Nicole Schmitt
Professor MSO
Molecular Cardiology and Membrane Proteins
Blegdamsvej 3
2200 København N.
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Novel Kv7.1-phosphatidylinositol 4,5-bisphosphate interaction sites uncovered by charge neutralization scanning
Eckey, K., Wrobel, E., Strutz-Seebohm, N., Pott, L., Schmitt, Nicole & Seebohm, G., 15 Aug 2014, In: The Journal of Biological Chemistry. 289, 33, p. 22749-58 10 p.Research output: Contribution to journal › Journal article › Research › peer-review
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Mutations in the potassium channel subunit KCNE1 are associated with early-onset familial atrial fibrillation
Olesen, M. S., Bentzen, Bo Hjorth, Nielsen, J. B., Steffensen, Annette Buur, David, J., Jabbari, J., Jensen, H., Haunsø, Stig, Svendsen, Jesper Hastrup & Schmitt, Nicole, 2012, In: B M C Medical Genetics. 13, p. 24Research output: Contribution to journal › Journal article › Research › peer-review
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Mutations in the Kv1.5 channel gene KCNA5 in cardiac arrest patients.
Nielsen, N. H., Winkel, B. G., Kanters, Jørgen K., Schmitt, Nicole, Hofman-Bang, J., Jensen, H. S., Bentzen, Bo Hjorth, Sigurd, B., Larsen, Lars Allan, Andersen, P. S., Kjeldsen, K., Grunnet, Morten, Christiansen, M., Olesen, Søren-Peter & Haunsø, Stig, 2007, In: Biochemical and Biophysical Research Communications. 354, 3, p. 776-82 6 p.Research output: Contribution to journal › Journal article › Research › peer-review
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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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Multiple genetic variations in sodium channel subunits in a case of sudden infant death syndrome
Denti, F., Bentzen, Bo Hjorth, Wojciak, J., Thomsen, N. M., Scheinman, M. & Schmitt, Nicole, 2018, In: Pacing and Clinical Electrophysiology. 41, 6, p. 620-626Research 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
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Modulation of ERG channels by XE991.
Elmedyb, P., Callø, Kirstine, Schmitt, Nicole, Hansen, R. S., Grunnet, Morten & Olesen, Søren-Peter, 2007, In: Basic & Clinical Pharmacology & Toxicology. 100, 5, p. 316-22 6 p.Research output: Contribution to journal › Journal article › Research › peer-review
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Long QT 1 mutation KCNQ1A344V increases local anesthetic sensitivity of the slowly activating delayed rectifier potassium current.
Siebrands, C. C., Binder, S., Eckhoff, U., Schmitt, Nicole & Friederich, P., 2006, In: Anesthesiology. 105, 3, p. 511-20 9 p.Research output: Contribution to journal › Journal article › Research › peer-review
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Local anesthetic interaction with human ether-a-go-go-related gene (HERG) channels: role of aromatic amino acids Y652 and F656.
Siebrands, C. C., Schmitt, Nicole & Friederich, P., 2005, In: Anesthesiology. 103, 1, p. 102-12 10 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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KCNQ1 mutation Q147R is associated with atrial fibrillation and prolonged QT interval.
Lundby, Alicia, Ravn, L. S., Svendsen, Jesper Hastrup, Olesen, Søren-Peter & Schmitt, Nicole, 2007, In: Heart Rhythm. 4, 12, p. 1532-41 9 p.Research output: Contribution to journal › Journal article › Research › peer-review
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KCNQ1 channels sense small changes in cell volume.
Grunnet, Morten, Jespersen, Thomas, MacAulay, Nanna, Jørgensen, N. K., Schmitt, Nicole, Pongs, O., Olesen, Søren-Peter & Klærke, Dan Arne, 2003, In: Journal of Physiology. 549, Pt 2, p. 419-27 8 p.Research output: Contribution to journal › Journal article › Research › peer-review
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KCNQ channels are involved in the regulatory volume decrease response in primary neonatal rat cardiomyocytes.
