Search Results - Argiropoulos, Bob

  • Showing 1 - 17 results of 17
Refine Results
  1. 1
    Site-Specific Recognition of a 70-Base-Pair Element Containing d(GA)(n) Repeats Mediates bithoraxoid Polycomb Group Response Element-Dependent Silencing

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

    Published 2001
    Get full text Get full text Get full text
    Text
    Save to List
    Saved in:
  2. 2
    Very Low Vitamin D in a Patient With a Novel Pathogenic Variant in the GC Gene That Encodes Vitamin D-Binding Protein

    Very Low Vitamin D in a Patient With a Novel Pathogenic Variant in the GC Gene That Encodes Vitamin D-Binding Protein by Banerjee, Ronadip R, Spence, Tara, Frank, Stuart J, Pandian, Raj, Hoofnagle, Andrew N, Argiropoulos, Bob, Marcadier, Julien L

    Published 2021
    Get full text Get full text Get full text
    Text
    Save to List
    Saved in:
  3. 3
    Hi-C detects genomic structural variants in peripheral blood of pediatric leukemia patients

    Hi-C detects genomic structural variants in peripheral blood of pediatric leukemia patients by Mallard, Claire, Johnston, Michael J., Bobyn, Anna, Nikolic, Ana, Argiropoulos, Bob, Chan, Jennifer A., Guilcher, Gregory M.T., Gallo, Marco

    Published 2022
    Get full text Get full text Get full text
    Text
    Save to List
    Saved in:
  4. 4
    Identification of E74-like factor 1 (ELF1) as a transcriptional regulator of the Hox co-factor MEIS1

    Identification of E74-like factor 1 (ELF1) as a transcriptional regulator of the Hox co-factor MEIS1 by Xiang, Ping, Lo, Chaoyu, Argiropoulos, Bob, Lai, C. Benjamin, Rouhi, Arefeh, Imren, Suzan, Jiang, Xiaoyan, Mager, Dixie, Humphries, R. Keith

    Published 2010
    Get full text Get full text Get full text
    Text
    Save to List
    Saved in:
  5. 5
    DELINEATING THE KEY REGIONS AND FUNCTIONS OF NUP98 CONTRIBUTING TO THE LEUKEMOGENIC ACTIVITY OF NUP98-HOX FUSIONS

    DELINEATING THE KEY REGIONS AND FUNCTIONS OF NUP98 CONTRIBUTING TO THE LEUKEMOGENIC ACTIVITY OF NUP98-HOX FUSIONS by Yung, Eric, Sekulovic, Sanja, Argiropoulos, Bob, Lai, Courteney K., Leung, Malina, Vollett, Sarah, Chang, Vicky Chi-Dan, Wan, Adrian, Wong, Sandy, Humphries, R. Keith

    Published 2010
    Get full text Get full text Get full text
    Text
    Save to List
    Saved in:
  6. 6
    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 Borys, Breanna S., Dang, Tiffany, So, Tania, Rohani, Leili, Revay, Tamas, Walsh, Tylor, Thompson, Madalynn, Argiropoulos, Bob, Rancourt, Derrick E., Jung, Sunghoon, Hashimura, Yas, Lee, Brian, Kallos, Michael S.

    Published 2021
    Get full text Get full text Get full text
    Text
    Save to List
    Saved in:
  7. 7
    Vitamin D–Binding Protein Deficiency and Homozygous Deletion of the GC Gene

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

    Published 2019
    Get full text Get full text Get full text
    Text
    Save to List
    Saved in:
  8. 8
    Molecular analysis distinguishes metastatic disease from second cancers in patients with retinoblastoma

    Molecular analysis distinguishes metastatic disease from second cancers in patients with retinoblastoma by Racher, Hilary, Soliman, Sameh, Argiropoulos, Bob, Chan, Helen S.L., Gallie, Brenda L., Perrier, Renée, Matevski, Donco, Rushlow, Diane, Piovesan, Beata, Shaikh, Furqan, MacDonald, Heather, Corson, Timothy W.

