Author
Mathias W. Seeliger
University of TübingenORCID 0000-0002-7879-6788Unclaimed ORCID profile · follow to get notified of new preprints
Biology Disciplines
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2020-2026 · peak 3/yrCo-Author Collaboration Network
10 top collaborators · 27 mutual co-author links8 papers
Recent·Most cited
- NeurosciencebioRxivPreprint
PGC-1α and PPARs cooperatively mediate photoreceptor neuroprotection in rd1 mouse inherited retinal degeneration
Lan Wang, Jie Yan, Javier Sancho-Pellúz…·François Paquet‐Durand
This study investigates the role of PPARs and PGC-1α in photoreceptor neuroprotection in rd1 mouse model of retinal degeneration, finding that their activation reduces photoreceptor death and PARP activity.
DOI 10.1101/2025.10.21.683632 - NeurosciencebioRxivPreprint
Ocular delivery of different VCP inhibitory formulations prevents retinal degeneration in rhodopsin 255 isoleucine deletion mice
Bowen Cao, Regine L. Mühlfriedel, Merve Sen…·Blanca Arango‐González
This study evaluates three VCP-targeted therapies in a mouse model of retinitis pigmentosa, finding that nanocarrier-encapsulated ML240 provides the best protection against photoreceptor degeneration.
DOI 10.1101/2025.06.25.661245 - Cell BiologyFrontiers in MedicinePeer-reviewed
A remarkable degree of conformance between the visual streak of the Mongolian gerbil and the human central retina
Alexander Günter, Mohamed Ali Jarboui, Regine Mühlfriedel, Mathias W. Seeliger
The paper compares the retinal structure of the Mongolian gerbil's visual streak to the human macula, finding similar features that suggest the gerbil as a model for studying the human central retina.
- PathologybioRxivPreprint
Autosomal dominant Retinitis Pigmentosa caused by the rhodopsin isoleucine 255 deletion features rapid neuroretinal degeneration, decreased synaptic connectivity, and neuroinflammation.
Bowen Cao, Yu Zhu, Alexander Günter…·Marius Ueffing
This paper introduces a novel mouse model of dominant retinitis pigmentosa caused by the RHO{Delta}I255 mutation, showing rapid photoreceptor degeneration, neuroinflammation, and disrupted neuronal connectivity.
4 citations - NeuroscienceCell Communication and SignalingPeer-reviewed
Inherited retinal degeneration: T-type voltage-gated channels, Na+/Ca2+-exchanger, and calpain-2 promote photoreceptor cell death.
Jie Yan, Lan Wang, Qianlu Yang…·François Paquet‐Durand
This study investigates the role of calcium signaling in photoreceptor cell death in IRD using mouse models and identifies calpain-2 as a key contributor to degeneration.
22 citations - Developmental BiologyCirculation ResearchPeer-reviewed
Mural cell SRF controls pericyte migration, vessel patterning and blood flow
Michael M. Orlich, Rodrigo Diéguez‐Hurtado, Regine L. Mühlfriedel…·Alfred Nordheim
This study investigates the role of SRF in mural cells, showing its importance in pericyte migration, vessel patterning, and blood flow during development and disease.
43 citations - NeurosciencebioRxivPreprint
Voltage-gated calcium channel subunit α2δ-3 shapes light responses of mouse retinal ganglion cells mainly in low and moderate light levels
Hartwig Seitter, Vithiyanjali Sothilingam, Boris Benkner…·Thomas A. Münch
This study investigates the role of 2δ-3 in mouse retinal ganglion cells, finding subtle changes in visual responses under low and moderate light levels but normal optokinetic reflexes.
DOI 10.1101/2020.02.10.941807