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Nanotechnology lighting the way for gene therapy in ophthalmopathy: from opportunities toward applications

Working synergistically, Bcrp, Mrp-2, and P-gp eliminate a multitude of drugs absorbed across tissue barriers (Chang et al., 2011)

Clinical Information autosomal recessive inborn error of methionine metabolism usually caused by a deficiency of cystathionine beta-synthase and associated with elevations of homocysteine in plasma and urine

But long-term GH replacement therapy (which produces similar GH/IGF-1 levels) has been studied for decades and is considered safe when properly monitored