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Referencias:

• Armstrong, L., Tilgner, K., Saretzki, G., Atkinson, S.P., Stojkovic, M., Moreno, R., Przyborski, S., Lako, M., Human induced pluripotent stem cell lines show stress defense mechanisms and mitochondrial regulation similar to those of human embryonic stem cells (2010) Stem Cells, 28, pp. 661-673
• Bigarella, C.L., Liang, R., Ghaffari, S., Stem cells and the impact of ROS signaling (2014) Development, pp. 4206-4218
• Boward, B., Wu, T., Dalton, S., Control of cell fate through cell cycle and pluripotency networks (2016) Stem Cells, 34
• Chen, X., Xu, H., Yuan, P., Fang, F., Huss, M., Vega, V.B., Wong, E., Ng, H.H., Integration of external signaling pathways with the core transcriptional network in embryonic stem cells (2008) Cell, 133, pp. 1106-1117. , https://doi.org/10.1016/j.cell.2008.04.043, https://doi.org/S0092-8674(08)00617-X, [pii]
• Cherepkova, M.Y., Sineva, G.S., Pospelov, V.A., Leukemia inhibitory factor (LIF) withdrawal activates mTOR signaling pathway in mouse embryonic stem cells through the MEK/ERK/TSC2 pathway (2016) Cell Death Dis., 7
• Cho, Y.M., Kwon, S., Pak, Y.K., Seol, H.W., Choi, Y.M., Park Do, J., Park, K.S., Lee, H.K., Dynamic changes in mitochondrial biogenesis and antioxidant enzymes during the spontaneous differentiation of human embryonic stem cells (2006) Biochem. Biophys. Res. Commun., 348, pp. 1472-1478. , https://doi.org/10.1016/j.bbrc.2006.08.020, https://doi.org/S0006-291X(06)01821-3, [pii]
• Circu, M.L., Aw, T.Y., Reactive oxygen species, cellular redox systems, and apoptosis (2010) Free Radic. Biol. Med., 48, pp. 749-762
• Davidson, K.C., Mason, E.A., Pera, M.F., The pluripotent state in mouse and human (2015) Development, 142, pp. 3090-3099
• Di Rienzo, J.A., Guzman, A.W., Casanoves, F., A multiple-comparisons method based on the distribution of the root node distance of a binary tree (2002) J. Agric. Biol. Environ. Stat., 7, pp. 129-142
• Di Rienzo, J.A., Casanoves, F., Balzarini, M.G., Gonzalez, L., Tablada, M., R., C.W., Infostat - Statistical software. Grupo InfoStat, FCA (2014), Universidad Nacional de Córdoba Argentina [WWW Document]; Elchuri, S., Oberley, T.D., Qi, W., Eisenstein, R.S., Jackson Roberts, L., Van Remmen, H., Epstein, C.J., Huang, T.-T., CuZnSOD deficiency leads to persistent and widespread oxidative damage and hepatocarcinogenesis later in life (2005) Oncogene, 24, pp. 367-380
• Huang, T.T., Yasunami, M., Carlson, E.J., Gillespie, A.M., Reaume, A.G., Hoffman, E.K., Chan, P.H., Epstein, C.J., Superoxide-mediated cytotoxicity in superoxide dismutase-deficient fetal fibroblasts (1997) Arch. Biochem. Biophys., 344, pp. 424-432
• Imamura, Y., Noda, S., Hashizume, K., Shinoda, K., Yamaguchi, M., Uchiyama, S., Shimizu, T., Tsubota, K., Drusen, choroidal neovascularization, and retinal pigment epithelium dysfunction in SOD1-deficient mice: a model of age-related macular degeneration (2006) Proc. Natl. Acad. Sci., 103, pp. 11282-11287
• Ito, K., Hirao, A., Arai, F., Takubo, K., Matsuoka, S., Miyamoto, K., Ohmura, M., Suda, T., Reactive oxygen species act through p38 MAPK to limit the lifespan of hematopoietic stem cells (2006) Nat. Med., 12, pp. 446-451. , https://doi.org/10.1038/nm1388, https://doi.org/nm1388, [pii]
• Jang, Y.Y., Sharkis, S.J., A low level of reactive oxygen species selects for primitive hematopoietic stem cells that may reside in the low-oxygenic niche (2007) Blood, 110, pp. 3056-3063. , https://doi.org/10.1182/blood-2007-05-087759, https://doi.org/blood-2007-05-087759, [pii]
• Losino, N., Luzzani, C., Solari, C., Boffi, J., Tisserand, M.L., Sevlever, G., Barañao, L., Guberman, A., Maintenance of murine embryonic stem cells’ self-renewal and pluripotency with increase in proliferation rate by a bovine granulosa cell line-conditioned medium (2011) Stem Cells Dev., 20, pp. 1439-1449
• Losino, N., Waisman, A., Solari, C., Luzzani, C., Espinosa, D.F., Sassone, A., Muro, A.F., Guberman, A., EDA-containing fibronectin increases proliferation of embryonic stem cells (2013) PLoS One, 8
• Luzzani, C., Solari, C., Losino, N., Ariel, W., Romorini, L., Bluguermann, C., Sevlever, G., Guberman, A., Modulation of chromatin modifying factors’ gene expression in embryonic and induced pluripotent stem cells (2011) Biochem. Biophys. Res. Commun., 410, pp. 816-822
• Miao, L., St. Clair, D.K., Regulation of superoxide dismutase genes: implcations in diseases (2010) Free Radic. Biol. Med., 47, pp. 344-356
• Muller, F.L., Song, W., Liu, Y., Chaudhuri, A., Pieke-Dahl, S., Strong, R., Huang, T.-T., Van Remmen, H., Absence of CuZn superoxide dismutase leads to elevated oxidative stress and acceleration of age-dependent skeletal muscle atrophy (2006) Free Radic. Biol. Med., 40, pp. 1993-2004
• Nugud, A., Sandeep, D., El-Serafi, A.T., Two faces of the coin: minireview for dissecting the role of reactive oxygen species in stem cell potency and lineage commitment (2018) J. Adv. Res.
