Výsledky vyhledávání - Martin Granzow

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  1. 1
    A Practical Approach to Microarray Data Analysis

    A Practical Approach to Microarray Data Analysis Autor Daniel Berrar, Werner Dubitzky, Martin Granzow

    Vydáno 2003
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  2. 2
    The RIN: an RNA integrity number for assigning integrity values to RNA measurements

    The RIN: an RNA integrity number for assigning integrity values to RNA measurements Autor Andreas Schröeder, Odilo Mueller, Susanne Stocker, Ruediger Salowsky, Michael J. Leiber, Marcus Gassmann, Samar Lightfoot, Wolfram Menzel, Martin Granzow, Thomas Ragg

    Vydáno 2006
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  3. 3
    Glycodelin: A New Biomarker with Immunomodulatory Functions in Non–Small Cell Lung Cancer

    Glycodelin: A New Biomarker with Immunomodulatory Functions in Non–Small Cell Lung Cancer Autor Marc A. Schneider, Martin Granzow, Arne Warth, Philipp A. Schnabel, Michael Thomas, Felix J.F. Herth, Hendrik Dienemann, Thomas Muley, Michael Meister

    Vydáno 2015
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  4. 4
    Progression in Smoldering Myeloma Is Independently Determined by the Chromosomal Abnormalities del(17p), t(4;14), Gain 1q, Hyperdiploidy, and Tumor Load

    Progression in Smoldering Myeloma Is Independently Determined by the Chromosomal Abnormalities del(17p), t(4;14), Gain 1q, Hyperdiploidy, and Tumor Load Autor Kai Neben, Anna Jauch, Thomas Hielscher, Jens Hillengaß, Nicola Lehners, Anja Seckinger, Martin Granzow, Marc S. Raab, Anthony D. Ho, Hartmut Goldschmidt, Dirk Hose

    Vydáno 2013
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  5. 5
    Translocation t(11;14) Is Associated With Adverse Outcome in Patients With Newly Diagnosed AL Amyloidosis When Treated With Bortezomib-Based Regimens

    Translocation t(11;14) Is Associated With Adverse Outcome in Patients With Newly Diagnosed AL Amyloidosis When Treated With Bortezomib-Based Regimens Autor Tilmann Bochtler, Ute Hegenbart, Christina Kunz, Martin Granzow, Axel Benner, Anja Seckinger, Christoph Kimmich, Hartmut Goldschmidt, Anthony D. Ho, Dirk Hose, Anna Jauch, Stefan Schönland

    Vydáno 2015
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  6. 6
    Hodgkin's lymphoma cell lines are characterized by frequent aberrations on chromosomes 2p and 9p including <i>REL</i> and <i>JAK2</i>

    Hodgkin's lymphoma cell lines are characterized by frequent aberrations on chromosomes 2p and 9p including <i>REL</i> and <i>JAK2</i> Autor Stefan Joos, Martin Granzow, Heidi Holtgreve‐Grez, Reiner Siebert, Lana Harder, José I. Martín‐Subero, Jürgen Wolf, Martyna Adamowicz, Thomas F.E. Barth, Peter Lichter, Anna Jauch

    Vydáno 2002
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  7. 7
    Prognostic impact of cytogenetic aberrations in AL amyloidosis patients after high-dose melphalan: a long-term follow-up study

    Prognostic impact of cytogenetic aberrations in AL amyloidosis patients after high-dose melphalan: a long-term follow-up study Autor Tilmann Bochtler, Ute Hegenbart, Christina Kunz, Axel Benner, Christoph Kimmich, Anja Seckinger, Dirk Hose, Hartmut Goldschmidt, Martin Granzow, Peter Dreger, Anthony D. Ho, Anna Jauch, Stefan Schönland

    Vydáno 2016
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  8. 8
    From latent disseminated cells to overt metastasis: Genetic analysis of systemic breast cancer progression

