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Steven S Scherer

Showing results (41-50 of 159) with videos related to

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Neurobiology of Disease|December 4, 2002
Diverse trafficking abnormalities of connexin32 mutants causing CMTXSabrina W Yum, Kleopas A Kleopa, Susan Shumas, et al.
The Journal of Cell Biology|October 31, 2002
Distinct claudins and associated PDZ proteins form different autotypic tight junctions in myelinating Schwann cellsSebastian Poliak, Sean Matlis, Christoph Ullmer, et al.
Glia|September 30, 2006
Pannexin1 is expressed by neurons and glia but does not form functional gap junctionsYan Huang, Judith B Grinspan, Charles K Abrams, et al.
The Journal of Comparative Neurology|October 30, 2004
Acute demyelination disrupts the molecular organization of peripheral nervous system nodesEdgardo J Arroyo, Erich E Sirkowski, Rohan Chitale, et al.
Annals of the New York Academy of Sciences|November 1, 2017
X-linked Charcot-Marie-Tooth Disease and Connexin32Kenneth H Fischbeck, Annette Abel, Grace S Lin, et al.
Journal of Neuro-Ophthalmology : the Official Journal of the North American Neuro-Ophthalmology Society|May 23, 2020
Optic Neuropathy in Charcot-Marie-Tooth DiseaseAli G Hamedani, James A Wilson, Robert A Avery, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|February 6, 2004
KCNQ2 is a nodal K+ channelJérôme J Devaux, Kleopas A Kleopa, Edward C Cooper, et al.
Annals of Neurology|December 30, 2009
A novel recessive Nefl mutation causes a severe, early-onset axonal neuropathySabrina W Yum, Junxian Zhang, Katie Mo, et al.
Journal of the Peripheral Nervous System : JPNS|January 18, 2018
A mutation in the heptad repeat 2 domain of MFN2 in a large CMT2A familyLois Dankwa, Jessica Richardson, William W Motley, et al.
Neurology(R) Neuroimmunology & Neuroinflammation|July 18, 2015
Caspr2 autoantibodies target multiple epitopesAbby L Olsen, Yongjie Lai, Josep Dalmau, et al.
Pageof 16

Showing results (41-50 of 159) with videos related to

Sort By:
Pageof 16
Neurobiology of Disease|December 4, 2002
Diverse trafficking abnormalities of connexin32 mutants causing CMTXSabrina W Yum, Kleopas A Kleopa, Susan Shumas, et al.
The Journal of Cell Biology|October 31, 2002
Distinct claudins and associated PDZ proteins form different autotypic tight junctions in myelinating Schwann cellsSebastian Poliak, Sean Matlis, Christoph Ullmer, et al.
Glia|September 30, 2006
Pannexin1 is expressed by neurons and glia but does not form functional gap junctionsYan Huang, Judith B Grinspan, Charles K Abrams, et al.
The Journal of Comparative Neurology|October 30, 2004
Acute demyelination disrupts the molecular organization of peripheral nervous system nodesEdgardo J Arroyo, Erich E Sirkowski, Rohan Chitale, et al.
Annals of the New York Academy of Sciences|November 1, 2017
X-linked Charcot-Marie-Tooth Disease and Connexin32Kenneth H Fischbeck, Annette Abel, Grace S Lin, et al.
Journal of Neuro-Ophthalmology : the Official Journal of the North American Neuro-Ophthalmology Society|May 23, 2020
Optic Neuropathy in Charcot-Marie-Tooth DiseaseAli G Hamedani, James A Wilson, Robert A Avery, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|February 6, 2004
KCNQ2 is a nodal K+ channelJérôme J Devaux, Kleopas A Kleopa, Edward C Cooper, et al.
Annals of Neurology|December 30, 2009
A novel recessive Nefl mutation causes a severe, early-onset axonal neuropathySabrina W Yum, Junxian Zhang, Katie Mo, et al.
Journal of the Peripheral Nervous System : JPNS|January 18, 2018
A mutation in the heptad repeat 2 domain of MFN2 in a large CMT2A familyLois Dankwa, Jessica Richardson, William W Motley, et al.
Neurology(R) Neuroimmunology & Neuroinflammation|July 18, 2015
Caspr2 autoantibodies target multiple epitopesAbby L Olsen, Yongjie Lai, Josep Dalmau, et al.
Pageof 16