Items where Author is "Weber, Bernhard"

Article

Grassmann, Felix and Weber, Bernhard (2017) Genetic risks and therapy development in retinal degeneration. MEDIZINISCHE GENETIK, 29 (2). pp. 195-201. ISSN 1863-5490

Moser, Christian and Lang, Sven A. and Hackl, Christina and Zhang, Hong and Lundgren, Karen and Hong, Victor and Mckenzie, Andres and Weber, Bernhard and Park, Jung S. and Schlitt, Hans J. and Geissler, Edward K. and Jung, Young D. and Stoeltzing, Oliver (2012) Oncogenic MST1R Activity in Pancreatic and Gastric Cancer Represents a Valid Target of HSP90 Inhibitors. ANTICANCER RESEARCH, 32 (2). pp. 427-437. ISSN 0250-7005, 1791-7530

Weigelt, Karin and Moehle, Christoph and Stempfl, Thomas and Weber, Bernhard and Langmann, Thomas (2008) An integrated workflow for analysis of ChIP-chip data. BIOTECHNIQUES, 45 (2). 131-+. ISSN 0736-6205, 1940-9818

Lommatzsch, Albrecht and Hermans, Pia and Weber, Bernhard and Pauleikhoff, Daniel (2007) Complement factor H variant Y402H and basal laminar deposits in exudative age-related macular degeneration. GRAEFES ARCHIVE FOR CLINICAL AND EXPERIMENTAL OPHTHALMOLOGY, 245 (11). pp. 1713-1716. ISSN 0721-832X

Conference or Workshop Item

Kellner, Simone and Stoehr, Heidi and Kiel, Christina and Weinitz, Silke and Farmand, Ghazaleh and Weber, Bernhard and Kellner, Ulrich (2023) Near-infrared autofluorescence in inherited retinal dystrophies. In: Annual Meeting of the Association for Research in Vision and Ophthalmology (ARVO), April 23-27, 2023, New Orleans, LA.

Berber, Patricia and Milenkovic, Andrea and Kiel, Christina and Michaelis, Lisa and Strunz, Tobias and Brandl, Caroline and Weber, Bernhard (2023) Patient-derived Retinal Organoid as a Disease Model for Adult-Onset Retinitis Pigmentosa 1. In: 55th European-Society of Human Genetics (ESHG) Conference, June 11-14, 2022, Vienna, Austria.

Kellner, Ulrich and Stoehr, Heidi and Kiel, Christina and Kellner, Simone and Weinitz, Silke and Farmand, Ghazaleh and Weber, Bernhard (2023) Wide-field optical coherence tomography in retinitis pigmentosa. In: Annual Meeting of the Association for Research in Vision and Ophthalmology (ARVO), April 23-27, 2023, New Orleans, LA.

Kiel, Christina and Strunz, Tobias and Hasler, Daniele and Meister, Gunter and Grassmann, Felix and Weber, Bernhard (2021) Allele-specific influence of seed polymorphism rs2168518 in hsa-miR-4513 on expression of neovascularization-associated genes. In: ARVO Annual Meeting 2021, Virtual meeting.

Other

Schaefer, Nicole and Busch, Catharina and Reinders, Joerg and Weber, Bernhard and Skerka, Christine and Pauly, Diana (2016) Newly generated antibodies affect the functional role of CFHR3 in complement and AMD. ASSOC RESEARCH VISION OPHTHALMOLOGY INC, ROCKVILLE.

Schaefer, Nicole and Foeckler, Renate and Eckert, Elfriede and Dannullis, Andrea and Reinders, Joerg and Weber, Bernhard and Skerka, Christine and Pauly, Diana (2015) Newly generated antibodies indicate CFHR3 function in the humane complement system. PERGAMON-ELSEVIER SCIENCE LTD, OXFORD.

Kellner, Ulrich and Kellner, Simone and Weinitz, Silke and Farmand, Gazaleh and Stoehr, Heidi and Weber, Bernhard (2013) Follow-up Of 36 Years In Autosomal Dominant Gyrate-Atrophy Like Choroidal Dystrophy. ASSOC RESEARCH VISION OPHTHALMOLOGY INC, ROCKVILLE.

Langmann, Thomas and Moehle, Christoph and Karlstetter, Marcus and Weber, Bernhard (2013) Loss of MicroRNA-124 and MicroRNA-126 expression regulates inflammatory microglial activation in inherited retinal degeneration. ASSOC RESEARCH VISION OPHTHALMOLOGY INC, ROCKVILLE.