Myelination: some receptors required

Por Scherer, Steven S.
Publicado em 2002

The debut of a rational treatment for an inherited neuropathy?

Por Scherer, Steven S.
Publicado em 2011

Molecular Mechanisms of Inherited Demyelinating Neuropathies

Por SCHERER, STEVEN S., WRABETZ, LAWRENCE
Publicado em 2008

Subtype-specific therapy for autoimmune neuropathies?

Por Lancaster, Eric, Scherer, Steven S.
Publicado no Neurol Neuroimmunol Neuroinflamm (2015)

Gap junctions in inherited human disorders of the central nervous system

Por Abrams, Charles K., Scherer, Steven S.
Publicado em 2011

Cx32 and Cx47 mediate oligodendrocyte:astrocyte and oligodendrocyte: oligodendrocyte gap junction coupling

Por Wasseff, Sameh K., Scherer, Steven S.
Publicado em 2011

X-linked Charcot-Marie-Tooth disease

Por Scherer, Steven S., Kleopa, Kleopas A.
Publicado em 2012

Neuronal cadherin (NCAD) increases sensory neurite formation and outgrowth on astrocytes

Por Ferguson, Toby A., Scherer, Steven S.
Publicado em 2012

Activated Microglia do not form Functional Gap Junctions in vivo

Por Wasseff, Sameh K., Scherer, Steven S.
Publicado em 2014

Kv7.5 is the Primary Kv7 Subunit Expressed in C-fibers

Por King, Chih H., Scherer, Steven S.
Publicado no J Comp Neurol (2012)

Activated Immune Response in an Inherited Leukodystrophy Disease Caused by the Loss of Oligodendrocyte Gap Junctions

Por Wasseff, Sameh K., Scherer, Steven S.
Publicado no Neurobiol Dis (2015)

Altered Ion Channels in an Animal Model of Charcot-Marie-Tooth Disease Type IA

Por Devaux, Jérôme J., Scherer, Steven S.
Publicado no J Neurosci (2005)

Microtubules, Axonal Transport, and Neuropathy

Por Holzbaur, Erika L.F., Scherer, Steven S.
Publicado em 2011

A patient with Neurofibromatosis type 1 and Charcot-Marie-Tooth Disease type 1B

Por Lancaster, Eric, Elman, Lauren B., Scherer, Steven S.
Publicado em 2010

Dominant connexin26 mutants associated with human hearing loss have trans-dominant effects on connexin30

Por Yum, Sabrina W., Zhang, Junxian, Scherer, Steven S.
Publicado em 2010

Dominant Cx26 mutants associated with hearing loss have dominant-negative effects on wild type Cx26

Por Zhang, Junxian, Scherer, Steven S., Yum, Sabrina W.
Publicado em 2010

A dominant connexin43 mutant does not have dominant effects on gap junction coupling in astrocytes

Por WASSEFF, SAMEH, ABRAMS, CHARLES K., SCHERER, STEVEN S.
Publicado em 2011

Isoform-specific loss of dystonin causes hereditary motor and sensory neuropathy

Por Motley, William W., Züchner, Stephan, Scherer, Steven S.
Publicado no Neurol Genet (2020)

How do Mutations in GJB1 Cause X-linked Charcot-Marie-Tooth Disease?

Por Kleopa, Kleopas A., Abrams, Charles K., Scherer, Steven S.
Publicado em 2012

Functional Gap Junctions in the Schwann Cell Myelin Sheath

Por Balice-Gordon, Rita J., Bone, Linda J., Scherer, Steven S.
Publicado em 1998