Michael Cheetham
University College London
H-index: 68
Europe-United Kingdom
Top articles of Michael Cheetham
Title | Journal | Author(s) | Publication Date |
|---|---|---|---|
Pluripotent stem cell-derived models of retinal disease: Elucidating pathogenesis, evaluating novel treatments, and estimating toxicity | Marzena Kurzawa-Akanbi Nikolaos Tzoumas Julio C Corral-Serrano Rosellina Guarascio David H Steel | 2024/5/1 | |
RP2-Associated X-linked Retinopathy: Clinical Findings, Molecular Genetics, and Natural History in a Large Cohort of Female Carriers | American Journal of Ophthalmology | Michalis Georgiou Anthony G Robson Sami H Uwaydat Marco H Ji Ahmed F Shakarchi | 2024/5/1 |
A Proximity Complementation Assay to Identify Small Molecules That Enhance the Traffic of ABCA4 Misfolding Variants | International Journal of Molecular Sciences | Davide Piccolo Christina Zarouchlioti James Bellingham Rosellina Guarascio Kalliopi Ziaka | 2024/4/20 |
Proof-of-concept for multiple AON delivery by a single U7snRNA vector to restore splicing defects in ABCA4 | Molecular Therapy | Nuria Suárez-Herrera Iris B Riswick Irene Vázquez-Domínguez Lonneke Duijkers Dyah W Karjosukarso | 2024/1/18 |
Tissue-Specific Dynamics of TCF4 Triplet Repeat Instability Revealed by Optical Genome Mapping | bioRxiv | Christina Zarouchlioti Stephanie Efthymiou Stefano Fracchini Natalia Dominik Nihar Bhattacharyya | 2024 |
Investigating the synaptic mechanisms of the spread of wild type and P301S 1N4R human tau in in vitro and in vivo models | Alzheimer's & Dementia | Chiara Panzi Laura Restani Elena Novelli Rosellina Guarascio Michael Cheetham | 2023/12 |
Use of iPSC-derived retinal ganglion cells to investigate cell specific OPA1 RNA processing | Investigative Ophthalmology & Visual Science | Joshua Harvey Neringa Jurkute Gavin Arno Patrick Yu-Wai-Man Michael E Cheetham | 2023/6/1 |
Late-onset autosomal dominant macular degeneration caused by deletion of the CRX gene | Ophthalmology | Samar Yahya Claire EL Smith James A Poulter Martin McKibbin Gavin Arno | 2023/1/1 |
Molecular insights and treatment of IFT140-mediated retinal dystrophy in iPSCs-derived retinal organoids and RPE | Investigative Ophthalmology & Visual Science | Julio Cesar Corral Serrano Nele Schwarz Karsten Boldt Katarina Jovanovic Daniele Ottaviani | 2023/6/1 |
CRISPR-Cas9 correction of a nonsense mutation in LCA5 rescues lebercilin expression and localization in human retinal organoids | Molecular Therapy-Methods & Clinical Development | Tess AV Afanasyeva Dimitra Athanasiou Pedro RL Perdigao Kae R Whiting Lonneke Duijkers | 2023/6/8 |
Deciphering novel TCF4-driven mechanisms underlying a common triplet repeat expansion-mediated disease | bioRxiv | Nihar Bhattacharyya Niuzheng Chai Nathaniel J Hafford-Tear Amanda N Sadan Anita Szabo | 2023/3/29 |
Eupatilin improves cilia defects in human CEP290 ciliopathy models | Cells | Julio C Corral-Serrano Paul E Sladen Daniele Ottaviani Olivia F Rezek Dimitra Athanasiou | 2023/6/7 |
Antisense oligonucleotide therapy corrects splicing in the common Stargardt disease type 1-causing variant ABCA4 c. 5461-10T> C | Molecular Therapy-Nucleic Acids | Melita Kaltak Petra de Bruijn Davide Piccolo Sang-Eun Lee Kalyan Dulla | 2023/3/14 |
Investigation of OPN1LW and OPN1MW interchange haplotypes in retinal organoids from patients with blue cone monochromacy | Investigative Ophthalmology & Visual Science | Owen Fernando Jessica C Gardner Julio Cesar Corral Serrano Michel Michaelides Michael E Cheetham | 2023/6/1 |
Transcriptome analyses of mouse models of rhodopsin retinitis pigmentosa using RNA-seq. | Investigative Ophthalmology & Visual Science | Kalliopi Ziaka Rosellina Guarascio Kwan Hau Rowan Asfahani Davide Piccolo | 2023/6/1 |
Multidisciplinary team directed analysis of whole genome sequencing reveals pathogenic non-coding variants in molecularly undiagnosed inherited retinal dystrophies | Human molecular genetics | Malena Daich Varela James Bellingham Fabiana Motta Neringa Jurkute Jamie M Ellingford | 2023/2/15 |
QR-1011 corrects splicing in the Stargardt disease type 1-causing variant ABCA4 c. 5461-10T> C | Investigative Ophthalmology & Visual Science | Melita Kaltak Petra de Bruijn Sang-Eun Lee Davide Piccolo Kalyan Dulla | 2022/6/1 |
Antisense oligonucleotides rescue aberrant splicing of ABCA4 | 2022/9/15 | ||
Intravitreal antisense oligonucleotide sepofarsen in Leber congenital amaurosis type 10: a phase 1b/2 trial | Nature medicine | Stephen R Russell Arlene V Drack Artur V Cideciyan Samuel G Jacobson Bart P Leroy | 2022/5 |
Characterising the disease mechanisms of RP17 structural variants | Investigative Ophthalmology & Visual Science | Vasileios Toulis Suzanne De Bruijn Uira S Melo Julio Corral-Serrano Kwan Hau | 2022/6/1 |
