KLEINLOGEL LAB

J. Kralik, S. Kleinlogel.

Functional Availability of ON-Bipolar Cells in the Degenerated Retina: Timing and Longevity of an Optogenetic Gene Therapy. Int. J. Mol. Sci. 2021

S. Kleinlogel, C. Vogl, M. Jeschke, J. Neef & T. Moser.

Emerging approaches for restoration of hearing and vision. Physiol. Rev. 2020

E. Hulliger, S. Hofstellter, S. Kleinlogel.

Empowering retinal gene therapy with a specific promoter for human rod and cone ON-bipolar cells. Mol Ther Methods Clin Dev. 2020

Jonas Streit, Sonja Kleinlogel.
Dynamic all-optical drug screening on cardiac voltage-gated ion channels. Sci Rep 8:1153, 2018

M. Perny, C.C Ting, S. Kleinlogel, P. Senn and M. Roccio.
Generation of Otic Sensory Neurons from Mouse Embryonic Stem Cells in 3D Culture. Front. Cell. Neurosci. 11:409, 2017

S. Kleinlogel.
Optogenetics for Vision Recovery: From Traditional to Designer Optogenetic Tools. Cambridge University Press Optogenetics: From Neuronal Function to Mapping and Disease Biology 337-355, 2017

M. van Wyk, E. C. Hulliger, L. Girod, A. Ebneter and S. Kleinlogel.
Present Molecular Limitations of ON-Bipolar Cell Targeted Gene Therapy. Front. Neuroscience 2017

M. Perny, L. Muri, H. Dawson and S. Kleinlogel.
Chronic activation of the D156A point mutant of Channelrhodopsin-2 signals apoptotic cell death: the good and the bad. Cell Death & Disease 7, e2447, 2016

A. Tscherter, M. Heidemann, S. Kleinlogel and J. Streit.
Embryonic Cell Grafts in a Culture Model of Spinal Cord Lesion: Neuronal Relay Formation Is Essential for Functional Regeneration. Front. Cell. Neurosci. 10:220, 2016

M. van Wyk, S. Kleinlogel.
Light-sensitive chimeric gpcr protein (WO 2012174674 A1, EP 2723767 B8). Patent 2016

S. Kleinlogel.
Optogenetic user’s guide to Opto-GPCRs. Front. Biosci. 21:794-805, 2016

M. van Wyk, J. Pielecka-Fortuna, S. Löwel, S. Kleinlogel.
Restoring the ON Switch in Blind Retinas: Opto-mGluR6, a Next-Generation, Cell-Tailored Optogenetic Tool. PLoS Biol 13(5):e1002143, 2015

M. van Wyk, S. Schneider, S. Kleinlogel.
Variable phenotypic expressivity in inbred retinal degeneration mouse lines: A comparative study of C3H/HeOu and FVB/N rd1 mice. Molecular Vision 21:811-827, 2015