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    Reductions of erythrocyte membrane viscoelastic coefficients reflect spectrin deficiencies in hereditary spherocytosis 

    Agre, Peter; Waugh, Richard E. (American Society for Clinical Investigation, 1988-01)
    Hereditary spherocytosis is a common hemolytic anemia associated with deficiencies in spectrin, the principal structural protein of the erythrocyte membrane-skeleton. We have examined 20 different individuals from 10 ...
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    Deficient red-cell spectrin in severe, recessively inherited spherocytosis 

    Agre, Peter; Bennett, Vann; Orringer, Eugene P. (Massachusetts Medical Society, 1982-05-13)
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    Inheritance pattern and clinical response to splenectomy as a reflection of erythrocyte spectrin deficiency in hereditary spherocytosis 

    Asimos, Andrew; Agre, Peter; McMillan, Campbell; Casella, James F. (Massachusetts Medical Society, 1986-12-18)
    To determine how various inheritance patterns and responses to splenectomy relate to erythrocyte spectrin deficiencies in hereditary spherocytosis, we measured the spectrin content of erythrocytes by radioimmunoassay in ...
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    Reductions of erythrocyte membrane viscoelastic coefficients reflect spectrin deficiencies in hereditary spherocytosis 

    Agre, Peter; Waugh, Richard E. (American Society for Clinical Investigation, 1988-01)
    Hereditary spherocytosis is a common hemolytic anemia associated with deficiencies in spectrin, the principal structural protein of the erythrocyte membrane-skeleton. We have examined 20 different individuals from 10 ...
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    Partial deficiency of erythrocyte spectrin in hereditary spherocytosis. 

    Bennett, Vann; McMillan, Campbell; Casella, James F.; Zinkham, William H.; Agre, Peter (Nature Publishing Group, 1985-03-28)
    Hereditary spherocytosis (HS) is a common, clinically heterogeneous haemolytic anaemia in which the primary erythrocyte defect is believed to be some abnormality in the spectrin-actin membrane skeleton, leading to loss of ...
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    Decreased membrane mechanical stability and in vivo loss of surface area reflect spectrin deficiencies in hereditary spherocytosis 

    Mohandas, Naria; Agre, Peter; Chasis, Joel Anne (American Society for Clinical Investigation, 1988-08)
    Whereas marked variations in the clinical manifestations of hereditary spherocytosis have long been recognized, we have only recently begun to define the molecular basis for this heterogeneity. An important unanswered ...

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    AuthorAgre, Peter (6)Bennett, Vann (2)Casella, James F. (2)McMillan, Campbell (2)Waugh, Richard E. (2)Asimos, Andrew (1)Chasis, Joel Anne (1)Mohandas, Naria (1)Orringer, Eugene P. (1)Zinkham, William H. (1)SubjectSpectrin/deficiency (6)
    Spherocytosis (6)
    Hereditary/blood (4)Erythrocyte Deformability (3)Erythrocyte Membrane/physiology (3)Hereditary/genetics (2)Erythocytes/ultrastructure (1)Erythrocyte Membrane/analysis (1)Erythrocytes/analysis (1)Membrane Proteins/deficiency (1)... View MoreDate Issued1988 (3)1982 (1)1985 (1)1986 (1)Has File(s)Yes (6)

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