    Published 2016
    Get full text Get full text Get full text
    Text
    Save to List
    Saved in:
  9. 9
    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 Borys, Breanna S., So, Tania, Colter, James, Dang, Tiffany, Roberts, Erin L., Revay, Tamas, Larijani, Leila, Krawetz, Roman, Lewis, Ian, Argiropoulos, Bob, Rancourt, Derrick E., Jung, Sunghoon, Hashimura, Yas, Lee, Brian, Kallos, Michael S.

    Published 2020
    Get full text Get full text Get full text
    Text
    Save to List
    Saved in:
  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 Machiraju, Pranav, Wang, Xuemei, Sabouny, Rasha, Huang, Joshua, Zhao, Tian, Iqbal, Fatima, King, Melissa, Prasher, Dimple, Lodha, Arijit, Jimenez-Tellez, Nerea, Ravandi, Amir, Argiropoulos, Bob, Sinasac, David, Khan, Aneal, Shutt, Timothy E., Greenway, Steven C.

    Published 2019
    Get full text Get full text Get full text
    Text
    Save to List
    Saved in:
  11. 11
    Rare copy number variations affecting the synaptic gene DMXL2 in neurodevelopmental disorders

    Rare copy number variations affecting the synaptic gene DMXL2 in neurodevelopmental disorders by Costain, Gregory, Walker, Susan, Argiropoulos, Bob, Baribeau, Danielle A., Bassett, Anne S., Boot, Erik, Devriendt, Koen, Kellam, Barbara, Marshall, Christian R., Prasad, Aparna, Serrano, Moises A., Stavropoulos, D. James, Twede, Hope, Vermeesch, Joris R., Vorstman, Jacob A. S., Scherer, Stephen W.

    Published 2019
    Get full text Get full text Get full text
    Text
    Save to List
    Saved in:
  12. 12
    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 Kuchenbauer, Florian, Morin, Ryan D., Argiropoulos, Bob, Petriv, Oleh I., Griffith, Malachi, Heuser, Michael, Yung, Eric, Piper, Jessica, Delaney, Allen, Prabhu, Anna-Liisa, Zhao, Yongjun, McDonald, Helen, Zeng, Thomas, Hirst, Martin, Hansen, Carl L., Marra, Marco A., Humphries, R. Keith

    Published 2008
    Get full text Get full text Get full text
    Text
    Save to List
    Saved in:
  13. 13
    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 Chénier, Sébastien, Yoon, Grace, Argiropoulos, Bob, Lauzon, Julie, Laframboise, Rachel, Ahn, Joo Wook, Ogilvie, Caroline Mackie, Lionel, Anath C, Marshall, Christian R, Vaags, Andrea K, Hashemi, Bita, Boisvert, Karine, Mathonnet, Géraldine, Tihy, Frédérique, So, Joyce, Scherer, Stephen W, Lemyre, Emmanuelle, Stavropoulos, Dimitri J

    Published 2014
    Get full text Get full text Get full text
    Text
    Save to List
    Saved in:
  14. 14
    Cell Fate Decisions in Malignant Hematopoiesis: Leukemia Phenotype Is Determined by Distinct Functional Domains of the MN1 Oncogene

    Cell Fate Decisions in Malignant Hematopoiesis: Leukemia Phenotype Is Determined by Distinct Functional Domains of the MN1 Oncogene by Lai, Courteney K., Moon, Yeonsook, Kuchenbauer, Florian, Starzcynowski, Daniel T., Argiropoulos, Bob, Yung, Eric, Beer, Philip, Schwarzer, Adrian, Sharma, Amit, Park, Gyeongsin, Leung, Malina, Lin, Grace, Vollett, Sarah, Fung, Stephen, Eaves, Connie J., Karsan, Aly, Weng, Andrew P., Humphries, R. Keith, Heuser, Michael

