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PIEZO1 loss-of-function compound heterozygous mutations in the rare congenital human disorder Prune Belly Syndrome Amado, Nathalia G.; Nosyreva, Elena D.; Thompson, David; Egeland, Thomas J.; Ogujiofor, Osita W.; Yang, Michelle; Fusco, Alexandria N.; Passoni, Niccolo; Mathews, Jeremy; Cantarel, Brandi; Baker, Linda A.; Syeda, Ruhma Share Save
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Chemical activation of the mechanotransduction channel Piezo1 Syeda, Ruhma; Xu, Jie; Dubin, Adrienne E.; Coste, Bertrand; Mathur, Jayanti; Truc Huynh; Matzen, Jason; Lao, Jianmin; Tully, David C.; Engels, Ingo H.; Petrassi, H. Michael; Schumacher, Andrew M.; Montal, Mauricio; Bandell, Michael; Patapoutian, Ardem Share Save
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Crystal structure of a voltage-gated K+ channel pore module in a closed state in lipid membranes (vol 287, pg 43063, 2012) Santos, Jose S.; Asmar-Rovira, Guillermo A.; Han, Gye Won; Liu, Wei; Syeda, Ruhma; Cherezov, Vadim; Baker, Kent A.; Stevens, Raymond C.; Montal, Mauricio Share Save
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