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

A xenotransplantation model for reactivation of paternal UBE3A using human-specific antisense oligonucleotides

利用人源特异性反义寡核苷酸激活父系UBE3A的异种移植模型

期刊:Scientific Reports
影响因子:3.9
doi:10.1038/s41598-026-41197-9
Smeenk, Hilde; Lendemeijer, Bas; Buurma, Mirle G; Forgione, Michell A; Slump, Denise E; Monshouwer, Roos A; Wallaard, Ilse; Mientjes, Edwin J; Hoogendijk, Witte J G; Elgersma, Ype; de Vrij, Femke M S; Kushner, Steven A
UBE3A
发表日期：2026
文献求助 收藏

Magnetoconductance Oscillations in Topological Crystalline Insulator Nanowires

拓扑晶体绝缘体纳米线中的磁导振荡

期刊:Nano Letters
影响因子:9.1
doi:10.1021/acs.nanolett.5c02643
van de Sande, Vince; Mientjes, Mathijs G C; Witmans, Femke J; Hulsen, Tim; Guan, Xin; Hoskam, Max S M; Ridderbos, Joost; Verheijen, Marcel A; Zwanenburg, Floris A; Brinkman, Alexander; Nichele, Fabrizio; Bakkers, Erik P A M
发表日期：2025
文献求助 收藏

UBE3A reinstatement restores behaviorand proteome in an Angelman syndrome mouse model of imprinting defects.

UBE3A 的恢复可以恢复 Angelman 综合征小鼠模型（印记缺陷）的行为和蛋白质组

期刊:Molecular Autism
影响因子:5.5
doi:10.1186/s13229-025-00675-z
Milazzo Claudia, Narayanan Ramanathan, Badillo Solveig, Wang Silvia, Almand Rosaisela, Monshouwer Roos, Tzouros Manuel, Golling Sabrina, Mientjes Edwin, Chamberlain Stormy, Kremer Thomas, Elgersma Ype
免疫/内分泌
Mouse
发表日期：2025
文献求助 收藏

Alignment of port policy to the context of the Physical Internet

端口策略与物理互联网环境的一致性

期刊:
影响因子:
doi:10.1080/03088839.2022.2147594
Fahim, Patrick B M; Mientjes, Gerjan; Rezaei, Jafar; van Binsbergen, Arjan; Montreuil, Benoit; Tavasszy, Lorant
发表日期：2024
文献求助 收藏

A loss of function variant in AGPAT3 underlies intellectual disability and retinitis pigmentosa (IDRP) syndrome

AGPAT3基因功能缺失变异是智力障碍和视网膜色素变性（IDRP）综合征的病因。

期刊:European Journal of Human Genetics
影响因子:4.6
doi:10.1038/s41431-023-01475-w
Malik, Madiha Amin; Saqib, Muhammad Arif Nadeem; Mientjes, Edwin; Acharya, Anushree; Alam, Muhammad Rizwan; Wallaard, Ilse; Schrauwen, Isabelle; Bamshad, Michael J; Santos-Cortez, Regie Lyn P; Elgersma, Ype; Leal, Suzanne M; Ansar, Muhammad
发表日期：2023
文献求助 收藏

A cross-species spatiotemporal proteomic analysis identifies UBE3A-dependent signaling pathways and targets

跨物种时空蛋白质组学分析确定了 UBE3A 依赖的信号通路和靶点

期刊:Molecular Psychiatry
影响因子:9.6
doi:10.1038/s41380-022-01484-z
Nikhil J Pandya #, Sonja Meier #, Stefka Tyanova #, Marco Terrigno, Congwei Wang, A Mattijs Punt, E J Mientjes, Audrey Vautheny, Ben Distel, Thomas Kremer, Ype Elgersma, Ravi Jagasia
信号转导
ELISA
发表日期：2022
文献求助 收藏

Secreted retrovirus-like GAG-domain-containing protein PEG10 is regulated by UBE3A and is involved in Angelman syndrome pathophysiology

分泌型逆转录病毒样GAG结构域蛋白PEG10受UBE3A调控，并参与Angelman综合征的病理生理过程。

期刊:Cell Reports Medicine
影响因子:11.7
doi:10.1016/j.xcrm.2021.100360
Nikhil J Pandya ,Congwei Wang ,Veronica Costa ,Paul Lopatta ,Sonja Meier ,F Isabella Zampeta ,A Mattijs Punt ,Edwin Mientjes ,Philip Grossen ,Tania Distler ,Manuel Tzouros ,Yasmina Martí ,Balazs Banfai ,Christoph Patsch ,Soren Rasmussen ,Marius Hoener ,Marco Berrera ,Thomas Kremer ,Tom Dunkley ,Martin Ebeling ,Ben Distel ,Ype Elgersma ,Ravi Jagasia
UBE3A
微生物学
信号转导
发表日期：2021
文献求助 收藏

Antisense oligonucleotide treatment rescues UBE3A expression and multiple phenotypes of an Angelman syndrome mouse model

反义寡核苷酸治疗可挽救Angelman综合征小鼠模型中的UBE3A表达和多种表型

期刊:JCI Insight
影响因子:6.1
doi:10.1172/jci.insight.145991
Milazzo, Claudia; Mientjes, Edwin J; Wallaard, Ilse; Rasmussen, Søren Vestergaard; Erichsen, Kamille Dumong; Kakunuri, Tejaswini; van der Sman, A S Elise; Kremer, Thomas; Miller, Meghan T; Hoener, Marius C; Elgersma, Ype
UBE3A
发表日期：2021
文献求助 收藏

Assessing the requirements of prenatal UBE3A expression for rescue of behavioral phenotypes in a mouse model for Angelman syndrome

评估产前 UBE3A 表达对挽救 Angelman 综合征小鼠模型中行为表型的要求

期刊:Molecular Autism
影响因子:6.3
doi:10.1186/s13229-020-00376-9
Monica Sonzogni, Peipei Zhai, Edwin J Mientjes, Geeske M van Woerden, Ype Elgersma
ACTC
发表日期：2020
文献求助 收藏

Loss of nuclear UBE3A causes electrophysiological and behavioral deficits in mice and is associated with Angelman syndrome

核 UBE3A 缺失导致小鼠电生理和行为缺陷，并与 Angelman 综合征有关

期刊:Nature Neuroscience
影响因子:21.2
doi:10.1038/s41593-019-0425-0
Rossella Avagliano Trezza #, Monica Sonzogni #, Stijn N V Bossuyt #, F Isabella Zampeta, A Mattijs Punt, Marlene van den Berg, Diana C Rotaru, Linda M C Koene, Shashini T Munshi, Jeffrey Stedehouder, Johan M Kros, Mark Williams, Helen Heussler, Femke M S de Vrij, Edwin J Mientjes, Geeske M van Woerd
信号转导
发表日期：2019
文献求助 收藏