6 results for author:"Goillot E." in Literature citations
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| Wnt4 participates in the formation of vertebrate neuromuscular junction. Strochlic L., Falk J., Goillot E., Sigoillot S., Bourgeois F., Delers P., Rouviere J., Swain A., Castellani V., Schaeffer L. et al. PLoS ONE 7:e29976-e29976(2012) · Mapped (3) |
| Interactome mapping of the phosphatidylinositol 3-kinase-mammalian target of rapamycin pathway identifies deformed epidermal autoregulatory factor-1 as a new glycogen synthase kinase-3 interactor. Pilot-Storck F., Chopin E., Rual J.F., Baudot A., Dobrokhotov P., Robinson-Rechavi M., Brun C., Cusick M.E., Hill D.E., Schaeffer L. et al. Mol. Cell Proteomics 9:1578-1593(2010) · Mapped (31) |
| Identification of an agrin mutation that causes congenital myasthenia and affects synapse function. Huze C., Bauche S., Richard P., Chevessier F., Goillot E., Gaudon K., Ben Ammar A., Chaboud A., Grosjean I., Lecuyer H.A. et al. Am. J. Hum. Genet. 85:155-167(2009) · UniProtKB (1) · Mapped (3) |
| MUSK, a new target for mutations causing congenital myasthenic syndrome. Chevessier F., Faraut B., Ravel-Chapuis A., Richard P., Gaudon K., Bauche S., Prioleau C., Herbst R., Goillot E., Ioos C. et al. Hum. Mol. Genet. 13:3229-3240(2004) · UniProtKB (1) · Mapped (12) |
| Role for the pleckstrin homology domain-containing protein CKIP-1 in phosphatidylinositol 3-kinase-regulated muscle differentiation. Safi A., Vandromme M., Caussanel S., Valdacci L., Baas D., Vidal M., Brun G., Schaeffer L., Goillot E. Mol. Cell. Biol. 24:1245-1255(2004) · UniProtKB (1) |
| Tumor induction and tissue atrophy in mice lacking E2F-1. Yamasaki L., Jacks T., Bronson R., Goillot E., Harlow E., Dyson N.J. Cell 85:537-548(1996) · Mapped (6) |