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

Descemet membrane endothelial keratoplasty in eyes with COL8A2-associated corneal dystrophy

Descemet膜内皮角膜移植术治疗COL8A2相关性角膜营养不良

Dzhaber, Daliya; Fliotsos, Michael J; Abousy, Mya; Kancherla, Swarupa; Siadati, Sepideh; Eberhart, Charles G; Gottsch, John D; Eghrari, Allen O

Pluripotent stem cell-derived corneal endothelial cells as an alternative to donor corneal endothelium in keratoplasty

多能干细胞衍生的角膜内皮细胞作为角膜移植术中供体角膜内皮的替代品

Muhammad Ali, Shahid Y Khan, John D Gottsch, Eric K Hutchinson, Aisha Khan, S Amer Riazuddin

Cigarette Smoke Triggers Loss of Corneal Endothelial Cells and Disruption of Descemet's Membrane Proteins in Mice

香烟烟雾导致小鼠角膜内皮细胞损失和 Descemet 膜蛋白破坏

Muhammad Ali, Shahid Y Khan, Yura Jang, Chan Hyun Na, C Conover Talbot Jr, John D Gottsch, James T Handa, S Amer Riazuddin

Attention control group activities and perceived benefit in a trial of a behavioral intervention for older adults

老年人行为干预试验中,注意力控制组的活动和感知获益

LaFave, Sarah E; Granbom, Marianne; Cudjoe, Thomas K M; Gottsch, Alex; Shorb, Gerard; Szanton, Sarah L

Monoclonal gammopathy of "ocular" significance

具有“眼部”意义的单克隆丙种球蛋白病

Karakus, Sezen; Gottsch, John D; Caturegli, Patrizio; Eghrari, Allen O

Generation and Proteome Profiling of PBMC-Originated, iPSC-Derived Corneal Endothelial Cells

PBMC 来源、iPSC 衍生的角膜内皮细胞的生成和蛋白质组分析

Muhammad Ali, Shahid Y Khan, Shivakumar Vasanth, Mariya R Ahmed, Ruiqiang Chen, Chan Hyun Na, Jason J Thomson, Caihong Qiu, John D Gottsch, S Amer Riazuddin

Pilot Study of Audiometric Patterns in Fuchs Corneal Dystrophy

Fuchs角膜营养不良患者听力图模式的初步研究

Reed, Nicholas S; Deal, Jennifer A; Huddle, Matthew G; Betz, Joshua F; Bailey, Bethany E; McGlumphy, Elyse J; Eghrari, Allen O; Riazuddin, S Amer; Lin, Frank R; Gottsch, John D

Automated Retroillumination Photography Analysis for Objective Assessment of Fuchs Corneal Dystrophy

用于客观评估 Fuchs 角膜营养不良的自动逆光照明摄影分析

Eghrari, Allen O; Mumtaz, Aisha A; Garrett, Brian; Rezaei, Mahsa; Akhavan, Mina S; Riazuddin, S Amer; Gottsch, John D

FOXE3 contributes to Peters anomaly through transcriptional regulation of an autophagy-associated protein termed DNAJB1

FOXE3 通过转录调控一种名为 DNAJB1 的自噬相关蛋白,参与 Peters 异常的发生。

Shahid Y Khan ,Shivakumar Vasanth ,Firoz Kabir ,John D Gottsch ,Arif O Khan ,Raghothama Chaerkady ,Mei-Chong W Lee ,Carmen C Leitch ,Zhiwei Ma ,Julie Laux ,Rafael Villasmil ,Shaheen N Khan ,Sheikh Riazuddin ,Javed Akram ,Robert N Cole ,C Conover Talbot ,Nader Pourmand ,Norann A Zaghloul ,J Fielding Hejtmancik ,S Amer Riazuddin

Mutations in phosphodiesterase 6 identified in familial cases of retinitis pigmentosa

在家族性视网膜色素变性病例中发现磷酸二酯酶 6 的突变

Ullah, Inayat; Kabir, Firoz; Gottsch, Clare Brooks S; Naeem, Muhammad Asif; Guru, Aditya A; Ayyagari, Radha; Khan, Shaheen N; Riazuddin, Sheikh; Akram, Javed; Riazuddin, S Amer