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

Rescue of neuropsychiatric phenotypes in a mouse model of 16p11.2 duplication syndrome by genetic correction of an epilepsy network hub

通过对癫痫网络中心进行基因校正来挽救 16p11.2 重复综合征小鼠模型中的神经精神表型

Marc P Forrest, Marc Dos Santos, Nicolas H Piguel, Yi-Zhi Wang, Nicole A Hawkins, Vikram A Bagchi, Leonardo E Dionisio, Sehyoun Yoon, Dina Simkin, Maria Dolores Martin-de-Saavedra, Ruoqi Gao, Katherine E Horan, Alfred L George Jr, Mark S LeDoux, Jennifer A Kearney, Jeffrey N Savas, Peter Penzes

Behavioral and molecular effects of Ubtf knockout and knockdown in mice

Ubtf 敲除和敲低对小鼠的行为和分子影响

Roderick T Hori, Mohammad Moshahid Khan, Jianfeng Xiao, Phillip W Hargrove, Tom Moss, Mark S LeDoux

The Importance of Emotional Regulation in Mental Health

情绪调节在心理健康中的重要性

Menefee, Deleene S; Ledoux, Tracey; Johnston, Craig A

Ribosomal DNA promoter recognition is determined in vivo by cooperation between UBTF1 and SL1 and is compromised in the UBTF-E210K neuroregression syndrome

核糖体 DNA 启动子识别在体内由 UBTF1 和 SL1 之间的合作决定,并且在 UBTF-E210K 神经退化综合征中受到损害

Michel G Tremblay, Dany S Sibai, Melissa Valère, Jean-Clément Mars, Frédéric Lessard, Roderick T Hori, Mohammad Moshahid Khan, Victor Y Stefanovsky, Mark S LeDoux, Tom Moss

Presynaptic PRRT2 Deficiency Causes Cerebellar Dysfunction and Paroxysmal Kinesigenic Dyskinesia

突触前 PRRT2 缺陷导致小脑功能障碍和阵发性运动源性运动障碍

Dylan J Calame, Jianfeng Xiao, Mohammad Moshahid Khan, T J Hollingsworth, Yi Xue, Abigail L Person, Mark S LeDoux

Lobular architecture of human adipose tissue defines the niche and fate of progenitor cells

人类脂肪组织的小叶结构决定了祖细胞的生态位和命运

D Estève, N Boulet, C Belles, A Zakaroff-Girard, P Decaunes, A Briot, Y Veeranagouda, M Didier, A Remaury, J C Guillemot, S Ledoux, C Dani, A Bouloumié, J Galitzky

Gnal haploinsufficiency causes genomic instability and increased sensitivity to haloperidol

Gnal 单倍体不足导致基因组不稳定,增加对氟哌啶醇的敏感性

Mohammad Moshahid Khan, Jianfeng Xiao, T J Hollingsworth, Damini Patel, Dana E Selley, Trevor L Ring, Mark S LeDoux

DNA damage and neurodegenerative phenotypes in aged Ciz1 null mice

老年 Ciz1 基因缺失小鼠的 DNA 损伤和神经退行性表型

Mohammad Moshahid Khan, Jianfeng Xiao, Damini Patel, Mark S LeDoux

Consequences of Cre-mediated deletion of Ciz1 exon 5 in mice

Cre 介导的 Ciz1 外显子 5 缺失对小鼠的影响

Jianfeng Xiao, Mohammad Moshahid Khan, Satya Vemula, Jun Tian, Mark S LeDoux

Whole-exome sequencing for variant discovery in blepharospasm

全外显子组测序用于发现眼睑痉挛的变异

Jun Tian, Satya R Vemula, Jianfeng Xiao, Enza Maria Valente, Giovanni Defazio, Simona Petrucci, Angelo Fabio Gigante, Monika Rudzińska-Bar, Zbigniew K Wszolek, Kathleen D Kennelly, Ryan J Uitti, Jay A van Gerpen, Peter Hedera, Elizabeth J Trimble, Mark S LeDoux