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Year | Number of Results |
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2011 | 1 |
2013 | 1 |
2017 | 1 |
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2024 | 0 |
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Juvenile cataract-associated mutation of solute carrier SLC16A12 impairs trafficking of the protein to the plasma membrane.
Invest Ophthalmol Vis Sci. 2011 Aug 29;52(9):6774-84. doi: 10.1167/iovs.10-6579.
Invest Ophthalmol Vis Sci. 2011.
PMID: 21778275
Free PMC article.
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.
Abplanalp J, et al.
Hum Mol Genet. 2013 Aug 15;22(16):3218-26. doi: 10.1093/hmg/ddt175. Epub 2013 Apr 10.
Hum Mol Genet. 2013.
PMID: 23578822
Free PMC article.
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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.
Stäubli A, et al.
Hum Mol Genet. 2017 Nov 1;26(21):4203-4214. doi: 10.1093/hmg/ddx310.
Hum Mol Genet. 2017.
PMID: 29088427
Free article.
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Molecular characterization of the orphan transporter SLC16A9, an extracellular pH- and Na+-sensitive creatine transporter.
Futagi Y, Narumi K, Furugen A, Kobayashi M, Iseki K.
Futagi Y, et al.
Biochem Biophys Res Commun. 2020 Feb 5;522(2):539-544. doi: 10.1016/j.bbrc.2019.11.137. Epub 2019 Nov 26.
Biochem Biophys Res Commun. 2020.
PMID: 31784090
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