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AORN Journal|October 18, 2002
Invitational theory and perioperative nursing preceptorshipsSusan D Finger, Tess M PapeThe Journal of Laboratory and Clinical Medicine|July 1, 1985
Cell heterogeneity in sickle cell disease: quantitation of the erythrocyte density profileG P Rodgers, A N Schechter, C T NoguchiProgress 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 SchechterThe Journal of Laboratory and Clinical Medicine|April 3, 2001
Rapid differentiation of five common alpha-thalassemia genotypes by polymerase chain reactionD C Tang, S Fucharoen, I Ding, et al.British Journal of Haematology|September 1, 1994
Reducing erythropoietin in cultures of human erythroid precursors elevates the proportion of fetal haemoglobinE Fibach, A N Schechter, C T Noguchi, et al.European Journal of Haematology|July 1, 1996
Monoclonal antibody-based methods for quantitation of hemoglobins: application to evaluating patients with sickle cell anemia treated with hydroxyureaN Epstein, M Epstein, A Boulet, et al.Hemoglobin|January 1, 1992
Hb Q-Thailand [alpha 74(EF3)Asp-->His]: gene organization, molecular structure, and DNA diagnosisF Y Zeng, S Fucharoen, S Z Huang, et al.Blood|July 1, 1997
Restoration of the CCAAT box or insertion of the CACCC motif activates [corrected] delta-globin gene expressionD C Tang, D Ebb, R C Hardison, et al.Nucleic Acids Research|July 25, 2000
The role of trans-acting factors and DNA-bending in the silencing of human beta-globin gene expressionL R Drew, D C Tang, P E Berg, et al.Pageof 13