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Department of Biomedicine

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Gytz Ammitzbøll, C., Steffensen, R., Jørgen Nielsen, H., Thiel, S., Stengaard-Pedersen, K., Bøgsted, M. & Jensenius, J. C. (2013). Polymorphisms in the MASP1 gene are associated with serum levels of MASP-1, MASP-3, and MAp44. PLOS ONE, 8(9), e73317. https://doi.org/10.1371/journal.pone.0073317

Haggerty, C. L., Klebanoff, M. A., Panum, I., Uldum, S. A., Bass, D. C., Olsen, J., Roberts, J. M. & Ness, R. B. (2013). Prenatal Chlamydia trachomatis infection increases the risk of preeclampsia. Pregnancy Hypertension, 3(3), 151-154. https://doi.org/10.1016/j.preghy.2013.03.002

Harsløf, T., Frost, M., Nielsen, T. L., Husted, L. B., Nyegaard, M., Brixen, K., Børglum, A. D., Mosekilde, L., Andersen, M., Rejnmark, L. & Langdahl, B. L. (2013). Polymorphisms of muscle genes are associated with bone mass and incident osteoporotic fractures in Caucasians. Calcified Tissue International, 92(5), 467-76. https://doi.org/10.1007/s00223-013-9702-1

Hartlev, L. B., Nyengaard, J. R., Thomsen, J. S., Boel, L. W. T., Stengaard-Pedersen, K. & Hauge, E. M. (2013). Application of design-based stereology for estimation of absolute volume and surface area of the articular and calcified cartilage compartments of undecalcified human femoral heads. Journal of Microscopy, 251(2), 133-143. https://doi.org/10.1111/jmi.12055

Hedegaard, E. R., Nielsen, B. D., Mogensen, S., Rembold, C. M., Frøbert, O. & Simonsen, U. (2013). Mechanisms involved in increased sensitivity to adenosine A2A receptor activation and hypoxia-induced vasodilatation in porcine coronary arteries. European Journal of Pharmacology. https://doi.org/10.1016/j.ejphar.2013.11.029

Hedegaard, C., Kjaer-Sorensen, K., Madsen, L. B., Henriksen, C., Momeni, J., Bendixen, C., Oxvig, C. & Larsen, K. E. (2013). Porcine synapsin 1: SYN1 gene analysis and functional characterization of the promoter. F E B S Open Bio, 3, 411–420. https://doi.org/10.1016/j.fob.2013.10.002

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

Hellfritzsch, M., Lassen, P. & Nielsen, L. P. (2013). Svær neurotoksicitet ved samtidig behandling med vincristin og fluconazol. Ugeskrift for Læger, 175(15), 1042-1043. http://ugeskriftet.dk/videnskab/svaer-neurotoksicitet-ved-samtidig-behandling-med-vincristin-og-fluconazol

Henriksen, C., Kjaer-Sorensen, K., Einholm, A. P., Madsen, L. B., Momeni, J., Bendixen, C., Oxvig, C., Vilsen, B. & Larsen, K. (2013). Molecular Cloning and Characterization of Porcine Na⁺/K⁺-ATPase Isoforms α1, α2, α3 and the ATP1A3 Promoter. P L o S One, 8(11), Article e79127. https://doi.org/10.1371/journal.pone.0079127

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).

Hollensen, A. K., Bak, R. O., Haslund, D. & Mikkelsen, J. G. (2013). Suppression of microRNAs by dual-targeting and clustered Tough Decoy inhibitors. RNA Biology, 10(3).

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

Horan, K. A., Hansen, K., Jakobsen, M. R., Holm, C. K., Søby, S., Unterholzner, L., Thompson, M., West, J. A., Iversen, M. B., Rasmussen, S. B., Ellermann-Eriksen, S., Kurt-Jones, E., Landolfo, S., Damania, B., Melchjorsen, J., Bowie, A. G., Fitzgerald, K. A. & Paludan, S. R. (2013). Proteasomal Degradation of Herpes Simplex Virus Capsids in Macrophages Releases DNA to the Cytosol for Recognition by DNA Sensors. Journal of Immunology, 190(5), 2311-2329. https://doi.org/10.4049/jimmunol.1202749

Horjales, E., Demontis, D., Lund, E. K., Vase, L., Finnerup, N. B., Børglum, A. D., Jensen, T. S. & Svensson, P. (2013). Emotional modulation of muscle pain is associated with polymorphisms in the serotonin transporter gene. Pain, 154(8), 1469-1476. https://doi.org/10.1016/j.pain.2013.05.011

Horjales, E., Demontis, D., Lund, E. K., Finnerup, N. B., Børglum, A. D., Jensen, T. S., Svensson, P. & Vase, L. (2013). Polymorphism in Serotonin Receptor 3B Is Associated with Pain Catastrophizing. PLOS ONE, 8(11), Article e78889. https://doi.org/10.1371/journal.pone.0078889

Høst, C., Gormsen, L. C., Christensen, B., Jessen, N., Hougaard, D. M., Christiansen, J. S., Pedersen, S. B., Jensen, M. D. & Gravholt, C. H. (2013). Independent Effects of Testosterone on Lipid Oxidation and VLDL-TG Production: A Randomized, Double-Blind, Placebo-Controlled, Crossover Study. Diabetes, 62(5), 1409-16. https://doi.org/10.2337/db12-0440

Husted, L. B., Harsløf, T., Stenkjær, L., Carstens, M., Jørgensen, N. R. & Langdahl, B. L. (2013). Functional polymorphisms in the P2X7 receptor gene are associated with osteoporosis. Osteoporosis International, 24(3), 949-59. https://doi.org/10.1007/s00198-012-2035-5

Husted, S. (2013). Optimal akut behandling af højrisikolungeemboli. Ugeskrift for Læger, 175(22), 1550.

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