Hypersensitivity to type I interferon as a cause of hydrocephalus development-Reference-Cited by-同舟云学术

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Hypersensitivity to type I interferon as a cause of hydrocephalus development

Published:2024-10 Issue: Volume:1840 Page:149082
ISSN:0006-8993
Container-title:Brain Research
language:en
Short-container-title:Brain Research

Author:

Arimoto Kei-ichiro,Zhang Yue^ORCID,Matsuura Shinobu^ORCID,Miyauchi Sayuri,Zhang Dong-Er

Funder

NIH

Publisher

Elsevier BV

Reference22 articles.

1. A mutation in Ccdc39 causes neonatal hydrocephalus with abnormal motile cilia development in mice;Abdelhamed;Development,2018

2. Hydrocephalus in weanling mice induced by a temperature-sensitive mutant of vesicular stomatitis virus;Ahdab-Barmada;J. Neuropathol. Exp. Neurol.,1982

3. JAK Inhibitor Therapy in a Child with Inherited USP18 Deficiency;Alsohime;N. Engl. J. Med.,2020

4. STAT2 is an essential adaptor in USP18-mediated suppression of type I interferon signaling;Arimoto;Nat. Struct. Mol. Biol.,2017

5. Expansion of interferon inducible gene pool via USP18 inhibition promotes cancer cell pyroptosis;Arimoto;Nat. Commun.,2023

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