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Biochemical and Biophysical Research Communications|May 16, 1983
A weak upstream promoter gives rise to long human beta-globin RNA moleculesT J Ley, A W NienhuisAnnual Review of Medicine|January 1, 1985
Induction of hemoglobin F synthesis in patients with beta thalassemiaT J Ley, A W NienhuisProceedings of the National Academy of Sciences of the United States of America|August 1, 1982
RNA processing errors in patients with beta-thalassemiaT J Ley, N P Anagnou, G Pepe, et al.Annals of Internal Medicine|January 1, 1985
Disseminated infection caused by Cunninghamella bertholletiae in a patient with beta-thalassemia. Case report and review of the literatureJ M Sands, A M Macher, T J Ley, et al.Journal of Clinical Apheresis|January 1, 1983
A trial of immunotherapy in aplastic anemia and pure red cell aplasiaN S Young, H G Klein, P Griffith, et al.Blood|July 1, 1984
Beta O-39 thalassemia gene: a premature termination codon causes beta-mRNA deficiency without affecting cytoplasmic beta-mRNA stabilityR K Humphries, T J Ley, N P Anagnou, et al.Progress in Clinical and Biological Research|January 1, 1983
DNA methylation and globin gene expression in patients treated with 5-azacytidineT J Ley, N P Anagnou, C T Noguchi, et al.British Journal of Haematology|June 1, 1989
Cyclosporine therapy of aplastic anaemia, congenital and acquired red cell aplasiaE M Leonard, E Raefsky, P Griffith, et al.Blood|August 1, 1983
5-Azacytidine increases gamma-globin synthesis and reduces the proportion of dense cells in patients with sickle cell anemiaT J Ley, J DeSimone, C T Noguchi, et al.Proceedings of the National Academy of Sciences of the United States of America|October 1, 1983
Acquired alpha-thalassemia in preleukemia is due to decreased expression of all four alpha-globin genesN P Anagnou, T J Ley, B Chesbro, et al.Pageof 133