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. 2016 Sep 28;44(20):9519–9529. doi: 10.1093/nar/gkw867

Figure 6.

Figure 6.

Ush1c.216A splicing in the inner ear of P22 mice dosed with ASO-Ush by amniotic cavity injection at E13-13.5. (A) Semi-quantitative radiolabeled RT-PCR analysis with primer sets specific for human USH1C (to specifically amplify only the knocked in human portion of the Ush1c216A allele (28)) and mouse Gapdh was performed on RNA isolated from the inner ear of P22 Ush1c216AA or Ush1c216GA mice treated with ASO-Ush at E13-13.5 by transuterine injection to the amniotic cavity (IA) (n = 3), or neonatal Ush1c216AA mice treated at P5 with ASO-Ush by intraperitoneal (IP) injection (n = 3), or untreated P22 Ush1c216AA (control)(n = 3) mice. (B) Quantification of correctly spliced mRNA from the Ush1c216A allele. Error bars represent s.e.m (n = 3). *P ≤ 0.05, one-tailed, two-sample t-test.