Amelioration of severe hereditary spherocytosis in nonablated adult mice by marrow transplantation
Author:
Publisher
Elsevier BV
Subject
Cancer Research,Cell Biology,Genetics,Hematology,Molecular Biology
Reference31 articles.
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3. Partial ankyrin and ankyrin deficiency in severe, atypical hereditary spherocytosis;Coetzer;N Engl J Med,1988
4. Spectrin deficient inherited hemolytic anemias in the mouse;Bodine;Cell,1984
5. The murine mutation jaundiced is caused by replacement of an arginine with a stop codon in the mRNA encoding the ninth repeat of β-spectrin;Bloom;Proc Natl Acad Sci U S A,1994
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2. An Adaptable Spectrin/Ankyrin-Based Mechanism for Long-Range Organization of Plasma Membranes in Vertebrate Tissues;Current Topics in Membranes;2016
3. Allo-hematopoietic stem cell transplantation is a potential treatment for a patient with a combined disorder of hereditary spherocytosis;CHINESE MED J-PEKING;2012
4. Potential Large Animal Models for Gene Therapy of Human Genetic Diseases of Immune and Blood Cell Systems;ILAR Journal;2009-01-01
5. Hereditary haemolytic anaemias: unexpected sequelae of mutations in the genes for erythroid membrane skeletal proteins;The Journal of Pathology;2004-10-19
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