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61 Although currently pursued primarily in oncology, these agents may ultimately enable more refined autophagy modulation in cardiovascular settings

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In 2009, 29% of 202 human alleles of GPR42 were shown to have an inactivating single nucleotide polymorphism (SNP) at W174, and 61% with an arginine in like GPR41, resulting in a fully functional receptor, differing from it by only 5 aminoacids (312)