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Aggregation of Normal and Sickle Hemoglobin in High Concentration Phosphate Buffer
Sickle cell disease is caused by a mutant form of hemoglobin, hemoglobin S, that polymerizes under hypoxic conditions. The extent and mechanism of polymerization are thus the subject of many studies of the pathophysiology of the disease and potential treatment strategies. To facilitate such studies,...
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| Main Authors: | , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Biophysical Society
2004
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC1304920/ https://ncbi.nlm.nih.gov/pubmed/15465861 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1529/biophysj.104.046482 |
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