• Ouyang, Z., Zhou, Q., Wong, W.H., ChIP-Seq of transcription factors predicts absolute and differential gene expression in embryonic stem cells (2009) Proc. Natl. Acad. Sci. U. S. A., 106, pp. 21521-21526
• Reaume, A.G., Elliott, J.L., Hoffman, E.K., Kowall, N.W., Ferrante, R.J., Siwek, D.R., Wilcox, H.M., Snider, W.D., Motor neurons in cu/Zn superoxide dismutase-deficient mice develop normally but exhibit enhanced cell death after axonal injury (1996) Nat. Genet., 13, pp. 43-47
• Saretzki, G., Armstrong, L., Leake, A., Lako, M., von Zglinicki, T., Stress defense in murine embryonic stem cells is superior to that of various differentiated murine cells (2004) Stem Cells, 22, pp. 962-971
• Saretzki, G., Walter, T., Atkinson, S., Passos, J.F., Bareth, B., Keith, W.N., Stewart, R., Lako, M., Downregulation of multiple stress defense mechanisms during differentiation of human embryonic stem cells (2008) Stem Cells, 26, pp. 455-464. , https://doi.org/10.1634/stemcells.2007-0628, https://doi.org/2007-0628, [pii]
• Sart, S., Song, L., Li, Y., Controlling redox status for stem cell survival, expansion, and differentiation (2015) Oxidative Med. Cell. Longev., p. 2015
• Schmelter, M., Ateghang, B., Helmig, S., Wartenberg, M., Sauer, H., Embryonic stem cells utilize reactive oxygen species as transducers of mechanical strain-induced cardiovascular differentiation (2006) FASEB J., 20, pp. 1182-1184. , https://doi.org/10.1096/fj.05-4723fje, https://doi.org/fj.05-4723fje, [pii]
• Solari, C., Vázquez Echegaray, C., Cosentino, M.S., Petrone, M.V., Waisman, A., Luzzani, C., Francia, M., Guberman, A., Manganese superoxide dismutase gene expression is induced by Nanog and Oct4, essential pluripotent stem Cells’ transcription factors (2015) PLoS One, 10
• Solari, C., Echegaray, C.V., Luzzani, C., Cosentino, M.S., Waisman, A., Petrone, M.V., Francia, M., Guberman, A., Protein arginine methyltransferase 8 gene is expressed in pluripotent stem cells and its expression is modulated by the transcription factor Sox2 (2016) Biochem. Biophys. Res. Commun., 473, pp. 6-11
• Stambrook, P.J., An ageing question: do embryonic stem cells protect their genomes? (2007) Mech. Ageing Dev., 128, pp. 31-35
• Trouillas, M., Saucourt, C., Guillotin, B., Gauthereau, X., Ding, L., Buchholz, F., Doss, M.X., Boeuf, H., Three LIF-dependent signatures and gene clusters with atypical expression profiles, identified by transcriptome studies in mouse ES cells and early derivatives (2009) BMC Genomics, 10, p. 73
• Ufer, C., Wang, C.C., The roles of glutathione peroxidases during embryo development (2011) Front. Mol. Neurosci., 4 (12)
• Waisman, A., Vazquez Echegaray, C., Solari, C., Cosentino, M.S., Martyn, I., Deglincerti, A., Ozair, M.Z., Guberman, A., Inhibition of cell division and DNA replication impair mouse-naïve pluripotency exit (2017) J. Mol. Biol.
• Zelko, I.N., Mariani, T.J., Folz, R.J., Superoxide dismutase multigene family: A comparison of the CuZn-SOD (SOD1), Mn-SOD (SOD2), and EC-SOD (SOD3) gene structures, evolution, and expression (2002) Free Radic. Biol. Med.

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