Publications

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Nielsen, M. F., Caumo, A., Aagaard, N. K., Chandramouli, V., Schumann, W. C., Landau, B. R., O., S. & Vilstrup, H. (2005). Contribution of defects in glucose uptake to carbohydrate intolerance in liver cirrhosis: Assessment during physiologic glucose and insulin concentrations. American Journal of Physiology, 288, G1135-43.
Nielsen, R. C., Sørensen, T. L., Møller, J. V., Nissen, P., Jidenko, M., le Maire, M. & Jaxel, C. (2005). Crystallization of a mammalian membrane protein overexpressed in S. cerevisiae. Proceedings of the National Academy of Sciences (PNAS), 102(11687-1191).
Nielsen, L. P. & Madsen, F. F. (2005). Farmakoterapi ved allergisk sygdom. Ugeskrift for Læger, 167(6), 661-663.
Nørregaard, R., Jensen, B. L., Li, C., Wang, W., Knepper, M. A., Nielsen, S. & Frøkiær, J. (2005). COX-2 inhibition prevents downregulation of key renal water and sodium transport proteins in response to bilateral ureteral obstruction. American Journal of Physiology, 289(2), F322-F333.
Nørskov-Lauritsen, N., Bruun, B. & Kilian, M. (2005). Multilocus sequence phylogenetic study of the genus Haemophilus with description of Haemophilus pittmaniae sp.nov. International Journal of Systematic and Evolutionary Microbiology, 55, 449-456.
Ohno, Y., Birn, H. & Christensen, E. I. (2005). In vivo confocal laser scanning microscopy and micropuncture in intact rat kidney. Nephron Experimental Nephrology, 99, e17-e25.
Olpin, S. E., Clark, S., Bischoff, C., Olsen, R. K. J., Gregersen, N., Chakrapani, A., Downing, M., Manning, N. J., Andresen, B. S., Sharrard, M., Bonham, J. R., Muntoni, F., Turnbull, D. N. & Pourfarzam, M. (2005). Biochemical, clinical and molecular findings in LCHAD and general mitochondrial trifunctional protein deficiency. Journal of Inherited Metabolic Disease, 28(4), 533-544.
Olsen, R. K. J., Andresen, B. S., Christensen, E., Mandel, H., Skovby, F., Nielsen, J. P., Knudsen, I., Vianey-Saban, C., Simonsen, H. & Gregersen, N. (2005). DNA-based prenatal diagnosis for severe and variant forms of multiple acyl-CoA dehydrogenation deficiency. Prenatal Diagnosis, 25(1), 60-64.
Olsen, R. K., Andresen, B. S., Christensen, E., Mandel, H., Skovby, F., Nielsen, J. P., Knudsen, I., Vianey-Saban, C., Simonsen, H. & Gregersen, N. (2005). DNA-based prenatal diagnosis for severe and variant forms of multiple acyl-CoA dehydrogenation deficiency. Prenat. Diagn., 25(1), 60-64.
Østergaard, J., Hansen, T. K., Thiel, S. & Flyvbjerg, A. (2005). Complement activation and diabetic vascular complications. Clin. Chim. Acta., 361, 10-19.
Ostergard, T., Ek, J., Hamid, Y., Pedersen, O. B., Hansen, T. & Schmitz, O. (2005). Influence of the PPAR-γ2 Pro12Ala and ACE I/D polymorphisms on insulin sensitivity and training effects in healthy offspring of type 2 diabetic subjects. Hormone and Metabolic Research, (37(2)), 99-105.
Overgaard, J., Wang, T., Nielsen, O. B. & Gesser, H. (2005). Extracellular determinants of cardiac contractility in the cold anoxic turtle. Physiological and Biochemical Zoology, 78(6), 976-995.