Nicole Schmitt
Professor MSO
Molecular Cardiology and Membrane Proteins
Blegdamsvej 3
2200 København N.
ORCID: 0000-0001-9482-9749
1 - 5 out of 5Page size: 500
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Cellular mechanisms for presynaptic inhibition of sensory afferents.
Perrier, Jean-Francois Marie, delgado-lezama, R., Christensen, R. K., Lind, B., Schmitt, Nicole, Loeza-Alcocer, E., petersen, A., Lauritzen, Martin & russo, R., 2011. 1 p.Research output: Contribution to conference › Poster › Research
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Mutations in sodium channel {beta}-subunit SCN3B are associated with early-onset lone atrial fibrillation
Olesen, M. S., Jespersen, Thomas, Nielsen, J. B., Liang, B., Møller, D. V., Hedley, P., Christiansen, M., Varro, A., Olesen, Søren-Peter, Haunsø, Stig, Schmitt, Nicole & Svendsen, Jesper Hastrup, 2011, In: Cardiovascular Research. 89, 4, p. 786-793 8 p.Research output: Contribution to journal › Journal article › Research › peer-review
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Letter by Olesen et al regarding article, "MOG1: a new susceptibility gene for Brugada syndrome"
Olesen, M. S., Holst, A. G. & Schmitt, Nicole, 2011, In: Circulation: Cardiovascular Genetics. 4, 5Research output: Contribution to journal › Journal article › Research › peer-review
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A Novel Nonsense Variant in Nav1.5 Cofactor MOG1 Eliminates Its Sodium Current Increasing Effect and May Increase the Risk of Arrhythmias
Olesen, M. S., Jensen, N. F., Holst, A. G., Nielsen, J. B., Tfelt-Hansen, Jacob, Jespersen, Thomas, Sajadieh, Ahmad, Haunsø, Stig, Lund, J. T., Callø, Kirstine, Schmitt, Nicole & Svendsen, Jesper Hastrup, 26 May 2011, In: Canadian Journal of Cardiology. 27, 4, p. 523.e17-23Research output: Contribution to journal › Journal article › Research › peer-review
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Multiple arrhythmic syndromes in a newborn, owing to a novel mutation in SCN5A
Calloe, K., Schmitt, Nicole, Grubb, Søren, Pfeiffer, R., David, J., Kanter, R., Cordeiro, J. M., Antzelevitch, C. & Callø, Kirstine, 2011, In: Canadian Journal of Physiology and Pharmacology. 89, 10, p. 723-36 14 p.Research output: Contribution to journal › Journal article › Research › peer-review
ID: 5624
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Dysfunction of the heteromeric KV7.3/KV7.5 potassium channel is associated with autism spectrum disorders
Research output: Contribution to journal › Journal article › Research › peer-review
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1497
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Characterization and mechanisms of action of novel NaV1.5 channel mutations associated with Brugada syndrome
Research output: Contribution to journal › Journal article › Research › peer-review
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256
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The anticonvulsant retigabine suppresses neuronal Kv2-mediated currents
Research output: Contribution to journal › Journal article › Research › peer-review
Published