Callø, Kirstine, Nielsen, Morten Schak, Grunnet, Morten, Schmitt, Nicole & Jorgensen, N. K., 2007, In: BBA General Subjects. 1773, 6, p. 764-73 9 p.Research output: Contribution to journal › Journal article › Research › peer-review
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KCNE3 mutation V17M identified in a patient with lone atrial fibrillation.
Lundby, Alicia, Ravn, L. S., Svendsen, J. H., Hauns, S., Olesen, Søren-Peter & Schmitt, Nicole, 2008, In: Cellular Physiology and Biochemistry. 21, 1-3, p. 47-54 7 p.Research output: Contribution to journal › Journal article › Research › peer-review
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Iron Overload Leading to Torsades de Pointes in β-Thalassemia and Long QT Syndrome
Refaat, M. M., El Hage, L., Steffensen, Annette Buur, Hotait, M., Schmitt, Nicole, Scheinman, M. & Badhwar, N., Mar 2016, In: Cardiac Electrophysiology Clinics. 8, 1, p. 247-256 10 p.Research output: Contribution to journal › Journal article › Research › peer-review
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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 journal › Journal article › Research › peer-review
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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. H1204-12Research output: Contribution to journal › Journal article › Research › peer-review
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Investigating gene-microRNA networks in atrial fibrillation patients with mitral valve regurgitation
Santos, J. L., Rodríguez, I., Olesen, Morten Steen Salling, Bentzen, Bo Hjorth & Schmitt, Nicole, 2020, In: PLoS ONE. 15, 5, 21 p., e0232719.Research output: Contribution to journal › Journal article › Research › peer-review
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In Vivo Phosphoproteomics Analysis Reveals the Cardiac Targets of β-Adrenergic Receptor Signaling
Lundby, Alicia, Andersen, M. N., Steffensen, Annette Buur, Horn, H., Kelstrup, C. D., Francavilla, C., Jensen, Lars Juhl, Schmitt, Nicole, Thomsen, Morten Bækgaard & Olsen, Jesper Velgaard, 4 Jun 2013, In: Science Signaling. 6, 278, p. rs11 13 p.Research output: Contribution to journal › Journal article › Research › peer-review
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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 journal › Journal article › Research › peer-review
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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 journal › Journal article › Research › peer-review
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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 journal › Journal article › Research › peer-review
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High Prevalence of Long QT Syndrome Associated SCN5A Variants in Patients with Early-Onset Lone Atrial Fibrillation
Olesen, M. S., Yuan, L., Liang, B., Holst, A. G., Nielsen, N., Nielsen, J. B., Hedley, P. L., Christiansen, M., Olesen, Søren-Peter, Haunsø, Stig, Schmitt, Nicole, Jespersen, Thomas & Svendsen, Jesper Hastrup, 2012, In: Circulation: Cardiovascular Genetics. 5, 4, p. 450-459 10 p.Research output: Contribution to journal › Journal article › Research › peer-review
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Gliadin Fragments and a Specific Gliadin 33-mer Peptide Close KATP Channels and Induce Insulin Secretion in INS-1E Cells and Rat Islets of Langerhans
Dall, M., Callø, Kirstine, Haupt-Jorgensen, M., Larsen, J., Schmitt, Nicole, Josefsen, K. & Buschard, K., 2013, In: PLOS ONE. 8, 6, p. 1-10 10 p., e66474.Research output: Contribution to journal › Journal article › Research › peer-review
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Genetic variation in the two-pore domain potassium channel, TASK-1, may contribute to an atrial substrate for arrhythmogenesis
Liang, B., Soka, M., Christensen, Alex Hørby, Olesen, Morten Steen Salling, Larsen, A. P., Knop, Filip Krag, Wang, F., Nielsen, J. B., Andersen, M. N., Humphreys, D., Mann, S. A., Huttner, I. G., Vandenberg, J. I., Svendsen, Jesper Hastrup, Haunsø, Stig, Preiss, T., Seebohm, G., Olesen, Søren-Peter, Schmitt, Nicole & Fatkin, D., 27 Dec 2013, In: Journal of Molecular and Cellular Cardiology. 67, p. 69-76 7 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
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Characterization and mechanisms of action of novel NaV1.5 channel mutations associated with Brugada syndrome
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The anticonvulsant retigabine suppresses neuronal Kv2-mediated currents
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