Search Results - Bob Argiropoulos

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  1. 1
    Unraveling the crucial roles of <i>Meis1</i> in leukemogenesis and normal hematopoiesis

    Unraveling the crucial roles of <i>Meis1</i> in leukemogenesis and normal hematopoiesis by Bob Argiropoulos, Eric Yung, R. Keith Humphries

    Published 2007
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  2. 2
    Site-Specific Recognition of a 70-Base-Pair Element Containing d(GA)<sub><i>n</i></sub> Repeats Mediates<i>bithoraxoid</i> Polycomb Group Response Element-Dependent Silencing

    Site-Specific Recognition of a 70-Base-Pair Element Containing d(GA)<sub><i>n</i></sub> Repeats Mediates<i>bithoraxoid</i> Polycomb Group Response Element-Dependent Silencing by Jacob W. Hodgson, Bob Argiropoulos, Hugh W. Brock

    Published 2001
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  3. 3
    Linkage of Meis1 leukemogenic activity to multiple downstream effectors including Trib2 and Ccl3

    Linkage of Meis1 leukemogenic activity to multiple downstream effectors including Trib2 and Ccl3 by Bob Argiropoulos, Lars Palmqvist, Eric Yung, Florian Kuchenbauer, Michael Heuser, Laura M. Sly, Adrian Wan, Gerald Krystal, R. Keith Humphries

    Published 2008
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  4. 4
    Overcoming bioprocess bottlenecks in the large-scale expansion of high-quality hiPSC aggregates in vertical-wheel stirred suspension bioreactors

    Overcoming bioprocess bottlenecks in the large-scale expansion of high-quality hiPSC aggregates in vertical-wheel stirred suspension bioreactors by Breanna S. Borys, Tiffany Dang, Tania So, Leili Rohani, Tamás Révay, Tylor Walsh, Madalynn Thompson, Bob Argiropoulos, Derrick E. Rancourt, Sunghoon Jung, Yas Hashimura, Brian Lee, Michael S. Kallos

    Published 2021
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  5. 5
    Vitamin D–Binding Protein Deficiency and Homozygous Deletion of the <i>GC</i> Gene

    Vitamin D–Binding Protein Deficiency and Homozygous Deletion of the <i>GC</i> Gene by Clark M. Henderson, Susan L. Fink, Hanan Bassyouni, Bob Argiropoulos, Lindsay Brown, Thomas J. Laha, Konner J. Jackson, R M Lewkonia, Patrick Ferreira, Andrew N. Hoofnagle, Julien L. Marcadier

    Published 2019
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  6. 6
    CBL Exon 8/9 Mutants Activate the FLT3 Pathway and Cluster in Core Binding Factor/11q Deletion Acute Myeloid Leukemia/Myelodysplastic Syndrome Subtypes

    CBL Exon 8/9 Mutants Activate the FLT3 Pathway and Cluster in Core Binding Factor/11q Deletion Acute Myeloid Leukemia/Myelodysplastic Syndrome Subtypes by Carola Reindl, Hilmar Quentmeier, Konstantin Petropoulos, Philipp A. Greif, Tobias Benthaus, Bob Argiropoulos, Gudrun Mellert, Sridhar Vempati, Justus Duyster, Christian Buske, Stefan K. Bohlander, R. Keith Humphries, Wolfgang Hiddemann, Karsten Spiekermann

    Published 2009
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  7. 7
    Optimized serial expansion of human induced pluripotent stem cells using low-density inoculation to generate clinically relevant quantities in vertical-wheel bioreactors

    Optimized serial expansion of human induced pluripotent stem cells using low-density inoculation to generate clinically relevant quantities in vertical-wheel bioreactors by Breanna S. Borys, Tania So, James Colter, Tiffany Dang, Erin L. Roberts, Tamás Révay, Leila Larijani, Roman Krawetz, Ian A. Lewis, Bob Argiropoulos, Derrick E. Rancourt, Sunghoon Jung, Yas Hashimura, Brian Lee, Michael S. Kallos

    Published 2020
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  8. 8
    MN1 overexpression induces acute myeloid leukemia in mice and predicts ATRA resistance in patients with AML

