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The Journal of Comparative Neurology
|
April 2, 2014
Kv7.2 regulates the function of peripheral sensory neurons
Chih H King, Eric Lancaster, Daniela Salomon, et al.
Neurology
|
December 10, 2003
The CNS phenotype of X-linked Charcot-Marie-Tooth disease: more than a peripheral problem
Robert A Taylor, Erin M Simon, Harold G Marks, et al.
Brain : a Journal of Neurology
|
April 15, 2006
Neuromyotonia and limbic encephalitis sera target mature Shaker-type K+ channels: subunit specificity correlates with clinical manifestations
Kleopas A Kleopa, Lauren B Elman, Bethan Lang, et al.
Ejhaem
|
January 28, 2025
Chronic Severe Neutropenia Associated With Intravenous Immunoglobulin for Multifocal Motor Neuropathy
Shannon Ugarte, Talia Gebhard, David R Cornblath, et al.
Journal of the Peripheral Nervous System : JPNS
|
November 9, 2019
Yield of next-generation neuropathy gene panels in axonal neuropathies
Diana C Lee, Lois Dankwa, Christyn Edmundson, et al.
Molecular and Cellular Neurosciences
|
March 9, 2007
Loss-of-function GJA12/Connexin47 mutations cause Pelizaeus-Merzbacher-like disease
Jennifer L Orthmann-Murphy, Alan D Enriquez, Charles K Abrams, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience
|
July 5, 2003
Connexins are critical for normal myelination in the CNS
Daniela M Menichella, Daniel A Goodenough, Erich Sirkowski, et al.
Glia
|
August 5, 2004
Unique distributions of the gap junction proteins connexin29, connexin32, and connexin47 in oligodendrocytes
Kleopas A Kleopa, Jennifer L Orthmann, Alan Enriquez, et al.
Experimental Neurology
|
June 26, 2018
Myelinated axons fail to develop properly in a genetically authentic mouse model of Charcot-Marie-Tooth disease type 2E
Eunjoo Lancaster, Jian Li, Taleen Hanania, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience
|
December 21, 2007
Two distinct heterotypic channels mediate gap junction coupling between astrocyte and oligodendrocyte connexins
Jennifer L Orthmann-Murphy, Mona Freidin, Esther Fischer, et al.
Page
of 16
Search research articles
Search
Showing results (51-60 of 159) with videos related to
Sort By:
Page
of 16
The Journal of Comparative Neurology
|
April 2, 2014
Kv7.2 regulates the function of peripheral sensory neurons
Chih H King, Eric Lancaster, Daniela Salomon, et al.
Neurology
|
December 10, 2003
The CNS phenotype of X-linked Charcot-Marie-Tooth disease: more than a peripheral problem
Robert A Taylor, Erin M Simon, Harold G Marks, et al.
Brain : a Journal of Neurology
|
April 15, 2006
Neuromyotonia and limbic encephalitis sera target mature Shaker-type K+ channels: subunit specificity correlates with clinical manifestations
Kleopas A Kleopa, Lauren B Elman, Bethan Lang, et al.
Ejhaem
|
January 28, 2025
Chronic Severe Neutropenia Associated With Intravenous Immunoglobulin for Multifocal Motor Neuropathy
Shannon Ugarte, Talia Gebhard, David R Cornblath, et al.
Journal of the Peripheral Nervous System : JPNS
|
November 9, 2019
Yield of next-generation neuropathy gene panels in axonal neuropathies
Diana C Lee, Lois Dankwa, Christyn Edmundson, et al.
Molecular and Cellular Neurosciences
|
March 9, 2007
Loss-of-function GJA12/Connexin47 mutations cause Pelizaeus-Merzbacher-like disease
Jennifer L Orthmann-Murphy, Alan D Enriquez, Charles K Abrams, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience
|
July 5, 2003
Connexins are critical for normal myelination in the CNS
Daniela M Menichella, Daniel A Goodenough, Erich Sirkowski, et al.
Glia
|
August 5, 2004
Unique distributions of the gap junction proteins connexin29, connexin32, and connexin47 in oligodendrocytes
Kleopas A Kleopa, Jennifer L Orthmann, Alan Enriquez, et al.
Experimental Neurology
|
June 26, 2018
Myelinated axons fail to develop properly in a genetically authentic mouse model of Charcot-Marie-Tooth disease type 2E
Eunjoo Lancaster, Jian Li, Taleen Hanania, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience
|
December 21, 2007
Two distinct heterotypic channels mediate gap junction coupling between astrocyte and oligodendrocyte connexins
Jennifer L Orthmann-Murphy, Mona Freidin, Esther Fischer, et al.
Page
of 16