At the physiological phenotype level, CRISPRa has also been used to increase the transcription of obesity risk genes SIM1 and MC4R , and to successfully rescue haploinsufficient obesity in mouse modelswith the effects persisting up to 9 months post-treatment [80]
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NHEK, renal proximal tubule epithelial cells (RPTEC), human umbilical vein endothelial cells (HUVEC) and human dermal microvascular endothelial cells (HDMEC), using a representative dimeric macrocycle, aMD5-PEG11 (Fig
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