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Conen, D, Popova, E, Wang, MK, Chan, MT, Landoni, G, Reimer, C, Srinathan, SK, Cata, JP, McLean, SR, Reyes, JT, Grande, AM, Tallada, AG, Sessler, DI, Fleischmann, E, Maziak, D, Kabon, B, Voltolini, L, Gutirrez-Soriano, L, Tandon, V, DuMerton, D, Kidane, B, Rajaram, R, Shargall, Y, Neary, JD, Wells, JR, McIntyre, WF, Blum, S, Ofori, SN, Vincent, J, Xu, L, Li, Z, Healey, JS, Garg, AX, Devereaux, PJ, Reiterer, C, Taschner, A, Horvath, K, Adamowitsch, N, Zotti, O, Hantkov, N, Hochreiter, B, Schmartz, D, Huybrechts, I, Cappeliez, S, Finley, C, Agzarian, J, Mehran, RJ, Sepesi, B, Walsh, GL, Rice, DC

Studies examining muscle protein synthesis, fiber hypertrophy in rodent models, and satellite cell biology have used IGF-1 LR3 as the standard research tool when sustained IGF1R activation is the experimental goal

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Other potential physiological substrates of MRP1 include the conjugated estrogens estradiol glucuronide and estrone sulfate, folic acid, GSH and its prooxidant metabolite GSH disulfide (GSSG) (see Fig

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