Nicole Schmitt
Professor MSO
Molecular Cardiology and Membrane Proteins
Blegdamsvej 3
2200 København N.
- 2022
- Published
A benzodiazepine activator locks Kv7.1 channels open by electro-mechanical uncoupling
Schreiber, J. A., Möller, M., Zaydman, M., Zhao, L., Beller, Z., Becker, S., Ritter, N., Hou, P., Shi, J., Silva, J., Wrobel, E., Strutz-Seebohm, N., Decher, N., Schmitt, Nicole, Meuth, S. G., Düfer, M., Wünsch, B., Cui, J. & Seebohm, G., 2022, In: Communications Biology . 5, 1, p. 1-13 301.Research output: Contribution to journal › Journal article › Research › peer-review
- 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 journal › Journal article › Research › peer-review
- 2021
- Published
The Tunicate Metabolite 2-(3,5-Diiodo-4-methoxyphenyl)ethan-1-amine Targets Ion Channels of Vertebrate Sensory Neurons
Paguigan, N. D., Yan, Y., Karthikeyan, M., Chase, K., Carter, J., Leavitt, L. S., Lim, A. L., Lin, Z., Memon, T., Christensen, S., Bentzen, Bo Hjorth, Schmitt, Nicole, Reilly, C. A., Teichert, R. W., Raghuraman, S., Olivera, B. M. & Schmidt, E. W., 2021, In: ACS chemical biology. 16, 9, p. 1654-1662Research output: Contribution to journal › Journal article › Research › peer-review
- 2020
- Published
A Novel Loss-of-Function Variant in the Chloride Ion Channel Gene Clcn2 Associates with Atrial Fibrillation
Hansen, T. H., Yan, Y., Ahlberg, G., Vad, O. B., Refsgaard, L., Dos Santos, J. L., Mutsaers, N., Svendsen, Jesper Hastrup, Olesen, Morten Steen Salling, Bentzen, Bo Hjorth & Schmitt, Nicole, 29 Jan 2020, In: Scientific Reports. 10, 1, 10 p., 1453.Research output: Contribution to journal › Journal article › Research › peer-review
- Published
Functional phenotype variations of two novel Kv 7.1 mutations identified in patients with Long QT syndrome
Bomholtz, Sofia Hammami, Refaat, M., Steffensen, Annette Buur, David, J., Espinosa, K., Nussbaum, R., Wojciak, J., Bentzen, Bo Hjorth, Scheinman, M. & Schmitt, Nicole, 2020, In: Pacing and Clinical Electrophysiology. 43, 2, p. 210-216 7 p.Research output: Contribution to journal › Journal article › Research › peer-review
- Published
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
- Published
Treatments for paroxysmal supraventricular tachycardia: A review of current practice
Rajan, D. & Schmitt, Nicole, 2020, In: World Heart Journal. 12, 3, p. 257-268Research output: Contribution to journal › Review › Research › peer-review
- 2019
- Published
Deletion in mice of X-linked, Brugada syndrome- and atrial fibrillation-associated Kcne5 augments ventricular KV currents and predisposes to ventricular arrhythmia
David, J., Lisewski, U., Crump, S. M., Jepps, Thomas Andrew Qvistgaard, Bocksteins, E., Wilck, N., Lossie, J., Roepke, T. K., Schmitt, Nicole & Abbott, G. W., Feb 2019, In: FASEB journal : official publication of the Federation of American Societies for Experimental Biology. 33, 2, p. 2537-2552 16 p.Research output: Contribution to journal › Journal article › Research › peer-review
- Published
Reappraisal of variants previously linked with sudden infant death syndrome: results from three population-based cohorts
Paludan-Müller, Christian, Ghouse, Jonas, Vad, O. B., Herfelt, C. B., Lundegaard, Pia Rengtved, Ahlberg, G., Schmitt, Nicole, Svendsen, Jesper Hastrup, Haunsø, Stig, Bundgård, Henning, Hansen, Torben, Kanters, Jørgen K. & Olesen, Morten Steen Salling, 2019, In: European Journal of Human Genetics. 27, 9, p. 1427-1435Research output: Contribution to journal › Journal article › Research › peer-review
- 2018
- 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 journal › Journal article › Research › peer-review
ID: 5624
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2572
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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
Published -
1470
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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
Published -
218
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The anticonvulsant retigabine suppresses neuronal Kv2-mediated currents
Research output: Contribution to journal › Journal article › Research › peer-review
Published