Disrupted alternative splicing for genes implicated in splicing and ciliogenesis causes PRPF31 retinitis pigmentosaAdriana Buskin, Majlinda Lako, Achim Treumann et al.|Nature Communications|2018Cited by 239
Decellularised extracellular matrix-derived peptides from neural retina and retinal pigment epithelium enhance the expression of synaptic markers and light responsiveness of human pluripotent stem cell derived retinal organoidsBirthe Dorgau, Majlinda Lako, Majed Felemban et al.|Biomaterials|2019Cited by 70
Extracellular matrix component expression in human pluripotent stem cell-derived retinal organoids recapitulates retinogenesis in vivo and reveals an important role for IMPG1 and CD44 in the development of photoreceptors and interphotoreceptor matrixMajed Felemban, Majlinda Lako, Birthe Dorgau et al.|Acta Biomaterialia|2018Cited by 49
Human iPSC-derived RPE and retinal organoids reveal impaired alternative splicing of genes involved in pre-mRNA splicing in PRPF31 autosomal dominant retinitis pigmentosaAdriana Buskin, Majlinda Lako, Lili Zhu et al.|bioRxiv (Cold Spring Harbor Laboratory)|2017Cited by 7
Splicing factor PRPF31 retinitis pigmentosa (RP11) is caused by disrupted alternative splicing programmes for genes implicated in pre-mRNA splicing, cellular adhesion and ciliogenesis.Adriana Buskin, Majlinda Lako, Valeria Chichagova et al.|Durham Research Online (Durham University)|2019Cited by 0