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

Christoph Lossin

Showing results (11-20 of 22) with videos related to

Pageof 3
Sort By:
The Journal of Pharmacology and Experimental Therapeutics|October 31, 2006
Inhibition of astroglial inwardly rectifying Kir4.1 channels by a tricyclic antidepressant, nortriptylineSuwen Su, Yukihiro Ohno, Christoph Lossin, et al.
Epilepsia|June 3, 2017
Abnormal γ-aminobutyric acid neurotransmission in a Kcnq2 model of early onset epilepsyTaku Uchida, Christoph Lossin, Yukiko Ihara, et al.
Neuron|June 28, 2002
Molecular basis of an inherited epilepsyChristoph Lossin, Dao W Wang, Thomas H Rhodes, et al.
Proceedings of the National Academy of Sciences of the United States of America|July 21, 2004
Noninactivating voltage-gated sodium channels in severe myoclonic epilepsy of infancyThomas H Rhodes, Christoph Lossin, Carlos G Vanoye, et al.
Plos One|December 11, 2013
Novel HCN2 mutation contributes to febrile seizures by shifting the channel's kinetics in a temperature-dependent mannerYuki Nakamura, Xiuyu Shi, Tomohiro Numata, et al.
Neurology|August 24, 2012
Altered fast and slow inactivation of the N440K Nav1.4 mutant in a periodic paralysis syndromeChristoph Lossin, Tai-Seung Nam, Shahab Shahangian, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|December 16, 2003
Epilepsy-associated dysfunction in the voltage-gated neuronal sodium channel SCN1AChristoph Lossin, Thomas H Rhodes, Reshma R Desai, et al.
Journal of Neurology|March 5, 2013
An algorithm for candidate sequencing in non-dystrophic skeletal muscle channelopathiesTai-Seung Nam, Christoph Lossin, Dong-Uk Kim, et al.
Annals of Neurology|February 25, 2015
Defective fast inactivation recovery of Nav 1.4 in congenital myasthenic syndromeW David Arnold, Daniel H Feldman, Sandra Ramirez, et al.
Molecular Brain|May 4, 2013
A human Dravet syndrome model from patient induced pluripotent stem cellsNorimichi Higurashi, Taku Uchida, Christoph Lossin, et al.
Pageof 3

Showing results (11-20 of 22) with videos related to

Sort By:
Pageof 3
The Journal of Pharmacology and Experimental Therapeutics|October 31, 2006
Inhibition of astroglial inwardly rectifying Kir4.1 channels by a tricyclic antidepressant, nortriptylineSuwen Su, Yukihiro Ohno, Christoph Lossin, et al.
Epilepsia|June 3, 2017
Abnormal γ-aminobutyric acid neurotransmission in a Kcnq2 model of early onset epilepsyTaku Uchida, Christoph Lossin, Yukiko Ihara, et al.
Neuron|June 28, 2002
Molecular basis of an inherited epilepsyChristoph Lossin, Dao W Wang, Thomas H Rhodes, et al.
Proceedings of the National Academy of Sciences of the United States of America|July 21, 2004
Noninactivating voltage-gated sodium channels in severe myoclonic epilepsy of infancyThomas H Rhodes, Christoph Lossin, Carlos G Vanoye, et al.
Plos One|December 11, 2013
Novel HCN2 mutation contributes to febrile seizures by shifting the channel's kinetics in a temperature-dependent mannerYuki Nakamura, Xiuyu Shi, Tomohiro Numata, et al.
Neurology|August 24, 2012
Altered fast and slow inactivation of the N440K Nav1.4 mutant in a periodic paralysis syndromeChristoph Lossin, Tai-Seung Nam, Shahab Shahangian, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|December 16, 2003
Epilepsy-associated dysfunction in the voltage-gated neuronal sodium channel SCN1AChristoph Lossin, Thomas H Rhodes, Reshma R Desai, et al.
Journal of Neurology|March 5, 2013
An algorithm for candidate sequencing in non-dystrophic skeletal muscle channelopathiesTai-Seung Nam, Christoph Lossin, Dong-Uk Kim, et al.
Annals of Neurology|February 25, 2015
Defective fast inactivation recovery of Nav 1.4 in congenital myasthenic syndromeW David Arnold, Daniel H Feldman, Sandra Ramirez, et al.
Molecular Brain|May 4, 2013
A human Dravet syndrome model from patient induced pluripotent stem cellsNorimichi Higurashi, Taku Uchida, Christoph Lossin, et al.
Pageof 3