Hydroxyurea therapy of a murine model of sickle cell anemia inhibits the progression of pneumococcal disease by down-modulating E-selectin
Author:
Affiliation:
1. Departments of Hematology,
2. Infectious Diseases, and
3. Animal Imaging Center, and
4. Department of Developmental Neurobiology, St Jude Children's Research Hospital, Memphis, TN
Abstract
Publisher
American Society of Hematology
Subject
Cell Biology,Hematology,Immunology,Biochemistry
Link
http://ashpublications.org/blood/article-pdf/119/8/1915/1355316/zh800812001915.pdf
Reference46 articles.
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2. The effect of prolonged administration of hydroxyurea on morbidity and mortality in adult patients with sickle cell syndromes: results of a 17-year, single-center trial (LaSHS).;Voskaridou;Blood,2010
3. Mortality in sickle cell disease. Life expectancy and risk factors for early death.;Platt;N Engl J Med,1994
4. Hydroxyurea and sickle cell anemia. Clinical utility of a myelosuppressive “switching” agent. The Multicenter Study of Hydroxyurea in Sickle Cell Anemia.;Charache;Medicine,1996
5. Effect of hydroxyurea on the frequency of painful crises in sickle cell anemia. Investigators of the Multicenter Study of Hydroxyurea in Sickle Cell Anemia.;Charache;N Engl J Med,1995
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