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

Syntaxin 3B Mediates Light-Dependent Interactions with STXBP1 and Arrestin 4: Distinct Roles in Rods and Cones

Syntaxin 3B 介导与 STXBP1 和 Arrestin 4 的光依赖性相互作用:在视杆细胞和视锥细胞中发挥不同的作用

Tebbe, Lars; Ikelle, Larissa; Makia, Mustafa S; Kakakhel, Mashal; Al-Ubaidi, Muayyad R; Naash, Muna I

Developmental riboflavin deficiency results in structural and functional changes in the neural retina and RPE.

发育过程中核黄素缺乏会导致神经视网膜和视网膜色素上皮的结构和功能发生变化

Zhao Xue, Makia Mustafa S, Naash Muna I, Al-Ubaidi Muayyad R

Sexual dysfunction among patients with type-2 diabetes mellitus attending diabetes clinics in primary healthcare centers in Bahrain-A cross-sectional study

巴林基层医疗中心糖尿病门诊就诊的2型糖尿病患者性功能障碍的横断面研究

Al Ubaidi, Basem Abbas A; Alawainati, Mahmood; Ali, Mohamed Shaikh; Alhalwaji, Mohamed; Mahdi, A Rasool; Husain, Hasan A; Al Matooq, Ahmed M

Author Correction: Downregulation of rhodopsin is an effective therapeutic strategy in ameliorating peripherin-2-associated inherited retinal disorders

作者更正:下调视紫红质是改善外周蛋白-2相关遗传性视网膜疾病的有效治疗策略。

Rutan Woods, Christian T; Makia, Mustafa S; Lewis, Tylor R; Crane, Ryan; Zeibak, Stephanie; Yu, Paul; Kakakhel, Mashal; Castillo, Carson M; Arshavsky, Vadim Y; Naash, Muna I; Al-Ubaidi, Muayyad R

Downregulation of rhodopsin is an effective therapeutic strategy in ameliorating peripherin-2-associated inherited retinal disorders

视紫红质下调是改善周围蛋白-2相关遗传性视网膜疾病的有效治疗策略

Christian T Rutan Woods, Mustafa S Makia, Tylor R Lewis, Ryan Crane, Stephanie Zeibak, Paul Yu, Mashal Kakakhel, Carson M Castillo, Vadim Y Arshavsky, Muna I Naash, Muayyad R Al-Ubaidi

Effective intravitreal gene delivery to retinal pigment epithelium with hyaluronic acid nanospheres

利用透明质酸纳米球有效地将基因传递到玻璃体内视网膜色素上皮

Ryan Crane, Mustafa S Makia, Stephanie Zeibak, Lars Tebbe, Larissa Ikele, Christian Rutan Woods, Shannon M Conley, Ghanashyam Acharya, Muna I Naash, Muayyad R Al-Ubaidi

The role of syntaxins in retinal function and health

突触蛋白在视网膜功能和健康中的作用

Tebbe, Lars; Kakakhel, Mashal; Al-Ubaidi, Muayyad R; Naash, Muna I

The usherin mutation c.2299delG leads to its mislocalization and disrupts interactions with whirlin and VLGR1

usherin 突变 c.2299delG 导致其错误定位并破坏与 whirlin 和 VLGR1 的相互作用

Lars Tebbe #, Maggie L Mwoyosvi #, Ryan Crane, Mustafa S Makia, Mashal Kakakhel, Dominic Cosgrove, Muayyad R Al-Ubaidi, Muna I Naash

Correction: Comparative study of PRPH2 D2 loop mutants reveals divergent disease mechanism in rods and cones

更正:PRPH2 D2环突变体的比较研究揭示了视杆细胞和视锥细胞中不同的疾病机制

Ikelle, Larissa; Makia, Mustafa; Lewis, Tylor; Crane, Ryan; Kakakhel, Mashal; Conley, Shannon M; Birtley, James R; Arshavsky, Vadim Y; Al-Ubaidi, Muayyad R; Naash, Muna I

Comparative study of PRPH2 D2 loop mutants reveals divergent disease mechanism in rods and cones

PRPH2 D2 环路突变体的比较研究揭示了视杆细胞和视锥细胞中不同的疾病机制

Larissa Ikelle #, Mustafa Makia #, Tylor Lewis, Ryan Crane, Mashal Kakakhel, Shannon M Conley, James R Birtley, Vadim Y Arshavsky, Muayyad R Al-Ubaidi, Muna I Naash