首页> bioRxiv : the preprint server for biology> Mechanisms of USP7/MAGEL2 Complex Assembly and Its Mutational Disruption in Neurodevelopmental Diseases.

Mechanisms of USP7/MAGEL2 Complex Assembly and Its Mutational Disruption in Neurodevelopmental Diseases.

导出 LinkOut

翻译打印收藏纠错

第一作者： Emilie J,Korchak

第一单位： Department of Molecular Biology and Biophysics, UCONN Health, Farmington, CT 06032, USA.

作者： Emilie J,Korchak ^[1] ; Gabriella A,Soriano ^[1] ; Irina,Semenova ^[1] ; Bing,Hao ^[1] ; Denis,Štepihar ^[2] ; Tara,Bayat ^[2] ; Klementina Fon,Tacer ^[2] ; Irina,Bezsonova ^[1]

作者单位： Department of Molecular Biology and Biophysics, UCONN Health, Farmington, CT 06032, USA. ^[1] School of Veterinary Medicine, Texas Tech University, 7671 Evans Dr., Amarillo, TX 79106, USA.;Texas Center for Comparative Cancer Research (TC3R), 7671 Evans Dr., Amarillo, TX 79106, USA. ^[2]

关键词 Co-IP Hao-Fountain syndrome ITC MAGEL2 NMR Prader-Willi syndrome Schaaf-Yang syndrome TRIM27 USP7 WASH pathway X-ray crystallography de-ubiquitination neurodevelopmental disorders pathogenic variants patient mutations

DOI 10.64898/2026.04.24.720667

PMID 42094436

发布时间 2026-05-25

翻译满意度评价：

准确一般字义偏差语意偏离译文作用小提交

浏览0

bioRxiv

相似文献

中文期刊
外文期刊
学位论文
会议论文

浏览0

点击下载本期目录封面

检索历史清除

Mechanisms of USP7/MAGEL2 Complex Assembly and Its Mutational Disruption in Neurodevelopmental Diseases.

bioRxiv

相似文献

同项目论文

bioRxiv

相关期刊

参考文献：
指定格式：	NoteExpress EndNote RefWorks NoteFirst

检索历史 清除

Mechanisms of USP7/MAGEL2 Complex Assembly and Its Mutational Disruption in Neurodevelopmental Diseases.

bioRxiv

相似文献

同项目论文

bioRxiv

相关期刊

检索历史清除