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Anzahl der Publikationen: 5
Zeitschriftenartikel
Lin, Hsiao-Chun Amy; Dean-Ben, Xose Luis; Reiss, Michael; Schöttle, Verena; Wahl-Schott, Christian A.; Efimov, Igor R. und Razansky, Daniel
(2018):
Ultrafast Volumetric Optoacoustic Imaging of Whole Isolated Beating Mouse Heart.
In: Scientific Reports, Bd. 8, 14132
[PDF, 2MB]
Chao, Yu-Kai; Schludi, Verena; Chen, Cheng-Chang; Butz, Elisabeth; Nguyen, O. N. Phuong; Müller, Martin; Krüger, Jens; Kammerbauer, Claudia; Ben-Johny, Manu; Vollmar, Angelika M.; Berking, Carola; Biel, Martin; Wahl-Schott, Christian A. und Grimm, Christian
(2017):
TPC2 polymorphisms associated with a hair pigmentation phenotype in humans result in gain of channel function by independent mechanisms.
In: Proceedings of the National Academy of Sciences of the United States of America, Bd. 114, Nr. 41, E8595-E8602
Koch, Susanne F.; Duong, Jimmy K.; Hsu, Chun-Wei; Tsai, Yi-Ting; Lin, Chyuan-Sheng; Wahl-Schott, Christian A. und Tsang, Stephen H.
(2017):
Genetic rescue models refute nonautonomous rod cell death in retinitis pigmentosa.
In: Proceedings of the National Academy of Sciences of the United States of America, Bd. 114, Nr. 20: S. 5259-5264
Michalakis, Stylianos; Shaltiel, Lior; Sothilingam, Vithiyanjali; Koch, Susanne; Schludi, Verena; Krause, Stefanie; Zeitz, Christina; Audo, Isabelle; Lancelot, Marie-Elise; Hamel, Christian; Meunier, Isabelle; Preising, Markus N.; Friedburg, Christoph; Lorenz, Birgit; Zabouri, Nawal; Haverkamp, Silke; Garcia Garrido, Marina; Tanimoto, Naoyuki; Seeliger, Mathias W.; Biel, Martin und Wahl-Schott, Christian A.
(2017):
Mosaic synaptopathy and functional defects in Cav1.4 heterozygous mice and human carriers of CSNB2 (vol 23, pg 1538, 2014).
In: Human Molecular Genetics, Bd. 26, Nr. 2: S. 466
Tanimoto, Naoyuki; Michalakis, Stylianos; Weber, Bernhard H. F.; Wahl-Schott, Christian A.; Hammes, Hans-Peter und Seeliger, Mathias W.
(2016):
In-Depth Functional Diagnostics of Mouse Models by Single-Flash and Flicker Electroretinograms without Adapting Background Illumination.
In: Retinal Degenerative Diseases: Mechanisms and Experimental therapy, Bd. 854: S. 619-625