    MN1 overexpression induces acute myeloid leukemia in mice and predicts ATRA resistance in patients with AML by Michael Heuser, Bob Argiropoulos, Florian Kuchenbauer, Eric Yung, Piper Jessica, Stephen Fung, Richard F. Schlenk, Konstanze Döhner, Tanja Hinrichsen, Cornelia Rudolph, Axel Schambach, Christopher Baum, Brigitte Schlegelberger, Hartmut Döhner, Arnold Ganser, R. Keith Humphries

    Published 2007
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  9. 9
    Modeling the functional heterogeneity of leukemia stem cells: role of STAT5 in leukemia stem cell self-renewal

    Modeling the functional heterogeneity of leukemia stem cells: role of STAT5 in leukemia stem cell self-renewal by Michael Heuser, Laura M. Sly, Bob Argiropoulos, Florian Kuchenbauer, Courteney Lai, Andrew P. Weng, Malina Leung, Grace Lin, Christy Brookes, Stephen Fung, Peter J.M. Valk, Ruud Delwel, Bob Löwenberg, Gerald Krystal, R. Keith Humphries

    Published 2009
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  10. 10
    SS-31 Peptide Reverses the Mitochondrial Fragmentation Present in Fibroblasts From Patients With DCMA, a Mitochondrial Cardiomyopathy

    SS-31 Peptide Reverses the Mitochondrial Fragmentation Present in Fibroblasts From Patients With DCMA, a Mitochondrial Cardiomyopathy by Pranav Machiraju, Xuemei Wang, Rasha Sabouny, Joshua Huang, Tian Zhao, Fatima Iqbal, Melissa A. King, Dimple Prasher, Arijit Lodha, Nerea Jiménez-Téllez, Amir Ravandi, Bob Argiropoulos, David S. Sinasac, Aneal Khan, Timothy E. Shutt, Steven C. Greenway

    Published 2019
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  11. 11
    In-depth characterization of the microRNA transcriptome in a leukemia progression model

    In-depth characterization of the microRNA transcriptome in a leukemia progression model by Florian Kuchenbauer, Ryan D. Morin, Bob Argiropoulos, Oleh I. Petriv, Malachi Griffith, Michael Heuser, Eric Yung, Jessica Piper, Allen Delaney, Anna‐Liisa Prabhu, Yongjun Zhao, Helen McDonald, Thomas Zeng, Martin Hirst, Carl L. Hansen, Marco A. Marra, R. Keith Humphries

    Published 2008
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  12. 12
    CHD2 haploinsufficiency is associated with developmental delay, intellectual disability, epilepsy and neurobehavioural problems

    CHD2 haploinsufficiency is associated with developmental delay, intellectual disability, epilepsy and neurobehavioural problems by Sébastien Chénier, Grace Yoon, Bob Argiropoulos, Julie Lauzon, Rachel Laframboise, Joo Wook Ahn, Caroline Mackie Ogilvie, Anath C. Lionel, Christian R. Marshall, Andrea K. Vaags, Bita Hashemi, Karine Boisvert, Géraldine Mathonnet, Frédérique Tihy, Joyce So, Stephen W. Scherer, Emmanuelle Lemyre, Dimitri J. Stavropoulos

    Published 2014
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  13. 13
    Cell of Origin in AML: Susceptibility to MN1-Induced Transformation Is Regulated by the MEIS1/AbdB-like HOX Protein Complex

    Cell of Origin in AML: Susceptibility to MN1-Induced Transformation Is Regulated by the MEIS1/AbdB-like HOX Protein Complex by Michael Heuser, Haiyang Yun, Tobias Berg, Eric Yung, Bob Argiropoulos, Florian Kuchenbauer, Gyeongsin Park, Iyas Hamwi, Lars Palmqvist, Courteney K. Lai, Malina Leung, Grace Lin, Anuhar Chaturvedi, Basant Kumar Thakur, Masayuki Iwasaki, Mikhail Bilenky, Nina Thiessen, Gordon Robertson, Martin Hirst, David G. Kent, Nicola K. Wilson, Berthold Göttgens, Connie J. Eaves, Michael L. Cleary, Marco A. Marra, Arnold Ganser, R. Keith Humphries

    Published 2011
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  14. 14
    Comprehensive analysis of mammalian miRNA* species and their role in myeloid cells

