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Abstract Among the priorities in neurology is the development of pathogenetic treatment for Parkinson’s disease (PD). Striatal neurons capable of expressing the tyrosine hydroxylase gene (Th) and containing this enzyme represent a potential target for such therapy. Transgenic mice with the green fluorescent protein gene under the Th promoter were used to model PD via 1‑methyl‑4‑phenyl‑1,2,3,6‑tetrahydropyridine neurotoxin.
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