Rikard Blunck, Ph.D.
Affiliations: | 2006- | Physics | Université de Montréal, Montréal, Canada |
Area:
Kv channels, pore forming toxins, iGluR, TRP, fluorescence, electrophysiologyWebsite:
http://www.biophys.umontreal.ca/bluncklabGoogle:
"Rikard Blunck"Mean distance: 16.05 (cluster 32) | S | N | B | C | P |
Parents
Sign in to add mentor| Ulf-Peter Hansen | grad student | 1994-1996 | Universität Kiel |
| Ulrich Seydel | grad student | 1996-1999 | Research Center Borstel |
| Francisco Bezanilla | post-doc | 2000-2006 | UCLA |
Children
Sign in to add trainee| Tanja Kalstrup | grad student | 2011- | Université de Montréal |
| Nicolas Groulx | grad student | 2012 | Université de Montréal |
| Georges A. Haddad | grad student | 2008-2012 | Université de Montréal |
| Dimitri Petitjean | grad student | 2011-2013 | Université de Montréal |
| Hugo McGuire | grad student | 2007-2014 | Université de Montréal |
| Élise Faure | grad student | 2007-2015 | Université de Montréal |
| Debanjan Tewari | post-doc | Université de Montréal | |
| Juan Zhao | post-doc | 2012- | Université de Montréal |
| Zarah Batulan | post-doc | 2009-2011 | Université de Montréal |
Collaborators
Sign in to add collaborator| Roberto Araya | collaborator | physics University of Montreal | |
| Derek Bowie | collaborator | 2008- | Université de Montréal |
BETA: Related publications
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Publications
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| Lacroix G, Bhat S, Shafia Z, et al. (2024) KCNG4 Genetic Variant Linked to Migraine Prevents Expression of KCNB1. International Journal of Molecular Sciences. 25 |
| Bhat S, Rousseau J, Michaud C, et al. (2024) Mono-allelic KCNB2 variants lead to a neurodevelopmental syndrome caused by altered channel inactivation. American Journal of Human Genetics |
| Bhat S, Blunck R. (2022) Characterising ion channel structure and dynamics using fluorescence spectroscopy techniques. Biochemical Society Transactions. 50: 1427-1445 |
| Dinoi G, Morin M, Conte E, et al. (2022) Clinical and Functional Study of a De Novo Variant in the PVP Motif of Kv1.1 Channel Associated with Epilepsy, Developmental Delay and Ataxia. International Journal of Molecular Sciences. 23 |
| McGuire H, Blunck R. (2022) Studying KcsA Channel Clustering Using Single Channel Voltage-Clamp Fluorescence Imaging. Frontiers in Physiology. 13: 863375 |
| Imbrici P, Conte E, Blunck R, et al. (2021) A Novel Variant in a Patient with Non-Progressive Congenital Ataxia and Epilepsy: Functional Characterization and Sensitivity to 4-Aminopyridine. International Journal of Molecular Sciences. 22 |
| Blunck R. (2021) Determining stoichiometry of ion channel complexes using single subunit counting. Methods in Enzymology. 653: 377-404 |
| Imbrici P, Accogli A, Blunck R, et al. (2021) Musculoskeletal Features without Ataxia Associated with a Novel de novo Mutation in Impairing the Voltage Sensitivity of Kv1.1 Channel. Biomedicines. 9 |
| Zhao J, Petitjean D, Haddad GA, et al. (2020) A Common Kinetic Property of Mutations Linked to Episodic Ataxia Type 1 Studied in the Shaker Kv Channel. International Journal of Molecular Sciences. 21 |
| Möller L, Regnier G, Labro AJ, et al. (2020) Determining the correct stoichiometry of Kv2.1/Kv6.4 heterotetramers, functional in multiple stoichiometrical configurations. Proceedings of the National Academy of Sciences of the United States of America |