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• W2775793583 startingPage "555" @default.
• W2775793583 abstract "β-Thalassemia is an inherited hematologic disorder caused by various mutations of the β-globin gene, thus resulting in a significant decrease in adult hemoglobin (HbA) production. An increase in fetal hemoglobin (HbF) levels by drug molecules is considered of great potential in β-thalassemia treatment and is expected to counterbalance the impaired production of HbA. In this work, based on a set of 129 experimentally tested biological inhibitors, we developed and validated a computational model for the prediction of K562 functional inhibition, possibly associated with HbF induction. To facilitate future advancements in the field, we incorporated our model into Enalos Cloud Platform, which enabled online access to our computational scheme (http://enalos.insilicotox.com/K562) through a user-friendly interface. This web service is offered to the wider community to promote in silico drug discovery through fast and reliable predictions." @default.
• W2775793583 created "2017-12-22" @default.
• W2775793583 creator A5005571764 @default.
• W2775793583 creator A5010261777 @default.
• W2775793583 creator A5053054748 @default.
• W2775793583 creator A5088194977 @default.
• W2775793583 date "2018-01-30" @default.
• W2775793583 modified "2023-09-27" @default.
• W2775793583 title "Consensus Predictive Model for Human K562 Cell Growth Inhibition through Enalos Cloud Platform" @default.
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• W2775793583 doi "https://doi.org/10.1002/cmdc.201700675" @default.
• W2775793583 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/29195008" @default.
• W2775793583 hasPublicationYear "2018" @default.
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