Charles K Abrams - JoVE Visualize

Search research articles

ABOUT JoVE

Overview Leadership Blog JoVE Help Center

AUTHORS

Publishing Process Editorial Board Scope & Policies Peer Review FAQ Submit

LIBRARIANS

Testimonials Subscriptions Access Resources Library Advisory Board FAQ

RESEARCH

JoVE Journal Methods Collections JoVE Encyclopedia of Experiments Archive

EDUCATION

JoVE Core JoVE Business JoVE Science Education JoVE Lab Manual Faculty Resource Center Faculty Site

Terms & Conditions of Use

Policies

Search research articles

ABOUT JoVE

Overview Leadership Blog JoVE Help Center

AUTHORS

Publishing Process Editorial Board Scope & Policies Peer Review FAQ Submit

LIBRARIANS

Testimonials Subscriptions Access Resources Library Advisory Board FAQ

RESEARCH

JoVE Journal Methods Collections JoVE Encyclopedia of Experiments Archive

EDUCATION

JoVE Core JoVE Business JoVE Science Education JoVE Lab Manual Faculty Resource Center Faculty Site

Terms & Conditions of Use

Policies

Filters

Charles K Abrams

Showing results (31-40 of 37) with videos related to

Pageof 4

Sort By:

You have reached the last page of results.This site can display upto 37 results.

Gene Therapy|February 5, 2021

AAV1.NT-3 gene therapy for X-linked Charcot-Marie-Tooth neuropathy type 1Burcak Ozes, Morgan Myers, Kyle Moss, et al.

Brain : a Journal of Neurology|December 6, 2008

Hereditary spastic paraplegia is a novel phenotype for GJA12/GJC2 mutationsJennifer L Orthmann-Murphy, Ettore Salsano, Charles K Abrams, et al.

The Journal of General Physiology|June 10, 2025

Molecular dynamics simulation of GJC2 mutants reveal pathogenic mechanisms of PMLD1 and SPG44David Gong, Jennifer L Orthmann-Murphy, Deepak Kumar, et al.

Journal of Neuroscience Research|November 1, 2007

Cx29 and Cx32, two connexins expressed by myelinating glia, do not interact and are functionally distinctMeejin Ahn, Jonathan Lee, Andreas Gustafsson, et al.

Human Molecular Genetics|June 19, 2013

Exome sequencing identification of a GJB1 missense mutation in a kindred with X-linked spinocerebellar ataxia (SCA-X1)Melody Caramins, James G Colebatch, Matthew N Bainbridge, et al.

Scientific Reports|May 15, 2026

Axonal dying back of upper motor neurons in human ALSHaley C Cropper, Fozia Mir, Jianguo Liu, et al.

Orphanet Journal of Rare Diseases|July 19, 2022

Genotype-phenotype correlations and disease mechanisms in PEX13-related Zellweger spectrum disordersPaola Borgia, Simona Baldassari, Nicoletta Pedemonte, et al.

Pageof 4

Search research articles

Showing results (31-40 of 37) with videos related to

Sort By:

Pageof 4

You have reached the last page of results.This site can display upto 37 results.

Gene Therapy|February 5, 2021

AAV1.NT-3 gene therapy for X-linked Charcot-Marie-Tooth neuropathy type 1Burcak Ozes, Morgan Myers, Kyle Moss, et al.

Brain : a Journal of Neurology|December 6, 2008

Hereditary spastic paraplegia is a novel phenotype for GJA12/GJC2 mutationsJennifer L Orthmann-Murphy, Ettore Salsano, Charles K Abrams, et al.

The Journal of General Physiology|June 10, 2025

Molecular dynamics simulation of GJC2 mutants reveal pathogenic mechanisms of PMLD1 and SPG44David Gong, Jennifer L Orthmann-Murphy, Deepak Kumar, et al.

Journal of Neuroscience Research|November 1, 2007

Cx29 and Cx32, two connexins expressed by myelinating glia, do not interact and are functionally distinctMeejin Ahn, Jonathan Lee, Andreas Gustafsson, et al.

Human Molecular Genetics|June 19, 2013

Exome sequencing identification of a GJB1 missense mutation in a kindred with X-linked spinocerebellar ataxia (SCA-X1)Melody Caramins, James G Colebatch, Matthew N Bainbridge, et al.

Scientific Reports|May 15, 2026

Axonal dying back of upper motor neurons in human ALSHaley C Cropper, Fozia Mir, Jianguo Liu, et al.

Orphanet Journal of Rare Diseases|July 19, 2022

Genotype-phenotype correlations and disease mechanisms in PEX13-related Zellweger spectrum disordersPaola Borgia, Simona Baldassari, Nicoletta Pedemonte, et al.

Pageof 4