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Progress in Clinical and Biological Research|January 1, 1987
Intracellular polymerization of sickle hemoglobin: disease severity and therapeutic goalsC T Noguchi, G P Rodgers, A N SchechterAmerican Journal of Hematology|September 1, 1985
Irreversibly sickled erythrocytes in sickle cell anemia: a quantitative reappraisalG P Rodgers, C T Noguchi, A N SchechterNucleic Acids Research|January 11, 2000
Quantitative analysis of globin gene induction in single human erythroleukemic cellsR D Smith, J D Malley, A N SchechterProceedings of the National Academy of Sciences of the United States of America|September 1, 1980
Determination of deoxyhemoglobin S polymer in sickle erythrocytes upon deoxygenationC T Noguchi, D A Torchia, A N SchechterBlood|June 1, 1984
Control of oxygen affinity of hemoglobin in K562 cells induced by heminY Wu, A Dean, W Egan, et al.The American Journal of Pediatric Hematology/Oncology|January 1, 1985
Noninvasive techniques to evaluate the vaso-occlusive manifestations of sickle cell diseaseG P Rodgers, C T Noguchi, A N SchechterThe Journal of Biological Chemistry|March 10, 1976
Antibodies to an NH2-terminal fragment of betaS globin. II. Specificity and isolation of antibodies for the sickle mutationJ G Curd, N S Young, A N SchechterProgress in Clinical and Biological Research|January 1, 1987
The development of non-invasive methods to evaluate sickle cell patients in the steady state and in crisisG P Rodgers, C T Noguchi, A N SchechterBlood|January 1, 1985
Hemoglobin S polymerization: primary determinant of the hemolytic and clinical severity of the sickling syndromesG M Brittenham, A N Schechter, C T NoguchiBailliere'S Clinical Haematology|March 1, 1993
Sickle cell disease pathophysiologyC T Noguchi, A N Schechter, G P RodgersPageof 15