    From latent disseminated cells to overt metastasis: Genetic analysis of systemic breast cancer progression Autor Oleg Schmidt‐Kittler, Thomas Ragg, Angela Daskalakis, Martin Granzow, A. Ahr, Thomas Blankenstein, Manfred Kaufmann, Joachim Diebold, H Arnholdt, Peter E. Müller, Joachim Bischoff, Detlev Harich, Günter Schlimok, Gert Riethmüller, Roland Eils, Christoph A. Klein

    Vydáno 2003
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  9. 9
    Impact of clinical exomes in neurodevelopmental and neurometabolic disorders

    Impact of clinical exomes in neurodevelopmental and neurometabolic disorders Autor Christina Evers, Christian Staufner, Martin Granzow, Nagarajan Paramasivam, Katrin Hinderhofer, Lilian Kaufmann, Christine Fischer, Christian Thiel, Thomas Opladen, Urania Kotzaeridou, Stefan Wiemann, Matthias Schlesner, Roland Eils, Stefan Kölker, Claus R. Bartram, Georg F. Hoffmann, Ute Moog

    Vydáno 2017
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  10. 10
    <i>DDX3X</i> mutations in two girls with a phenotype overlapping Toriello–Carey syndrome

    <i>DDX3X</i> mutations in two girls with a phenotype overlapping Toriello–Carey syndrome Autor Nicola Dikow, Martin Granzow, Luitgard Graul‐Neumann, Stephanie Karch, Katrin Hinderhofer, Nagarajan Paramasivam, Laura‐Jane Behl, Lilian Kaufmann, Christine Fischer, Christina Evers, Matthias Schlesner, Roland Eils, Guntram Borck, Christiane Zweier, Claus R. Bartram, John C. Carey, Ute Moog

    Vydáno 2017
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  11. 11
    Marker chromosomes can arise from chromothripsis and predict adverse prognosis in acute myeloid leukemia

    Marker chromosomes can arise from chromothripsis and predict adverse prognosis in acute myeloid leukemia Autor Tilmann Bochtler, Martin Granzow, Friedrich Stölzel, Christina Kunz, Brigitte Mohr, Mutlu Kartal‐Kaess, Katrin Hinderhofer, Christoph E. Heilig, Michael Krämer, Christian Thiede, Volker Endris, Martina Kirchner, Albrecht Stenzinger, Axel Benner, Martin Bornhäuser, Gerhard Ehninger, Anthony D. Ho, Anna Jauch, Alwin Krämer

    Vydáno 2017
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  12. 12
    miR-16 and miR-125b are involved in barrier function dysregulation through the modulation of claudin-2 and cingulin expression in the jejunum in IBS with diarrhoea

    miR-16 and miR-125b are involved in barrier function dysregulation through the modulation of claudin-2 and cingulin expression in the jejunum in IBS with diarrhoea Autor Cristina Martínez, Bruno K. Rodiño‐Janeiro, Beatriz Lobo, Megan L. Stanifer, Bernd Klaus, Martin Granzow, Ana María González-Castro, Eloísa Salvo‐Romero, Carmen Alonso, Marc Pigrau, Ralph Roeth, Gudrun Rappold, Wolfgang Huber, Rosa González-Silos, Justo Lorenzo, Inés de Torres, Fernando Azpiroz, Steeve Boulant, María Vicario, Beate Niesler, Javier Santos

    Vydáno 2017
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  13. 13
    Recurrent CDKN1B (p27) mutations in hairy cell leukemia

    Recurrent CDKN1B (p27) mutations in hairy cell leukemia Autor Sascha Dietrich, Jennifer Hüllein, Stanley Chun-Wei Lee, Barbara Hutter, David González, Sandrine Jayne, Martin J.S. Dyer, Małgorzata Oleś, Monica Else, Xiyang Liu, Mikołaj Słabicki, Bian Wu, Xavier Troussard, Jan Dürig, Mindaugas Andrulis, Claire Dearden, Christof von Kalle, Martin Granzow, Anna Jauch, Stefan Fröhling, Wolfgang Huber, Manja Meggendorfer, Torsten Haferlach, Anthony D. Ho, Daniela Richter, Benedikt Brors, Hanno Glimm, Estella Matutes, Omar Abdel Wahab, Thorsten Zenz

