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The isolated nucleic acid of claim 1, 2, or 3, wherein the encoded modified tetracycline repressor binds to a tetracycline operator sequence in a prokaryotic organism with a greater affinity in the presence of tetracycline or a tetracycline analog than in the absence of tetracycline or the tetracycline analog with a greater affinity at 37° C. The language “effective amount” of the compound is that amount necessary or sufficient to treat or prevent a tetracycline compound responsive state. Only 1 HSV-1 isolate (0.1%) was resistant to acyclovir (IC 50 ⩾8.8 μ M); this isolate was also resistant to penciclovir (IC 50 ⩾8.8 μ M).
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"Increased glutamatergic neurotransmission and oxidative stress after alcohol withdrawal". In yet other embodiments, the stable lisinopril powder formulations have about 3% w/w total impurities or related substances.
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