Anzahl der Einträge: 9.
2012
2008
Janssen, A.,
Min, S. H.,
Molday, L. .,
Tanimoto, N.,
Seeliger, N. W.,
Hauswirth, W. W.,
Molday, R. S. und
Weber, Bernhard H. F.
(2008)
Effect of Late-stage Therapy on Disease Progression in AAV-mediated Rescue of Photoreceptor Cells in the Retinoschisin-deficient Mouse.
Molecular Therapy 16, S. 1010-1017.
2006
Molday, L. L.,
Min, S. H.,
Seeliger, M. W.,
Wu, W. W.,
Dinculescu, A.,
Timmers, A. M.,
Janssen, A.,
Tonagel, F.,
Hudl, K.,
Weber, Bernhard H. F. ,
Hauswirth, W. W. und
Molday, R. S.
(2006)
Disease mechanisms and gene therapy in a mouse model for x-linked retinoschisis.
Advances in experimental medicine and biology 572, S. 283-289.
Volltext nicht vorhanden.
2005
Stöhr, H.,
Molday, L. L.,
Molday, R. S.,
Weber, Bernhard H. F. ,
Biedermann, B.,
Reichenbach, A. und
Krämer, F.
(2005)
Membrane-associated guanylate kinase proteins MPP4 and MPP5 associate with Veli3 at distinct intercellular junctions of the neurosensory retina.
The Journal of Comparative Neurology 481 (1), S. 31-41.
Min, S. H.,
Molday, L. L.,
Seeliger, M. W.,
Dinculescu, A.,
Timmers, A. M.,
Janssen, A.,
Tonagel, F.,
Tanimoto, N.,
Weber, Bernhard H. F. ,
Molday, R. S. und
Hauswirth, W. W.
(2005)
Prolonged recovery of retinal structure/function after gene therapy in an Rs1h-deficient mouse model of X-linked juvenile retinoschisis.
Molecular Therapy 12 (4), S. 644-651.
2002
Weber, Bernhard H. F. ,
Schrewe, H.,
Molday, L. L.,
Gehrig, A.,
White, K. L.,
Seeliger, M. W.,
Jaissle, G. B.,
Friedburg, C.,
Tamm, E. und
Molday, R. S.
(2002)
Inactivation of the murine X-linked juvenile retinoschisis gene, Rs1h, suggests a role of retinoschisin in retinal cell layer organization and synaptic structure.
Proceedings of the National Academy of Sciences of the United States of America : PNAS 99 (9), S. 6222-6227.
2001
1999
Zack, D. J.,
Dean, M.,
Molday, R. S.,
Nathans, J.,
Redmont, T. M.,
Stone, E. M.,
Swaroop, A.,
Valle, D. und
Weber, Bernhard H. F.
(1999)
What can we learn about age-related macular degeneration from other retinal diseases?
Molecular vision 5, S. 30.
1998
Nasonkin, I.,
Illing, M.,
Koehler, M. R.,
Schmid, M.,
Molday, R. S. und
Weber, Bernhard H. F.
(1998)
Mapping of the rod photoreceptor ABC transporter (ABCR) to 1p21–p22.1 and identification of novel mutations in Stargardt’s disease.
Human Genetics 102 (1), S. 21-26.
Volltext nicht vorhanden.
Diese Liste wurde erzeugt am Sun Oct 20 00:53:06 2024 CEST.