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pro vyhledávání: '"J Ford Burns"'
Autor:
Jonathan W. Stocker, Lucia De Franceschi, Grant A McNaughton-Smith, J Ford Burns, Gregory Cooksey Rigdon, Tara Shelton, Christopher Creech, Susan Arrington
Publikováno v:
Journal of medicinal chemistry. 51(4)
Sickle cell disease (SCD) is a hereditary condition characterized by deformation of red blood cells (RBCs). This phenomenon is due to the presence of abnormal hemoglobin that polymerizes upon deoxygenation. This effect is exacerbated when dehydrated
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::52785fc3214275905e515ac31dd4eb03
https://pubmed.ncbi.nlm.nih.gov/18232633
https://pubmed.ncbi.nlm.nih.gov/18232633
Autor:
Grant A. McNaughton-Smith, J. Ford Burns, Gregory C. Rigdon, Christopher Creech, Susan Arrington, Tara Shelton, Lucia de Franceschi, Jonathan W. Stocker
Publikováno v:
Journal of Medicinal Chemistry; Jan2008, Vol. 51 Issue 4, p976-982, 7p