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I Tamai

Showing results (121-130 of 124) with videos related to

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The Journal of Pharmacy and Pharmacology|December 1, 1999
Immunohistochemical and functional characterization of pH-dependent intestinal absorption of weak organic acids by the monocarboxylic acid transporter MCT1I Tamai, Y Sai, A Ono, et al.
Human Molecular Genetics|November 5, 1999
Genetic epidemiology of the carnitine transporter OCTN2 gene in a Japanese population and phenotypic characterization in Japanese pedigrees with primary systemic carnitine deficiencyA Koizumi, J Nozaki, T Ohura, et al.
Hepatology (Baltimore, Md.)|September 25, 1999
Loss of wild-type carrier-mediated L-carnitine transport activity in hepatocytes of juvenile visceral steatosis miceK Yokogawa, M Yonekawa, I Tamai, et al.
Nature Genetics|January 23, 1999
Primary systemic carnitine deficiency is caused by mutations in a gene encoding sodium ion-dependent carnitine transporterJ Nezu, I Tamai, A Oku, et al.
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Showing results (121-130 of 124) with videos related to

Sort By:
Pageof 13
You have reached the last page of results.This site can display upto 124 results.
The Journal of Pharmacy and Pharmacology|December 1, 1999
Immunohistochemical and functional characterization of pH-dependent intestinal absorption of weak organic acids by the monocarboxylic acid transporter MCT1I Tamai, Y Sai, A Ono, et al.
Human Molecular Genetics|November 5, 1999
Genetic epidemiology of the carnitine transporter OCTN2 gene in a Japanese population and phenotypic characterization in Japanese pedigrees with primary systemic carnitine deficiencyA Koizumi, J Nozaki, T Ohura, et al.
Hepatology (Baltimore, Md.)|September 25, 1999
Loss of wild-type carrier-mediated L-carnitine transport activity in hepatocytes of juvenile visceral steatosis miceK Yokogawa, M Yonekawa, I Tamai, et al.
Nature Genetics|January 23, 1999
Primary systemic carnitine deficiency is caused by mutations in a gene encoding sodium ion-dependent carnitine transporterJ Nezu, I Tamai, A Oku, et al.
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