Mutations of CNTNAP1 led to defects in neuronal development-Reference-Cited by-同舟云学术

Mutations of CNTNAP1 led to defects in neuronal development

Published:2020-11-05 Issue:21 Volume:5 Page:
ISSN:2379-3708
Container-title:JCI Insight
language:en
Short-container-title:

Author:

Li Wanxing^ORCID,Yang Lin,Tang Chuanqing,Liu Kaiyi,Lu Yulan^ORCID,Wang Huijun^ORCID,Yan Kai,Qiu Zilong,Zhou Wenhao

Funder

the National Key Research and Development Program of China

Foundation of Shanghai Municipal Commission of Health and Family Planning

Shanghai Shen Kang Hospital Development Center

National Natural Science Foundation of China

Shanghai Brain-Intelligence Project from STCSM

Strategic Priority Research Program of the Chinese Academy of Sciences

Program of Shanghai Academic Research Leader, the Open Large Infrastructure Research of Chinese Academy of Sciences, and the Shanghai Municipal Science and Technology Major Project

Publisher

American Society for Clinical Investigation

Subject

General Medicine

Link

https://insight.jci.org/articles/view/135697/files/pdf

Reference48 articles.

1. Neurexin IV, caspr and paranodin—novel members of the neurexin family: encounters of axons and glia

2. Axon-Glia Interactions and the Domain Organization of Myelinated Axons Requires Neurexin IV/Caspr/Paranodin

3. Juxtaparanodal clustering of Shaker-like K+ channels in myelinated axons depends on Caspr2 and TAG-1

4. Organization of Myelinated Axons by Caspr and Caspr2 Requires the Cytoskeletal Adapter Protein 4.1B

5. Organization and maintenance of molecular domains in myelinated axons

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