Glial pathology in a novel spontaneous mutant mouse of the Eif2b5 gene: a vanishing white matter disease model-Reference-Cited by-同舟云学术

Glial pathology in a novel spontaneous mutant mouse of the Eif2b5 gene: a vanishing white matter disease model

Published:2019-10-28 Issue:1 Volume:154 Page:25-40
ISSN:0022-3042
Container-title:Journal of Neurochemistry
language:en
Short-container-title:J. Neurochem.

Author:

Terumitsu‐Tsujita Mika¹²³^ORCID,Kitaura Hiroki¹⁴,Miura Ikuo⁵,Kiyama Yuji²,Goto Fumiko²,Muraki Yoshiko¹,Ominato Shiho¹,Hara Norikazu⁶^ORCID,Simankova Anna⁷,Bizen Norihisa⁷,Kashiwagi Kazuhiro⁸^ORCID,Ito Takuhiro⁸^ORCID,Toyoshima Yasuko⁴,Kakita Akiyoshi⁴,Manabe Toshiya²,Wakana Shigeharu⁵,Takebayashi Hirohide⁷⁹^ORCID,Igarashi Hironaka¹

Affiliation:

1. Center for Integrated Human Brain Science Brain Research Institute Niigata University Niigata Japan

2. Division of Neuronal Network The Institute of Medical Science The University of Tokyo Tokyo Japan

3. Administrative Section of Radiation Protection National Center of Neurology and Psychiatry National Institute of Neuroscience Kodaira Tokyo Japan

4. Department of Pathology Brain Research Institute Niigata University Niigata Japan

5. Technology and Development Team for Mouse Phenotype Analysis The Japan Mouse Clinic RIKEN BioResource Research Center Ibaraki Japan

6. Department of Molecular Genetics Brain Research Institute Niigata University Niigata Japan

7. Division of Neurobiology and Anatomy Graduate School of Medical and Dental Sciences Niigata University Niigata Japan

8. Laboratory for Translation Structural Biology RIKEN Center for Biosystems Dynamics Research Tsurumi‐ku Yokohama Japan

9. Center for Coordination of Research Facilities Niigata University Niigata Japan

Funder

University of Tokyo

Publisher

Wiley

Subject

Cellular and Molecular Neuroscience,Biochemistry

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/jnc.14887

Reference56 articles.

1. Integrated stress response deregulation underlies vanishing white matter and is a target for therapy;Abbink T. E. M.;BioRxiv,2018

2. Not(ch) just development: Notch signalling in the adult brain

3. Gene Expression Regulation by Upstream Open Reading Frames and Human Disease

4. EIF2B5 mutations compromise GFAP+ astrocyte generation in vanishing white matter leukodystrophy

5. Astrocytes are central in the pathomechanisms of vanishing white matter

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