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It relieves symptoms and improves patients 'quality of life Genetic diseases related to abnormal glycine metabolism non-ketotic hyperglycinemia Non-ketotic hyperglycinemia is a rare genetic disease characterized by abnormally elevated levels of glycine in the blood

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the newly developed angiotensin IV agonist ligand Dihexa has been shown to facilitate acquisition of a spatial learning and memory task in scopolamine treated rats (data not shown)

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If solution storage is necessary, researchers commonly use sterile buffers around pH 56, aliquot to reduce freezethaw exposure, and store refrigerated shortterm (often referenced as up to ~30 days at ~4C (39F) as general guidance), freezing when not in use depending on the protocol