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

A Minassian

Showing results (211-220 of 324) with videos related to

Pageof 33
Sort By:
Seizure|September 3, 2019
The best evidence for progressive myoclonic epilepsy: A pathway to precision therapyAlessandro Orsini, Angelo Valetto, Veronica Bertini, et al.
Journal of Cellular Physiology|February 1, 1984
In vitro characteristics of the lipid-filled interstitial cell associated with postnatal lung growth: evidence for fibroblast heterogeneityH J Maksvytis, R M Niles, L Simanovsky, et al.
Human Molecular Genetics|November 10, 2005
Sacred disease secrets revealed: the genetics of human epilepsyJulie Turnbull, Hannes Lohi, Jennifer A Kearney, et al.
Neurotherapeutics : the Journal of the American Society for Experimental Neurotherapeutics|April 8, 2021
Targeting Gys1 with AAV-SaCas9 Decreases Pathogenic Polyglucosan Bodies and Neuroinflammation in Adult Polyglucosan Body and Lafora Disease Mouse ModelsEmrah Gumusgoz, Dikran R Guisso, Sahba Kasiri, et al.
Neurology|December 10, 2003
Skin biopsy in Lafora disease: genotype-phenotype correlations and diagnostic pitfallsD M Andrade, C A Ackerley, T S C Minett, et al.
Molecular Neurobiology|April 3, 2013
Laforin prevents stress-induced polyglucosan body formation and Lafora disease progression in neuronsYin Wang, Keli Ma, Peixiang Wang, et al.
Annals of Neurology|January 15, 2014
PTG protein depletion rescues malin-deficient Lafora disease in mouseJulie Turnbull, Jonathan R Epp, Danielle Goldsmith, et al.
Journal of Neurochemistry|September 6, 2020
Ppp1r3d deficiency preferentially inhibits neuronal and cardiac Lafora body formation in a mouse model of the fatal epilepsy Lafora diseaseLori Israelian, Silvia Nitschke, Peixiang Wang, et al.
Human Molecular Genetics|July 29, 2005
Sacred disease secrets revealed: the genetics of human epilepsyJulie Turnbull, Hannes Lohi, Jennifer A Kearney, et al.
Molecular and Cellular Biology|October 1, 2008
Laforin negatively regulates cell cycle progression through glycogen synthase kinase 3beta-dependent mechanismsRunhua Liu, Lizhong Wang, Chong Chen, et al.
Pageof 33

Showing results (211-220 of 324) with videos related to

Sort By:
Pageof 33
Seizure|September 3, 2019
The best evidence for progressive myoclonic epilepsy: A pathway to precision therapyAlessandro Orsini, Angelo Valetto, Veronica Bertini, et al.
Journal of Cellular Physiology|February 1, 1984
In vitro characteristics of the lipid-filled interstitial cell associated with postnatal lung growth: evidence for fibroblast heterogeneityH J Maksvytis, R M Niles, L Simanovsky, et al.
Human Molecular Genetics|November 10, 2005
Sacred disease secrets revealed: the genetics of human epilepsyJulie Turnbull, Hannes Lohi, Jennifer A Kearney, et al.
Neurotherapeutics : the Journal of the American Society for Experimental Neurotherapeutics|April 8, 2021
Targeting Gys1 with AAV-SaCas9 Decreases Pathogenic Polyglucosan Bodies and Neuroinflammation in Adult Polyglucosan Body and Lafora Disease Mouse ModelsEmrah Gumusgoz, Dikran R Guisso, Sahba Kasiri, et al.
Neurology|December 10, 2003
Skin biopsy in Lafora disease: genotype-phenotype correlations and diagnostic pitfallsD M Andrade, C A Ackerley, T S C Minett, et al.
Molecular Neurobiology|April 3, 2013
Laforin prevents stress-induced polyglucosan body formation and Lafora disease progression in neuronsYin Wang, Keli Ma, Peixiang Wang, et al.
Annals of Neurology|January 15, 2014
PTG protein depletion rescues malin-deficient Lafora disease in mouseJulie Turnbull, Jonathan R Epp, Danielle Goldsmith, et al.
Journal of Neurochemistry|September 6, 2020
Ppp1r3d deficiency preferentially inhibits neuronal and cardiac Lafora body formation in a mouse model of the fatal epilepsy Lafora diseaseLori Israelian, Silvia Nitschke, Peixiang Wang, et al.
Human Molecular Genetics|July 29, 2005
Sacred disease secrets revealed: the genetics of human epilepsyJulie Turnbull, Hannes Lohi, Jennifer A Kearney, et al.
Molecular and Cellular Biology|October 1, 2008
Laforin negatively regulates cell cycle progression through glycogen synthase kinase 3beta-dependent mechanismsRunhua Liu, Lizhong Wang, Chong Chen, et al.
Pageof 33