Publikationen von Wolfgang Berger

Zeitz, C.; Scherthan, H.; Freier, S.; Feil, S.; Suckow, V.; Schweiger, S.; Berger, W.: NYX (Nyctalopin on chromosome X), the gene mutated in congenital stationary night blindness, encodes a cell surface protein. Investigative Ophthalmology & Visual Science 44 (10), S. 4184 - 4191 (2003)

Pesch, K.; Zeitz, C.; Fries, J. E.; Muenscher, S.; Pusch, C. M.; Kohler, K.; Berger, W.; Wissinger, B.: Isolation of the mouse nyctalopin gene Nyx and expression studies in mouse and rat retina. Investigative Ophthalmology & Visual Science 44 (5), S. 2260 - 2266 (2003)

Lenzner, S.; Prietz, S.; Feil, S.; Nuber, U. A.; Ropers, H. H.; Berger, W.: Global Gene Expression Analysis in a Mouse Model for Norrie Disease: Late Involvement of Photoreceptor Cells. Investigative Ophthalmology & Visual Science 43 (9), S. 2825 - 2833 (2002)

Rehm, H. L.; Zhang, D.-S.; Brown, M. C.; Burgess, B.; Halpin, C.; Berger, W.; Morton, C. C.; Corey, D. P.; Chen, Z.-Y.: Vascular Defects and Sensorineural Deafness in a Mouse Model of Norrie Disease. Journal of Neuroscience 22 (11), S. 4286 - 4292 (2002)