Hasil Pencarian - Tim Ripperger

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  1. 1
    Managing individuals with propensity to myeloid malignancies due to germline RUNX1 deficiency

    Managing individuals with propensity to myeloid malignancies due to germline RUNX1 deficiency oleh Tim Ripperger, Marcel Tauscher, Detlef Haase, Frank Griesinger, Brigitte Schlegelberger, Doris Steinemann

    Diterbitkan 2011-12-01
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  2. 2
    Induced G1 phase arrest of fast-dividing cells improves the quality of genomic profiles generated by array-CGH

    Induced G1 phase arrest of fast-dividing cells improves the quality of genomic profiles generated by array-CGH oleh Georgi Manukjan, Marcel Tauscher, Tim Ripperger, Adrian Schwarzer, Brigitte Schlegelberger, Doris Steinemann

    Diterbitkan 2012-10-01
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  3. 3
    SPECTRUM OF CLINICAL PHENOTYPES AND SOMATIC VARIANTS IN RUNX1-ASSOCIATED FAMILIAL PLATELET DISORDER WITH PREDISPOSITION TO HEMATOLOGIC MALIGNANCIES

    SPECTRUM OF CLINICAL PHENOTYPES AND SOMATIC VARIANTS IN RUNX1-ASSOCIATED FAMILIAL PLATELET DISORDER WITH PREDISPOSITION TO HEMATOLOGIC MALIGNANCIES oleh Alisa Förster, Melanie Decker, Yvonne L. Behrens, Gudrun Göhring, Brigitte Schlegelberger, Tim Ripperger

    Diterbitkan 2023-12-01
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  4. 4
    FUNCTIONAL ANALYSES OF RUNX1 VARIANTS IN THE CONTEXT OF FAMILIAL PLATELET DISORDER WIT PREDISPOSITION TO HEMATOLOGIC MALIGNANCIES

    FUNCTIONAL ANALYSES OF RUNX1 VARIANTS IN THE CONTEXT OF FAMILIAL PLATELET DISORDER WIT PREDISPOSITION TO HEMATOLOGIC MALIGNANCIES oleh Melanie Decker, Förster Alisa, Prüne Alina, Anne Seebacher, Alena Wittstock, Thomas Illig, Brigitte Schlegelberger, Tim Ripperger

    Diterbitkan 2023-12-01
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  5. 5
    GABP is necessary for stem/progenitor cell maintenance and myeloid differentiation in human hematopoiesis and chronic myeloid leukemia

    GABP is necessary for stem/progenitor cell maintenance and myeloid differentiation in human hematopoiesis and chronic myeloid leukemia oleh Georgi Manukjan, Tim Ripperger, Letizia Venturini, Michael Stadler, Gudrun Göhring, Axel Schambach, Brigitte Schlegelberger, Doris Steinemann

    Diterbitkan 2016-05-01
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  6. 6
    Constitutional mismatch repair deficiency and childhood leukemia/lymphoma – report on a novel biallelic MSH6 mutation

    Constitutional mismatch repair deficiency and childhood leukemia/lymphoma – report on a novel biallelic MSH6 mutation oleh Tim Ripperger, Carmela Beger, Nils Rahner, Karl W. Sykora, Clemens L. Bockmeyer, Ulrich Lehmann, Hans H. Kreipe, Brigitte Schlegelberger

    Diterbitkan 2010-05-01
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  7. 7
    Progressive Immunodeficiency with Gradual Depletion of B and CD4<sup>+</sup> T Cells in Immunodeficiency, Centromeric Instability and Facial Anomalies Syndrome 2 (ICF2)

    Progressive Immunodeficiency with Gradual Depletion of B and CD4<sup>+</sup> T Cells in Immunodeficiency, Centromeric Instability and Facial Anomalies Syndrome 2 (ICF2) oleh Georgios Sogkas, Natalia Dubrowinskaja, Anke K. Bergmann, Jana Lentes, Tim Ripperger, Mykola Fedchenko, Diana Ernst, Alexandra Jablonka, Robert Geffers, Ulrich Baumann, Reinhold E. Schmidt, Faranaz Atschekzei

    Diterbitkan 2019-04-01
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  8. 8
    MDS1 and EVI1 complex locus (MECOM): a novel candidate gene for hereditary hematological malignancies

    MDS1 and EVI1 complex locus (MECOM): a novel candidate gene for hereditary hematological malignancies oleh Tim Ripperger, Winfried Hofmann, Jan C. Koch, Katayoon Shirneshan, Detlef Haase, Gerald Wulf, Peter R. Issing, Matthias Karnebogen, Gunnar Schmidt, Bernd Auber, Brigitte Schlegelberger, Thomas Illig, Birgit Zirn, Doris Steinemann

    Diterbitkan 2018-02-01
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  9. 9
    Breast cancer patients suggestive of Li-Fraumeni syndrome: mutational spectrum, candidate genes, and unexplained heredity

