Search Results - Hartmut Peters

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  1. 1
    Missense mutations in the forkhead domain of FOXL2 lead to subcellular mislocalization, protein aggregation and impaired transactivation

    Missense mutations in the forkhead domain of FOXL2 lead to subcellular mislocalization, protein aggregation and impaired transactivation by Diane Beysen, Lara Moumné, Reiner A. Veitia, Hartmut Peters, Bart P. Leroy, Anne De Paepe, Elfride De Baere

    Published 2008
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  2. 2
    The Gene for Cherubism Maps to Chromosome 4p16

    The Gene for Cherubism Maps to Chromosome 4p16 by Valdenize Tiziani, Ernst Reichenberger, Celso Luiz Buzzo, Sadia Niazi, Naomi Fukai, Michael Stiller, Hartmut Peters, Francisco M. Salzano, Cassio Menezes Raposo do Amaral, Bjørn R. Olsen

    Published 1999
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  3. 3
    Minor Lesion Mutational Spectrum of the Entire NF1 Gene Does Not Explain Its High Mutability but Points to a Functional Domain Upstream of the GAP-Related Domain

    Minor Lesion Mutational Spectrum of the Entire NF1 Gene Does Not Explain Its High Mutability but Points to a Functional Domain Upstream of the GAP-Related Domain by Raimund Fahsold, Sven Hoffmeyer, Claudia Mischung, Christoph Gille, Christian Ehlers, Nazan Kücükceylan, Maher Abdel-Nour, Andreas Gewies, Hartmut Peters, Dieter Kaufmann, Annegret Buske, Sigrid Tinschert, Peter Nürnberg

    Published 2000
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  4. 4
    Deletions of the RUNX2 gene are present in about 10% of individuals with cleidocranial dysplasia

    Deletions of the RUNX2 gene are present in about 10% of individuals with cleidocranial dysplasia by Claus‐Eric Ott, Gundula Leschik, Fabienne Trotier, Louise Brueton, Han G. Brunner, Wim Brussel, Encarna Guillén‐Navarro, Claudia M. Haase, Juergen Kohlhase, Dieter Kotzot, Andrew Lane, Min Ae Lee‐Kirsch, Susanne Morlot, Marleen Simon, Elisabeth Steichen‐Gersdorf, David Tegay, Hartmut Peters, Stefan Mundlos, Eva Klopocki

    Published 2010
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  5. 5
    Multiple giant cell lesions in patients with Noonan syndrome and cardio-facio-cutaneous syndrome

    Multiple giant cell lesions in patients with Noonan syndrome and cardio-facio-cutaneous syndrome by Thomas Neumann, Judith Allanson, Ines Kavamura, Bronwyn Kerr, Giovanni Neri, Jacqueline A. Noonan, Viviana Cordeddu, Kate Gibson, Andreas Tzschach, Gabriele Krüger, Maria Hoeltzenbein, Timm O. Goecke, Hans-Gerd Kehl, Beate Albrecht, Klaudiusz Łuczak, Maria Sąsiadek, Luciana Musante, Rohan Laurie, Hartmut Peters, Marco Tartaglia, Martin Zenker, Vera M. Kalscheuer

    Published 2008
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