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

AAV gene therapy rescues hearing and balance in a model of CLIC5 deafness.

AAV基因疗法在CLIC5耳聋模型中恢复了听力和平衡能力。

Hahn Roni, Taiber Shahar, Shubina-Oleinik Olga, Géléoc Gwenaëlle S G, Holt Jeffrey R, Avraham Karen B

A sound vision: MYO7A gene therapy reaches the inner ear

清晰的愿景:MYO7A基因疗法抵达内耳

Taiber, Shahar; Avraham, Karen B

The dynamics of stomatal closure of Arabidopsis thaliana determined by terahertz spectroscopy and a water transport model

利用太赫兹光谱和水传输模型测定拟南芥气孔关闭的动态过程

Taiber, Jochen; Helminiak, Jan; Hernandez-Cardoso, Goretti G; Mach, Cornelius; Jäckel, Alexander; Naranjo-Montoya, Oscar A; Castro-Camus, Enrique; Ache, Peter; Hedrich, Rainer; Koch, Martin

Precise alternating cellular pattern in the inner ear by coordinated hopping intercalations and delaminations.

内耳中通过协调的跳跃式插入和分离形成精确的交替细胞模式。

Cohen Roie, Taiber Shahar, Loza Olga, Kasirer Shahar, Woland Shiran, Sprinzak David

Bats experience age-related hearing loss (presbycusis)

蝙蝠会经历与年龄相关的听力丧失(老年性耳聋)。

Tarnovsky, Yifat Chaya; Taiber, Shahar; Nissan, Yomiran; Boonman, Arjan; Assaf, Yaniv; Wilkinson, Gerald S; Avraham, Karen B; Yovel, Yossi

The Genomics of Auditory Function and Disease

听觉功能和疾病的基因组学

Taiber, Shahar; Gwilliam, Kathleen; Hertzano, Ronna; Avraham, Karen B

A Nesprin-4/kinesin-1 cargo model for nuclear positioning in cochlear outer hair cells

Nesprin-4/kinesin-1 货物模型用于耳蜗外毛细胞的核定位

Shahar Taiber, Oren Gozlan, Roie Cohen, Leonardo R Andrade, Ellen F Gregory, Daniel A Starr, Yehu Moran, Rebecca Hipp, Matthew W Kelley, Uri Manor, David Sprinzak, Karen B Avraham

Neonatal AAV gene therapy rescues hearing in a mouse model of SYNE4 deafness

新生儿 AAV 基因治疗挽救了 SYNE4 耳聋小鼠模型的听力

Shahar Taiber, Roie Cohen, Ofer Yizhar-Barnea, David Sprinzak, Jeffrey R Holt, Karen B Avraham

Broadband wide-angle terahertz antenna based on the application of transformation optics to a Luneburg lens

基于变换光学原理的吕讷堡透镜宽带广角太赫兹天线

Amarasinghe, Yasith; Mendis, Rajind; Shrestha, Rabi; Guerboukha, Hichem; Taiber, Jochen; Koch, Martin; Mittleman, Daniel M

Homozygote loss-of-function variants in the human COCH gene underlie hearing loss

人类 COCH 基因的纯合功能丧失变异是听力损失的根本原因

Nada Danial-Farran, Elena Chervinsky, Prathamesh T Nadar-Ponniah, Eran Cohen Barak, Shahar Taiber, Morad Khayat, Karen B Avraham, Stavit A Shalev