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The Journal of Biological Chemistry|February 25, 1985
A particle-associated ATP-dependent proteolytic activity in erythroleukemia cellsR F Rieder, A Ibrahim, J D EtlingerBlood|May 1, 1986
A soluble adenosine triphosphate-dependent proteolytic system in human peripheral red blood cellsR F Rieder, A Ibrahim, J D EtlingerAmerican Journal of Hematology|March 1, 1992
Studies on the in vitro and in vivo expression of a dysfunctional alpha-globin geneS Safaya, D R Trauber, R F RiederBlood|May 1, 1981
Rapid destruction of newly synthesized excess beta-globin chains in HbH diseaseG B Sancar, M M Cedeno, R F RiederBritish Journal of Haematology|February 1, 1976
The interaction of alpha-thalassaemia and haemoglobin G PhiladelphiaR F Rieder, D H Woodbury, D L RucknagelThe Johns Hopkins Medical Journal|June 1, 1980
The varied arrangement of the alpha globin genes in alpha thalassemia and Hb H disease in American blacksG B Sancar, M M Cedeno, R F RiederBlood|February 1, 1985
Plasmodium falciparum in vitro: diminished growth in hemoglobin H disease erythrocytesT C Ifediba, A Stern, A Ibrahim, et al.Proceedings of the National Academy of Sciences of the United States of America|November 1, 1980
Proportion of hemoglobin G Philadelphia (alpha 268 Asn leads to Lys beta 2) in heterozygotes is determined by alpha-globin gene deletionsG B Sancar, B Tatsis, M M Cedeno, et al.Blood|March 1, 1985
The leftward deletion alpha-thal-2 haplotype in a black subject with hemoglobin SSS H Embury, M A Gholson, P Gillette, et al.Hemoglobin|January 1, 1982
Interaction of chromosomes bearing 1, 2 or 3 alpha-globin genes in an American black family with alpha-thalassemiaG B Sancar, M M Cedeno, R Bellevue, et al.Pageof 4