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Potential role of LSD1 inhibitors in the treatment of sickle cell disease: a review of preclinical animal model data

Sickle cell disease (SCD) is caused by a mutation of the β-globin gene (Ingram VM. Nature 180: 326–328, 1957), which triggers the polymerization of deoxygenated sickle hemoglobin (HbS). Approximately 100,000 SCD patients in the United States and millions worldwide (Piel FB, et al. PLoS Med 10: e1001...

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Опубликовано в: :Am J Physiol Regul Integr Comp Physiol
Главные авторы: Rivers, Angela, Jagadeeswaran, Ramasamy, Lavelle, Donald
Формат: Artigo
Язык:Inglês
Опубликовано: American Physiological Society 2018
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Online-ссылка:https://ncbi.nlm.nih.gov/pmc/articles/PMC6734057/
https://ncbi.nlm.nih.gov/pubmed/30067082
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1152/ajpregu.00440.2017
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