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

Recreating pathophysiology of CLN2 disease and demonstrating reversion by TPP1 gene therapy in hiPSC-derived retinal organoids and retina-on-chip.

在hiPSC衍生的视网膜类器官和芯片视网膜中重现CLN2疾病的病理生理,并证明TPP1基因治疗可逆转该疾病

Corti Serena, Kim Kwi Hye, Chen Ting, Botezatu Adelina, Cora Virginia, Ma Ke, Pashkovskaia Natalia, Bernal Vergara Anamaria, Sperlich Denise, Dave Kaushambee, Tolone Arianna, Reddinger Ryan M, Tully Christopher B, Higgins Mikayla, Kleger Alexander, Breunig Markus, Lopatta Paul, Wingerter Svenja, Cipriano Madalena, Bolz Sylvia, Ueffing Marius, Buss Nicholas, Loskill Peter, Liebau Stefan, Achberger Kevin

Outer retina micro-inflammation is driven by T cell responses prior to retinal degeneration in early age-related macular degeneration

在早期年龄相关性黄斑变性中,视网膜变性之前,T细胞反应会驱动外层视网膜微炎症。

Stürzbecher, Lucas; Bartolomaeus, Hendrik; Bartolomaeus, Theda U P; Bolz, Sylvia; Sekulic, Andjela; Ueffing, Marius; Clark, Simon J; Reichhart, Nadine; Crespo-Garcia, Sergio; Wilck, Nicola; Strauß, Olaf

Ciliopathy-Associated Missense Mutations in IFT140 are Tolerated by the Inherent Resilience of the IFT Machinery.

IFT140 中与纤毛病相关的错义突变可通过 IFT 机制的固有弹性而被容忍

Beyer Tina, Diwan Gaurav D, Leonhard Tobias, Dahlke Katrin, Klose Franziska, Stehle Isabel F, Seda Marian, Bolz Sylvia, Woerz Franziska, Russell Robert B, Jenkins Dagan, Ueffing Marius, Boldt Karsten

Sustained Extracellular Electrical Stimulation Modulates the Permeability of Gap Junctions in rd1 Mouse Retina with Photoreceptor Degeneration

持续的细胞外电刺激调节rd1小鼠视网膜光感受器退化中缝隙连接的通透性

Stürmer, Sophie; Bolz, Sylvia; Zrenner, Eberhart; Ueffing, Marius; Haq, Wadood

Pharmacokinetics of Pullulan-Dexamethasone Conjugates in Retinal Drug Delivery

普鲁兰-地塞米松缀合物在视网膜药物递送中的药代动力学

Kicková, Eva; Sadeghi, Amir; Puranen, Jooseppi; Tavakoli, Shirin; Sen, Merve; Ranta, Veli-Pekka; Arango-Gonzalez, Blanca; Bolz, Sylvia; Ueffing, Marius; Salmaso, Stefano; Caliceti, Paolo; Toropainen, Elisa; Ruponen, Marika; Urtti, Arto

A nonsense mutation in PDE6H causes autosomal-recessive incomplete achromatopsia

PDE6H基因的无义突变会导致常染色体隐性遗传的不完全性色盲。

Kohl, Susanne; Coppieters, Frauke; Meire, Françoise; Schaich, Simone; Roosing, Susanne; Brennenstuhl, Christina; Bolz, Sylvia; van Genderen, Maria M; Riemslag, Frans C C; Lukowski, Robert; den Hollander, Anneke I; Cremers, Frans P M; De Baere, Elfride; Hoyng, Carel B; Wissinger, Bernd

Effects of combined ketamine/xylazine anesthesia on light induced retinal degeneration in rats

氯胺酮/赛拉嗪联合麻醉对大鼠光致视网膜变性的影响

Arango-Gonzalez, Blanca; Schatz, Andreas; Bolz, Sylvia; Eslava-Schmalbach, Javier; Willmann, Gabriel; Zhour, Ahmad; Zrenner, Eberhart; Fischer, M Dominik; Gekeler, Florian

Structural and functional protein network analyses predict novel signaling functions for rhodopsin

结构和功能蛋白质网络分析预测视紫红质具有新的信号传导功能

Kiel, Christina; Vogt, Andreas; Campagna, Anne; Chatr-aryamontri, Andrew; Swiatek-de Lange, Magdalena; Beer, Monika; Bolz, Sylvia; Mack, Andreas F; Kinkl, Norbert; Cesareni, Gianni; Serrano, Luis; Ueffing, Marius