Publications and communications of Christine Grill

Grill, C., Benzekri, L., Rubod, A., Aktary, Z., Ezzedine, K., Taïeb, A., Gauthier, Y., Larue, L., & Delmas, V. (May 2018). Epidermal melanocytes in segmental vitiligo show altered expression of E-cadherin, but not P-cadherin. British Journal of Dermatology, 178 (5), 1204 - 1206. doi:10.1111/bjd.16352

Sohier, P., Legrand, L., Aktary, Z., Grill, C., Delmas, V., Bernex, F., Reyes-Gomez, E., Larue, L., & Vergier, B. (May 2018). A histopathological classification system of Tyr::NRASQ61K murine melanocytic lesions: A reproducible simplified classification. Pigment Cell and Melanoma Research, 31 (3), 423 - 431. doi:10.1111/pcmr.12677

Grill, C., & Larue, L. (January 2016). What's up NF1? Pigment Cell and Melanoma Research, 29 (1), 4-5. doi:10.1111/pcmr.12423

Grill, C., & Larue, L. (2016). NRAS, NRAS, Which Mutation Is Fairest of Them All? Journal of Investigative Dermatology, 136 (10), 1936-1938. doi:10.1016/j.jid.2016.06.011

Praetorius, C., Grill, C., Stacey, S. N., Metcalf, A. M., Gorkin, D. U., Robinson, K. C., Van Otterloo, E., Kim, R. S. Q., Bergsteinsdottir, K., Ogmundsdottir, M. H., Magnusdottir, E., Mishra, P. J., Davis, S. R., Guo, T., Zaidi, M. R., Helgason, A. S., Sigurdsson, M. I., Meltzer, P. S., Merlino, G., ... Steingrimsson, E. (21 November 2013). A polymorphism in IRF4 affects human pigmentation through a tyrosinase-dependent MITF/TFAP2A pathway. Cell, 155 (5), 1022-33. doi:10.1016/j.cell.2013.10.022

Grill, C., Bergsteinsdóttir, K., Ogmundsdóttir, M. H., Pogenberg, V., Schepsky, A., Wilmanns, M., Pingault, V., & Steingrímsson, E. (01 November 2013). MITF mutations associated with pigment deficiency syndromes and melanoma have different effects on protein function. Human Molecular Genetics, 22 (21), 4357-67. doi:10.1093/hmg/ddt285

Grill, C., Sunitsch, S., Hatz, M., Hauser-Kronberger, C., Leuschner, I., Hoefler, G., & Guertl, B. (December 2011). Activation of beta-catenin is a late event in the pathogenesis of nephroblastomas and rarely correlated with genetic changes of the APC gene. Pathology, 43 (7), 702-6. doi:10.1097/PAT.0b013e32834bf65c

Grill, C., Guelly, C., Ebner, B., Leuschner, I., Hauser-Kronberger, C., Hoefler, G., & Guertl, B. (August 2010). Loss of PTEN/MMAC1 activity is a rare and late event in the pathogenesis of nephroblastomas. Human Pathology, 41 (8), 1172-7. doi:10.1016/j.humpath.2009.10.024