Helmholtz Gemeinschaft

Search
Browse
Statistics
Feeds

Browse by Journal Title

Up a level
Export as [feed] Atom [feed] RSS 1.0 [feed] RSS 2.0
Group by: Date | Item Type
Jump to: 2015 | 2014 | 2012 | 2009 | 2008 | 2006 | 2005 | 2004 | 2002 | 2001

2015

Comparison of standard versus wide-field composite images of the corneal subbasal layer by In vivo confocal microscopy.
Kheirkhah, A. and Muller, R. and Mikolajczak, J. and Ren, A. and Kadas, E.M. and Zimmermann, H. and Pruess, H. and Paul, F. and Brandt, A.U. and Hamrah, P.
Investigative Ophthalmology & Visual Science 56 (10): 5801-5807. 1 September 2015

2014

Retinal segmentation to demonstrate hyperplasia in ataxia of charlevoix-saguenay: critique on study methodology and results.
Albrecht, P. and Balk, L. and Oberwahrenbrock, T. and Petzold, A. and Paul, F.
Investigative Ophthalmology & Visual Science 55 (8): 4728. 4 August 2014

2012

Sleeping Beauty transposon-mediated transfection of retinal and iris pigment epithelial cells.
Johnen, S. and Izsvak, Z. and Stocker, M. and Harmening, N. and Salz, A.K. and Walter, P. and Thumann, G.
Investigative Ophthalmology & Visual Science 53 (8): 4787-4796. 18 July 2012

Mutations in RD3 are associated with an extremely rare and severe form of early onset retinal dystrophy.
Preising, M.N. and Hausotter-Will, N. and Solbach, M.C. and Friedburg, C. and Rueschendorf, F. and Lorenz, B.
Investigative Ophthalmology & Visual Science 53 (7): 3463-3472. 8 June 2012

2009

A new Fgf10 mutation in the mouse leads to atrophy of the harderian gland and slit-eye phenotype in heterozygotes: a novel model for dry-eye disease?
Puk, O. and Esposito, I. and Soeker, T. and Loester, J. and Budde, B. and Nuernberg, P. and Michel-Soewarto, D. and Fuchs, H. and Wolf, E. and Hrabe de Angelis, M. and Graw, J.
Investigative Ophthalmology & Visual Science 50 (9): 4311-4318. September 2009

2008

Mutation in a novel connexin-like gene (Gjf1) in the mouse affects early lens development and causes a variable small-eye phenotype.
Puk, O. and Loester, J. and Dalke, C. and Soewarto, D. and Fuchs, H. and Budde, B. and Nuernberg, P. and Wolf, E. and de Angelis, M.H. and Graw, J.
Investigative Ophthalmology & Visual Science 49 (4): 1525-1532. April 2008

2006

Structural and functional abnormalities of retinal ribbon synapses due to Cacna2d4 mutation.
Wycisk, K.A. and Budde, B. and Feil, S. and Skosyrski, S. and Buzzi, F. and Neidhardt, J. and Glaus, E. and Nuernberg, P. and Ruether, K. and Berger, W.
Investigative Ophthalmology & Visual Science 47 : 3523-3530. August 2006

2005

Three novel Pax6 alleles in the mouse leading to the same small-eye phenotype caused by different consequences at target promoters.
Graw, J. and Loester, J. and Puk, O. and Muenster, D. and Haubst, N. and Soewarto, D. and Fuchs, H. and Meyer, B. and Nuernberg, P. and Pretsch, W. and Selby, P. and Favor, J. and Wolf, E. and de Angelis, M.H.
Investigative Ophthalmology & Visual Science 46 (12): 4671-4683. 1 December 2005

2004

OPA1, the disease gene for autosomal dominant optic atrophy, is specifically expressed in ganglion cells and intrinsic neurons of the retina.
Pesch, U.E.A. and Fries, J.E. and Bette, S. and Kalbacher, H. and Wissinger, B. and Alexander, C. and Kohler, K.
Investigative Ophthalmology & Visual Science 45 (11): 4217-4225. 1 January 2004

2002

A comprehensive survey of mutations in the OPA1 gene in patients with autosomal dominant optic atrophy.
Thiselton, D.L. and Alexander, C. and Taanman, J.W. and Brooks, S. and Rosenberg, T. and Eiberg, H. and Andreasson, S. and Van Regemorter, N. and Munier, F.L. and Moore, A.T. and Bhattacharya, S.S. and Votruba, M.
Investigative Ophthalmology & Visual Science 43 : 1715-1724. 1 June 2002

2001

Characterization of a new, dominant V124E mutation in the mouse alphaA-crystallin-encoding gene.
Graw, J. and Loester, J. and Soewarto, D. and Fuchs, H. and Meyer, B. and Reis, A. and Wolf, E. and Balling, R. and de Angelis, M.H.
Investigative Ophthalmology & Visual Science 42 : 2909-2915. 1 January 2001

Aey2, a new mutation in thebetaB2-crystallin-encoding gene of the mouse.
Graw, J. and Loester, J. and Soewarto, D. and Fuchs, H. and Reis, A. and Wolf, E. and Balling, R. and de Angelis, M.H.
Investigative Ophthalmology & Visual Science 42 : 1574-1580. 1 January 2001

This list was generated on Mon Sep 24 10:12:15 2018 CEST.
Open Access
MDC Library