Ngā hua rapu - Martin Granzow

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  1. 1
    A Practical Approach to Microarray Data Analysis

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

    I whakaputaina 2003
    Whiwhi kuputuhi katoa
    Livro
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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 mā Andreas Schröeder, Odilo Mueller, Susanne Stocker, Ruediger Salowsky, Michael J. Leiber, Marcus Gassmann, Samar Lightfoot, Wolfram Menzel, Martin Granzow, Thomas Ragg

    I whakaputaina 2006
    Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
    Artigo
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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 mā Marc A. Schneider, Martin Granzow, Arne Warth, Philipp A. Schnabel, Michael Thomas, Felix J.F. Herth, Hendrik Dienemann, Thomas Muley, Michael Meister

    I whakaputaina 2015
    Whiwhi kuputuhi katoa
    Artigo
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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 mā Kai Neben, Anna Jauch, Thomas Hielscher, Jens Hillengaß, Nicola Lehners, Anja Seckinger, Martin Granzow, Marc S. Raab, Anthony D. Ho, Hartmut Goldschmidt, Dirk Hose

    I whakaputaina 2013
    Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
    Artigo
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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 mā 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

    I whakaputaina 2015
    Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
    Artigo
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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> mā 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

    I whakaputaina 2002
    Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
    Artigo
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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 mā 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

    I whakaputaina 2016
    Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
    Artigo
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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 mā 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

    I whakaputaina 2003
    Whiwhi kuputuhi katoa
    Artigo
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  9. 9
    Impact of clinical exomes in neurodevelopmental and neurometabolic disorders

    Impact of clinical exomes in neurodevelopmental and neurometabolic disorders mā 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

    I whakaputaina 2017
    Whiwhi kuputuhi katoa
    Artigo
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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 mā 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

    I whakaputaina 2017
    Whiwhi kuputuhi katoa
    Artigo
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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 mā 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

    I whakaputaina 2017
    Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
    Artigo
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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 mā 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

    I whakaputaina 2017
    Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
    Artigo
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  13. 13
    Recurrent CDKN1B (p27) mutations in hairy cell leukemia

    Recurrent CDKN1B (p27) mutations in hairy cell leukemia mā 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

    I whakaputaina 2015
    Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
    Artigo
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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 mā 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

    I whakaputaina 2017
    Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
    Artigo
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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 mā 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

    I whakaputaina 2017
    Whiwhi kuputuhi katoa
    Artigo
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