Ngā hua rapu - Kerstin Nagel‐Wolfrum

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  1. 1
    Ataluren for the Treatment of Usher Syndrome 2A Caused by Nonsense Mutations

    Ataluren for the Treatment of Usher Syndrome 2A Caused by Nonsense Mutations mā A. Samanta, Katarína Štingl, Susanne Kohl, Jessica Ries, Joshua Linnert, Kerstin Nagel‐Wolfrum

    I whakaputaina 2019
    Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
    Artigo
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  2. 2
    The Interaction of Specific Peptide Aptamers With the DNA Binding Domain and the Dimerization Domain of the Transcription Factor Stat3 Inhibits Transactivation and Induces Apoptosis in Tumor Cells

    The Interaction of Specific Peptide Aptamers With the DNA Binding Domain and the Dimerization Domain of the Transcription Factor Stat3 Inhibits Transactivation and Induces Apoptosi... mā Kerstin Nagel‐Wolfrum, Claudia Buerger, Ilka Wittig, Karin Butz, Felix Hoppe‐Seyler, Bernd Groner

    I whakaputaina 2004
    Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
    Artigo
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  3. 3
    Characterization of the ternary Usher syndrome SANS/ush2a/whirlin protein complex

    Characterization of the ternary Usher syndrome SANS/ush2a/whirlin protein complex mā Nasrin Sorusch, Katharina Bauß, Janet Plutniok, A. Samanta, Barbara Knapp, Kerstin Nagel‐Wolfrum, Uwe Wolfrum

    I whakaputaina 2017
    Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
    Artigo
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  4. 4
    Sequence-specific Peptide Aptamers, Interacting with the Intracellular Domain of the Epidermal Growth Factor Receptor, Interfere with Stat3 Activation and Inhibit the Growth of Tumor Cells

    Sequence-specific Peptide Aptamers, Interacting with the Intracellular Domain of the Epidermal Growth Factor Receptor, Interfere with Stat3 Activation and Inhibit the Growth of Tum... mā Claudia Buerger, Kerstin Nagel‐Wolfrum, Christian Künz, Ilka Wittig, Karin Butz, Felix Hoppe‐Seyler, Bernd Groner

    I whakaputaina 2003
    Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
    Artigo
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  5. 5
    The retinitis pigmentosa protein RP2 links pericentriolar vesicle transport between the Golgi and the primary cilium

    The retinitis pigmentosa protein RP2 links pericentriolar vesicle transport between the Golgi and the primary cilium mā R. Jane Evans, Nele Schwarz, Kerstin Nagel‐Wolfrum, Uwe Wolfrum, Alison J. Hardcastle, Michael E. Cheetham

    I whakaputaina 2010
    Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
    Artigo
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  6. 6
    A comparative evaluation of NB30, NB54 and PTC124 in translational read‐through efficacy for treatment of an <i>USH1C</i> nonsense mutation

    A comparative evaluation of NB30, NB54 and PTC124 in translational read‐through efficacy for treatment of an <i>USH1C</i> nonsense mutation mā Tobias Goldmann, Nora Overlack, Fabian Möller, Valery Belakhov, Michiel van Wyk, Timor Baasov, Uwe Wolfrum, Kerstin Nagel‐Wolfrum

    I whakaputaina 2012
    Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
    Artigo
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  7. 7
    Disruption of the retinitis pigmentosa 28 gene Fam161a in mice affects photoreceptor ciliary structure and leads to progressive retinal degeneration

    Disruption of the retinitis pigmentosa 28 gene Fam161a in mice affects photoreceptor ciliary structure and leads to progressive retinal degeneration mā Marcus Karlstetter, Nasrin Sorusch, Albert Caramoy, Katharina Dannhausen, Alexander Aslanidis, Sascha Fauser, Michael Boesl, Kerstin Nagel‐Wolfrum, Ernst R. Tamm, Herbert Jägle, Heidi Stoehr, Uwe Wolfrum, Thomas Langmann

    I whakaputaina 2014
    Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
    Artigo
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  8. 8
    A Homozygous Mutation in the<i><scp>TUB</scp></i>Gene Associated with Retinal Dystrophy and Obesity

    A Homozygous Mutation in the<i><scp>TUB</scp></i>Gene Associated with Retinal Dystrophy and Obesity mā Arundhati Dev Borman, Laura R. Pearce, Donna S. Mackay, Kerstin Nagel‐Wolfrum, Alice E. Davidson, Robert Henderson, Sumedha Garg, Naushin Waseem, Andrew R. Webster, Vincent Plagnol, Uwe Wolfrum, I. Sadaf Farooqi, Anthony T. Moore

    I whakaputaina 2013
    Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
    Artigo
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  9. 9
    PEX6 is Expressed in Photoreceptor Cilia and Mutated in Deafblindness with Enamel Dysplasia and Microcephaly

