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Usage Information

Preferential Binding of βS Globin Chains Associated with Stroma in Sickle Cell Disorders
Arthur Bank, … , Joyce V. O'Donnell, Clayton Natta
Arthur Bank, … , Joyce V. O'Donnell, Clayton Natta
Published October 1, 1974
Citation Information: J Clin Invest. 1974;54(4):805-809. https://doi.org/10.1172/JCI107820.
View: Text | PDF
Research Article

Preferential Binding of βS Globin Chains Associated with Stroma in Sickle Cell Disorders

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Abstract

Sickle cell anemia (SS) is associated with abnormalities of the red cell membrane and decreased red cell deformability. The present study assesses globin chain binding to stroma in SS, sickle cell trait (AS), and nonsickling (AA) cells. The results indicate that there is preferential binding of newly synthesized βS globin to red cell stroma in SS cells and preferential binding of βS to stroma compared to βA in AS cells. These studies show that βS globin binding to stroma accompanies the membrane abnormalities in SS and AS patients.

Authors

Arthur Bank, Gregory Mears, Robert Weiss, Joyce V. O'Donnell, Clayton Natta

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Usage data is cumulative from May 2024 through May 2025.

Usage JCI PMC
Text version 106 3
PDF 52 11
Scanned page 155 1
Citation downloads 47 0
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