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

Charles K Abrams

Showing results (21-30 of 37) with videos related to

Pageof 4
Sort By:
Glia|April 9, 2021
Investigating oligodendrocyte connexins: Heteromeric interactions between Cx32 and mutant or wild-type forms of Cx47 do not contribute to or modulate gap junction functionCharles K Abrams, Rafael E Flores-Obando, Gabriel D Dungan, et al.
Experimental Neurology|November 20, 2022
Knock-in mouse models for CMTX1 show a loss of function phenotype in the peripheral nervous systemCharles K Abrams, Eunjoo Lancaster, Jian J Li, et al.
Scientific Reports|January 11, 2017
Loss of Coupling Distinguishes GJB1 Mutations Associated with CNS Manifestations of CMT1X from Those Without CNS ManifestationsCharles K Abrams, Mikhail Goman, Sarah Wong, et al.
Acta Neuropathologica Communications|September 3, 2016
Systemic inflammation disrupts oligodendrocyte gap junctions and induces ER stress in a model of CNS manifestations of X-linked Charcot-Marie-Tooth diseaseMargarita Olympiou, Irene Sargiannidou, Kyriaki Markoullis, et al.
Glia|October 17, 2018
Regulatory role of oligodendrocyte gap junctions in inflammatory demyelinationChristos P Papaneophytou, Elena Georgiou, Christos Karaiskos, et al.
American Journal of Physiology. Cell Physiology|July 26, 2018
Alterations at Arg<sup>76</sup> of human connexin 46, a residue associated with cataract formation, cause loss of gap junction formation but preserve hemichannel functionCharles K Abrams, Alejandro Peinado, Rola Mahmoud, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|November 25, 2003
Pathogenesis of X-linked Charcot-Marie-Tooth disease: differential effects of two mutations in connexin 32Charles K Abrams, Mona Freidin, Feliksas Bukauskas, et al.
ACS Pharmacology & Translational Science|February 17, 2023
Pharmacologic Targeting of the C-Terminus of Heat Shock Protein 90 Improves Neuromuscular Function in Animal Models of Charcot Marie Tooth X1 DiseaseSukhmanjit Kaur, Xinyue Zhang, Sugandha Patel, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 22, 2006
Properties of human connexin 31, which is implicated in hereditary dermatological disease and deafnessCharles K Abrams, Mona M Freidin, Vytas K Verselis, et al.
Journal of Neurology|July 26, 2014
A new mutation in GJC2 associated with subclinical leukodystrophyCharles K Abrams, Steven S Scherer, Rafael Flores-Obando, et al.
Pageof 4

Showing results (21-30 of 37) with videos related to

Sort By:
Pageof 4
Glia|April 9, 2021
Investigating oligodendrocyte connexins: Heteromeric interactions between Cx32 and mutant or wild-type forms of Cx47 do not contribute to or modulate gap junction functionCharles K Abrams, Rafael E Flores-Obando, Gabriel D Dungan, et al.
Experimental Neurology|November 20, 2022
Knock-in mouse models for CMTX1 show a loss of function phenotype in the peripheral nervous systemCharles K Abrams, Eunjoo Lancaster, Jian J Li, et al.
Scientific Reports|January 11, 2017
Loss of Coupling Distinguishes GJB1 Mutations Associated with CNS Manifestations of CMT1X from Those Without CNS ManifestationsCharles K Abrams, Mikhail Goman, Sarah Wong, et al.
Acta Neuropathologica Communications|September 3, 2016
Systemic inflammation disrupts oligodendrocyte gap junctions and induces ER stress in a model of CNS manifestations of X-linked Charcot-Marie-Tooth diseaseMargarita Olympiou, Irene Sargiannidou, Kyriaki Markoullis, et al.
Glia|October 17, 2018
Regulatory role of oligodendrocyte gap junctions in inflammatory demyelinationChristos P Papaneophytou, Elena Georgiou, Christos Karaiskos, et al.
American Journal of Physiology. Cell Physiology|July 26, 2018
Alterations at Arg<sup>76</sup> of human connexin 46, a residue associated with cataract formation, cause loss of gap junction formation but preserve hemichannel functionCharles K Abrams, Alejandro Peinado, Rola Mahmoud, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|November 25, 2003
Pathogenesis of X-linked Charcot-Marie-Tooth disease: differential effects of two mutations in connexin 32Charles K Abrams, Mona Freidin, Feliksas Bukauskas, et al.
ACS Pharmacology & Translational Science|February 17, 2023
Pharmacologic Targeting of the C-Terminus of Heat Shock Protein 90 Improves Neuromuscular Function in Animal Models of Charcot Marie Tooth X1 DiseaseSukhmanjit Kaur, Xinyue Zhang, Sugandha Patel, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 22, 2006
Properties of human connexin 31, which is implicated in hereditary dermatological disease and deafnessCharles K Abrams, Mona M Freidin, Vytas K Verselis, et al.
Journal of Neurology|July 26, 2014
A new mutation in GJC2 associated with subclinical leukodystrophyCharles K Abrams, Steven S Scherer, Rafael Flores-Obando, et al.
Pageof 4