檢索結果 - Michael Zeschnigk

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  1. 1
    A novel real-time PCR assay for quantitative analysis of methylated alleles (QAMA): analysis of the retinoblastoma locus

    A novel real-time PCR assay for quantitative analysis of methylated alleles (QAMA): analysis of the retinoblastoma locus 由 Michael Zeschnigk

    出版 2004
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  2. 2
    Expression pattern of M‐cadherin in normal, denervated, and regenerating mouse muscles

    Expression pattern of M‐cadherin in normal, denervated, and regenerating mouse muscles 由 Andrey Irintchev, Michael Zeschnigk, Anna Starzinski‐Powitz, A. Wernig

    出版 1994
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  3. 3
    Molecular pathology of uveal melanoma

    Molecular pathology of uveal melanoma 由 Sarah E. Coupland, Sarah L. Lake, Michael Zeschnigk, Bertil Damato

    出版 2012
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  4. 4
    Imprinted Segments in the Human Genome: Different Dna Methylation Patterns in the Prader-Willi/Angelman Syndrome Region As Determined by the Genomic Sequencing Method

    Imprinted Segments in the Human Genome: Different Dna Methylation Patterns in the Prader-Willi/Angelman Syndrome Region As Determined by the Genomic Sequencing Method 由 Michael Zeschnigk, Birgit Schmitz, Bärbel Dittrich, Karin Buiting, B. Horsthemke, Walter Doerfler

    出版 1997
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  5. 5
    Prognostic significance of chromosome 3 alterations determined by microsatellite analysis in uveal melanoma: a long-term follow-up study

    Prognostic significance of chromosome 3 alterations determined by microsatellite analysis in uveal melanoma: a long-term follow-up study 由 Stefanie M. Thomas, Carolin Pütter, Stefanie Weber, Norbert Bornfeld, Dietmar Lohmann, Michael Zeschnigk

    出版 2012
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  6. 6
    Ultradeep sequencing detects <scp><i>GNAQ</i></scp> and <scp><i>GNA11</i></scp> mutations in cell‐free <scp>DNA</scp> from plasma of patients with uveal melanoma

    Ultradeep sequencing detects <scp><i>GNAQ</i></scp> and <scp><i>GNA11</i></scp> mutations in cell‐free <scp>DNA</scp> from plasma of patients with uveal melanoma 由 Claudia H.D. Metz, M. E. Scheulen, Norbert Bornfeld, Dietmar Lohmann, Michael Zeschnigk

    出版 2013
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  7. 7
    Somatic mosaicism in patients with Angelman syndrome and an imprinting defect

    Somatic mosaicism in patients with Angelman syndrome and an imprinting defect 由 Hülya Nazlican, Michael Zeschnigk, Uwe Claussen, Susanne Michel, Stefan Böehringer, Gabriele Gillessen‐Kaesbach, Karin Buiting, Bernhard Horsthemke

    出版 2004
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  8. 8
    Relevance of Foxp3<sup>+</sup> regulatory T cells for early and late phases of murine sepsis

    Relevance of Foxp3<sup>+</sup> regulatory T cells for early and late phases of murine sepsis 由 Marina Tatura, Michael Zeschnigk, Wiebke Hansen, Joerg Steinmann, Pedrina Gonçalves Vidigal, Marina Hutzler, Eva Pastille, Astrid M. Westendorf, Jan Buer, Jan Kehrmann

    出版 2015
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  9. 9
    Methylation and Silencing of the Retinoic Acid Receptor- 2 Gene in Breast Cancer

    Methylation and Silencing of the Retinoic Acid Receptor- 2 Gene in Breast Cancer 由 Martin Widschwendter, Jennifer Berger, Martin Hermann, Hanna M. Müller, Albert Amberger, Michael Zeschnigk, Andreas Widschwendter, Burghard Abendstein, AG Zeimet, G. Daxenbichler, C Marth

    出版 2000
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  10. 10
    TERT promoter mutations in ocular melanoma distinguish between conjunctival and uveal tumours

    TERT promoter mutations in ocular melanoma distinguish between conjunctival and uveal tumours 由 Klaus Griewank, Rajmohan Murali, Bastian Schilling, Simone L. Scholz, Antje Sucker, Mingxia Song, Daniela Süßkind, Florian Grabellus, Lisa Zimmer, Uwe Hillen, Steuhl Kp, Dirk Schadendorf, Henrike Westekemper, Michael Zeschnigk

    出版 2013
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  11. 11
    eIF1A residues implicated in cancer stabilize translation preinitiation complexes and favor suboptimal initiation sites in yeast

    eIF1A residues implicated in cancer stabilize translation preinitiation complexes and favor suboptimal initiation sites in yeast 由 Pilar Martín-Marcos, Fujun Zhou, Charm Karunasiri, Fan Zhang, Jinsheng Dong, Jagpreet S. Nanda, Shardul D. Kulkarni, Neelam Dabas Sen, Mercedes Tamame, Michael Zeschnigk, Jon R. Lorsch, Alan G. Hinnebusch

    出版 2017
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  12. 12
    Exome sequencing identifies recurrent somatic mutations in EIF1AX and SF3B1 in uveal melanoma with disomy 3

