Disruption of Src Is Associated with Phenotypes Related to Williams-Beuren Syndrome and Altered Cellular Localization of TFII-I-Reference-Cited by-同舟云学术

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Disruption of Src Is Associated with Phenotypes Related to Williams-Beuren Syndrome and Altered Cellular Localization of TFII-I

Published:2015-03 Issue:2 Volume:2 Page:ENEURO.0016-14.2015
ISSN:2373-2822
Container-title:eneuro
language:en
Short-container-title:eneuro

Author:

Sinai Laleh,Ivakine Evgueni A.,Lam Emily,Deurloo Marielle,Dida Joana,Zirngibl Ralph A.,Jung Cynthia,Aubin Jane E.^ORCID,Feng Zhong-Ping,Yeomans John,Roderick R. McInnes,Osborne Lucy R.^ORCID,Roder John C.

Publisher

Society for Neuroscience

Subject

General Medicine,General Neuroscience

Cited by 9 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. Neutralizing peripheral circulating IL1β slows the progression of ALS in a lentivirus‐infected OPTN ^E478G mouse model;Animal Models and Experimental Medicine;2022-12-27

2. Functions of Gtf2i and Gtf2ird1 in the developing brain: transcription, DNA binding and long-term behavioral consequences;Human Molecular Genetics;2020-04-21

3. Functions of Gtf2i and Gtf2ird1 in the developing brain: transcription, DNA-binding, and long term behavioral consequences;2019-11-25

4. ALS-Associated E478G Mutation in Human OPTN (Optineurin) Promotes Inflammation and Induces Neuronal Cell Death;Frontiers in Immunology;2018-11-14

5. The contribution of GTF2I haploinsufficiency to Williams syndrome;Molecular and Cellular Probes;2018-08

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