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

Steven S Scherer

Showing results (21-30 of 159) with videos related to

Pageof 16
Sort By:
Neuromolecular Medicine|June 16, 2006
Molecular genetics of X-linked Charcot-Marie-Tooth diseaseKleopas A Kleopa, Steven S Scherer
Biochimica Et Biophysica Acta|August 30, 2011
Gap junctions in inherited human disorders of the central nervous systemCharles K Abrams, Steven S Scherer
Neurologic Clinics|November 16, 2002
Inherited neuropathiesKleopas A Kleopa, Steven S Scherer
Neuroscience Letters|June 16, 2012
Neuronal cadherin (NCAD) increases sensory neurite formation and outgrowth on astrocytesToby A Ferguson, Steven S Scherer
Neurobiology of Disease|March 15, 2011
Cx32 and Cx47 mediate oligodendrocyte:astrocyte and oligodendrocyte:oligodendrocyte gap junction couplingSameh K Wasseff, Steven S Scherer
The New England Journal of Medicine|December 16, 2011
Microtubules, axonal transport, and neuropathyErika L F Holzbaur, Steven S Scherer
Molecular and Cellular Neurosciences|November 3, 2010
Dominant Cx26 mutants associated with hearing loss have dominant-negative effects on wild type Cx26Junxian Zhang, Steven S Scherer, Sabrina W Yum
Neurobiology of Disease|January 26, 2010
Dominant connexin26 mutants associated with human hearing loss have trans-dominant effects on connexin30Sabrina W Yum, Junxian Zhang, Steven S Scherer
Neurology. Genetics|August 18, 2020
Isoform-specific loss of dystonin causes hereditary motor and sensory neuropathyWilliam W Motley, Stephan Züchner, Steven S Scherer
Journal of the Peripheral Nervous System : JPNS|April 12, 2021
A recurrent MORC2 mutation causes Charcot-Marie-Tooth disease type 2ZDragan Vujovic, David R Cornblath, Steven S Scherer
Pageof 16

Showing results (21-30 of 159) with videos related to

Sort By:
Pageof 16
Neuromolecular Medicine|June 16, 2006
Molecular genetics of X-linked Charcot-Marie-Tooth diseaseKleopas A Kleopa, Steven S Scherer
Biochimica Et Biophysica Acta|August 30, 2011
Gap junctions in inherited human disorders of the central nervous systemCharles K Abrams, Steven S Scherer
Neurologic Clinics|November 16, 2002
Inherited neuropathiesKleopas A Kleopa, Steven S Scherer
Neuroscience Letters|June 16, 2012
Neuronal cadherin (NCAD) increases sensory neurite formation and outgrowth on astrocytesToby A Ferguson, Steven S Scherer
Neurobiology of Disease|March 15, 2011
Cx32 and Cx47 mediate oligodendrocyte:astrocyte and oligodendrocyte:oligodendrocyte gap junction couplingSameh K Wasseff, Steven S Scherer
The New England Journal of Medicine|December 16, 2011
Microtubules, axonal transport, and neuropathyErika L F Holzbaur, Steven S Scherer
Molecular and Cellular Neurosciences|November 3, 2010
Dominant Cx26 mutants associated with hearing loss have dominant-negative effects on wild type Cx26Junxian Zhang, Steven S Scherer, Sabrina W Yum
Neurobiology of Disease|January 26, 2010
Dominant connexin26 mutants associated with human hearing loss have trans-dominant effects on connexin30Sabrina W Yum, Junxian Zhang, Steven S Scherer
Neurology. Genetics|August 18, 2020
Isoform-specific loss of dystonin causes hereditary motor and sensory neuropathyWilliam W Motley, Stephan Züchner, Steven S Scherer
Journal of the Peripheral Nervous System : JPNS|April 12, 2021
A recurrent MORC2 mutation causes Charcot-Marie-Tooth disease type 2ZDragan Vujovic, David R Cornblath, Steven S Scherer
Pageof 16