Myelination: some receptors required

por Scherer, Steven S.
Publicado 2002

The debut of a rational treatment for an inherited neuropathy?

por Scherer, Steven S.
Publicado 2011

Molecular Mechanisms of Inherited Demyelinating Neuropathies

por SCHERER, STEVEN S., WRABETZ, LAWRENCE
Publicado 2008

Subtype-specific therapy for autoimmune neuropathies?

por Lancaster, Eric, Scherer, Steven S.
Publicado en Neurol Neuroimmunol Neuroinflamm (2015)

A MT-ATP6 Mutation Causes a Slowly Progressive Myeloneuropathy

por Bardakjian, Tanya, Scherer, Steven S.
Publicado en J Neuromuscul Dis (2019)

Gap junctions in inherited human disorders of the central nervous system

por Abrams, Charles K., Scherer, Steven S.
Publicado 2011

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

por Wasseff, Sameh K., Scherer, Steven S.
Publicado 2011

X-linked Charcot-Marie-Tooth disease

por Scherer, Steven S., Kleopa, Kleopas A.
Publicado 2012

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

por Ferguson, Toby A., Scherer, Steven S.
Publicado 2012

Activated Microglia do not form Functional Gap Junctions in vivo

por Wasseff, Sameh K., Scherer, Steven S.
Publicado 2014

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

por King, Chih H., Scherer, Steven S.
Publicado en 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 en 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 en J Neurosci (2005)

Microtubules, Axonal Transport, and Neuropathy

por Holzbaur, Erika L.F., Scherer, Steven S.
Publicado 2011

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

por Lancaster, Eric, Elman, Lauren B., Scherer, Steven S.
Publicado 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 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 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 2011

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

por Motley, William W., Züchner, Stephan, Scherer, Steven S.
Publicado en 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 2012