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).
Nørregaard, R., Jensen, B. L., Li, C., Wang, W., Knepper, M. A.
, Nielsen, S. & Frøkiaer, 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: Renal Physiology,
289(2), F322-33.
https://doi.org/10.1152/ajprenal.00061.2005
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.
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.
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.