Hanne Borger Rasmussen

Hanne Borger Rasmussen

Associate Professor


  1. Published

    Requirement of subunit co-assembly and ankyrin-G for M-channel localization at the axon initial segment.

    Rasmussen, Hanne Borger, Frøkjær-Jensen, Christian, Jensen, C. S., Jensen, H. S., Jørgensen, N. K., Misonou, H., Trimmer, J. S., Olesen, Søren-Peter & Schmitt, Nicole, 2007, In: Journal of Cell Science. 120, Pt 6, p. 953-63 10 p.

    Research output: Contribution to journalJournal articlepeer-review

  2. Published

    The Voltage-Dependent K+ Channel Family

    Rasmussen, Hanne Borger & Trimmer, J. S., 2019, The Oxford Handbool of Neuronal Ion Channels. Bhattacharjee (ed.). Oxford University Press, 47 p.

    Research output: Chapter in Book/Report/Conference proceedingBook chapterResearchpeer-review

  3. Published

    Subcellular localization of the delayed rectifier K(+) channels KCNQ1 and ERG1 in the rat heart.

    Rasmussen, Hanne Borger, Møller, Morten, Knaus, H., Jensen, B. S., Olesen, Søren-Peter & Jørgensen, N. K., 2003, In: American Journal of Physiology: Heart and Circulatory Physiology. 286, 4, p. H1300-9

    Research output: Contribution to journalJournal articlepeer-review

  4. Published

    Pharmacological investigation of the role of ion channels in salivary secretion.

    Stummann, T. C., Poulsen, J. H., Hay-Schmidt, Anders, Grunnet, Morten, Klærke, Dan Arne, Rasmussen, Hanne Borger, Olesen, Søren-Peter & Jorgensen, N. K., 2003, In: Pflügers Archiv: European Journal of Physiology. 446, 1, p. 78-87 9 p.

    Research output: Contribution to journalJournal articlepeer-review

  5. Published

    Ventricular tachycardia in a Brugada syndrome patient caused by a novel deletion in SCN5A

    Tfelt-Hansen, J., Jespersen, Thomas, Hofman-Bang, J., Rasmussen, Hanne Borger, Cedergreen, P., Skovby, F., Abriel, H., Svendsen, Jesper Hastrup, Olesen, S., Christiansen, M. & Haunso, S., 2009, In: Canadian Journal of Cardiology. 25, 3, p. 156-60 4 p.

    Research output: Contribution to journalJournal articlepeer-review

  6. Published

    Identification of a Kir3.4 Mutation in Congenital Long QT Syndrome

    Yang, Y., Yang, Y., Liang, B., Liu, J., Li, J., Grunnet, M., Olesen, S-P., Rasmussen, H. B., Ellinor, P. T., Gao, L., Lin, X., Li, L., Wang, L., Xiao, J., Liu, Y., Liu, Y., Zhang, S., Liang, D., Peng, L., Jespersen, T. & 1 others, Chen, Y., 2010, In: American Journal of Human Genetics. 86, 6, p. 872-80 9 p.

    Research output: Contribution to journalJournal articlepeer-review

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