    Published 2014
    Get full text Get full text Get full text
    Text
    Save to List
    Saved in:
  15. 15
    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 Heuser, Michael, Yun, Haiyang, Berg, Tobias, Yung, Eric, Argiropoulos, Bob, Kuchenbauer, Florian, Park, Gyeongsin, Hamwi, Iyas, Palmqvist, Lars, Lai, Courteney K., Leung, Malina, Lin, Grace, Chaturvedi, Anuhar, Thakur, Basant Kumar, Iwasaki, Masayuki, Bilenky, Mikhail, Thiessen, Nina, Robertson, Gordon, Hirst, Martin, Kent, David, Wilson, Nicola K., Göttgens, Bertie, Eaves, Connie, Cleary, Michael L., Marra, Marco, Ganser, Arnold, Humphries, R. Keith

    Published 2011
    Get full text Get full text Get full text
    Text
    Save to List
    Saved in:
  16. 16
    MicroRNA-223 dose levels fine tune proliferation and differentiation in human cord blood progenitors and acute myeloid leukemia

    MicroRNA-223 dose levels fine tune proliferation and differentiation in human cord blood progenitors and acute myeloid leukemia by Gentner, Bernhard, Pochert, Nicole, Rouhi, Arefeh, Boccalatte, Francesco, Plati, Tiziana, Berg, Tobias, Sun, Su Ming, Mah, Sarah M., Mirkovic-Hösle, Milijana, Ruschmann, Jens, Muranyi, Andrew, Leierseder, Simon, Argiropoulos, Bob, Starczynowski, Daniel T., Karsan, Aly, Heuser, Michael, Hogge, Donna, Camargo, Fernando D., Engelhardt, Stefan, Döhner, Hartmut, Buske, Christian, Jongen-Lavrencic, Mojca, Naldini, Luigi, Humphries, R. Keith, Kuchenbauer, Florian

    Published 2015
    Get full text Get full text Get full text
    Text
    Save to List
    Saved in:
  17. 17
    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 Lionel, Anath C., Tammimies, Kristiina, Vaags, Andrea K., Rosenfeld, Jill A., Ahn, Joo Wook, Merico, Daniele, Noor, Abdul, Runke, Cassandra K., Pillalamarri, Vamsee K., Carter, Melissa T., Gazzellone, Matthew J., Thiruvahindrapuram, Bhooma, Fagerberg, Christina, Laulund, Lone W., Pellecchia, Giovanna, Lamoureux, Sylvia, Deshpande, Charu, Clayton-Smith, Jill, White, Ann C., Leather, Susan, Trounce, John, Melanie Bedford, H., Hatchwell, Eli, Eis, Peggy S., Yuen, Ryan K.C., Walker, Susan, Uddin, Mohammed, Geraghty, Michael T., Nikkel, Sarah M., Tomiak, Eva M., Fernandez, Bridget A., Soreni, Noam, Crosbie, Jennifer, Arnold, Paul D., Schachar, Russell J., Roberts, Wendy, Paterson, Andrew D., So, Joyce, Szatmari, Peter, Chrysler, Christina, Woodbury-Smith, Marc, Brian Lowry, R., Zwaigenbaum, Lonnie, Mandyam, Divya, Wei, John, MacDonald, Jeffrey R., Howe, Jennifer L., Nalpathamkalam, Thomas, Wang, Zhuozhi, Tolson, Daniel, Cobb, David S., Wilks, Timothy M., Sorensen, Mark J., Bader, Patricia I., An, Yu, Wu, Bai-Lin, Musumeci, Sebastiano Antonino, Romano, Corrado, Postorivo, Diana, Nardone, Anna M., Monica, Matteo Della, Scarano, Gioacchino, Zoccante, Leonardo, Novara, Francesca, Zuffardi, Orsetta, Ciccone, Roberto, Antona, Vincenzo, Carella, Massimo, Zelante, Leopoldo, Cavalli, Pietro, Poggiani, Carlo, Cavallari, Ugo, Argiropoulos, Bob, Chernos, Judy, Brasch-Andersen, Charlotte, Speevak, Marsha, Fichera, Marco, Ogilvie, Caroline Mackie, Shen, Yiping, Hodge, Jennelle C., Talkowski, Michael E., Stavropoulos, Dimitri J., Marshall, Christian R., Scherer, Stephen W.

    Published 2014
    Get full text Get full text Get full text
    Text
    Save to List
    Saved in:

Search Tools: