Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Karin Jurkat-Rott

Showing results (41-50 of 82) with videos related to

Pageof 9
Sort By:
Muscle & Nerve|June 17, 2015
Painful cramps and giant myotonic discharges in a family with the Nav1.4-G1306A mutationTorberg Torbergsen, Karin Jurkat-Rott, Erik V Stålberg, et al.
Journal of Neural Transmission (Vienna, Austria : 1996)|December 25, 2013
Myotonia in DNM2-related centronuclear myopathyRon Dabby, Menachem Sadeh, Ronit Gilad, et al.
Scientific Reports|February 10, 2021
Relevance of pathogenicity prediction tools in human RYR1 variants of unknown significanceKerstin Hoppe, Karin Jurkat-Rott, Stefanie Kranepuhl, et al.
Biophysical Journal|January 13, 2009
A CaV1.1 Ca2+ channel splice variant with high conductance and voltage-sensitivity alters EC coupling in developing skeletal musclePetronel Tuluc, Natalia Molenda, Bettina Schlick, et al.
Neuromuscular Disorders : NMD|December 27, 2011
A Becker myotonia patient with compound heterozygosity for CLCN1 mutations and Prinzmetal angina pectorisDaniel Zielonka, Karin Jurkat-Rott, Paweł Stachowiak, et al.
Scientific Reports|July 12, 2018
Na<sub>V</sub>1.4 DI-S4 periodic paralysis mutation R222W enhances inactivation and promotes leak current to attenuate action potentials and depolarize muscle fibersLandon Bayless-Edwards, Vern Winston, Frank Lehmann-Horn, et al.
Brain : a Journal of Neurology|March 26, 2002
Enhanced inactivation and pH sensitivity of Na(+) channel mutations causing hypokalaemic periodic paralysis type IIAlexey Kuzmenkin, Vanesa Muncan, Karin Jurkat-Rott, et al.
The Journal of Physiology|November 17, 2007
Neutralization of a negative charge in the S1-S2 region of the KV7.2 (KCNQ2) channel affects voltage-dependent activation in neonatal epilepsyThomas V Wuttke, Johann Penzien, Michael Fauler, et al.
Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology|May 2, 2003
Acute hypokalemic tetraparesis induced by intravenous methotrexatePeter C Thuss-Patience, Uwe Peters, Karin Jurkat-Rott, et al.
Brain : a Journal of Neurology|February 20, 2014
NaV1.4 mutations cause hypokalaemic periodic paralysis by disrupting IIIS4 movement during recoveryJames R Groome, Frank Lehmann-Horn, Chunxiang Fan, et al.
Pageof 9

Showing results (41-50 of 82) with videos related to

Sort By:
Pageof 9
Muscle & Nerve|June 17, 2015
Painful cramps and giant myotonic discharges in a family with the Nav1.4-G1306A mutationTorberg Torbergsen, Karin Jurkat-Rott, Erik V Stålberg, et al.
Journal of Neural Transmission (Vienna, Austria : 1996)|December 25, 2013
Myotonia in DNM2-related centronuclear myopathyRon Dabby, Menachem Sadeh, Ronit Gilad, et al.
Scientific Reports|February 10, 2021
Relevance of pathogenicity prediction tools in human RYR1 variants of unknown significanceKerstin Hoppe, Karin Jurkat-Rott, Stefanie Kranepuhl, et al.
Biophysical Journal|January 13, 2009
A CaV1.1 Ca2+ channel splice variant with high conductance and voltage-sensitivity alters EC coupling in developing skeletal musclePetronel Tuluc, Natalia Molenda, Bettina Schlick, et al.
Neuromuscular Disorders : NMD|December 27, 2011
A Becker myotonia patient with compound heterozygosity for CLCN1 mutations and Prinzmetal angina pectorisDaniel Zielonka, Karin Jurkat-Rott, Paweł Stachowiak, et al.
Scientific Reports|July 12, 2018
Na<sub>V</sub>1.4 DI-S4 periodic paralysis mutation R222W enhances inactivation and promotes leak current to attenuate action potentials and depolarize muscle fibersLandon Bayless-Edwards, Vern Winston, Frank Lehmann-Horn, et al.
Brain : a Journal of Neurology|March 26, 2002
Enhanced inactivation and pH sensitivity of Na(+) channel mutations causing hypokalaemic periodic paralysis type IIAlexey Kuzmenkin, Vanesa Muncan, Karin Jurkat-Rott, et al.
The Journal of Physiology|November 17, 2007
Neutralization of a negative charge in the S1-S2 region of the KV7.2 (KCNQ2) channel affects voltage-dependent activation in neonatal epilepsyThomas V Wuttke, Johann Penzien, Michael Fauler, et al.
Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology|May 2, 2003
Acute hypokalemic tetraparesis induced by intravenous methotrexatePeter C Thuss-Patience, Uwe Peters, Karin Jurkat-Rott, et al.
Brain : a Journal of Neurology|February 20, 2014
NaV1.4 mutations cause hypokalaemic periodic paralysis by disrupting IIIS4 movement during recoveryJames R Groome, Frank Lehmann-Horn, Chunxiang Fan, et al.
Pageof 9