    Breast cancer patients suggestive of Li-Fraumeni syndrome: mutational spectrum, candidate genes, and unexplained heredity oleh Judith Penkert, Gunnar Schmidt, Winfried Hofmann, Stephanie Schubert, Maximilian Schieck, Bernd Auber, Tim Ripperger, Karl Hackmann, Marc Sturm, Holger Prokisch, Ursula Hille-Betz, Dorothea Mark, Thomas Illig, Brigitte Schlegelberger, Doris Steinemann

    Diterbitkan 2018-08-01
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  10. 10
    Promoter methylation of PARG1, a novel candidate tumor suppressor gene in mantle cell lymphomas

    Promoter methylation of PARG1, a novel candidate tumor suppressor gene in mantle cell lymphomas oleh Tim Ripperger, Nils von Neuhoff, Kathrin Kamphues, Makito Emura, Ulrich Lehmann, Marcel Tauscher, Margit Schraders, Patricia Groenen, Britta Skawran, Cornelia Rudolph, Evelyne Callet-Bauchu, Johan H.J.M. van Krieken, Brigitte Schlegelberger, Doris Steinemann

    Diterbitkan 2007-04-01
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  11. 11
    Plasma Metabolome Signature Indicative of BRCA1 Germline Status Independent of Cancer Incidence

    Plasma Metabolome Signature Indicative of BRCA1 Germline Status Independent of Cancer Incidence oleh Judith Penkert, Andre Märtens, Martin Seifert, Bernd Auber, Katja Derlin, Ursula Hille-Betz, Philipp Hörmann, Norman Klopp, Jana Prokein, Lisa Schlicker, Frank Wacker, Hannah Wallaschek, Brigitte Schlegelberger, Karsten Hiller, Karsten Hiller, Tim Ripperger, Thomas Illig, Thomas Illig

    Diterbitkan 2021-04-01
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  12. 12
    The RUNX1 database (RUNX1db): establishment of an expert curated RUNX1 registry and genomics database as a public resource for familial platelet disorder with myeloid malignancy

    The RUNX1 database (RUNX1db): establishment of an expert curated RUNX1 registry and genomics database as a public resource for familial platelet disorder with myeloid malignancy oleh Claire C. Homan, Sarah L. King-Smith, David M. Lawrence, Peer Arts, Jinghua Feng, James Andrews, Mark Armstrong, Thuong Ha, Julia Dobbins, Michael W. Drazer, Kai Yu, Csaba Bödör, Alan Cantor, Mario Cazzola, Erin Degelman, Courtney D. DiNardo, Nicolas Duployez, Remi Favier, Stefan Fröhling, Jude Fitzgibbon, Jeffery M. Klco, Alwin Krämer, Mineo Kurokawa, Joanne Lee, Luca Malcovati, Neil V. Morgan, Georges Natsoulis, Carolyn Owen, Keyur P. Patel, Claude Preudhomme, Hana Raslova, Hugh Rienhoff, Tim Ripperger, Rachael Schulte, Kiran Tawana, Elvira Velloso, Benedict Yan, Paul Liu, Lucy A. Godley, Andreas W. Schreiber, Christopher N. Hahn, Hamish S. Scott, Anna L. Brown

    Diterbitkan 2021-07-01
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  13. 13
    The complex genetic landscape of familial MDS and AML reveals pathogenic germline variants

    The complex genetic landscape of familial MDS and AML reveals pathogenic germline variants oleh Ana Rio-Machin, Tom Vulliamy, Nele Hug, Amanda Walne, Kiran Tawana, Shirleny Cardoso, Alicia Ellison, Nikolas Pontikos, Jun Wang, Hemanth Tummala, Ahad Fahad H. Al Seraihi, Jenna Alnajar, Findlay Bewicke-Copley, Hannah Armes, Michael Barnett, Adrian Bloor, Csaba Bödör, David Bowen, Pierre Fenaux, Andrew Green, Andrew Hallahan, Henrik Hjorth-Hansen, Upal Hossain, Sally Killick, Sarah Lawson, Mark Layton, Alison M. Male, Judith Marsh, Priyanka Mehta, Rogier Mous, Josep F. Nomdedéu, Carolyn Owen, Jiri Pavlu, Elspeth M. Payne, Rachel E. Protheroe, Claude Preudhomme, Nuria Pujol-Moix, Aline Renneville, Nigel Russell, Anand Saggar, Gabriela Sciuccati, David Taussig, Cynthia L. Toze, Anne Uyttebroeck, Peter Vandenberghe, Brigitte Schlegelberger, Tim Ripperger, Doris Steinemann, John Wu, Joanne Mason, Paula Page, Susanna Akiki, Kim Reay, Jamie D. Cavenagh, Vincent Plagnol, Javier F. Caceres, Jude Fitzgibbon, Inderjeet Dokal

    Diterbitkan 2020-02-01
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