M
Mathias W. Seeliger
Researcher at University of Tübingen
Publications - 173
Citations - 11275
Mathias W. Seeliger is an academic researcher from University of Tübingen. The author has contributed to research in topics: Retina & Retinal. The author has an hindex of 56, co-authored 172 publications receiving 10313 citations.
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Journal ArticleDOI
Genetic Reactivation of Cone Photoreceptors Restores Visual Responses in Retinitis Pigmentosa
Volker Busskamp,Jens Duebel,D. Balya,Mathias Fradot,Mathias Fradot,Mathias Fradot,Tim J. Viney,Sandra Siegert,Anna C. Groner,Erik Cabuy,Valérie Forster,Valérie Forster,Valérie Forster,Mathias W. Seeliger,Martin Biel,Peter Humphries,Michel Paques,Saddek Mohand-Said,Didier Trono,Karl Deisseroth,José-Alain Sahel,Serge Picaud,Botond Roska +22 more
TL;DR: It is shown that expression of archaebacterial halorhodopsin in light-insensitive cones can substitute for the native phototransduction cascade and restore light sensitivity in mouse models of retinitis pigmentosa.
Journal ArticleDOI
HIF-1-induced erythropoietin in the hypoxic retina protects against light-induced retinal degeneration
Christian Grimm,Andreas Wenzel,Matthias Groszer,Helmut Mayser,Mathias W. Seeliger,Marijana Samardzija,Christian Bauer,Max Gassmann,Charlotte E. Remé +8 more
TL;DR: It is shown in the adult mouse retina that acute hypoxia dose-dependently stimulates expression of Epo, fibroblast growth factor 2 and vascular endothelial growth factor via Hypoxia-inducible factor-1α (HIF-1 α) stabilization.
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Mutation of CDH23, encoding a new member of the cadherin gene family, causes Usher syndrome type 1D
Hanno J. Bolz,von Brederlow B,Alfredo Ramirez,Elizabeth C. Bryda,Kerstin Kutsche,Hans Gerd Nothwang,Mathias W. Seeliger,del C-Salcedó Cabrera M,Vila Mc,Molina Op,Andreas Gal,Christian Kubisch +11 more
TL;DR: The data show that different mutations in CDH23 result in USH1D with a variable retinal phenotype, and it is shown that mutations in the mouse ortholog cause disorganization of inner ear stereocilia and deafness in the waltzer mouse.
Journal ArticleDOI
Genetic disorders of vision revealed by a behavioral screen of 400 essential loci in zebrafish.
Stephan C.F. Neuhauss,Oliver Biehlmaier,Mathias W. Seeliger,Tilak Das,Konrad Kohler,William A. Harris,Herwig Baier +6 more
TL;DR: The mutations uncovered by behavioral assays of 450 zebrafish mutants provide distinct entry points for the study of visual pathways and set the stage for a genetic dissection of vertebrate vision.
Journal ArticleDOI
Guidelines for basic multifocal electroretinography (mfERG)
TL;DR: Department of Ophthalmology, Stanford University School of Medicine, Stanford, California, USA; andDepartment of Psychology, Columbia University, New York, NewYork, USA, for the International Society for Clinical Electrophysiology of Vision.