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We carried out serial-tangential cryosectioning with immunoblotting [27] to examine the expression of IGF-1R in rod and cone photoreceptors of wild-type and rod Igf-1r / mice, using rhodopsin as a photoreceptor marker (Fig

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Where feasible, single wavelength data for which NADPH was titrated were fit using numerical integration in KinTek explorer software to descriptive models derived from conclusions drawn from analytical fitting to both single and multi-wavelength datasets

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