日期:
2020 年 — 2026 年
2020
2021
2022
2023
2024
2025
2026
影响因子:

Genetic Analysis of Choroideremia-Related Rab Escort Proteins.

脉络膜萎缩症相关Rab护送蛋白的基因分析

Xing Zhuo, Wu Fuguo, Cortes-Gomez Eduardo, Pao Annie, Gao Lingqiu, Douglas Avrium, Li Yichen, Spernyak Joseph A, Wong G William, Singh Prashant K, Wang Jianmin, Liu Song, Thanavala Yasmin, MacDonald Ian M, Mu Xiuqian, Yu Y Eugene

Dissection of a Down syndrome-associated trisomy to separate the gene dosage-dependent and -independent effects of an extra chromosome

对唐氏综合征相关三体进行解剖,以区分额外染色体的基因剂量依赖性效应和非剂量依赖性效应

Xing, Zhuo; Li, Yichen; Cortes-Gomez, Eduardo; Jiang, Xiaoling; Gao, Shuang; Pao, Annie; Shan, Jidong; Song, Yinghui; Perez, Amanda; Yu, Tao; Highsmith, Max R; Boadu, Frimpong; Conroy, Jeffrey M; Singh, Prashant K; Bakin, Andrei V; Cheng, Jianlin; Duan, Zhijun; Wang, Jianmin; Liu, Song; Tycko, Benjamin; Yu, Y Eugene

Genetic and epigenetic pathways in Down syndrome: Insights to the brain and immune system from humans and mouse models

唐氏综合征的遗传和表观遗传通路:来自人类和小鼠模型的关于大脑和免疫系统的启示

Yu, Y Eugene; Xing, Zhuo; Do, Catherine; Pao, Annie; Lee, Eun Joon; Krinsky-McHale, Sharon; Silverman, Wayne; Schupf, Nicole; Tycko, Benjamin

Mouse-based genetic modeling and analysis of Down syndrome

基于小鼠的唐氏综合征遗传建模与分析

Xing, Zhuo; Li, Yichen; Pao, Annie; Bennett, Abigail S; Tycko, Benjamin; Mobley, William C; Yu, Y Eugene

Genetic dissection of the Down syndrome critical region

唐氏综合征关键区域的基因解析

Jiang, Xiaoling; Liu, Chunhong; Yu, Tao; Zhang, Li; Meng, Kai; Xing, Zhuo; Belichenko, Pavel V; Kleschevnikov, Alexander M; Pao, Annie; Peresie, Jennifer; Wie, Sarah; Mobley, William C; Yu, Y Eugene

Human chromosome 21 orthologous region on mouse chromosome 17 is a major determinant of Down syndrome-related developmental cognitive deficits

小鼠17号染色体上与人类21号染色体同源的区域是唐氏综合征相关发育认知缺陷的主要决定因素。

Zhang, Li; Meng, Kai; Jiang, Xiaoling; Liu, Chunhong; Pao, Annie; Belichenko, Pavel V; Kleschevnikov, Alexander M; Josselyn, Sheena; Liang, Ping; Ye, Ping; Mobley, William C; Yu, Y Eugene

Genetic analysis of Down syndrome facilitated by mouse chromosome engineering

利用小鼠染色体工程技术进行唐氏综合征的遗传分析

Zhang, Li; Fu, Dawei; Belichenko, Pavel V; Liu, Chunhong; Kleschevnikov, Alexander M; Pao, Annie; Liang, Ping; Clapcote, Steven J; Mobley, William C; Yu, Y Eugene

Genetic analysis of Down syndrome-associated heart defects in mice

对小鼠唐氏综合征相关心脏缺陷的基因分析

Liu, Chunhong; Morishima, Masae; Yu, Tao; Matsui, Sei-Ichi; Zhang, Li; Fu, Dawei; Pao, Annie; Costa, Alberto C; Gardiner, Katheleen J; Cowell, John K; Nowak, Norma J; Parmacek, Michael S; Liang, Ping; Baldini, Antonio; Yu, Y Eugene

A mouse model of Down syndrome trisomic for all human chromosome 21 syntenic regions

一种唐氏综合征小鼠模型,其所有人类21号染色体同源区域均为三体。

Yu, Tao; Li, Zhongyou; Jia, Zhengping; Clapcote, Steven J; Liu, Chunhong; Li, Shaomin; Asrar, Suhail; Pao, Annie; Chen, Rongqing; Fan, Ni; Carattini-Rivera, Sandra; Bechard, Allison R; Spring, Shoshana; Henkelman, R Mark; Stoica, George; Matsui, Sei-Ichi; Nowak, Norma J; Roder, John C; Chen, Chu; Bradley, Allan; Yu, Y Eugene

Lgi1 null mutant mice exhibit myoclonic seizures and CA1 neuronal hyperexcitability

Lgi1基因敲除突变小鼠表现出肌阵挛性癫痫发作和CA1区神经元过度兴奋。

Yu, Y Eugene; Wen, Lei; Silva, Jeane; Li, Zhongyou; Head, Karen; Sossey-Alaoui, Khalid; Pao, Annie; Mei, Lin; Cowell, John K