Analysis of the red cell membrane in a family with hereditary elliptocytosis — total or partial of protein 4.1
Author:
Publisher
Springer Science and Business Media LLC
Subject
Genetics (clinical),Genetics
Link
http://link.springer.com/content/pdf/10.1007/BF00278857.pdf
Reference16 articles.
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3. Dodge JT, Mitchell C, Hanahan DJ (1963) The preparation and chemical characteristics of hemoglobin free ghosts of human erythrocytes. Arch Biochem Biophys 100:119–130
4. Fairbanks G, Steck TL, Wallach DFH (1971) Electrophoretic analysis of the major polypeptides of the human erythrocyte membrane. Biochemistry 10:2606–2617
5. Greenquist AC, Shohet SB (1976) Phosphorylation in erythrocyte membranes form abnormally shaped cells. Blood 48:877–886
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1. Homozygous deletion of EPB41 genuine AUG-containing exons results in mRNA splicing defects, NMD activation and protein 4.1R complete deficiency in hereditary elliptocytosis;Blood Cells, Molecules, and Diseases;2011-10
2. Red cell membrane alteration involving protein 4.1 and protein 3 in a case of recessively inherited haemolytic anaemia;European Journal of Haematology;2009-04-24
3. Nectin-like molecule 1 is a protein 4.1N associated protein and recruits protein 4.1N from cytoplasm to the plasma membrane;Biochimica et Biophysica Acta (BBA) - Biomembranes;2005-05
4. Une forme particulière d'anémie constitutionnelle chez un nourrisson de deux mois : l'elliptocytose;Archives de Pédiatrie;2005-02
5. Characterization of zebrafish merlot/chablis as non-mammalian vertebrate models for severe congenital anemia due to protein 4.1 deficiency;Development;2002-09-15
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