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Plos One|May 8, 2015
New mutation in the mouse Xpd/Ercc2 gene leads to recessive cataractsSarah Kunze, Claudia Dalke, Helmut Fuchs, et al.Mutation Research. Reviews in Mutation Research|December 7, 2016
Ionizing radiation induced cataracts: Recent biological and mechanistic developments and perspectives for future researchElizabeth A Ainsbury, Stephen Barnard, Scott Bright, et al.Journal of Proteome Research|October 29, 2019
CREB Signaling Mediates Dose-Dependent Radiation Response in the Murine Hippocampus Two Years after Total Body ExposureDaniela Hladik, Claudia Dalke, Christine von Toerne, et al.Molecular Vision|August 10, 2005
An ENU-induced mutation in Rs1h causes disruption of retinal structure and functionMonica M Jablonski, Claudia Dalke, XiaoFei Wang, et al.Genetics|July 23, 2003
Mutation in intron 6 of the hamster Mitf gene leads to skipping of the subsequent exon and creates a novel animal model for the human Waardenburg syndrome type IIJochen Graw, Walter Pretsch, Jana LösterInvestigative Ophthalmology & Visual Science|May 1, 2002
Altered Na,K-ATPase pattern in gamma-crystallin mutant miceAmy Moseley, Jochen Graw, Nicholas A DelamereInternational Journal of Cancer|September 25, 2008
Cancer-retina antigens as potential paraneoplastic antigens in melanoma-associated retinopathyAlexandr V Bazhin, Claudia Dalke, Nadine Willner, et al.Investigative Ophthalmology & Visual Science|January 28, 2004
Electroretinography as a screening method for mutations causing retinal dysfunction in miceClaudia Dalke, Jana Löster, Helmut Fuchs, et al.Biochemical and Biophysical Research Communications|June 5, 2018
Crybb2 associates with Tmsb4X and is crucial for dendrite morphogenesisMinxuan Sun, Nafees Ahmad, Ruobing Zhang, et al.Mammalian Genome : Official Journal of the International Mammalian Genome Society|May 18, 2013
Longitudinal fundus and retinal studies with SD-OCT: a comparison of five mouse inbred strainsOliver Puk, Martin Hrabĕ de Angelis, Jochen GrawPageof 13