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

Impaired nucleocytoplasmic transport in SOD1-mediated ALS.

SOD1介导的ALS中核质转运受损。

Argueti-Ostrovsky Shirel, Lim Su Min, Arogundade Olubankole A, Diaz-Garcia Sandra, Yunisova Gulshan, Meng Alex, Hermann Anita, Ong Kailee, Eremenko Ekaterina, Bravo-Hernandez Mariana, Driscoll Shawn P, Lee Chao-Zong, Jiang Xin, Stavsky Alexandra, Barel Shir, Shani Tom, Kahn Joy, Pfaff Samuel L, Monsonego Alon, Marsala Martin, Ravits John, Lagier-Tourenne Clotilde, Israelson Adrian

Generating a Synthetic Lumbar CT from a Standard MRI Protocol

利用标准 MRI 方案生成合成腰椎 CT 图像

Shilo, Yehiel; Phillips, Frank M; Witham, Timothy F; Poelstra, Kornelis; Hodeda, Lital; Stavsky, Moshe

Do All Fractures in the Ankylotic Spine Really Require Surgical Intervention?

脊柱强直引起的所有骨折真的都需要手术治疗吗?

Stavsky, Moshe; Harats, Elad; Sharabati, Ahmad; Hamad, Amjad; Arzi, Harel; Qutteineh, Bilal; Barzilay, Yair

Synapsin E-domain is essential for α-synuclein function

突触蛋白E结构域对α-突触核蛋白的功能至关重要。

Stavsky, Alexandra; Parra-Rivas, Leonardo A; Tal, Shani; Riba, Jen; Madhivanan, Kayalvizhi; Roy, Subhojit; Gitler, Daniel

ASIC1a senses lactate uptake to regulate metabolism in neurons

ASIC1a感知乳酸摄取以调节神经元代谢

Ivana Savic Azoulay ,Xin Qi ,Maya Rozenfeld ,Fan Liu ,Qin Hu ,Tsipi Ben Kasus Nissim ,Alexandra Stavsky ,Michael X Zhu ,Tian-Le Xu ,Israel Sekler

Essential role of the mitochondrial Na+/Ca2+ exchanger NCLX in mediating PDE2-dependent neuronal survival and learning

线粒体 Na+/Ca2+ 交换器 NCLX 在介导 PDE2 依赖性神经元存活和学习中的重要作用

Maya Rozenfeld, Ivana Savic Azoulay, Tsipi Ben Kasus Nissim, Alexandra Stavsky, Moran Melamed, Grace Stutzmann, Michal Hershfinkel, Ora Kofman, Israel Sekler

Frequency- and spike-timing-dependent mitochondrial Ca(2+) signaling regulates the metabolic rate and synaptic efficacy in cortical neurons

频率和脉冲时间依赖性的线粒体Ca(2+)信号传导调节皮层神经元的代谢率和突触效能

Stoler, Ohad; Stavsky, Alexandra; Khrapunsky, Yana; Melamed, Israel; Stutzmann, Grace; Gitler, Daniel; Sekler, Israel; Fleidervish, Ilya

CDH2 mutation affecting N-cadherin function causes attention-deficit hyperactivity disorder in humans and mice

CDH2基因突变影响N-钙黏蛋白功能,导致人类和小鼠出现注意力缺陷多动障碍。

D Halperin #,A Stavsky #,R Kadir,M Drabkin,O Wormser,Y Yogev,V Dolgin,R Proskorovski-Ohayon,Y Perez,H Nudelman,O Stoler,B Rotblat,T Lifschytz,A Lotan,G Meiri,D Gitler,O S Birk

Aberrant activity of mitochondrial NCLX is linked to impaired synaptic transmission and is associated with mental retardation

线粒体 NCLX 的异常活动与突触传递受损有关,并与智力障碍有关

Alexandra Stavsky, Ohad Stoler, Marko Kostic, Tomer Katoshevsky, Essam A Assali, Ivana Savic, Yael Amitai, Holger Prokisch, Steffen Leiz, Cornelia Daumer-Haas, Ilya Fleidervish, Fabiana Perocchi, Daniel Gitler #, Israel Sekler #

Author Correction: Aberrant activity of mitochondrial NCLX is linked to impaired synaptic transmission and is associated with mental retardation

作者更正:线粒体NCLX的异常活性与突触传递受损有关,并与智力低下相关。

Stavsky, Alexandra; Stoler, Ohad; Kostic, Marko; Katoshevsky, Tomer; Assali, Essam A; Savic, Ivana; Amitai, Yael; Prokisch, Holger; Leiz, Steffen; Daumer-Haas, Cornelia; Fleidervish, Ilya; Perocchi, Fabiana; Gitler, Daniel; Sekler, Israel