Articles dans des revues avec comité de lecture (10)
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Igoillo Esteve, M., Martins Oliveira, A. F., Cosentino, C., Fantuzzi, F., Demarez, C., Toivonen, S., Hu, A., Chintawar, S., Lopes, M., Pachera, N., Cai, Y., Abdulkarim, B., Rai, M., Marselli, L., Marchetti, P., Tariq, M., Jonas, J.-C. J., Boscolo, M., Pandolfo, M., Eizirik, D. L., & Cnop, M. (2019). Exenatide induces frataxin expression and improves mitochondrial function in Friedreich ataxia. JCI insight. doi:10.1172/jci.insight.1342212.
Igoillo Esteve, M., Gurgul-Convey, E., Hu, A., Romagueira Bichara Dos Santos, L. R., Abdulkarim, B., Chintawar, S., Marselli, L., Jonas, J.-C. J., Eizirik, D. L., Pandolfo, M., & Cnop, M. (2015). Unveiling a common mechanism of apoptosis in β-cells and neurons in Friedreich’s ataxia. Human molecular genetics, 24, 2274-86. doi:10.1093/hmg/ddu7453.
Dibbens, L. M., De Vries, B., Donatello, S., Heron, S. E., Hodgson, B. L., Chintawar, S., Crompton, D. E., Hughes, J. N., Bellows, S. T., Klein, K. M., Callenbach, P. M., Corbett, M. A., Gardner, A. E., Kivity, S., Iona, X., Regan, B. M., Weller, C. M., Crimmins, D., O'Brien, T. J., Guerrero-López, R., Mulley, J. C., Dubeau, F., Licchetta, L., Bisulli, F., Cossette, P., Thomas, P. Q., Gecz, J., Serratosa, J. M., Brouwer, O., Andermann, F., Andermann, E., Van den Maagdenberg, A. M., Pandolfo, M., Berkovic, S. F., & Scheffer, I. E. (2013). Mutations in DEPDC5 cause familial focal epilepsy with variable foci. Nature genetics. doi:10.1038/ng.25994.
Hick, A., Wattenhofer-Donzé, M., Chintawar, S., Tropel, P., Simard, J. P., Vaucamps, N., Gall, D., Lambot, L., André, C., Reutenauer, L., Rai, M., Teletin, M., Messaddeq, N., Schiffmann, S. N., Viville, S., Pearson, C. E., Pandolfo, M., & Puccio, H. (2013). Neurons and cardiomyocytes derived from induced pluripotent stem cells as a model for mitochondrial defects in Friedreich's ataxia. Disease Models and Mechanisms, 6(3), 608-621. doi:10.1242/dmm.0109006.
Jäderstad, J., Jäderstad, L. M., Li, J., Chintawar, S., Salto, C., Pandolfo, M., Ourednik, V., Teng, Y. D., Sidman, R. L., Arenas, E., Snyder, E. Y., & Herlenius, E. (2010). Communication via gap junctions underlies early functional and beneficial interactions between grafted neural stem cells and the host. Proceedings of the National Academy of Sciences of the United States of America, 107(11), 5184-5189. doi:10.1073/pnas.09151341077.
Chintawar, S., Hourez, R., Ravella, A. B., Gall, D., Orduz Perez, D., Rai, M., Bishop, D. P., Geuna, S., Schiffmann, S. N., & Pandolfo, M. (2009). Grafting neural precursor cells promotes functional recovery in an SCA1 mouse model. The Journal of neuroscience, 29(42), 13126-13135. doi:10.1523/JNEUROSCI.0647-09.20098.
Chintawar, S., Hourez, R., Ravella, A. B., Gall, D., Orduz Perez, D., Rai, M., Bishop, D. P., Geuna, S., Schiffmann, S. N., & Pandolfo, M. (2009). Grafting neural precursor cells promotes functional recovery in an SCA1 mouse model. The Journal of neuroscience, 29(42), 13126-13135. doi:10.1523/JNEUROSCI.0647-09.20099.
Chintawar, S., Cayrol, R., Antel, J., Pandolfo, M., & Prats, A. C. (2009). Blood-brain barrier promotes differentiation of human fetal neural precursor cells. Stem cells, 27(4), 838-846. doi:10.1002/stem.2510.
De Windt, A., Rai, M., Bernier, L., Thelen, K. M., Soini, J., Lefebvre, C., Chintawar, S., Lavigne, J., Saarinen, L., Kytömäki, L., Munzer, J. S., Lütjohann, D., Pandolfo, M., Davignon, J., Seidah, N. G., & Laaksonen, R. (2007). Gene set enrichment analysis reveals several globally affected pathways due to SKI-1/S1P inhibition in HepG2 cells. DNA and cell biology, 26(11), 765-772. doi:10.1089/dna.2007.0624 Thèses et mémoires (1)