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Therefore, the metabolic phenotype of NKCC2A KO mice likely stems from complex, age-dependent and long-term functional interactions between the brain, pancreatic islets, kidneys and intestines as well as other tissues where NKCC2 may be expressed, even in minimal quantities relative to the kidneys

(62) In contrast to these results, another study has found increased incidence of the ALDH2 * 1 variant in patients with alcoholic cirrhosis

Unless otherwise specified, the following siRNAs (siGENOME

Huerga Encabo, H

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