Leonie Kinder and Moritz Lindner @MoritzLindner2 investigate Expression of Osteopontin in M2 and M4 Intrinsically Photosensitive Retinal Ganglion Cells in the Mouse Retina, https://t.co/jxTP60UQz0.
How would optogenetic gene therapy function in individuals with residual visual function? We used ERG+VEP recordings and a mouse model to address this question! read our latest preprint at #biorxiv_neursci: https://t.co/3PSeGjSF74
Great collab of @Uni_MR@UniofOxford@OfficialUoM
Enhanced restoration of visual code after targeting on bipolar cells compared to retinal ganglion cells with optogenetic therapy https://t.co/BbqO6MED7V #biorxiv_neursci
Some #biophysics from our lab! Fresh from the bench and published in @SpringerNature s CMLS: Silent-KvS, like those involved in Kcnv2-associated retinopathy may form complexes also with Kv7 channels! Read more: https://t.co/cgTNF2AXJT
#Neuroscience#patchclamp
With this picture of (most of) the current SPP2127 members, we are closing our first in-person meeting of this funding period.
After two days of great minds, great ideas and great fun, we are looking forward to more meetings and amazing science!
New year! New hire! Are you interested in innate immune response and epithelial wound healing using Drosophila as a genetic model system? We have an open postdoc position. Come and join us! Further info here: https://t.co/iERKG20M7x
PIs please retweet!
PhD and postdoc positions in immune cell response and wound closure dynamics available - Bogdan lab at the Philipps-University of Marburg. If you are interested in, please apply via [email protected]. PIs please retweet!
#DOG2022: Am Freitag wurde die Auszeichnung mit dem Deutschen Förderprogramm für #Augenheilkunde von @BayerPharma für die Jahre 2021 & 22 verliehen. Wir gratulieren Sumit Biswas (Marburg) & Dr. Anne Wolf (Köln). Mehr zu den geförderten Projekten: https://t.co/9g5FAQWEzR
DPhil opportunity in the @eyeMacLaren research group at @NDCNOxford evaluating patient iPSC-derived retinal organoids as an in vitro model of inherited retinal disease, for applicants qualifying for tuition fees at the Home rate https://t.co/KHcelycUNc
Usher Syndrome Awareness Day is September 17. Usher syndrome is a rare disease and leading genetic cause of deaf-blindness. Those with Usher begin by losing vision in dim light first followed by loss of peripheral vision leading to tunnel vision. #TakeBackTheLight#USHDay2022