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The Journal of Clinical Investigation|December 1, 1970
Hemoglobin stability: observations on the denaturation of normal and abnormal hemoglobins by oxidant dyes, heat, and alkaliR F RiederThe Journal of Clinical Investigation|February 1, 1971
Synthesis of hemoglobin Gun Hill: increased synthesis of the heme-free beta-GH globin chain and subunit exchange with a free alpha-chain poolR F RiederThe Journal of Clinical Investigation|February 1, 1972
Translation of -globin m-RNA in -thalassemia and the S and C hemoglobinopathiesR F RiederThe Journal of Biological Chemistry|March 25, 1988
Dysfunctional alpha-globin gene in hemoglobin H disease in blacks. A dinucleotide deletion produces a frameshift and a termination codonS Safaya, R F RiederBlood|March 1, 1976
Translation of human globin mRNA: globin synthesis in cells containing Hb LeidenR F Rieder, G W JamesThe Journal of Clinical Investigation|October 1, 1974
Imbalance in alpha and beta globin synthesis associated with a hemoglobinopathyR F Rieder, G W JamesBlood|December 1, 1994
Augmentation of gamma-globin gene promoter activity by carboxylic acids and components of the human beta-globin locus control regionS Safaya, A Ibrahim, R F RiederAmerican Journal of Hematology|December 1, 1987
Dysfunctional alpha-globin genes in hemoglobin H disease in blacks: variation in restriction fragment size permits the detection of the -alpha/-alpha T genotypeS Safaya, P Mullaney, R F RiederBritish Journal of Haematology|February 1, 1979
Alpha thalassaemia in American blacks: a study of a family with five cases of haemoglobin H diseaseR Bellevue, H Dosik, R F RiederPageof 4