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Our identification and mapping of the cyclin D-Rb docking interaction provides an additional target for cancer drugs because deregulation of the G1/S transition and the cyclin D-CDK4/6-Rb pathway is a hallmark of many cancer cells 13

The prevalence of zinc deficiency in 6-month to 12-year old children in Bandar Abbas in 2013

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Structural characteristics of the peptide-binding GPCRs and structure-based drug development Many peptide-binding GPCRs are well-known therapeutic targets 14,85 (Table 1)