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106. A mutation in SLC22A4 encoding an organic cation transporter expressed in the cochlea strial endothelium causes human recessive non-syndromic hearing loss DFNB60

127. Accurate Evaluation of Hepatocyte Metabolisms on a Noble Oxygen-Permeable Material With Low Sorption Characteristics

129. Molecular Genetic Typing of Yersinia enterocolitica Serovar O:8 Isolated in Japan

137. Genome-wide association study of clinically defined gout identifies multiple risk loci and its association with clinical subtypes

146. Cryopreserved human hepatocytes culture optimization on polymethylpentene oxygen permeable membranes for drug screening purposes

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