Articles dans des revues avec comité de lecture (7)
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Lytrivi, M., Senée, V., Salpea, P., Fantuzzi, F., Philippi, A., Abdulkarim, B., Sawatani, T., Marin Canas, S., Pachera, N., Degavre, A., Singh, P., Derbois, C., Lechner, D., Ladrière, L., Igoillo Esteve, M., Cosentino, C., Marselli, L., Deleuze, J. F., Marchetti, P., Eizirik, D. L., Nicolino, M., Chaussenot, A., Julier, C., & Cnop, M. (2021). DNAJC3 deficiency induces β-cell mitochondrial apoptosis and causes syndromic young-onset diabetes. European journal of endocrinology, 184(3), 455-468. doi:10.1530/EJE-20-06362.
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.1342213.
Abdulkarim, B., Hernangomez Herrero, M., Igoillo Esteve, M., Andrade Da Cunha, D., Marselli, L., Marchetti, P., Ladrière, L., & Cnop, M. (2017). Guanabenz Sensitizes Pancreatic β Cells to Lipotoxic Endoplasmic Reticulum Stress and Apoptosis. Endocrinology, 158(6), 1659-1670. doi:10.1210/en.2016-17734.
Abdulkarim, B., Nicolino, M., Igoillo Esteve, M., Daures, M., Romero, S., Philippi, A., Senée, V., Lopes, M., Andrade Da Cunha, D., Harding, H. P., Derbois, C., Bendelac, N., Hattersley, A. T., Eizirik, D., Ron, D., Cnop, M., & Julier, C. (2015). A Missense Mutation in PPP1R15B Causes a Syndrome Including Diabetes, Short Stature, and Microcephaly. Diabetes (New York, N.Y.), 64(11), 3951-3962. doi:10.2337/db15-04775.
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/ddu7456.
Cnop, M., Abdulkarim, B., Bottu, G., Andrade Da Cunha, D., Igoillo Esteve, M., Masini, M., Turatsinze, J. V., Griebel, T., Villate, O., Santin Gomez, I., Bugliani, M., Ladrière, L., Marselli, L., McCarthy, M. I., Marchetti, P., Sammeth, M., & Eizirik, D. L. (2014). RNA-sequencing identifies dysregulation of the human pancreatic islet transcriptome by the saturated fatty acid palmitate. Diabetes (New York, N.Y.), 63, 1978-93. doi:10.2337/db13-13837.
Igoillo Esteve, M., Genin, A., Lambert, N., Désir, J., Pirson, I., Abdulkarim, B., Simonis, N., Drielsma, A., Marselli, L., Marchetti, P., Vanderhaeghen, P., Eizirik, D. L., Wuyts, W., Julier, C., Chakera, A. J., Ellard, S., Hattersley, A. T., Abramowicz, M., & Cnop, M. (2013). tRNA methyltransferase homolog gene TRMT10A mutation in young onset diabetes and primary microcephaly in human. PLoS genetics, 9. doi:10.1371/journal.pgen.1003888 Participations à des congrès et colloques internationaux (2)
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Igoillo Esteve, M., Genin, A., Lambert, N., Désir, J., Pirson, I., Abdulkarim, B., Simonis, N., Drielsma, A., Marselli, L., Marchetti, P., Vanderhaeghen, P., Eizirik, D. L., Wuyts, W., Julier, C., Chakera, A. J., Ellard, S., Hattersley, A. T., & Abramowicz, M. (2013). Loss-of-function of TRMT10A causes young onset diabetes and microcephaly. Paper session presented at 23rd Meeting of the Belgian Endocrine Society (2013: Ghent, Belgium).2.
Igoillo Esteve, M., Genin, A., Lambert, N., Désir, J., Pirson, I., Abdulkarim, B., Simonis, N., Drielsma, A., Marselli, L., Marchetti, P., Vanderhaeghen, P., Eizirik, D. L., Wuyts, W., Julier, C., Chakera, A. J., Ellard, S., Hattersley, A. T., & Abramowicz, M. (2013). tRNA methyltransferase homolog gene TRMT10A mutation in young onset diabetes and primary microcephaly in humans. Paper session presented at Belgian Medical Genomics Initiative (BeMGI) Kickoff Meeting (2013: Leuven, Belgium). Thèses et mémoires (1)