Search Results - Zenker, Martin

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  1. 1
    Oculopharyngeal muscular dystrophy as a rare differential diagnosis for unexplained dysphagia: a case report

    Oculopharyngeal muscular dystrophy as a rare differential diagnosis for unexplained dysphagia: a case report by Bumm, Klaus, Zenker, Martin, Bozzato, Alessandro

    Published 2009
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  2. 2
    Clinical utility gene card for: Johanson–Blizzard syndrome

    Clinical utility gene card for: Johanson–Blizzard syndrome by Sukalo, Maja, Mayerle, Julia, Zenker, Martin

    Published 2014
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  3. 3
    Noonan syndrome and clinically related disorders

    Noonan syndrome and clinically related disorders by Tartaglia, Marco, Gelb, Bruce D., Zenker, Martin

    Published 2011
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  4. 4
    An unexpected new role of mutant Ras: perturbation of human embryonic development

    An unexpected new role of mutant Ras: perturbation of human embryonic development by Kratz, Christian P., Niemeyer, Charlotte M., Zenker, Martin

    Published 2007
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  5. 5
    Long-term Culture of EBV-induced Human Lymphoblastoid Cell Lines Reveals Chromosomal Instability

    Long-term Culture of EBV-induced Human Lymphoblastoid Cell Lines Reveals Chromosomal Instability by Volleth, Marianne, Zenker, Martin, Joksic, Ivana, Liehr, Thomas

    Published 2020
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  6. 6
    Johanson-Blizzard syndrome

    Johanson-Blizzard syndrome by Almashraki, Nabeel, Abdulnabee, Mukarram Zainuddin, Sukalo, Maja, Alrajoudi, Abdullah, Sharafadeen, Iman, Zenker, Martin

    Published 2011
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  7. 7
    Clinical and Genetic Distinction of Schimke Immuno-Osseous Dysplasia and Cartilage-Hair Hypoplasia

    Clinical and Genetic Distinction of Schimke Immuno-Osseous Dysplasia and Cartilage-Hair Hypoplasia by Baradaran-Heravi, Alireza, Thiel, Christian, Rauch, Anita, Zenker, Martin, Boerkoel, Cornelius F., Kaitila, Ilkka

    Published 2008
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  8. 8
    Johanson-Blizzard syndrome with mild phenotypic features confirmed by UBR1 gene testing

    Johanson-Blizzard syndrome with mild phenotypic features confirmed by UBR1 gene testing by Alkhouri, Naim, Kaplan, Barbara, Kay, Marsha, Shealy, Amy, Crowe, Carol, Bauhuber, Susanne, Zenker, Martin

    Published 2008
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  9. 9
    A Dual Phenotype of Periventricular Nodular Heterotopia and Frontometaphyseal Dysplasia in One Patient Caused by a Single FLNA Mutation Leading to Two Functionally Different Aberrant Transcripts

    A Dual Phenotype of Periventricular Nodular Heterotopia and Frontometaphyseal Dysplasia in One Patient Caused by a Single FLNA Mutation Leading to Two Functionally Different Aberra... by Zenker, Martin, Rauch, Anita, Winterpacht, Andreas, Tagariello, Andreas, Kraus, Cornelia, Rupprecht, Thomas, Sticht, Heinrich, Reis, André

    Published 2004
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  10. 10
    Neonatal progeria: increased ratio of progerin to lamin A leads to progeria of the newborn

    Neonatal progeria: increased ratio of progerin to lamin A leads to progeria of the newborn by Reunert, Janine, Wentzell, Rüdiger, Walter, Michael, Jakubiczka, Sibylle, Zenker, Martin, Brune, Thomas, Rust, Stephan, Marquardt, Thorsten

    Published 2012
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  11. 11
    Germline PTPN11 and somatic PIK3CA variant in a boy with megalencephaly-capillary malformation syndrome (MCAP) - pure coincidence?

