Insertion of mutant proteolipid protein results in missorting of myelin proteins-Reference-Cited by-同舟云学术

Insertion of mutant proteolipid protein results in missorting of myelin proteins

Published:2003-11-26 Issue:6 Volume:54 Page:769-780
ISSN:0364-5134
Container-title:Annals of Neurology
language:en
Short-container-title:Ann Neurol.

Author:

Vaurs-Barriere Catherine,Wong Kondi,Weibel Thais D.,Abu-Asab Mones,Weiss Michael D.,Kaneski Christine R.,Mixon Tong-Hui,Bonavita Simona,Creveaux Isabelle,Heiss John D.,Tsokos Maria,Goldin Ehud,Quarles Richard H.,Boespflug-Tanguy Odile,Schiffmann Raphael

Publisher

Wiley

Subject

Neurology (clinical),Neurology

Reference49 articles.

1. The proteolipid protein gene and myelin disorders in man and animal models

2. Oligodendrocytes expressing exclusively the DM20 isoform of the proteolipid protein gene: Myelination and development

3. Assembly of CNS Myelin in the Absence of Proteolipid Protein

4. The Pathobiology of Myelin Mutants Reveal Novel Biological Functions of the MBP and PLP Genes

5. Genotype–phenotype correlation in inherited brain myelination defects due to proteolipid protein gene mutations

Cited by 21 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. PLP1 gene mutations cause spastic paraplegia type 2 in three families;Annals of Clinical and Translational Neurology;2023-01-09

2. Advances in Clinical Features and Pathogenesis of Pelizaeus-Merzbacher Disease;PROG BIOCHEM BIOPHYS;2022

3. Genotype–phenotype correlation and natural history analyses in a Chinese cohort with pelizaeus–merzbacher disease;Orphanet Journal of Rare Diseases;2022-03-28

4. Proteolipid protein modulates preservation of peripheral axons and premature death when myelin protein zero is lacking;Glia;2015-09-22

5. Epidemiological, clinical, and genetic landscapes of hypomyelinating leukodystrophies;Journal of Neurology;2014-02-16