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XB-GENEPAGE-1012783
Papers associated with slc16a12
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Contribution of monocarboxylate transporter 12 to blood supply of creatine on the sinusoidal membrane of the hepatocytes., Jomura R, Tanno Y, Akanuma SI, Kubo Y, Tachikawa M, Hosoya KI., Am J Physiol Gastrointest Liver Physiol. August 1, 2021; 321 (2): G113-G122. |
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Monocarboxylate transporter 12 as a guanidinoacetate efflux transporter in renal proximal tubular epithelial cells., Jomura R, Tanno Y, Akanuma SI, Kubo Y, Tachikawa M, Hosoya KI., Biochim Biophys Acta Biomembr. November 1, 2020; 1862 (11): 183434. |
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Functional characterization of monocarboxylate transporter 12 (SLC16A12/MCT12) as a facilitative creatine transporter., Takahashi M, Kishimoto H, Shirasaka Y, Inoue K., Drug Metab Pharmacokinet. June 1, 2020; 35 (3): 281-287. |
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Identification of a selective inhibitor of human monocarboxylate transporter 4., Futagi Y, Kobayashi M, Narumi K, Furugen A, Iseki K., Biochem Biophys Res Commun. January 1, 2018; 495 (1): 427-432. |
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Abnormal creatine transport of mutations in monocarboxylate transporter 12 (MCT12) found in patients with age-related cataract can be partially rescued by exogenous chaperone CD147., Stäubli A, Capatina N, Fuhrer Y, Munier FL, Labs S, Schorderet DF, Tiwari A, Verrey F, Heon E, Cheng CY, Wong TY, Berger W, Camargo SMR, Kloeckener-Gruissem B., Hum Mol Genet. November 1, 2017; 26 (21): 4203-4214. |
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Renal localization and regulation by dietary phosphate of the MCT14 orphan transporter., Knöpfel T, Atanassoff A, Hernando N, Biber J, Wagner CA., PLoS One. June 29, 2017; 12 (6): e0177942.  |
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Mutation in the Monocarboxylate Transporter 12 Gene Affects Guanidinoacetate Excretion but Does Not Cause Glucosuria., Dhayat N, Simonin A, Anderegg M, Pathare G, Lüscher BP, Deisl C, Albano G, Mordasini D, Hediger MA, Surbek DV, Vogt B, Sass JO, Kloeckener-Gruissem B, Fuster DG., J Am Soc Nephrol. May 1, 2016; 27 (5): 1426-36. |
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The cataract and glucosuria associated monocarboxylate transporter MCT12 is a new creatine transporter., Abplanalp J, Laczko E, Philp NJ, Neidhardt J, Zuercher J, Braun P, Schorderet DF, Munier FL, Verrey F, Berger W, Camargo SM, Kloeckener-Gruissem B., Hum Mol Genet. August 15, 2013; 22 (16): 3218-26.  |
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