Publications

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Ma, X., Wildgruber, R., Bauer, J., Weber, G., Infanger, M., Grosse, J. & Grimm, D. G. (2012). The use of sigmoid pH gradients in free-flow isoelectric focusing of human endothelial cell proteins. Electrophoresis, 33(9-10), 1349-55. https://doi.org/10.1002/elps.201100598
Mak, T. N., Fischer, N., Laube, B., Brinkmann, V., Metruccio, M. M. E., Sfanos, K. S., Mollenkopf, H.-J., Meyer, T. F. & Brüggemann, H. (2012). Propionibacterium acnes host cell tropism contributes to vimentin-mediated invasion and induction of inflammation. Cellular Microbiology Online, 14(11), 1720-33. https://doi.org/10.1111/j.1462-5822.2012.01833.x
Marchegiani, F., Spazzafumo, L., Cardelli, M., Provinciali, M., Lescai, F., Franceschi, C. & Antonicelli, R. (2012). Paraoxonase-1 55 LL genotype is associated with No ST-Elevation Myocardial Infarction and with high levels of myoglobin. Journal of Lipids, 601796.
Marques, R. D., de Bruijn, P. I. A., Sørensen, M. V., Bleich, M., Prætorius, H. & Leipziger, J. G. (2012). Basolateral P2X receptors mediate inhibition of NaCl transport in mouse medullary thick ascending limb (mTAL). American Journal of Physiology: Renal Physiology, 302, F487-94 .
Matrone, C., Luvisetto, S., La Rosa, L. R., Tamayev, R., Pignataro, A., Canu, N., Yang, L., Barbagallo, A. P. M., Biundo, F., Lombino, F., Zheng, H., Ammassari-Teule, M. & D'Adamio, L. (2012). Tyr682 in the Aβ-precursor protein intracellular domain regulates synaptic connectivity, cholinergic function, and cognitive performance. Aging Cell. https://doi.org/10.1111/acel.12009
Møller, P. H., Brolin, C. & Gissel, H. (2012). Calcium influx determines the muscular response to electrotransfer. American Journal of Physiology: Regulatory, Integrative and Comparative Physiology, 302(4), R446-53. https://doi.org/10.1152/ajpregu.00383.2011
Møller, L. B., Lenartowicz, M., Zabot, M.-T., Josiane, A., Burglen, L., Bennett, C., Riconda, D., Fisher, R., Janssens, S., Mohammed, S., Ausems, M., Tümer, Z., Horn, N. & Jensen, T. G. (2012). Clinical expression of Menkes disease in females with normal karyotype. Orphanet Journal of Rare Diseases, 7, 6. https://doi.org/10.1186/1750-1172-7-6