Publications

Sort by: Date | Author | Title

Hejl, J. L., Skals, M., Leipziger, J. & Praetorius, H. A. (2013). P2X receptor stimulation amplifies complement-induced haemolysis. Pflügers Archiv - European Journal of Physiology, 465(4), 529-41. https://doi.org/10.1007/s00424-012-1174-z
Hjel, J. L., Skals, M. G., Leipziger, J. G. & Prætorius, H. (2013). P2X receptor stimulation amplifies complement-induced haemolysis. Pflügers Archiv - European Journal of Physiology, 465, 529-41.
Hollegaard, M. V., Grauholm, J., Nielsen, R., Grove, J., Mandrup, S. & Hougaard, D. M. (2013). Archived neonatal dried blood spot samples can be used for accurate whole genome and exome-targeted next-generation sequencing. Molecular Genetics and Metabolism, 110(1-2), 65-72. https://doi.org/10.1016/j.ymgme.2013.06.004
Hollegaard, M. V., Skogstrand, K., Thorsen, P., Nørgaard-Petersen, B., Hougaard, D. & Grove, J. (2013). Joint analysis of SNPs and proteins identifies regulatory IL18 gene variations decreasing the chance of spastic cerebral palsy. Human Mutation, 34(1).
Hooli, B. V., Kovacs-Vajna, Z. M., Mullin, K., Blumenthal, M. A., Mattheisen, M., Zhang, C., Lange, C., Mohapatra, G., Bertram, L. & Tanzi, R. E. (2013). Rare autosomal copy number variations in early-onset familial Alzheimer's disease. Molecular Psychiatry. https://doi.org/10.1038/mp.2013.77
Husted, S. (2013). Optimal akut behandling af højrisikolungeemboli. Ugeskrift for Læger, 175(22), 1550.
Ishima, Y., Shinagawa, T., Yoneshige, S., Kragh-Hansen, U., Ohya, Y., Inomata, Y., Kai, T., Otagiri, M. & Maruyama, T. (2013). UW solution improved with high anti-apoptotic activity by S-nitrosated human serum albumin. Nitric Oxide: Biology and Chemistry, 30, 36-42.