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2. Altered spectrin association and membrane fragility without abnormal spectrin heat sensitivity in a case of congenital hemolytic anemia. Ravindranath Y, Johnson RM. Am J Hematol; 1985 Sep; 20(1):53-65. PubMed ID: 4025321 [Abstract] [Full Text] [Related]
18. Molecular basis of spectrin deficiency in hereditary pyropoikilocytosis. Hanspal M, Hanspal JS, Sahr KE, Fibach E, Nachman J, Palek J. Blood; 1993 Sep 01; 82(5):1652-60. PubMed ID: 8364214 [Abstract] [Full Text] [Related]
19. Heterogeneity of the molecular basis of hereditary pyropoikilocytosis and hereditary elliptocytosis associated with increased levels of the spectrin alpha I/74-kilodalton tryptic peptide. Floyd PB, Gallagher PG, Valentino LA, Davis M, Marchesi SL, Forget BG. Blood; 1991 Sep 01; 78(5):1364-72. PubMed ID: 1878597 [Abstract] [Full Text] [Related]
20. Dependence of spectrin organization in red blood cell membranes on cell metabolism: implications for control of red cell shape, deformability, and surface area. Palek J, Liu SC. Semin Hematol; 1979 Jan 01; 16(1):75-93. PubMed ID: 154737 [No Abstract] [Full Text] [Related] Page: [Next] [New Search]