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Institute of Human Genetics

The focus of the research group of Bernhard Weber is on disease mechanisms in hereditary as well as multifactorial retinal degenerations

Methodology

  • Generation of mouse models – transgene, knock-in, knock-out
  • Genetic, biochemistry, cell biology, functional assays

Scientific Cooperations

  • Cooperation 1
    Robert, S. Molday, Department of Biochemistry and Molecular Bioloqv, University of British Columbia, Vancouver, B.C., Canada
  • Cooperation 2
    William W. Hauswirth, Ophthalmology, University of Florida, Gainesville, FL
  • Cooperation 3
    Rando Allikmets, Departments of Ophthalmology and Pathology & Cell Biology, Columbia University, New York, NY
  • Cooperation 4
    Sheila A. Fisher, Department of Medical and Molecular Genetics, Guy's King's and St Thomas' School of Medicine, King's College London, London, United Kingdom
  • Cooperation 5
    Ulrich Kellner, EyeCentre Siegburg, Siegburg-Bonn, Germany

Group Leader

Bernhard Weber
[more information]

Contact

University of Regensburg

Franz-Josef-Strauss-Allee 11
D-93053 Regensburg
Germany

Phone: +49-941 944 5400
Fax: +49-941 944 5402

Email:
bweb[at]klinik.uni-regensburg.de

Website:
www-huge.uni-regensburg.de/Humangenetik.shtml

Current Research Projects

  • Project 1
    Function of bestrophin-1 and molecular pathology of Best disease mutations
  • Project 2
    The role of retinoschisin - Identification of interacting partners
  • Project 3
    Therapeutic approaches in hereditary retinal degeneration – the retinoschisin-deficient mouse as a model
  • Project 4
    Genetics of age-related macular degeneration – Understanding disease pathology

Research Groups

People

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age-related macular degeneration
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cell membrane/membrane specializations
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degenerations/dystrophies
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inner retina dysfunction: biochemistry and cell biology
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macular dystrophy, inherited
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molecular diagnostics
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proteins encoded by disease genes
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retinal degenerations: hereditary
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retinal pigment epithelium
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transcription factors
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transgenics/knock-outs
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hereditary retinal dystrophy
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case /control association studies
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genetic mouse model
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functional studies
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