Knock-in mouse models for CMTX1 show a loss of function phenotype in the peripheral nervous system-Reference-Cited by-同舟云学术

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Knock-in mouse models for CMTX1 show a loss of function phenotype in the peripheral nervous system

Published:2023-02 Issue: Volume:360 Page:114277
ISSN:0014-4886
Container-title:Experimental Neurology
language:en
Short-container-title:Experimental Neurology

Author:

Abrams Charles K.,Lancaster Eunjoo,Li Jian J.,Dungan Gabriel,Gong David,Scherer Steven S.,Freidin Mona M.

Funder

Muscular Dystrophy Association

Publisher

Elsevier BV

Subject

Developmental Neuroscience,Neurology

Reference75 articles.

1. Assessing functional performance in the mdx mouse model;Aartsma-Rus;J. Vis. Exp.,2014

2. Studies in transgenic mice indicate a loss of connexin32 function in X-linked Charcot-Marie-Tooth disease;Abel;J. Neuropathol. Exp. Neurol.,1999

3. Gap junctions in inherited human disorders of the central nervous system;Abrams;Biochim. Biophys. Acta,2012

4. Pathogenesis of X-linked Charcot-Marie-Tooth disease: differential effects of two mutations in connexin 32;Abrams;J. Neurosci.,2003

5. Functional requirement for a highly conserved charged residue at position 75 in the gap junction protein connexin 32;Abrams;J. Biol. Chem.,2013

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2. Peripheral Nervous System (PNS) Myelin Diseases;Cold Spring Harbor Perspectives in Biology;2024-01-22

3. Assessment of blood–brain barrier leakage and brain oxygenation in Connexin‐32 knockout mice with systemic neuroinflammation using pulse electron paramagnetic resonance imaging techniques;Magnetic Resonance in Medicine;2024-01-09

4. Proteostasis plays an important role in demyelinating Charcot Marie Tooth disease;Biochemical Pharmacology;2023-10

5. Gene replacement therapy in two Golgi-retained CMT1X mutants before and after the onset of demyelinating neuropathy;Molecular Therapy - Methods & Clinical Development;2023-09

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