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Mediating ERK1/2 signaling rescues congenital heart defects in a mouse model of Noonan syndrome

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Figure

Figure 1Developmental stage–specific transgene expression of normal or
Figure 2Histological findings. (A) Four-chamber view of the hearts at E16.5 (original magnification, ×4)
Table 1
Figure 4Reduction of ERK1/2 hyperphosphorylation rescues Q79R-induced heart disease. Western blot analysis (
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