Abnormal junctions and permeability of myelin in PMP22-deficient nerves-Reference-Cited by-同舟云学术

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Abnormal junctions and permeability of myelin in PMP22-deficient nerves

Published:2014-02 Issue:2 Volume:75 Page:255-265
ISSN:0364-5134
Container-title:Annals of Neurology
language:en
Short-container-title:Ann Neurol.

Author:

Guo Jiasong¹,Wang Leiming²¹,Zhang Yang¹,Wu Jiawen¹,Arpag Sezgi¹,Hu Bo¹,Imhof Beat A.³,Tian Xinxia²,Carter Bruce D.⁴,Suter Ueli⁵,Li Jun¹⁶

Affiliation:

1. Department of Neurology, Center for Human Genetics Research; Vanderbilt Brain Institute, Vanderbilt University School of Medicine; Nashville TN

2. Department of Pathology; Peking University Health Science Center; Beijing China

3. Department of Pathology and Immunology; University of Geneva School of Medicine; Geneva Switzerland

4. Department of Biochemistry; Vanderbilt University School of Medicine; Nashville TN

5. Department of Biology; Institute of Molecular Health Sciences, ETH Zurich; Zurich Switzerland

6. Tennessee Valley Healthcare System-Nashville VA; Nashville TN

Publisher

Wiley

Subject

Clinical Neurology,Neurology

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/ana.24086/fullpdf

Reference32 articles.

1. Activity-dependent conduction block in multifocal motor neuropathy;Kaji;Brain,2000

2. Rapid conduction and the evolution of giant axons and myelinated fibers;Hartline;Curr Biol,2007

3. The PMP22 gene and its related diseases;Li;Mol Neurobiol,2013

4. Loss-of-function phenotype of hereditary neuropathy with liability to pressure palsies;Li;Muscle Nerve,2004

5. Deletions of chromosome 17p11.2 in multifocal neuropathies;Tyson;Ann Neurol,1996

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1. PMP22 associates with MPZ via their transmembrane domains and disrupting this interaction causes a loss-of-function phenotype similar to hereditary neuropathy associated with liability to pressure palsies (HNPP);2023-12-24

2. Hereditary neuropathy associated with liability to pressure palsies: a 24-year experience with carpal and cubital tunnel surgery;Journal of Hand Surgery (European Volume);2023-09-17

3. Myelin barrier breakdown, mechanical hypersensitivity, and painfulness in polyneuropathy with claudin-12 deficiency;Neurobiology of Disease;2023-09

4. Schwann cell‐specific RhoA knockout accelerates peripheral nerve regeneration via promoting Schwann cell dedifferentiation;Glia;2023-03-27

5. How T118M peripheral myelin protein 22 predisposes humans to Charcot–Marie–Tooth disease;Journal of Biological Chemistry;2023-02

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