    Exome sequencing identifies recurrent somatic mutations in EIF1AX and SF3B1 in uveal melanoma with disomy 3 由 Marcel Martin, Lars Maßhöfer, Petra Temming, Sven Rahmann, Claudia H.D. Metz, Norbert Bornfeld, Johannes van de Nes, Ludger Klein‐Hitpaß, Alan G. Hinnebusch, Bernhard Horsthemke, Dietmar Lohmann, Michael Zeschnigk

    出版 2013
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  13. 13
    Pancreatic cancer acquires resistance to MAPK pathway inhibition by clonal expansion and adaptive DNA hypermethylation

    Pancreatic cancer acquires resistance to MAPK pathway inhibition by clonal expansion and adaptive DNA hypermethylation 由 Laura Godfrey, Jan Förster, Sven‐Thorsten Liffers, Christopher Schröder, Johannes Köster, Leonie Henschel, Kerstin U. Ludwig, David Lähnemann, Marija Trajkovic‐Arsic, Diana Behrens, Aldo Scarpa, Rita T. Lawlor, Kathrin E. Witzke, Barbara Sitek, Steven A. Johnsen, Sven Rahmann, Bernhard Horsthemke, Michael Zeschnigk, Jens T. Siveke

    出版 2024
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  14. 14
    Acquired IFNγ resistance impairs anti-tumor immunity and gives rise to T-cell-resistant melanoma lesions

    Acquired IFNγ resistance impairs anti-tumor immunity and gives rise to T-cell-resistant melanoma lesions 由 Antje Sucker, Fang Zhao, Natalia Pieper, Christina Heeke, Raffaela Maltaner, Nadine Stadtler, Birgit Real, Nicola Bielefeld, Sebastian Howe, Benjamin Weide, Ralf Gutzmer, Jochen Utikal, Carmen Loquai, Helen Gogas, Ludger Klein‐Hitpaß, Michael Zeschnigk, Astrid M. Westendorf, Mirko Trilling, Susanne Horn, Bastian Schilling, Dirk Schadendorf, Klaus Griewank, Annette Paschen

    出版 2017
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  15. 15
    Compound Heterozygosity of Low-Frequency Promoter Deletions and Rare Loss-of-Function Mutations in TXNL4A Causes Burn-McKeown Syndrome

    Compound Heterozygosity of Low-Frequency Promoter Deletions and Rare Loss-of-Function Mutations in TXNL4A Causes Burn-McKeown Syndrome 由 Dagmar Wieczorek, William G. Newman, Thomas Wieland, Tea Berulava, Maria Kaffe, D. Falkenstein, Christian Beetz, Elisabeth Graf, Thomas Schwarzmayr, Sofia Douzgou, Jill Clayton‐Smith, Sarah B. Daly, Simon G. Williams, Sanjeev S. Bhaskar, Jill Urquhart, Beverley Anderson, James O’Sullivan, Odile Boute, Jasmin Gundlach, Johanna Christina Czeschik, Anthonie J. van Essen, Fılız Hazan, Sarah Park, Anne Hing, Alma Kuechler, Dietmar Lohmann, Kerstin U. Ludwig, Elisabeth Mangold, Laura Steenpaß, Michael Zeschnigk, Johannes R. Lemke, Charles Marques Lourenço, Ute Hehr, Eva-Christina Prott, Mélanie Waldenberger, Anne C. Böhmer, Bernhard Horsthemke, Raymond T. O’Keefe, Thomas Meitinger, John Burn, H.-J. Lüdecke, Tim M. Strom

    出版 2014
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  16. 16
    A comprehensive molecular study on Coffin–Siris and Nicolaides–Baraitser syndromes identifies a broad molecular and clinical spectrum converging on altered chromatin remodeling

    A comprehensive molecular study on Coffin–Siris and Nicolaides–Baraitser syndromes identifies a broad molecular and clinical spectrum converging on altered chromatin remodeling 由 Dagmar Wieczorek, Nina Bögershausen, Filippo Beleggia, Sabine Steiner-Haldenstätt, Esther Pohl, Yun Li, Esther Milz, Marcel Martin, Holger Thiele, Janine Altmüller, Yasemin Alanay, Hülya Kayserili, Ludger Klein‐Hitpaß, Stefan Böhringer, Andreas Wollstein, Beate Albrecht, Koray Boduroğlu, Almuth Caliebe, Krystyńa Chrzańowska, Özgür Çoğulu, Francesca Cristofoli, Johanna Christina Czeschik, Koenraad Devriendt, Maria Teresa Dotti, Nursel Elçioğlu, Blanca Gener, Timm O. Goecke, Małgorzata Krajewska‐Walasek, Encarna Guillén‐Navarro, Joussef Hayek, Gunnar Houge, Esra KAYA KILIÇ, Pelin Özlem Şimşek‐Kiper, Vanesa López‐González, Alma Kuechler, Stanislas Lyonnet, Francesca Mari, Annabella Marozza, Michèle Mathieu Dramard, Barbara Mikat, G Morin, Fanny Morice‐Picard, Ferda Özkınay, Anita Rauch, Alessandra Renieri, Sigrid Tinschert, Gülen Eda Ütine, Catheline Vilain, Rossella Vivarelli, Christiane Zweier, Peter Nürnberg, Sven Rahmann, Joris Vermeesch, Hermann‐Josef Lüdecke, Michael Zeschnigk, Bernd Wollnik

    出版 2013
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