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

Deciphering the heterogeneity of differentiating hPSC-derived corneal limbal stem cells through single-cell RNA sequencing

通过单细胞 RNA 测序揭示分化 hPSC 衍生的角膜缘干细胞的异质性

Meri Vattulainen, Jos G A Smits, Julian A Arts, Dulce Lima Cunha, Tanja Ilmarinen, Heli Skottman, Huiqing Zhou

Identification of the regulatory circuit governing corneal epithelial fate determination and disease

识别调控角膜上皮细胞命运决定和疾病的调控回路

Jos G A Smits ,Dulce Lima Cunha ,Maryam Amini ,Marina Bertolin ,Camille Laberthonnière ,Jieqiong Qu ,Nicholas Owen ,Lorenz Latta ,Berthold Seitz ,Lauriane N Roux ,Tanja Stachon ,Stefano Ferrari ,Mariya Moosajee ,Daniel Aberdam ,Nora Szentmary ,Simon J van Heeringen ,Huiqing Zhou

Restoration of functional PAX6 in aniridia patient iPSC-derived ocular tissue models using repurposed nonsense suppression drugs

使用重新利用的无义抑制药物恢复无虹膜患者 iPSC 衍生眼组织模型中的功能性 PAX6

Dulce Lima Cunha, Hajrah Sarkar, Jonathan Eintracht, Philippa Harding, Jo Huiqing Zhou, Mariya Moosajee

PAX6 disease models for aniridia

PAX6 无虹膜症疾病模型

Abdolkarimi, Dorsa; Cunha, Dulce Lima; Lahne, Manuela; Moosajee, Mariya

Efficient embryoid-based method to improve generation of optic vesicles from human induced pluripotent stem cells

基于胚状体的有效方法来改善人类诱导多能干细胞视泡的生成

Jonathan Eintracht #, Philippa Harding #, Dulce Lima Cunha, Mariya Moosajee

REP1 deficiency causes systemic dysfunction of lipid metabolism and oxidative stress in choroideremia

REP1 缺乏会导致脉络膜萎缩症中脂质代谢和氧化应激的系统性功能障碍。

Cunha, Dulce Lima; Richardson, Rose; Tracey-White, Dhani; Abbouda, Alessandro; Mitsios, Andreas; Horneffer-van der Sluis, Verena; Takis, Panteleimon; Owen, Nicholas; Skinner, Jane; Welch, Ailsa A; Moosajee, Mariya

Longitudinal genotype-phenotype analysis in 86 patients with PAX6-related aniridia

对 86 例 PAX6 相关无虹膜症患者进行纵向基因型-表型分析

Kit, Vivienne; Cunha, Dulce Lima; Hagag, Ahmed M; Moosajee, Mariya

Generation of human iPSC line (UCLi013-A) from a patient with microphthalmia and aniridia, carrying a heterozygous missense mutation c.372C>A p.(Asn124Lys) in PAX6

从患有小眼畸形和无虹膜症的患者体内生成人类 iPSC 系 (UCLi013-A),该患者携带 PAX6 中的杂合错义突变 c.372C>A p.(Asn124Lys)

Philippa Harding, Dulce Lima Cunha, Cécile Méjécase, Jonathan Eintracht, Lyes Toualbi, Hajrah Sarkar, Mariya Moosajee

Generation of two human iPSC lines from patients with autosomal dominant retinitis pigmentosa (UCLi014-A) and autosomal recessive Leber congenital amaurosis (UCLi015-A), associated with RDH12 variants

从患有常染色体显性视网膜色素变性 (UCLi014-A) 和常染色体隐性莱伯先天性黑蒙 (UCLi015-A) 的患者中生成两种人类 iPSC 系,与 RDH12 变异有关

Hajrah Sarkar, Cécile Méjécase, Philippa Harding, Jonathan Eintracht, Lyes Toualbi, Dulce Lima Cunha, Mariya Moosajee

hiPSC-Derived Epidermal Keratinocytes from Ichthyosis Patients Show Altered Expression of Cornification Markers

鱼鳞病患者 hiPSC 衍生的表皮角质形成细胞显示角质化标志物的表达发生改变

Dulce Lima Cunha, Amanda Oram, Robert Gruber, Roswitha Plank, Arno Lingenhel, Manoj K Gupta, Janine Altmüller, Peter Nürnberg, Matthias Schmuth, Johannes Zschocke, Tomo Šarić, Katja M Eckl, Hans C Hennies