Differences in residual CFTR-mediated current across the rs7512462 genotypes in the cultures with vehicle only (DMSO, n = 10) did not reach statistical significance ( P = 0.09, -0.17 μA/cm 2 ΔI eq -forskolin per C protective allele, Fig. 3B , red).
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Cystic fibrosis gene modifier SLC26A9 modulates airway response to CFTR-directed therapeutics.
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