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

A ciliopathy combining Joubert syndrome and Oro-Facial-Digital syndrome caused by bi-allelic 5'-UTR loss-of-function CEP83 variant

由双等位基因 5'-UTR 功能丧失的 CEP83 变异引起的纤毛病,同时伴有 Joubert 综合征和口面指综合征。

Matan M Jean ,Anan Yunis ,Tzofit Elbaz-Biton ,Vadim Dolgin ,Ginat Narkis ,Analia Michaelovsky ,Marina Eskin-Schwartz ,Alexandra A Tsitrina ,Nadav Agam ,Tomer Poleg ,Amit Safran ,Ofek Freund ,Noam Hadar ,Dan Levy ,Ilan Shelef ,Khalil El Amour ,Hagit Flusser ,Ohad S Birk

SMARCA4 mutation causes human otosclerosis and a similar phenotype in mice

SMARCA4基因突变会导致人类耳硬化症,并在小鼠中产生类似的表型。

Max Drabkin,Matan M Jean,Yael Noy,Daniel Halperin,Yuval Yogev,Ohad Wormser,Regina Proskorovski-Ohayon,Vadim Dolgin,Noam Levaot,Vlad Brumfeld,Shira Ovadia,Mor Kishner,Udi Kazenell,Karen B Avraham,Ilan Shelef,Ohad S Birk

Circulating isomiRs May Be Superior Biomarkers Compared to Their Corresponding miRNAs: A Pilot Biomarker Study of Using isomiR-Ome to Detect Coronary Calcium-Based Cardiovascular Risk in Patients with NAFLD

循环 isomiR 可能比其对应的 miRNA 更具有优势:一项利用 isomiR-Ome 检测 NAFLD 患者冠状动脉钙化心血管风险的试点生物标志物研究

Nataly Makarenkov, Uri Yoel, Yulia Haim, Yair Pincu, Nikhil S Bhandarkar, Aryeh Shalev, Ilan Shelef, Idit F Liberty, Gal Ben-Arie, David Yardeni, Assaf Rudich, Ohad Etzion, Isana Veksler-Lublinsky

Limb girdle muscular disease caused by HMGCR mutation and statin myopathy treatable with mevalonolactone

由 HMGCR 突变引起的肢带肌疾病和他汀类肌病可用甲瓦龙内酯治疗

Yuval Yogev, Zamir Shorer, Arie Koifman, Ohad Wormser, Max Drabkin, Daniel Halperin, Vadim Dolgin, Regina Proskorovski-Ohayon, Noam Hadar, Geula Davidov, Hila Nudelman, Raz Zarivach, Ilan Shelef, Yonatan Perez, Ohad S Birk

Slow blood-to-brain transport underlies enduring barrier dysfunction in American football players

血脑运输缓慢是美式足球运动员长期屏障功能障碍的根本原因

Ronel Veksler, Udi Vazana, Yonatan Serlin, Ofer Prager, Jonathan Ofer, Nofar Shemen, Andrew M Fisher, Olga Minaeva, Ning Hua, Rotem Saar-Ashkenazy, Itay Benou, Tammy Riklin-Raviv, Ellen Parker, Griffin Mumby, Lyna Kamintsky, Steven Beyea, Chris V Bowen, Ilan Shelef, Eoin O'Keeffe, Matthew Campbell, 

Paroxysmal slow cortical activity in Alzheimer's disease and epilepsy is associated with blood-brain barrier dysfunction

阿尔茨海默病和癫痫中的阵发性皮质活动缓慢与血脑屏障功能障碍有关

Dan Z Milikovsky, Jonathan Ofer, Vladimir V Senatorov Jr, Aaron R Friedman, Ofer Prager, Liron Sheintuch, Netta Elazari, Ronel Veksler, Daniel Zelig, Itai Weissberg, Guy Bar-Klein, Evyatar Swissa, Erez Hanael, Gal Ben-Arie, Osnat Schefenbauer, Lyna Kamintsky, Rotem Saar-Ashkenazy, Ilan Shelef, Merav

Mutations in the microtubule-associated protein MAP11 (C7orf43) cause microcephaly in humans and zebrafish

微管相关蛋白 MAP11(C7orf43)突变导致人类和斑马鱼出现小头畸形

Yonatan Perez, Reut Bar-Yaacov, Rotem Kadir, Ohad Wormser, Ilan Shelef, Ohad S Birk, Hagit Flusser, Ramon Y Birnbaum

Effector-Invariant Movement Encoding in the Human Motor System

人类运动系统中效应器不变的运动编码

Haar, Shlomi; Dinstein, Ilan; Shelef, Ilan; Donchin, Opher

Interleukin-1β regulates fat-liver crosstalk in obesity by auto-paracrine modulation of adipose tissue inflammation and expandability

白细胞介素-1β通过自身旁分泌调节脂肪组织炎症和扩张性来调节肥胖中的脂肪肝串扰

Ori Nov, Hagit Shapiro, Hilla Ovadia, Tanya Tarnovscki, Irit Dvir, Elad Shemesh, Julia Kovsan, Ilan Shelef, Yaron Carmi, Elena Voronov, Ron N Apte, Eli Lewis, Yulia Haim, Daniel Konrad, Nava Bashan, Assaf Rudich