Resultados de procura - Mathias Woidy

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  1. 1
    Mapping the functional landscape of frequent<i>phenylalanine hydroxylase</i>(<i>PAH</i>) genotypes promotes personalised medicine in phenylketonuria

    Mapping the functional landscape of frequent<i>phenylalanine hydroxylase</i>(<i>PAH</i>) genotypes promotes personalised medicine in phenylketonuria por Marta K. Danecka, Mathias Woidy, Johannes Zschocke, François Feillet, Ania C. Muntau, Søren W. Gersting

    Publicado 2015
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  2. 2
    The interplay between genotype, metabolic state and cofactor treatment governs phenylalanine hydroxylase function and drug response

    The interplay between genotype, metabolic state and cofactor treatment governs phenylalanine hydroxylase function and drug response por Michael Staudigl, Søren W. Gersting, Marta K. Danecka, Dunja D. Messing, Mathias Woidy, D.M. Pinkas, Kristina Kemter, Nenad Blau, Ania C. Muntau

    Publicado 2011
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  3. 3
    Accumulation of α-synuclein mediates podocyte injury in Fabry nephropathy

    Accumulation of α-synuclein mediates podocyte injury in Fabry nephropathy por Fabian Braun, Ahmed H. Abed, Dominik Sellung, Manuel Rogg, Mathias Woidy, Øystein Eikrem, Nicola Wanner, Jessica Gambardella, Sandra D. Laufer, Fabian Haas, Milagros N. Wong, Bernhard Dumoulin, Paula Franziska Rischke, Anne K. Mühlig, Wiebke Sachs, Katharina von Cossel, Kristina Schulz, Nicole Muschol, Søren W. Gersting, Ania C. Muntau, Oliver Kretz, Oliver Hahn, Markus M. Rinschen, Michael Mauer, Tillmann Bork, Florian Grahammer, Wei Liang, Thorsten Eierhoff, Winfried Römer, Arne Hansen, Catherine Meyer-Schwesinger, Guido Iaccarino, Camilla Tøndel, Hans‐Peter Marti, Behzad Najafian, Victor G. Puelles, Christoph Schell, Tobias B. Huber

    Publicado 2023
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