Scale Adjustments to Facilitate Two-Dimensional Measurements in OCT Images

Por Garcia Garrido, Marina, Mühlfriedel, Regine L., Beck, Susanne C., Wallrapp, Christine, Seeliger, Mathias W.
Publicado no PLoS One (2015)

Towards a Quantitative OCT Image Analysis

Por Garcia Garrido, Marina, Beck, Susanne C., Mühlfriedel, Regine, Julien, Sylvie, Schraermeyer, Ulrich, Seeliger, Mathias W.
Publicado em 2014

Degeneration of the mouse retina upon dysregulated activity of serum response factor

Por Sandström, Jenny, Heiduschka, Peter, Beck, Susanne C., Philippar, Ulrike, Seeliger, Matthias W., Schraermeyer, Ulrich, Nordheim, Alfred
Publicado em 2011

Successful Subretinal Delivery and Monitoring of MicroBeads in Mice

Por Fischer, M. Dominik, Goldmann, Tobias, Wallrapp, Christine, Mühlfriedel, Regine, Beck, Susanne C., Stern-Schneider, Gabi, Ueffing, Marius, Wolfrum, Uwe, Seeliger, Mathias W.
Publicado em 2013

AAV-Mediated Gene Supplementation Therapy in Achromatopsia Type 2: Preclinical Data on Therapeutic Time Window and Long-Term Effects

Por Mühlfriedel, Regine, Tanimoto, Naoyuki, Schön, Christian, Sothilingam, Vithiyanjali, Garcia Garrido, Marina, Beck, Susanne C., Huber, Gesine, Biel, Martin, Seeliger, Mathias W., Michalakis, Stylianos
Publicado no Front Neurosci (2017)

Spectral Domain Optical Coherence Tomography in Mouse Models of Retinal Degeneration

Por Huber, Gesine, Beck, Susanne C., Grimm, Christian, Sahaboglu-Tekgoz, Ayse, Paquet-Durand, Francois, Wenzel, Andreas, Humphries, Peter, Redmond, T. Michael, Seeliger, Mathias W., Fischer, M. Dominik
Publicado em 2009

Elk3 Deficiency Causes Transient Impairment in Post-Natal Retinal Vascular Development and Formation of Tortuous Arteries in Adult Murine Retinae

Por Weinl, Christine, Wasylyk, Christine, Garcia Garrido, Marina, Sothilingam, Vithiyanjali, Beck, Susanne C., Riehle, Heidemarie, Stritt, Christine, Roux, Michel J., Seeliger, Mathias W., Wasylyk, Bohdan, Nordheim, Alfred
Publicado em 2014

Long-term consequences of developmental vascular defects on retinal vessel homeostasis and function in a mouse model of Norrie disease

Por Beck, Susanne C., Feng, Yuxi, Sothilingam, Vithiyanjali, Garcia Garrido, Marina, Tanimoto, Naoyuki, Acar, Niyazi, Shan, Shenliang, Seebauer, Britta, Berger, Wolfgang, Hammes, Hans-Peter, Seeliger, Mathias W.
Publicado no PLoS One (2017)

Retinal Degenerative and Hypoxic Ischemic Disease

Por Fulton, Anne B., Akula, James D., Mocko, Julie A., Hansen, Ronald M., Benador, Ilan Y., Beck, Susanne C., Fahl, Edda, Seeliger, Mathias W., Moskowitz, Anne, Harris, Maureen E.
Publicado em 2008

Novel Rodent Models for Macular Research

Por Huber, Gesine, Heynen, Severin, Imsand, Coni, vom Hagen, Franziska, Muehlfriedel, Regine, Tanimoto, Naoyuki, Feng, Yuxi, Hammes, Hans-Peter, Grimm, Christian, Peichl, Leo, Seeliger, Mathias W., Beck, Susanne C.
Publicado em 2010

Cystoid edema, neovascularization and inflammatory processes in the murine Norrin-deficient retina

Por Beck, Susanne C., Karlstetter, Marcus, Garcia Garrido, Marina, Feng, Yuxi, Dannhausen, Katharina, Mühlfriedel, Regine, Sothilingam, Vithiyanjali, Seebauer, Britta, Berger, Wolfgang, Hammes, Hans-Peter, Seeliger, Mathias W., Langmann, Thomas
Publicado no Sci Rep (2018)

Alterations of the Tunica Vasculosa Lentis in the Rat Model of Retinopathy of Prematurity

Por Favazza, Tara L, Tanimoto, Naoyuki, Munro, Robert J., Beck, Susanne C., Garrido, Marina G., Seide, Christina, Sothilingam, Vithiyanjali, Hansen, Ronald M., Fulton, Anne B., Seeliger, Mathias W., Akula, James D
Publicado em 2013

Targeted Ablation of the Pde6h Gene in Mice Reveals Cross-species Differences in Cone and Rod Phototransduction Protein Isoform Inventory

Por Brennenstuhl, Christina, Tanimoto, Naoyuki, Burkard, Markus, Wagner, Rebecca, Bolz, Sylvia, Trifunovic, Dragana, Kabagema-Bilan, Clement, Paquet-Durand, Francois, Beck, Susanne C., Huber, Gesine, Seeliger, Mathias W., Ruth, Peter, Wissinger, Bernd, Lukowski, Robert
Publicado no J Biol Chem (2015)

