NCA Publications

New NCA Publications

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Henrik, H., Kwon, T.-H., Vinnikova, A. K., Masilamini, S., Frøkiær, J., Knepper, M. A. & Nielsen, S. (2001). Immunocytichemical and immunoelectron microscopical localization of alfa, beta and gamma-ENac in rat kidney. Am J Physiol, Renal Fluid and Electrolyte Physiol, 280, 1093-1106.
Elkjær, M.-L., Nejsum, L. N., Gresz, V., Kwon, T. H., Jensen, U. B., Frøkiaer, J. & Nielsen, S. (2001). Immunolocalization of aquaporin-8 in rat kidney, gastrointestinal tract, testis, and airways. American Journal of Physiology: Renal Physiology, 281(6), F1047-57.
Nielsen, J. E., Jennum, P., Fenger, K., Sørensen, S. A. & Fuglsang-Frederiksen, A. (2001). Increased intracortical facilitation in patients with autosomal dominant pure spastic paraplegia linked to chromosome 2p. European Journal of Neurology, 8, 335-339.
Dirac, A. G. & Kjems, J. (2001). Mapping DNA sites of HIV-1 integrase by protein footprinting. FEBS journal, 268, 743-751.
Jennum, P., Neerup Jensen, L., Fenger, K., Nielsen, J. E. & Fuglsang-Frederiksen, A. (2001). Motor evoked potentials from the external anal sphincter in patients with autosomal dominant pure spastic paraplegia linked to chromosome 2p. J. Neurol. Neurosurg. Psychiatry, 71, 561-562.
Andersen, P. S., Havndrup, O., Bundgaard, H., Moolman-Smook, J. C., Larsen, L. A., Mogensen, J., Brink, P. A., Børglum, A. D., Corfield, V. A., Kjeldsen, K., Vuust, J. & Christiansen, M. (2001). Myosin light chain mutations in familial hypertrophic cardiomyopathy: phenotypic presentation and frequency in Danish and South African populations. Journal of Medical Genetics, 38(12), E43.
Tranebjærg, L., Jensen, P. K. A., Van Ghelue, M., Vnencak-Jones, C. L., Sund, S., Elgjo, K., Jakobsen, J., Lindal, S., Warburg, M., Fuglsang-Frederiksen, A. & Skullerud, K. (2001). Neuronal cell death in the visual cortex is a prominent feature of the X-linked ressessive mitochondrial deafness-dystonia syndrome caused by mutations in the TIMM8a gene. Ophtalmic Genetics, 22, 207-223.