Infantile Neuroaxonal Dystrophy: Diagnosis and Possible Treatments-Reference-Cited by-同舟云学术

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Infantile Neuroaxonal Dystrophy: Diagnosis and Possible Treatments

Published:2018-12-10 Issue: Volume:9 Page:
ISSN:1664-8021
Container-title:Frontiers in Genetics
language:
Short-container-title:Front. Genet.

Author:

Babin Patricia L.,Rao Sudheendra N. R.,Chacko Anita,Alvina Fidelia B.,Panwala Anil,Panwala Leena,Fumagalli Danielle C.

Publisher

Frontiers Media SA

Subject

Genetics(clinical),Genetics,Molecular Medicine

Reference37 articles.

1. Inhibition of calcium-independent phospholipase A2 prevents arachidonic acid incorporation and phospholipid remodeling in P388D1 macrophages.;Balsinde;Proc. Natl. Acad. Sci. U.S.A.,1995

2. Neuroaxonal dystrophy in calcium-independent phospholipase A2beta deficiency results from insufficient remodeling and degeneration of mitochondrial and presynaptic membranes.;Beck;J. Neurosci.,2011

3. Efficient CNS targeting in adult mice by intrathecal infusion of single-stranded AAV9-GFP for gene therapy of neurological disorders.;Bey;Gene Ther.,2017

4. CRISPR-Cas9 for in vivo gene therapy: promise and hurdles.;Dai;Mol. Ther. Nucleic Acids,2016

5. Catalytic function of PLA2G6 is impaired by mutations associated with infantile neuroaxonal dystrophy but not dystonia-parkinsonism.;Engel;PLoS One,2010

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