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Molecular Vision|February 8, 2012
Analysis of mitochondrial DNA variations in Indian patients with congenital cataractMascarenhas Roshan, Shama Prasada Kabekkodu, Pai H Vijaya, et al.
Molecular Vision|April 18, 2013
Novel small-eye allele in paired box gene 6 (Pax6) is caused by a point mutation in intron 7 and creates a new exonOliver Puk, Xiaohe Yan, Sibylle Sabrautzki, et al.
The International Journal of Developmental Biology|December 6, 2013
Pitx3 directly regulates Foxe3 during early lens developmentNafees Ahmad, Muhammad Aslam, Doris Muenster, et al.
BMC Ophthalmology|December 26, 2014
Characterization of ex vivo cultured neuronal- and glial- like cells from human idiopathic epiretinal membranesSofija Andjelić, Xhevat Lumi, Xiaohe Yan, et al.
The Journal of Comparative Neurology|August 14, 2012
Visualizing corticotropin-releasing hormone receptor type 1 expression and neuronal connectivities in the mouse using a novel multifunctional alleleClaudia Kühne, Oliver Puk, Jochen Graw, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|September 13, 2002
V76D mutation in a conserved gD-crystallin region leads to dominant cataracts in miceJochen Graw, Jana Löster, Dian Soewarto, et al.
BMC Developmental Biology|April 10, 2010
Relative roles of the different Pax6 domains for pancreatic alpha cell developmentPetra Dames, Ramona Puff, Michaela Weise, et al.
Human Molecular Genetics|June 5, 2014
Peroxidasin is essential for eye development in the mouseXiaohe Yan, Sibylle Sabrautzki, Marion Horsch, et al.
Molecular Vision|July 25, 2006
Identification of a novel, putative cataract-causing allele in CRYAA (G98R) in an Indian familySathiyavedu T Santhiya, Torben Soker, Norman Klopp, et al.
Plos One|August 23, 2011
The pathologic effect of a novel neomorphic Fgf9(Y162C) allele is restricted to decreased vision and retarded lens growthOliver Puk, Gabriele Möller, Arie Geerlof, et al.
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