of the New York Academy of Sciences|January 1, 1985
Metabolism of structurally abnormal mRNAs resulting from beta-thalassemia mutationsE J Benz, K Takeshita, A L Scarpa
Proceedings of the National Academy of Sciences of the United States of America|September 1, 1977
Relative stability of alpha- and beta-globin messenger RNAs in homozygous beta+ thalassemiaA W Nienhuis, P Turner, E J Benz
Pageof 12

Showing results (21-30 of 115) with videos related to

Sort By:
Pageof 12
Annual Review of Medicine|January 1, 1982
The thalassemia syndromes: models for the molecular analysis of human diseaseE J Benz, B G Forget
Proceedings of the National Academy of Sciences of the United States of America|April 11, 1992
Beta-globin nonsense mutation: deficient accumulation of mRNA occurs despite normal cytoplasmic stabilityS J Baserga, E J Benz
Pathobiology Annual|January 1, 1980
Pathogenesis of the thalassemia syndromesE J Benz, B G Forget
Hematologic Pathology|January 1, 1988
Antenatal diagnosis of the hemoglobinopathiesA I Radin, E J Benz
The New England Journal of Medicine|December 22, 1977
Regulation of hemoglobin synthesis during the development of the red cell. (Second of three parts)A W Nienhuis, E J Benz
The New England Journal of Medicine|December 15, 1977
Regulation of hemoglobin synthesis during the development of the red cell (first of three parts)A W Nienhuis, E J Benz
The Journal of Clinical Investigation|December 1, 1971
Defect in messenger RNA for human hemoglobin synthesis in beta thalassemiaE J Benz, B G Forget
The Journal of Biological Chemistry|November 15, 1992
Differential translation of the Na,K-ATPase subunit mRNAsP Devarajan, M Gilmore-Hebert, E J Benz
Annals of the New York Academy of Sciences|January 1, 1985
Metabolism of structurally abnormal mRNAs resulting from beta-thalassemia mutationsE J Benz, K Takeshita, A L Scarpa
Proceedings of the National Academy of Sciences of the United States of America|September 1, 1977
Relative stability of alpha- and beta-globin messenger RNAs in homozygous beta+ thalassemiaA W Nienhuis, P Turner, E J Benz
Pageof 12