    Vydáno 2015
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  14. 14
    miR-16 and miR-103 impact 5-HT4 receptor signalling and correlate with symptom profile in irritable bowel syndrome

    miR-16 and miR-103 impact 5-HT4 receptor signalling and correlate with symptom profile in irritable bowel syndrome Autor Carolin Wohlfarth, Stefanie Schmitteckert, Janina D. Härtle, Lesley A. Houghton, Harsh Dweep, Marina Fortea, Ghazaleh Assadi, Alexander Braun, Tanja Mederer, Sarina Pöhner, Philip P. Becker, Christine Fischer, Martin Granzow, Hubert Mönnikes, Emeran A. Mayer, Gregory S. Sayuk, Guy E. Boeckxstaens, Mira M. Wouters, Magnus Simrén, Greger Lindberg, Bodil Ohlsson, Peter T. Schmidt, Aldona Dlugosz, Lars Agréus, Anna Andréasson, Mauro D’Amato, Barbara Burwinkel, Justo Lorenzo Bermejo, Ralph Röth, Felix Lasitschka, María Vicario, Marco Metzger, Javier Santos, Gudrun Rappold, Cristina Martínez, Beate Niesler

    Vydáno 2017
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  15. 15
    De Novo Mutations in Protein Kinase Genes CAMK2A and CAMK2B Cause Intellectual Disability

    De Novo Mutations in Protein Kinase Genes CAMK2A and CAMK2B Cause Intellectual Disability Autor Sébastien Küry, Geeske M. van Woerden, Thomas Besnard, Martina Proietti Onori, Xénia Latypova, Meghan C. Towne, Megan T. Cho, Trine Prescott, Melissa A. Ploeg, Stephan Sanders, Holly A.F. Stessman, Aurora Pujol, Ben Distel, Laurie Robak, Jonathan A. Bernstein, Anne‐Sophie Denommé‐Pichon, Gaëtan Lesca, Elizabeth A. Sellars, Jonathan Berg, Wilfrid Carré, Øyvind L. Busk, Bregje W.M. van Bon, Jeff L. Waugh, Matthew A. Deardorff, George Hoganson, Katherine B. Bosanko, Diana Johnson, Tabib Dabir, Øystein L. Holla, Ajoy Sarkar, Kristian Tveten, Julitta de Bellescize, Geir J. Braathen, Paulien A. Terhal, Dorothy K. Grange, Arie van Haeringen, Christina Lam, Ghayda Mirzaa, Jennifer Burton, Elizabeth Bhoj, Jessica Douglas, Avni Santani, Addie I. Nesbitt, Katherine L. Helbig, Marisa V. Andrews, Amber Begtrup, Sha Tang, Koen L.I. van Gassen, Jane Juusola, Kimberly Foss, Gregory M. Enns, Ute Moog, Katrin Hinderhofer, Nagarajan Paramasivam, Sharyn A. Lincoln, Brandon H. Kusako, Pierre Lindenbaum, Éric Charpentier, C. Nowak, Elouan Chérot, Thomas Simonet, Claudia Ruivenkamp, Sihoun Hahn, Donna M. Brown, Fan Xia, Sébastien Schmitt, Wallid Deb, Dominique Bonneau, Mathilde Nizon, Delphine Quinquis, Jamel Chelly, Gabrielle Rudolf, Damien Sanlaville, Philippe Parent, Brigitte Gilbert‐Dussardier, Annick Toutain, V. Reid Sutton, Jenny Thies, Lisenka E.L.M. Peart-Vissers, Pierre Boisseau, Marie Vincent, Andreas M. Grabrucker, Christèle Dubourg, Wen‐Hann Tan, Nienke E. Verbeek, Martin Granzow, Gijs W.E. Santen, Jay Shendure, Bertrand Isidor, Laurent Pasquier, Richard Redon, Yaping Yang, Matthew W. State, Tjitske Kleefstra, Benjamin Cogné, Slavé Petrovski, Kyle Retterer, Evan E. Eichler, Jill A. Rosenfeld, Pankaj B. Agrawal

    Vydáno 2017
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