Phosphatidylserine Ameliorates Neurodegenerative Symptoms and Enhances Axonal Transport in a Mouse Model of Familial Dysautonomia-Reference-Cited by-同舟云学术

Phosphatidylserine Ameliorates Neurodegenerative Symptoms and Enhances Axonal Transport in a Mouse Model of Familial Dysautonomia

Published:2016-12-20 Issue:12 Volume:12 Page:e1006486
ISSN:1553-7404
Container-title:PLOS Genetics
language:en
Short-container-title:PLoS Genet

Author:

Naftelberg Shiran,Abramovitch Ziv,Gluska Shani,Yannai Sivan,Joshi Yuvraj,Donyo Maya,Ben-Yaakov Keren,Gradus Tal,Zonszain Jonathan,Farhy Chen,Ashery-Padan Ruth,Perlson Eran,Ast Gil

Funder

Dysautonomia Foundation

Israel Science Foundation

Teva Pharmaceutical Industries

European Research Council

Publisher

Public Library of Science (PLoS)

Subject

Cancer Research,Genetics(clinical),Genetics,Molecular Biology,Ecology, Evolution, Behavior and Systematics

Reference99 articles.

1. Screening for familial dysautonomia in Israel: evidence for higher carrier rate among Polish Ashkenazi Jews;O Lehavi;Genet Test,2003

2. Survival in familial dysautonomia: Impact of early intervention;FB Axelrod;J Pediatr,2002

3. Central autonomic dysfunction with defective lacrimation; report of five cases;CM Riley;Pediatrics,1949

4. Clinical neurological aspects of familial dysautonomia;M Mahloudji;J Neurol Sci,1970

5. Current treatments in familial dysautonomia;JA Palma;Expert Opin Pharmacother,2014

Cited by 32 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. ELP1, the Gene Mutated in Familial Dysautonomia, Is Required for Normal Enteric Nervous System Development and Maintenance and for Gut Epithelium Homeostasis;The Journal of Neuroscience;2024-08-13

2. Elp1 function in placode-derived neurons is critical for proper trigeminal ganglion development;2024-07-16

3. Transcriptome analysis in a humanized mouse model of familial dysautonomia reveals tissue-specific gene expression disruption in the peripheral nervous system;Scientific Reports;2024-01-04

4. Transcriptome analysis in a humanized mouse model of familial dysautonomia reveals tissue-specific gene expression disruption in the peripheral nervous system;2023-09-29

5. Loss of the m6A methyltransferase METTL3 in monocyte-derived macrophages ameliorates Alzheimer’s disease pathology in mice;PLOS Biology;2023-03-07