    Germline PTPN11 and somatic PIK3CA variant in a boy with megalencephaly-capillary malformation syndrome (MCAP) - pure coincidence? by Döcker, Dennis, Schubach, Max, Menzel, Moritz, Spaich, Christiane, Gabriel, Heinz-Dieter, Zenker, Martin, Bartholdi, Deborah, Biskup, Saskia

    Published 2015
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  12. 12
    KRAS Mutation in an Implant-associated Peripheral Giant Cell Granuloma of the Jaw: Implications of Genetic Analysis of the Lesion for Treatment Concept and Surveillance

    KRAS Mutation in an Implant-associated Peripheral Giant Cell Granuloma of the Jaw: Implications of Genetic Analysis of the Lesion for Treatment Concept and Surveillance by FRIEDRICH, REINHARD E., WÜSTHOFF, FALK, LUEBKE, ANDREAS M., KOHLRUSCH, FELIX K., WIELAND, ILSE, ZENKER, MARTIN, GOSAU, MARTIN

    Published 2021
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  13. 13
    Three-dimensional morphometric analysis of the lateral clavicle and acromion: Implications for surgical treatment using subacromial support

    Three-dimensional morphometric analysis of the lateral clavicle and acromion: Implications for surgical treatment using subacromial support by Zenker, Martin, Shamsollahi, Javad, Galm, André, Hoyen, Harry A, Jiang, Chunyan, Lambert, Simon, Nijs, Stefaan, Jaeger, Martin

    Published 2022
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  14. 14
    Genomic Duplication of PTPN11 is an Uncommon Cause of Noonan Syndrome

    Genomic Duplication of PTPN11 is an Uncommon Cause of Noonan Syndrome by Graham, John M., Kramer, Nancy, Bejjani, Bassem A., Thiel, Christian T., Carta, Claudio, Neri, Giovanni, Tartaglia, Marco, Zenker, Martin

    Published 2009
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  15. 15
    Profiling of the Bacterial Microbiota along the Murine Alimentary Tract

    Profiling of the Bacterial Microbiota along the Murine Alimentary Tract by Vilchez-Vargas, Ramiro, Salm, Franz, Znalesniak, Eva B., Haupenthal, Katharina, Schanze, Denny, Zenker, Martin, Link, Alexander, Hoffmann, Werner

    Published 2022
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  16. 16
    Outcomes in growth hormone-treated Noonan syndrome children: impact of PTPN11 mutation status

    Outcomes in growth hormone-treated Noonan syndrome children: impact of PTPN11 mutation status by Jorge, Alexander A L, Edouard, Thomas, Maghnie, Mohamad, Pietropoli, Alberto, Kelepouris, Nicky, Romano, Alicia, Zenker, Martin, Horikawa, Reiko

    Published 2022
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  17. 17
    Clinical and Molecular Findings of Tunisian Patients with RASopathies

    Clinical and Molecular Findings of Tunisian Patients with RASopathies by Louati, Rim, Abdelmoula, N. Bouayed, Trabelsi, Imen, Abid, Dorra, Lissewski, Christina, Kharrat, Najla, Kamoun, Samir, Zenker, Martin, Rebai, Tarek

    Published 2014
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  18. 18
    Biochemical and Functional Characterization of Germ Line KRAS Mutations

    Biochemical and Functional Characterization of Germ Line KRAS Mutations by Schubbert, Suzanne, Bollag, Gideon, Lyubynska, Natalya, Nguyen, Hoa, Kratz, Christian P., Zenker, Martin, Niemeyer, Charlotte M., Molven, Anders, Shannon, Kevin

    Published 2007
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  19. 19
    Germline KRAS Mutations Cause Aberrant Biochemical and Physical Properties Leading to Developmental Disorders

    Germline KRAS Mutations Cause Aberrant Biochemical and Physical Properties Leading to Developmental Disorders by Gremer, Lothar, Merbitz-Zahradnik, Torsten, Dvorsky, Radovan, Cirstea, Ion C., Kratz, Christian Peter, Zenker, Martin, Wittinghofer, Alfred, Ahmadian, Mohammad Reza

    Published 2010
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  20. 20
    RIT1 controls actin dynamics via complex formation with RAC1/CDC42 and PAK1

    RIT1 controls actin dynamics via complex formation with RAC1/CDC42 and PAK1 by Meyer zum Büschenfelde, Uta, Brandenstein, Laura Isabel, von Elsner, Leonie, Flato, Kristina, Holling, Tess, Zenker, Martin, Rosenberger, Georg, Kutsche, Kerstin

    Published 2018
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