检索结果 - Argiropoulos, Bob

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

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

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

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

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

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

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Vitamin D–Binding Protein Deficiency and Homozygous Deletion of the GC Gene 由 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.

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Molecular analysis distinguishes metastatic disease from second cancers in patients with retinoblastoma 由 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.

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Optimized serial expansion of human induced pluripotent stem cells using low‐density inoculation to generate clinically relevant quantities in vertical‐wheel bioreactors 由 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.

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

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Rare copy number variations affecting the synaptic gene DMXL2 in neurodevelopmental disorders 由 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.

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In-depth characterization of the microRNA transcriptome in a leukemia progression model 由 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

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CHD2 haploinsufficiency is associated with developmental delay, intellectual disability, epilepsy and neurobehavioural problems 由 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

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Cell Fate Decisions in Malignant Hematopoiesis: Leukemia Phenotype Is Determined by Distinct Functional Domains of the MN1 Oncogene 由 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

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Cell of origin in AML: Susceptibility to MN1-induced transformation is regulated by the MEIS1/AbdB-like HOX protein complex 由 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

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MicroRNA-223 dose levels fine tune proliferation and differentiation in human cord blood progenitors and acute myeloid leukemia 由 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

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

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