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. 1965 Aug;44(8):1417–1424. doi: 10.1172/JCI105247

Adenosine Triphosphate Metabolism in Hereditary Spherocytosis^{^*}

Daniel N Mohler ^1,^†

PMCID: PMC292619 PMID: 14322046

1417

Selected References

These references are in PubMed. This may not be the complete list of references from this article.

BERTLES J. F. Sodium transport across the surface membrane of red blood cells in hereditary spherocytosis. J Clin Invest. 1957 Jun;36(6 Pt 1):816–824. doi: 10.1172/JCI103487. [DOI] [PMC free article] [PubMed] [Google Scholar]
DUNHAM E. T., GLYNN I. M. Adenosinetriphosphatase activity and the active movements of alkali metal ions. J Physiol. 1961 Apr;156:274–293. doi: 10.1113/jphysiol.1961.sp006675. [DOI] [PMC free article] [PubMed] [Google Scholar]
DUNN I., IBSEN K. H., COE E. L., SCHNEIDER A. S., WEINSTEIN I. M. ERYTHROCYTE CARBOHYDRATE METABOLISM IN HEREDITARY SPHEROCYTOSIS. J Clin Invest. 1963 Oct;42:1535–1541. doi: 10.1172/JCI104838. [DOI] [PMC free article] [PubMed] [Google Scholar]
HARRIS E. J., PRANKERD T. A. The rate of sodium extrusion from human erythrocytes. J Physiol. 1953 Sep;121(3):470–486. doi: 10.1113/jphysiol.1953.sp004959. [DOI] [PMC free article] [PubMed] [Google Scholar]
JACOB H. S., JANDL J. H. INCREASED CELL MEMBRANE PERMEABILITY IN THE PATHOGENESIS OF HEREDITARY SPHEROCYTOSIS. J Clin Invest. 1964 Aug;43:1704–1720. doi: 10.1172/JCI105046. [DOI] [PMC free article] [PubMed] [Google Scholar]
JAFFE E. R. The reduction of methemoglobin in human erythrocytes incubated with purine nucleosides. J Clin Invest. 1959 Sep;38:1555–1563. doi: 10.1172/JCI103934. [DOI] [PMC free article] [PubMed] [Google Scholar]
MURPHY J. R. Erythrocyte metabolism. V. Active cation transport and glycolysis. J Lab Clin Med. 1963 Apr;61:567–577. [PubMed] [Google Scholar]
POST R. L., MERRITT C. R., KINSOLVING C. R., ALBRIGHT C. D. Membrane adenosine triphosphatase as a participant in the active transport of sodium and potassium in the human erythrocyte. J Biol Chem. 1960 Jun;235:1796–1802. [PubMed] [Google Scholar]
PRANKERD T. A. Studies on the pathogenesis of haemolysis in hereditary spherocytosis. Q J Med. 1960 Apr;29:199–208. [PubMed] [Google Scholar]
ROBINSON M. A., LODER P. B., DE GRUCHY G. C. Red-cell metabolism in non-spherocytic congenital haemolytic anaemia. Br J Haematol. 1961 Jul;7:327–339. doi: 10.1111/j.1365-2141.1961.tb00343.x. [DOI] [PubMed] [Google Scholar]
SELWYN J. G., DACIE J. V. Autohemolysis and other changes resulting from the incubation in vitro of red cells from patients with congenital hemolytic anemia. Blood. 1954 May;9(5):414–438. [PubMed] [Google Scholar]
SHAFER A. W. THE PHOSPHORYLATED CARBOHYDRATE INTERMEDIATES FROM ERYTHROCYTES IN HEREDITARY SPHEROCYTOSIS. Blood. 1964 Apr;23:417–426. [PubMed] [Google Scholar]
WHITTAM R. Potassium movements and ATP in human red cells. J Physiol. 1958 Mar 11;140(3):479–497. [PMC free article] [PubMed] [Google Scholar]

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