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Steven S Scherer

Showing results (71-80 of 159) with videos related to

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Neuron Glia Biology|May 25, 2006
Identification of novel cell-adhesion molecules in peripheral nerves using a signal-sequence trapIvo Spiegel, Konstantin Adamsky, Menahem Eisenbach, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|February 11, 2005
Transgenic expression of human connexin32 in myelinating Schwann cells prevents demyelination in connexin32-null miceSteven S Scherer, Yi-Tian Xu, Albee Messing, et al.
Glia|May 28, 2011
Paranodal permeability in "myelin mutants"Seema Shroff, Amanda Mierzwa, Steven S Scherer, et al.
American Journal of Physiology. Cell Physiology|July 7, 2007
Human connexin26 and connexin30 form functional heteromeric and heterotypic channelsSabrina W Yum, Junxian Zhang, Virginijus Valiunas, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|November 27, 2002
Identification of genes that are downregulated in the absence of the POU domain transcription factor pou3f1 (Oct-6, Tst-1, SCIP) in sciatic nerveJohn R Bermingham, Susan Shumas, Tom Whisenhunt, 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.
Neuromuscular Disorders : NMD|January 16, 2019
A novel MFN2 mutation causes variable clinical severity in a multi-generational CMT2 familyLois Dankwa, Jessica Richardson, William W Motley, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|October 27, 2006
Genetic and physiological evidence that oligodendrocyte gap junctions contribute to spatial buffering of potassium released during neuronal activityDaniela M Menichella, Marta Majdan, Rajeshwar Awatramani, et al.
Neurobiology of Disease|March 25, 2020
A recessive Trim2 mutation causes an axonal neuropathy in miceJian J Li, Nicolas Sarute, Eunjoo Lancaster, et al.
Pageof 16

Showing results (71-80 of 159) with videos related to

Sort By:
Pageof 16
Neuron Glia Biology|May 25, 2006
Identification of novel cell-adhesion molecules in peripheral nerves using a signal-sequence trapIvo Spiegel, Konstantin Adamsky, Menahem Eisenbach, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|February 11, 2005
Transgenic expression of human connexin32 in myelinating Schwann cells prevents demyelination in connexin32-null miceSteven S Scherer, Yi-Tian Xu, Albee Messing, et al.
Glia|May 28, 2011
Paranodal permeability in "myelin mutants"Seema Shroff, Amanda Mierzwa, Steven S Scherer, et al.
American Journal of Physiology. Cell Physiology|July 7, 2007
Human connexin26 and connexin30 form functional heteromeric and heterotypic channelsSabrina W Yum, Junxian Zhang, Virginijus Valiunas, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|November 27, 2002
Identification of genes that are downregulated in the absence of the POU domain transcription factor pou3f1 (Oct-6, Tst-1, SCIP) in sciatic nerveJohn R Bermingham, Susan Shumas, Tom Whisenhunt, 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.
Neuromuscular Disorders : NMD|January 16, 2019
A novel MFN2 mutation causes variable clinical severity in a multi-generational CMT2 familyLois Dankwa, Jessica Richardson, William W Motley, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|October 27, 2006
Genetic and physiological evidence that oligodendrocyte gap junctions contribute to spatial buffering of potassium released during neuronal activityDaniela M Menichella, Marta Majdan, Rajeshwar Awatramani, et al.
Neurobiology of Disease|March 25, 2020
A recessive Trim2 mutation causes an axonal neuropathy in miceJian J Li, Nicolas Sarute, Eunjoo Lancaster, et al.
Pageof 16