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

A stable NTN1 fluorescent reporter chicken reveals cell specific molecular signatures during optic fissure closure.

稳定的 NTN1 荧光报告鸡揭示了视裂闭合过程中细胞特异性的分子特征

Ho Ching Chan Brian, Hardy Holly, Requena Teresa, Findlay Amy, Ioannidis Jason, Meunier Dominique, Toms Maria, Moosajee Mariya, Raper Anna, McGrew Mike J, Rainger Joe

A Novel De Novo Missense Variant in Netrin-1 (NTN1) Associated With Chorioretinal Coloboma, Sensorineural Hearing Loss and Polydactyly.

Netrin-1 (NTN1) 中的一种新的从头错义变异与脉络膜视网膜缺损、感觉神经性听力损失和多指畸形相关

Toms Maria, Heppell Cara, Owen Nicholas, Malka Samantha, Moosajee Mariya

Oxidative Stress, Inflammation and Altered Glucose Metabolism Contribute to the Retinal Phenotype in the Choroideremia Zebrafish

氧化应激、炎症和葡萄糖代谢改变共同导致了脉络膜萎缩斑马鱼的视网膜表型。

Méjécase, Cécile; Nair, Neelima; Sarkar, Hajrah; Soro-Barrio, Pablo; Toms, Maria; Halliday, Sophia; Linkens, Katy; Jaroszynska, Natalia; Maurer, Constance; Owen, Nicholas; Moosajee, Mariya

Nuclear Receptor Subfamily 2 Group E Member 3 (NR2E3): Role in Retinal Development and Disease

核受体亚家族2 E组成员3 (NR2E3):在视网膜发育和疾病中的作用

Toms, Maria; Ward, Natasha; Moosajee, Mariya

Changes in Mitochondrial Size and Morphology in the RPE and Photoreceptors of the Developing and Ageing Zebrafish

斑马鱼发育和衰老过程中视网膜色素上皮细胞和感光细胞线粒体大小和形态的变化

Burgoyne, Thomas; Toms, Maria; Way, Chris; Tracey-White, Dhani; Futter, Clare E; Moosajee, Mariya

Longitudinal Study to Assess the Quantitative Use of Fundus Autofluorescence for Monitoring Disease Progression in Choroideremia

一项纵向研究旨在评估眼底自发荧光定量检测在脉络膜萎缩症疾病进展监测中的应用。

Dubis, Adam M; Lim, Wei S; Jolly, Jasleen K; Toms, Maria; MacLaren, Robert E; Webster, Andrew R; Moosajee, Mariya

The Use of Induced Pluripotent Stem Cells as a Model for Developmental Eye Disorders

利用诱导多能干细胞作为发育性眼病模型

Eintracht, Jonathan; Toms, Maria; Moosajee, Mariya

USH2A-retinopathy: From genetics to therapeutics

USH2A视网膜病变:从遗传学到治疗

Toualbi, Lyes; Toms, Maria; Moosajee, Mariya

Usher syndrome: clinical features, molecular genetics and advancing therapeutics

Usher综合征:临床特征、分子遗传学和最新治疗进展

Toms, Maria; Pagarkar, Waheeda; Moosajee, Mariya

Missense variants in the conserved transmembrane M2 protein domain of KCNJ13 associated with retinovascular changes in humans and zebrafish

KCNJ13 保守跨膜 M2 蛋白结构域中的错义变异与人类和斑马鱼的视网膜血管变化相关

Toms, Maria; Dubis, Adam M; Lim, Wei Sing; Webster, Andrew R; Gorin, Michael B; Moosajee, Mariya