    Comprehensive analysis of mammalian miRNA* species and their role in myeloid cells by Florian Kuchenbauer, Sarah M. Mah, Michael Heuser, Andrew McPherson, Jens Rüschmann, A. MAUREEN ROUHI, Tobias Berg, Lars Bullinger, Bob Argiropoulos, Ryan D. Morin, David Lai, Daniel T. Starczynowski, Aly Karsan, Connie J. Eaves, Akira Watahiki, Yuzhuo Wang, Samuel Aparício, Arnold Ganser, Jürgen Krauter, Hartmut Döhner, Konstanze Döhner, Marco A. Marra, Fernando D. Camargo, Lars Palmqvist, Christian Buske, R. Keith Humphries

    Published 2011
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  15. 15
    DYRK1A haploinsufficiency causes a new recognizable syndrome with microcephaly, intellectual disability, speech impairment, and distinct facies

    DYRK1A haploinsufficiency causes a new recognizable syndrome with microcephaly, intellectual disability, speech impairment, and distinct facies by Jianling Ji, Hane Lee, Bob Argiropoulos, Naghmeh Dorrani, John Mann, Julián A. Martínez-Agosto, Natalia Gomez‐Ospina, Natalie M. Gallant, Jonathan A. Bernstein, Louanne Hudgins, Leah Slattery, Bertrand Isidor, Cédric Le Caignec, Albert David, Ewa Obersztyn, Barbara Wiśniowiecka‐Kowalnik, Michelle Fox, Joshua L. Deignan, Éric Vilain, Emily Hendricks, Margaret Harr, Sarah E. Noon, Jessi R Jackson, Alisha Wilkens, Ghayda Mirzaa, Noriko Salamon, Jeff Abramson, Elaine H. Zackai, Ian D. Krantz, A. Micheil Innes, Stanley F. Nelson, Wayne W. Grody, Fabiola Quintero‐Rivera

    Published 2015
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  16. 16
    Disruption of the ASTN2/TRIM32 locus at 9q33.1 is a risk factor in males for autism spectrum disorders, ADHD and other neurodevelopmental phenotypes

    Disruption of the ASTN2/TRIM32 locus at 9q33.1 is a risk factor in males for autism spectrum disorders, ADHD and other neurodevelopmental phenotypes by A. C. Lionel, Kristiina Tammimies, Andrea K. Vaags, Jill A. Rosenfeld, Joo Wook Ahn, Daniele Merico, Abdul Noor, Cassandra Runke, Vamsee Pillalamarri, M. T. Carter, Matthew J. Gazzellone, Bhooma Thiruvahindrapuram, Christina Fagerberg, Lone Walentin Laulund, Giovanna Pellecchia, Sylvia Lamoureux, Charu Deshpande, Jill Clayton‐Smith, A. Clinton White, Susan Leather, J Q Trounce, H. Melanie Bedford, Eli Hatchwell, Peggy S. Eis, Ryan K. C. Yuen, Susan Walker, Mohammed Uddin, Michael T. Geraghty, Sarah M. Nikkel, Eva Tomiak, Bridget A. Fernandez, Noam Soreni, Jennifer Crosbie, Paul Arnold, Russell Schachar, Wendy Roberts, Andrew D. Paterson, Jonathan So, Péter Szatmári, Christina Chrysler, Marc Woodbury‐Smith, R. Brian Lowry, Lonnie Zwaigenbaum, D. Mandyam, John Wei, Jeffrey R. MacDonald, Jennifer Howe, Thomas Nalpathamkalam, Z. Wang, Debbie Tolson, Donna Cobb, Timothy Wilks, Merete Juul Sørensen, Patricia I. Bader, Yu An, Bai-Lin Wu, S Musumeci, Corrado Romano, Diana Postorivo, A. Nardone, Matteo Della Monica, Gioacchino Scarano, Leonardo Zoccante, Francesca Novara, Orsetta Zuffardi, Roberto Ciccone, Vincenzo Antona, Massimo Carella, Leopoldo Zelante, Pietro Cavalli, Carlo Poggiani, Ugo Cavallari, Bob Argiropoulos, Judy Chernos, Charlotte Brasch‐Andersen, Marsha Speevak, Marco Fichera, Caroline Mackie Ogilvie, Ya Shen, JM Hodge, Michael E. Talkowski, Dimitri J. Stavropoulos, Christian R. Marshall, Stephen W. Scherer

    Published 2013
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