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

Intersection of mitochondrial dysfunction and myelination: An overlooked aspect in neurodevelopmental disorders

线粒体功能障碍与髓鞘形成之间的交集:神经发育障碍中一个被忽视的方面

Sade, Ariel Nir; Wiener, Gal; Barak, Boaz

Early-Age Cuprizone Exposure Induces Region-Specific Demyelination and Neuroinflammation in Mice.

幼年时期接触铜嗪可诱导小鼠出现区域特异性脱髓鞘和神经炎症。

Rokach May, Levy Gilad, Elad-Sfadia Galit, Barak Boaz

Gtf2i-encoded transcription factor Tfii-i regulates myelination via Sox10 and Mbp regulatory elements.

Gtf2i 编码的转录因子 Tfii-i 通过 Sox10 和 Mbp 调控元件调节髓鞘形成。

Levy Gilad, Rokach May, Fischer Inbar, Kimchi-Feldhorn Omri, Shoob Shiri, Bar Ela, Rosenberg Tali, Bartman Joanna, Parnas Hadar, Grad Meitar, Israel-Elgali Ifat, Sfadia Galit E, Trangle Sari S, Vainshtein Anna, Eisenbach Yael Eshed, Jahn Olaf, Siems Sophie B, Werner Hauke B, Shomron Noam, Assaf Yaniv, Peles Elior, Slutsky Inna, Marco Asaf, Barak Boaz

Long-Term Excessive Alcohol Consumption Enhances Myelination in the Mouse Nucleus Accumbens.

长期过量饮酒会增强小鼠伏隔核的髓鞘形成

Liran Mirit, Fischer Inbar, Elboim May, Rahamim Nofar, Gordon Tamar, Urshansky Nataly, Assaf Yaniv, Barak Boaz, Barak Segev

Remote inspection of adversary-controlled environments

对敌方控制环境进行远程检查

Tobisch, Johannes; Philippe, Sébastien; Barak, Boaz; Kaplun, Gal; Zenger, Christian; Glaser, Alexander; Paar, Christof; Rührmair, Ulrich

Postnatal therapeutic approaches in genetic neurodevelopmental disorders

遗传性神经发育障碍的产后治疗方法

Levy, Gilad; Barak, Boaz

MyelTracer: A Semi-Automated Software for Myelin g-Ratio Quantification

MyelTracer:一种用于髓鞘g比率定量分析的半自动软件

Kaiser, Tobias; Allen, Harrison Mitchell; Kwon, Ohyoon; Barak, Boaz; Wang, Jing; He, Zhigang; Jiang, Minqing; Feng, Guoping

Systematic comparison of single-cell and single-nucleus RNA-sequencing methods

单细胞和单核RNA测序方法的系统比较

Ding, Jiarui; Adiconis, Xian; Simmons, Sean K; Kowalczyk, Monika S; Hession, Cynthia C; Marjanovic, Nemanja D; Hughes, Travis K; Wadsworth, Marc H; Burks, Tyler; Nguyen, Lan T; Kwon, John Y H; Barak, Boaz; Ge, William; Kedaigle, Amanda J; Carroll, Shaina; Li, Shuqiang; Hacohen, Nir; Rozenblatt-Rosen, Orit; Shalek, Alex K; Villani, Alexandra-Chloé; Regev, Aviv; Levin, Joshua Z

Shank3 mutation in a mouse model of autism leads to changes in the S-nitroso-proteome and affects key proteins involved in vesicle release and synaptic function

在自闭症小鼠模型中,Shank3基因突变导致S-亚硝基蛋白质组发生改变,并影响参与囊泡释放和突触功能的关键蛋白。

Amal, Haitham; Barak, Boaz; Bhat, Vadiraja; Gong, Guanyu; Joughin, Brian A; Wang, Xin; Wishnok, John S; Feng, Guoping; Tannenbaum, Steven R

Neurobiology of social behavior abnormalities in autism and Williams syndrome

自闭症和威廉姆斯综合征社交行为异常的神经生物学

Barak, Boaz; Feng, Guoping