A retinal model of cerebral malaria

Por Paquet-Durand, François, Beck, Susanne C., Das, Soumyaparna, Huber, Gesine, Le Chang, Schubert, Timm, Tanimoto, Naoyuki, Garcia-Garrido, Marina, Mühlfriedel, Regine, Bolz, Sylvia, Hoffmann, Wolfgang, Schraermeyer, Ulrich, Mordmüller, Benjamin, Seeliger, Mathias W.
Publicado no Sci Rep (2019)

Noninvasive, In Vivo Assessment of Mouse Retinal Structure Using Optical Coherence Tomography

Por Fischer, M. Dominik, Huber, Gesine, Beck, Susanne C., Tanimoto, Naoyuki, Muehlfriedel, Regine, Fahl, Edda, Grimm, Christian, Wenzel, Andreas, Remé, Charlotte E., van de Pavert, Serge A., Wijnholds, Jan, Pacal, Marek, Bremner, Rod, Seeliger, Mathias W.
Publicado em 2009

PALS1 Is Essential for Retinal Pigment Epithelium Structure and Neural Retina Stratification

Por Park, Bokyung, Alves, Celso Henrique, Lundvig, Ditte M., Tanimoto, Naoyuki, Beck, Susanne C., Huber, Gesine, Richard, Fabrice, Klooster, Jan, Andlauer, Till F. M., Swindell, Eric C., Jamrich, Milan, Le Bivic, André, Seeliger, Mathias W., Wijnholds, Jan
Publicado no J Neurosci (2011)

Restoration of Cone Vision in the CNGA3(−/−) Mouse Model of Congenital Complete Lack of Cone Photoreceptor Function

Por Michalakis, Stylianos, Mühlfriedel, Regine, Tanimoto, Naoyuki, Krishnamoorthy, Vidhyasankar, Koch, Susanne, Fischer, M Dominik, Becirovic, Elvir, Bai, Lin, Huber, Gesine, Beck, Susanne C, Fahl, Edda, Büning, Hildegard, Paquet-Durand, François, Zong, Xiangang, Gollisch, Tim, Biel, Martin, Seeliger, Mathias W
Publicado em 2010

Targeted Ablation of Crb1 and Crb2 in Retinal Progenitor Cells Mimics Leber Congenital Amaurosis

Por Pellissier, Lucie P., Alves, Celso Henrique, Quinn, Peter M., Vos, Rogier M., Tanimoto, Naoyuki, Lundvig, Ditte M. S., Dudok, Jacobus J., Hooibrink, Berend, Richard, Fabrice, Beck, Susanne C., Huber, Gesine, Sothilingam, Vithiyanjali, Garcia Garrido, Marina, Le Bivic, André, Seeliger, Mathias W., Wijnholds, Jan
Publicado em 2013

Accessory heterozygous mutations in cone photoreceptor CNGA3 exacerbate CNG channel–associated retinopathy

Por Burkard, Markus, Kohl, Susanne, Krätzig, Timm, Tanimoto, Naoyuki, Brennenstuhl, Christina, Bausch, Anne E., Junger, Katrin, Reuter, Peggy, Sothilingam, Vithiyanjali, Beck, Susanne C., Huber, Gesine, Ding, Xi-Qin, Mayer, Anja K., Baumann, Britta, Weisschuh, Nicole, Zobor, Ditta, Hahn, Gesa-Astrid, Kellner, Ulrich, Venturelli, Sascha, Becirovic, Elvir, Charbel Issa, Peter, Koenekoop, Robert K., Rudolph, Günther, Heckenlively, John, Sieving, Paul, Weleber, Richard G., Hamel, Christian, Zong, Xiangang, Biel, Martin, Lukowski, Robert, Seeliger, Matthias W., Michalakis, Stylianos, Wissinger, Bernd, Ruth, Peter
Publicado no J Clin Invest (2018)

Mutations in the unfolded protein response regulator ATF6 cause the cone dysfunction disorder achromatopsia

Por Kohl, Susanne, Zobor, Ditta, Chiang, Wei-Chieh, Weisschuh, Nicole, Staller, Jennifer, Menendez, Irene Gonzalez, Chang, Stanley, Beck, Susanne C, Garrido, Marina Garcia, Sothilingam, Vithiyanjali, Seeliger, Mathias W, Stanzial, Franco, Benedicenti, Francesco, Inzana, Francesca, Héon, Elise, Vincent, Ajoy, Beis, Jill, Strom, Tim M, Rudolph, Günther, Roosing, Susanne, den Hollander, Anneke I, Cremers, Frans P M, Lopez, Irma, Ren, Huanan, Moore, Anthony T, Webster, Andrew R, Michaelides, Michel, Koenekoop, Robert K, Zrenner, Eberhart, Kaufman, Randal J, Tsang, Stephen H, Wissinger, Bernd, Lin, Jonathan H
Publicado no Nat Genet (2015)