Nicole Schmitt

Nicole Schmitt

Professor MSO


  1. Published

    Investigations of the Navβ1b sodium channel subunit in human ventricle; functional characterization of the H162P Brugada Syndrome mutant

    Yuan, L., Koivumaki, J., Liang, B., Lorentzen, L. G., Tang, C., Andersen, M. N., Svendsen, Jesper Hastrup, Tfelt-Hansen, J., Maleckar, M., Schmitt, Nicole, Olesen, Morten Steen Salling & Jespersen, Thomas, 21 Feb 2014, In: American Journal of Physiology: Heart and Circulatory Physiology. 306, 8, p. H1204-12

    Research output: Contribution to journalJournal articlepeer-review

  2. Published

    Investigations of the Navβ1b sodium channel subunit in human ventricle; functional characterization of the H162P Brugada syndrome mutant.

    Yuan, L., Koivumäki, J., Liang, B., Lorentzen, Lasse Gøbel, Tang, C., Andersen, M., Svendsen, J., Tfelt-Hansen, Jacob, Maleckar, M., Schmitt, Nicole, Olesen, M. & Jespersen, Thomas, Feb 2014, In: American journal of physiology. Heart and circulatory physiology.

    Research output: Contribution to journalJournal articlepeer-review

  3. Published

    Whole-Exome Sequencing Implicates Neuronal Calcium Channel with Familial Atrial Fibrillation

    Vad, Oliver Tim Bundgaard, Yan, Y., Denti, F., Ahlberg, Gustav, Refsgaard, L., Bomholtz, Sofia Hammami, Santos, J. L., Rasmussen, Simon, Haunsø, Stig, Svendsen, Jesper Hastrup, Christophersen, I. E., Schmitt, Nicole, Olesen, Morten Steen Salling & Bentzen, Bo Hjorth, 2022, In: Frontiers in Genetics. 13, 8 p., 806429.

    Research output: Contribution to journalJournal articlepeer-review

  4. Published

    A Common Structural Component for β-Subunit Mediated Modulation of Slow Inactivation in Different KV Channels

    Strutz-Seebohm, N., Henrion, U., Schmitt, Nicole, Schulze-Bahr, E. & Seebohm, G., 26 Jun 2013, In: Cellular Physiology and Biochemistry. 31, 6, p. 968-980 13 p.

    Research output: Contribution to journalJournal articlepeer-review

  5. Published

    PKD Phosphorylation as Novel Pathway of KV11.1 Regulation

    Steffensen, Annette Buur, Bomholtz, Sofia Hammami, Andersen, M. N., Olsen, Jesper Velgaard, Mutsaers, N., Lundegaard, Pia Rengtved, Lundby, Alicia & Schmitt, Nicole, 2018, In: Cellular Physiology and Biochemistry. 47, 4, p. 1742-1750 9 p.

    Research output: Contribution to journalJournal articlepeer-review

  6. Published

    High incidence of functional ion-channel abnormalities in a consecutive Long QT cohort with novel missense genetic variants of unknown significance

    Steffensen, Annette Buur, Refaat, M. M., David, J., Mujezinovic, A., Callø, Kirstine, Wojciak, J., Nussbaum, R. L., Scheinman, M. M. & Schmitt, Nicole, 12 Jun 2015, In: Scientific Reports. 5, p. 1-13 13 p., 10009.

    Research output: Contribution to journalJournal articlepeer-review

  7. Published

    IKs Gain- and Loss-of-Function In Early-Onset Lone Atrial Fibrillation

    Steffensen, Annette Buur, Refsgaard, L., Andersen, M. N., Vallet, C., Mujezinovic, A., Haunsø, Stig, Svendsen, Jesper Hastrup, Olesen, Søren-Peter, Olesen, Morten Steen Salling & Schmitt, Nicole, 2015, In: Journal of Cardiovascular Electrophysiology. 26, 7, p. 715-23 9 p.

    Research output: Contribution to journalJournal articlepeer-review

  8. Published

    SUMO co-expression modifies KV 11.1 channel activity

    Steffensen, Annette Buur, Andersen, M. N., Mutsaers, N., Mujezinovic, A. & Schmitt, Nicole, Mar 2018, In: Acta Physiologica (Print). 222, 3, 11 p., e12974.

    Research output: Contribution to journalJournal articlepeer-review

  9. Published

    The anticonvulsant retigabine suppresses neuronal Kv2-mediated currents

    Stas, J. I., Bocksteins, E., Jensen, C. S., Schmitt, Nicole & Snyders, D. J., 13 Oct 2016, In: Scientific Reports. 6, 12 p., 35080.

    Research output: Contribution to journalJournal articlepeer-review

  10. Published

    Homozygosity for SCN4A Arg1142Gln causes congenital myopathy with variable disease expression

    Sloth, C. K., Denti, F., Schmitt, Nicole, Bentzen, Bo Hjorth, Fagerberg, C., Vissing, John & Gaist, D., Oct 2018, In: Neurology: Genetics. 4, 5, p. e267 3 p.

    Research output: Contribution to journalJournal articlepeer-review

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