    PEX6 is Expressed in Photoreceptor Cilia and Mutated in Deafblindness with Enamel Dysplasia and Microcephaly mā Maha S. Zaki, Raoul Heller, Michaela Thoenes, Gudrun Nürnberg, Gabi Stern-Schneider, Peter Nürnberg, Srikanth Karnati, Daniel Swan, Ekram Fateen, Kerstin Nagel‐Wolfrum, Mostafa I. Mostafa, Hölger Thiele, Uwe Wolfrum, Eveline Baumgart‐Vogt, Hanno J. Bolz

    I whakaputaina 2015
    Whiwhi kuputuhi katoa
    Artigo
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  10. 10
    Translational read-through of the RP2 Arg120stop mutation in patient iPSC-derived retinal pigment epithelium cells

    Translational read-through of the RP2 Arg120stop mutation in patient iPSC-derived retinal pigment epithelium cells mā Nele Schwarz, Amanda‐Jayne F. Carr, Amelia Lane, Fabian Moeller, Li Chen, Mònica Aguilà, Britta Nommiste, Manickam Nick Muthiah, Naheed Kanuga, Uwe Wolfrum, Kerstin Nagel‐Wolfrum, Lyndon da Cruz, Peter Coffey, Michael E. Cheetham, Alison J. Hardcastle

    I whakaputaina 2014
    Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
    Artigo
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  11. 11
    Human brain organoids assemble functionally integrated bilateral optic vesicles

    Human brain organoids assemble functionally integrated bilateral optic vesicles mā Elke Gabriel, Walid Albanna, Giovanni Pasquini, Anand Ramani, Nataša Josipović, Aruljothi Mariappan, Friedrich Schinzel, Celeste M. Karch, Guobin Bao, Marco Gottardo, Ata Alp Suren, Jürgen Hescheler, Kerstin Nagel‐Wolfrum, Veronica Persico, Silvio O. Rizzoli, Janine Altmüller, Maria Giovanna Riparbelli, Giuliano Callaini, Olivier Goureau, Argyris Papantonis, Volker Busskamp, Toni Schneider, Jay Gopalakrishnan

    I whakaputaina 2021
    Whiwhi kuputuhi katoa
    Artigo
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  12. 12
    Next-generation sequencing reveals the mutational landscape of clinically diagnosed Usher syndrome: copy number variations, phenocopies, a predominant target for translational read-through, and<i>PEX26</i>mutated in Heimler syndrome

    Next-generation sequencing reveals the mutational landscape of clinically diagnosed Usher syndrome: copy number variations, phenocopies, a predominant target for translational read... mā Christine Neuhaus, Tobias Eisenberger, Christian Decker, Sandra Nagl, Cornelia Blank, Markus Pfister, Ingo Kennerknecht, Cornelie Müller-Hofstede, Peter Charbel Issa, Raoul Heller, Bodo B. Beck, Klaus Rüther, Diana Mitter, Klaus Rohrschneider, Ute Steinhauer, Heike Korbmacher, Dagmar Huhle, Solaf M. Elsayed, Hesham M. Taha, Shahid Mahmood Baig, Heidi Stöhr, Markus N. Preising, Susanne Markus, Fabian Moeller, Birgit Lorenz, Kerstin Nagel‐Wolfrum, Arif O. Khan, Hanno J. Bolz

    I whakaputaina 2017
    Whiwhi kuputuhi katoa
    Artigo
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  13. 13
    Early disruption of photoreceptor cell architecture and loss of vision in a humanized pig model of usher syndromes

    Early disruption of photoreceptor cell architecture and loss of vision in a humanized pig model of usher syndromes mā Sophia Grotz, Jessica Schäfer, Kirsten A. Wunderlich, Zdeňka Ellederová, Hannah Auch, Andrea Bähr, Petra Vochozková, Janet Fadl, Vanessa Arnold, Taras Ardan, Miroslav Veith, Gianluca Santamaria, G. Dhom, Wolfgang Hitzl, Barbara Keßler, C. Eckardt, Joshua P. Klein, Anna Brýmová, Joshua Linnert, Mayuko Kurome, Valeri Zakharchenko, Andrea Fischer, Andreas Blutke, Anna Döring, Stepanka Suchankova, Jiří Popelář, Eduardo Rodríguez‐Bocanegra, Julia Dlugaiczyk, Hans Straka, Helen May‐Simera, Weiwei Wang, Karl‐Ludwig Laugwitz, Luk H. Vandenberghe, Eckhard Wolf, Kerstin Nagel‐Wolfrum, Tobias Peters, Jan Motlík, M. Dominik Fischer, Uwe Wolfrum, Nikolai Klymiuk

    I whakaputaina 2022
    Whiwhi kuputuhi katoa
    Artigo
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