List of works - Charles K. Abrams

A Threat to the Citizen Volunteer?

scientific article published in 1959

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

scientific article published on March 4, 2011

A new mutation in GJC2 associated with subclinical leukodystrophy

scientific article

Acetylation of C-terminal lysines modulates protein turnover and stability of Connexin-32

scientific article published on 29 September 2018

Acute demyelinating neuropathy in a patient with neurolymphomatosis

scientific article published on 05 March 2018

Alterations at Arg76 of human connexin 46, a residue associated with cataract formation, cause loss of gap junction formation but preserve hemichannel function

scientific article published on 25 July 2018

Connexin 32 increases the proliferative response of Schwann cells to neuregulin-1 (Nrg1)

scientific article

Cx29 and Cx32, two connexins expressed by myelinating glia, do not interact and are functionally distinct

scientific article published on April 2008

Diseases of connexins expressed in myelinating glia

scientific article published on 22 May 2017

Exome sequencing identification of a GJB1 missense mutation in a kindred with X-linked spinocerebellar ataxia (SCA-X1).

scientific article published on 16 June 2013

Functional Requirement for a Highly Conserved Charged Residue at Position 75 in the Gap Junction Protein Connexin 32 ⬇️

scientific article published on December 3, 2012

GJB1-associated X-linked Charcot-Marie-Tooth disease, a disorder affecting the central and peripheral nervous systems

scientific article

Gap junctions couple astrocytes and oligodendrocytes

scientific article

Gap junctions in inherited human disorders of the central nervous system ⬇️

scientific article published on August 16, 2011

Gene expression profiling studies in regenerating nerves in a mouse model for CMT1X: uninjured Cx32-knockout peripheral nerves display expression profile of injured wild type nerves

scientific article

Genotype–phenotype correlations and disease mechanisms in PEX13-related Zellweger spectrum disorders

scientific article published in 2022

Hereditary spastic paraplegia is a novel phenotype for GJA12/GJC2 mutations

scientific article

How do mutations in GJB1 cause X-linked Charcot-Marie-Tooth disease?

scientific article

Human oligodendrocytes express Cx31.3: function and interactions with Cx32 mutants

scientific article

Increase in chemokines CXCL10 and CCL2 in blood from pigs infected with high compared to low virulence African swine fever virus isolates

scientific article published on October 2013

Loss of Coupling Distinguishes GJB1 Mutations Associated with CNS Manifestations of CMT1X from Those Without CNS Manifestations

scientific article published on 10 January 2017

Loss-of-function GJA12/Connexin47 mutations cause Pelizaeus-Merzbacher-like disease

scientific article

Normalization of nomenclature for peptide motifs as ligands of modular protein domains

scientific article

Pannexin1 is expressed by neurons and glia but does not form functional gap junctions

scientific article published in January 2007

Pathogenesis of X-linked Charcot-Marie-Tooth disease: differential effects of two mutations in connexin 32

scientific article published in November 2003

Patterns of Spontaneous Local Network Activity in Developing Cerebral Cortex: Relationship to Adult Cognitive Function

scientific article published on 22 June 2015

Properties of human connexin 31, which is implicated in hereditary dermatological disease and deafness.

scholarly article

Rapid and Specific Immunomagnetic Isolation of Mouse Primary Oligodendrocytes.

scientific article

Regulatory role of oligodendrocyte gap junctions in inflammatory demyelination

scientific article published on 16 October 2018

Systemic inflammation disrupts oligodendrocyte gap junctions and induces ER stress in a model of CNS manifestations of X-linked Charcot-Marie-Tooth disease

scientific article

The Legal Basis for Reorganizing Metropolitan Areas in a Free Society

scientific article

The MyD116 African swine fever virus homologue interacts with the catalytic subunit of protein phosphatase 1 and activates its phosphatase activity.

scientific article published on 10 January 2007

The Rising Challenge to Minority Advance

scientific article published in 1959

The challenge of profound hypoglycorrhachia: two cases of sarcoidosis and review of the literature

scientific article published on 26 August 2011

Two distinct heterotypic channels mediate gap junction coupling between astrocyte and oligodendrocyte connexins.

scientific article published in December 2007

List of works by Charles K. Abrams

A Threat to the Citizen Volunteer?

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

A new mutation in GJC2 associated with subclinical leukodystrophy

Acetylation of C-terminal lysines modulates protein turnover and stability of Connexin-32

Acute demyelinating neuropathy in a patient with neurolymphomatosis

Alterations at Arg76 of human connexin 46, a residue associated with cataract formation, cause loss of gap junction formation but preserve hemichannel function

Connexin 32 increases the proliferative response of Schwann cells to neuregulin-1 (Nrg1)

Cx29 and Cx32, two connexins expressed by myelinating glia, do not interact and are functionally distinct

Diseases of connexins expressed in myelinating glia

Exome sequencing identification of a GJB1 missense mutation in a kindred with X-linked spinocerebellar ataxia (SCA-X1).

Functional Requirement for a Highly Conserved Charged Residue at Position 75 in the Gap Junction Protein Connexin 32 ⬇️

GJB1-associated X-linked Charcot-Marie-Tooth disease, a disorder affecting the central and peripheral nervous systems

Gap junctions couple astrocytes and oligodendrocytes

Gap junctions in inherited human disorders of the central nervous system ⬇️

Gene expression profiling studies in regenerating nerves in a mouse model for CMT1X: uninjured Cx32-knockout peripheral nerves display expression profile of injured wild type nerves

Genotype–phenotype correlations and disease mechanisms in PEX13-related Zellweger spectrum disorders

Hereditary spastic paraplegia is a novel phenotype for GJA12/GJC2 mutations

How do mutations in GJB1 cause X-linked Charcot-Marie-Tooth disease?

Human oligodendrocytes express Cx31.3: function and interactions with Cx32 mutants

Increase in chemokines CXCL10 and CCL2 in blood from pigs infected with high compared to low virulence African swine fever virus isolates

Loss of Coupling Distinguishes GJB1 Mutations Associated with CNS Manifestations of CMT1X from Those Without CNS Manifestations

Loss-of-function GJA12/Connexin47 mutations cause Pelizaeus-Merzbacher-like disease

Normalization of nomenclature for peptide motifs as ligands of modular protein domains

Pannexin1 is expressed by neurons and glia but does not form functional gap junctions

Pathogenesis of X-linked Charcot-Marie-Tooth disease: differential effects of two mutations in connexin 32

Patterns of Spontaneous Local Network Activity in Developing Cerebral Cortex: Relationship to Adult Cognitive Function

Properties of human connexin 31, which is implicated in hereditary dermatological disease and deafness.

Rapid and Specific Immunomagnetic Isolation of Mouse Primary Oligodendrocytes.

Regulatory role of oligodendrocyte gap junctions in inflammatory demyelination

Systemic inflammation disrupts oligodendrocyte gap junctions and induces ER stress in a model of CNS manifestations of X-linked Charcot-Marie-Tooth disease

The Legal Basis for Reorganizing Metropolitan Areas in a Free Society

The MyD116 African swine fever virus homologue interacts with the catalytic subunit of protein phosphatase 1 and activates its phosphatase activity.

The Rising Challenge to Minority Advance

The challenge of profound hypoglycorrhachia: two cases of sarcoidosis and review of the literature

Two distinct heterotypic channels mediate gap junction coupling between astrocyte and oligodendrocyte connexins.