Articles dans des revues avec comité de lecture (63)
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Ansseau, E., Gerbaux, C., Cloet, S., Wauters, A., Zorbo, S., Meyer, P., Pirson, I., Laoudj-Chenivesse, D., Wattiez, R., Harper, S. S., Belayew, A., Eidahl, J. J., Coppee, F., Lancelot, C., Tassin, A., Matteotti, C., Yip, C., Liu, J., Leroy, B., & Hubeau, C. (2016). Homologous transcription factors DUX4 and DUX4c associate with cytoplasmic proteins during muscle differentiation. PloS one, 11(1), e0146893. doi:10.1371/journal.pone.014689315.
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.100388816.
Genin, A., Désir, J., Lambert, N., Biervliet, M., Van Der Aa, N., Pierquin, G., Killian, A., Tosi, M., Urbina, M., Lefort, A., Libert, F., Pirson, I., & Abramowicz, M. (2012). Kinetochore KMN network gene CASC5 mutated in primary microcephaly. Human molecular genetics, 21(24), 5306-5317. doi:10.1093/hmg/dds38617.
Drielsma, A., Jalas, C., Simonis, N., Désir, J., Simanovsky, N., Pirson, I., Elpeleg, O., Abramowicz, M., & Edvardson, S. (2012). Two novel CCDC88C mutations confirm the role of DAPLE in autosomal recessive congenital hydrocephalus. Journal of medical genetics, 49(11), 708-712. doi:10.1136/jmedgenet-2012-10119018.
Burniat, A., Pirson, I., Vilain, C., Kulik, W., Afink, G., Moreno Reyes, M. R., Corvilain, B., & Abramowicz, M. (2012). Iodotyrosine deiodinase defect identified via genome-wide approach. The Journal of clinical endocrinology and metabolism, 97(7), E1276-E1283. doi:10.1210/jc.2011-331419.
Erneux, C., Elong Edimo, W., Deneubourg, L., & Pirson, I. (2011). SHIP2 multiple functions: a balance between a negative control of PtdIns(3,4,5)P₃ level, a positive control of PtdIns(3,4)P₂ production, and intrinsic docking properties. Journal of cellular biochemistry, 112(9), 2203-2209. doi:10.1002/jcb.2314620.
Azizieh, N.-R., Orduz Perez, D., Van Bogaert, P., Bouschet, T., Rodriguez, W., Schiffmann, S. N., Pirson, I., & Abramowicz, M. (2011). Progressive myoclonic epilepsy-associated gene KCTD7 is a regulator of potassium conductance in neurons. Molecular neurobiology, 44(1), 111-121. doi:10.1007/s12035-011-8194-021.
Vilain, C., Rens, C., Aeby, A., Balériaux, D., Van Bogaert, P., Remiche, G., Smet, J., Van Coster, R., Abramowicz, M., & Pirson, I. (2011). A novel NDUFV1 gene mutation in complex I deficiency in consanguineous siblings with brainstem lesions and Leigh syndrome. Clinical genetics, 82(3), 264-270. doi:10.1111/j.1399-0004.2011.01743.x22.
De Schutter, J., Guillabert, A., Imbault, V., Degraef, C., Erneux, C., Communi, D., & Pirson, I. (2009). SHIP2 (SH2 domain-containing inositol phosphatase 2) SH2 domain negatively controls SHIP2 monoubiquitination in response to epidermal growth factor. The Journal of biological chemistry, 284(52), 36062-36076. doi:10.1074/jbc.M109.06492323.
Onnockx, S., Xie, J., Degraef, C., Erneux, C., & Pirson, I. (2009). Insulin increase in MAP kinase phosphorylation is shifted to early time-points by overexpressing APS, while Akt phosphorylation is not influenced. Experimental cell research, 315(15), 2479-2486. doi:10.1016/j.yexcr.2009.06.00624.
Montagut, G., Onnockx, S., Vaqué, M., Bladé, C., Blay, M., Fernández-Larrea, J., Pujadas, G., Salvadó, M. J., Arola, L., Pirson, I., Ardévol, A., & Pinent, M. (2009). Oligomers of grape-seed procyanidin extract activate the insulin receptor and key targets of the insulin signaling pathway differently from insulin. Journal of nutritional biochemistry. doi:10.1016/j.jnutbio.2009.02.003