Myelination: some receptors required

od Scherer, Steven S.
Wydane 2002

The debut of a rational treatment for an inherited neuropathy?

od Scherer, Steven S.
Wydane 2011

Molecular Mechanisms of Inherited Demyelinating Neuropathies

od SCHERER, STEVEN S., WRABETZ, LAWRENCE
Wydane 2008

Subtype-specific therapy for autoimmune neuropathies?

od Lancaster, Eric, Scherer, Steven S.
Wydane w Neurol Neuroimmunol Neuroinflamm (2015)

A MT-ATP6 Mutation Causes a Slowly Progressive Myeloneuropathy

od Bardakjian, Tanya, Scherer, Steven S.
Wydane w J Neuromuscul Dis (2019)

Gap junctions in inherited human disorders of the central nervous system

od Abrams, Charles K., Scherer, Steven S.
Wydane 2011

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

od Wasseff, Sameh K., Scherer, Steven S.
Wydane 2011

X-linked Charcot-Marie-Tooth disease

od Scherer, Steven S., Kleopa, Kleopas A.
Wydane 2012

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

od Ferguson, Toby A., Scherer, Steven S.
Wydane 2012

Activated Microglia do not form Functional Gap Junctions in vivo

od Wasseff, Sameh K., Scherer, Steven S.
Wydane 2014

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

od King, Chih H., Scherer, Steven S.
Wydane w J Comp Neurol (2012)

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

od Wasseff, Sameh K., Scherer, Steven S.
Wydane w Neurobiol Dis (2015)

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

od Devaux, Jérôme J., Scherer, Steven S.
Wydane w J Neurosci (2005)

Microtubules, Axonal Transport, and Neuropathy

od Holzbaur, Erika L.F., Scherer, Steven S.
Wydane 2011

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

od Lancaster, Eric, Elman, Lauren B., Scherer, Steven S.
Wydane 2010

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

od Yum, Sabrina W., Zhang, Junxian, Scherer, Steven S.
Wydane 2010

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

od Zhang, Junxian, Scherer, Steven S., Yum, Sabrina W.
Wydane 2010

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

od WASSEFF, SAMEH, ABRAMS, CHARLES K., SCHERER, STEVEN S.
Wydane 2011

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

od Motley, William W., Züchner, Stephan, Scherer, Steven S.
Wydane w Neurol Genet (2020)

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

od Kleopa, Kleopas A., Abrams, Charles K., Scherer, Steven S.
Wydane 2012