Defective spectrin dimer-dimer association with hereditary elliptocytosis.-Reference-Cited by-同舟云学术

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Defective spectrin dimer-dimer association with hereditary elliptocytosis.

Published:1982-03-01 Issue:6 Volume:79 Page:2072-2076
ISSN:0027-8424
Container-title:Proceedings of the National Academy of Sciences
language:en
Short-container-title:Proceedings of the National Academy of Sciences

Author:

Liu S. C.,Palek J.,Prchal J. T.

Publisher

Proceedings of the National Academy of Sciences

Subject

Multidisciplinary

Cited by 77 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Vesiculation of healthy and defective red blood cells;Physical Review E;2015-07-21

2. Variations in Both a-Spectrin(SPTA1)and �-Spectrin (SPTB) in a Neonate with Prolonged Jaundice in a Family where Nine Individuals Had Hereditary Elliptocytosis;Neonatology;2014

3. A genomic deletion causes truncation of α-spectrin and ellipto-poikilocytosis;Blood Cells, Molecules, and Diseases;2011-03

4. Detection of hereditary pyropoikilocytosis by the eosin-5-maleimide (EMA)-binding test is attributable to a marked reduction in EMA-reactive transmembrane proteins;International Journal of Laboratory Hematology;2010-11-03

5. Defective spectrin dimer self-association in thalassemic red cells;European Journal of Haematology;2009-04-24

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