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26. Molecular cloning and functional characterization of the OCTN2 transporter at the RBE4 cells, an in vitro model of the blood-brain barrier. Friedrich A; Prasad PD; Freyer D; Ganapathy V; Brust P Brain Res; 2003 Apr; 968(1):69-79. PubMed ID: 12644265 [TBL] [Abstract][Full Text] [Related]
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28. Functional and pharmacological characterization of human Na(+)-carnitine cotransporter hOCTN2. Wagner CA; Lükewille U; Kaltenbach S; Moschen I; Bröer A; Risler T; Bröer S; Lang F Am J Physiol Renal Physiol; 2000 Sep; 279(3):F584-91. PubMed ID: 10966938 [TBL] [Abstract][Full Text] [Related]
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31. Age-associated cardiomyopathy in heterozygous carrier mice of a pathological mutation of carnitine transporter gene, OCTN2. Xiaofei E; Wada Y; Dakeishi M; Hirasawa F; Murata K; Masuda H; Sugiyama T; Nikaido H; Koizumi A J Gerontol A Biol Sci Med Sci; 2002 Jul; 57(7):B270-8. PubMed ID: 12084797 [TBL] [Abstract][Full Text] [Related]
32. A missense mutation of mouse OCTN2, a sodium-dependent carnitine cotransporter, in the juvenile visceral steatosis mouse. Lu Km; Nishimori H; Nakamura Y; Shima K; Kuwajima M Biochem Biophys Res Commun; 1998 Nov; 252(3):590-4. PubMed ID: 9837751 [TBL] [Abstract][Full Text] [Related]
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