Genetic disorders of the red cell membrane☆
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Partial Splenectomy for Hereditary Spherocytosis
2008, Pediatric Clinics of North AmericaCitation Excerpt :Although some children and adults who have HS have a mild clinical phenotype, many patients develop clinically significant and eventually severe clinical consequences, such as anemia, hemolytic crises, splenic sequestration, and gallstones, which traditionally have led to the recommendation of total splenectomy. The shortened lifespan of RBCs in HS is related to a deficiency or dysfunction of constituents within the RBC cytoskeleton [1,19,20]. The erythrocyte cytoskeleton is a spectrin-based 2-D network of cell membrane proteins, with each spectrin moiety (α- or β-subunit) consisting of repeating polypeptide domains that fold into repeating helices.
Partial splenectomy for children with congenital hemolytic anemia and massive splenomegaly
2008, Journal of Pediatric SurgeryCitation Excerpt :Congenital hemolytic anemia (CHA) frequently leads to severe hemolysis because of splenic sequestration of abnormal erythrocytes [1].
An alternative domain containing a leucine-rich sequence regulates nuclear cytoplasmic localization of protein 4.1R
2003, Journal of Biological Chemistry4.1R proteins associate with interphase microtubules in human T cells: A 4.1R constitutive region is involved in tubulin binding
2001, Journal of Biological ChemistryThe Prototypical 4.1R-10-kDa Domain and the 4.1G-10-kDa Paralog Mediate Fodrin-Actin Complex Formation
2001, Journal of Biological Chemistry
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This paper was reviewed by Bernard Forget, M.D., Hematology Section, Yale University School of Medicine, New Haven, CT 06510, USA.