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Red cell membrane remodeling in sickle cell anemia. Sequestration of membrane lipids and proteins in Heinz bodies.

In red cells from patients with sickle cell anemia, hemoglobin S denatures and forms Heinz bodies. Binding of Heinz bodies to the inner surface of the sickle cell membrane promotes clustering and colocalization of the membrane protein band 3, outer surface-bound autologous IgG and, to some extent, t...

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Hlavní autoři: Liu, S C, Yi, S J, Mehta, J R, Nichols, P E, Ballas, S K, Yacono, P W, Golan, D E, Palek, J
Médium: Artigo
Jazyk:Inglês
Vydáno: 1996
Témata:
On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC507059/
https://ncbi.nlm.nih.gov/pubmed/8550846
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