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  1. Jüschke, Christoph [Author]; Wächter, Andrea [Author]; Schwappach, Blanche [Author]; Seedorf, Matthias [Author]

    SEC18/NSF-independent, protein-sorting pathway from the yeast cortical ER to the plasma membrane

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    2005

    Published in: The journal of cell biology ; 169(2005), 4, Seite 613-622

  2. Swirski, Sebastian [Author]; May, Oliver [Author]; Ahlers, Malte Thorsten [Author]; Wissinger, Bernd [Author]; Greschner, Martin [Author]; Jüschke, Christoph [Author]; Neidhardt, John [Author]

    In vivo efficacy and safety evaluations of therapeutic splicing correction using U1 snRNA in the mouse retina

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    2023

    Published in: Cells ; 12(2023), 6, Artikel-ID 955, Seite 1-19

  3. Jüschke, Christoph [Author]; Klopstock, Thomas [Author]; Catarino, Claudia B. [Author]; Owczarek-Lipska, Marta [Author]; Wissinger, Bernd [Author] ; Neidhardt, John [Other]

    Autosomal dominant optic atrophy : a novel treatment for OPA1 splice defects using U1 snRNA adaption

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    2021

    Published in: Molecular therapy. Nucleic Acids ; 26(2021), Seite 1186-1197

  4. Vössing, Christine [Author]; Owczarek-Lipska, Marta [Author]; Nagel-Wolfrum, Kerstin [Author]; Reiff, Charlotte [Author]; Jüschke, Christoph [Author]; Neidhardt, John [Author]

    Translational read-through therapy of RPGR nonsense mutations

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    2020

    Published in: International journal of molecular sciences ; Volume 21 (2020), issue 22, Artikel-Nummer 8418, Seite 1-16

  5. Vössing, Christine [Author]; Owczarek-Lipska, Marta [Author]; Nagel-Wolfrum, Kerstin [Author]; Reiff, Charlotte M. [Author]; Jüschke, Christoph [Author]; Neidhardt, John [Author]

    Translational read-through therapy of RPGR nonsense mutations

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    Basel: MDPI AG, 2020

    Published in: International journal of molecular sciences ; 21, 22 (2020), 8418

  6. Usman, Muhammad [Author]; Jüschke, Christoph [Author]; Song, Fei [Author]; Kastrati, Dennis [Author]; Owczarek-Lipska, Marta [Author]; Eilers, Jannis [Author]; Pauleikhoff, Laurenz [Author]; Lange, Clemens [Author]; Neidhardt, John [Author]

    Skewed X-inactivation is associated with retinal dystrophy in female carriers of RPGR mutations

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    2023

    Published in: Life science alliance ; 6(2023), 10, Artikel-ID e202201814, Seite 1-12

  7. Reiff, Charlotte [Author]; Owczarek-Lipska, Marta [Author]; Spital, Georg [Author]; Röger, Carsten [Author]; Hinz, Hebke [Author]; Jüschke, Christoph [Author]; Thiele, Holger [Author]; Altmüller, Janine [Author]; Nürnberg, Peter [Author]; Da Costa, Romain [Author]; Neidhardt, John [Author]

    The mutation p.E113K in the Schiff base counterion of rhodopsin is associated with two distinct retinal phenotypes within the same family

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    Carl von Ossietzky Universität Oldenburg: /oops/ - Oldenburger Online-Publikations-Server, 2016

  8. Usman, Muhammad; Jüschke, Christoph; Song, Fei; Kastrati, Dennis; Owczarek-Lipska, Marta; Eilers, Jannis; Pauleikhoff, Laurenz; Lange, Clemens; Neidhardt, John

    Skewed X-inactivation is associated with retinal dystrophy in female carriers ofRPGRmutations

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    Life Science Alliance, LLC, 2023

    Published in: Life Science Alliance, 6 (2023) 10, Seite e202201814