Hoda Shamsnajafabadi ๐๏ธ๐ง
@hodashamss
Neuroscientist, Postdoc research scientist at Optogenetic gene therapy of retinal disease @NDCNOxford @UniofOxford @eyeMacLaren
ID: 1716102519208689664
https://www.ndcn.ox.ac.uk/team/hoda-shamsnajafabadi 22-10-2023 14:41:48
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Age-related macular degeneration: suitability of optogenetic therapy for geographic atrophy Frontiers - Neuroscience A great team effort Hoda Shamsnajafabadi ๐๏ธ๐ง , Benjamin W.J. Ng, Kanmin Xue, Samantha de Silva, Susan M. Downes, MacLaren Research Group Oxford, Jasmina Kapetanovic frontiersin.org/journals/neuroโฆ
Oxford Ophthalmology Congress 2024 #OOC2024 with amazing Doyne Lecture by Robert MacLaren MacLaren Research Group Oxford, Hertford college gala dinner and so excited to share our research on optogenetic gene therapy on retinal human organoid.
An incredible time at Optogenetics Gordon Research Conference conference, filled with insightful discussions, innovative ideas and dynamic networking. Proud to be part of such a talented and forward-thinking community. #OptoGRC2024
Excited to share my latest article on CRISPR-Cas mediated base editing approaches for CRB1-related retinal dystrophy! A must-read for anyone passionate about base editing gene therapy of retinal disease! Jasmina Kapetanovic MacLaren Research Group Oxford mdpi.com/2073-4425/15/5โฆ
Excited to share our last publication on โGenetic therapies and potential therapeutic applications of CRISPR activators in the eyeโ. Huge thanks to our entire team Jasmina Kapetanovic MacLaren Research Group Oxford for their support and hard work. Well done, Ben! sciencedirect.com/science/articlโฆ
Annual lab dinner 2024. Vary proud to be a member of Robert MacLaren Research Group Oxford and Jasmina Jasmina Kapetanovic retina research lab.
On the 2nd of September at the University of Oxfordโs Divinity School, we celebrated a milestone with Professor Robert McLarenโs lab MacLaren Research Group Oxford achieving an advancement in gene therapies for treating retinal eye diseases caused by a mutation in the CDHR1 gene.