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Platelet transcriptome analysis in patients with germline RUNX1 mutations
Palma-Barqueros, Verónica, Bastida, José María, López Andreo, María José, Zámora-Cánovas, Ana, Zaninetti, Carlo, Ruiz-Pividal, Juan Francisco, Bohdan, Natalia, Padilla, José, Teruel-Montoya, Raúl, Marín-Quilez, Ana, Revilla, Nuria, Sánchez-Fuentes, Ana, Rodriguez-Alen, Agustín, Benito, Rocío, Vicente, Vicente, Iturbe, Teodoro, Greinacher, Andreas, Lozano, María Luisa, Rivera, José
Published in Journal of thrombosis and haemostasis (01.05.2023)
Published in Journal of thrombosis and haemostasis (01.05.2023)
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The creatine kinase pathway is a metabolic vulnerability in EVI1-positive acute myeloid leukemia
Fenouille, Nina, Bassil, Christopher F, Ben-Sahra, Issam, Benajiba, Lina, Alexe, Gabriela, Ramos, Azucena, Pikman, Yana, Conway, Amy S, Burgess, Michael R, Li, Qing, Luciano, Frédéric, Auberger, Patrick, Galinsky, Ilene, DeAngelo, Daniel J, Stone, Richard M, Zhang, Yi, Perkins, Archibald S, Shannon, Kevin, Hemann, Michael T, Puissant, Alexandre, Stegmaier, Kimberly
Published in Nature medicine (01.03.2017)
Published in Nature medicine (01.03.2017)
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Long Noncoding RNA RUNXOR Promotes Myeloid-Derived Suppressor Cell Expansion and Functions via Enhancing Immunosuppressive Molecule Expressions during Latent HIV Infection
Zhang, Jinyu, Thakuri, Bal Krishna Chand, Zhao, Juan, Nguyen, Lam N, Nguyen, Lam N T, Khanal, Sushant, Cao, Dechao, Dang, Xindi, Schank, Madison, Lu, Zeyuan, Wu, Xiao Y, Morrison, Zheng D, El Gazzar, Mohamed, Jiang, Yong, Ning, Shunbin, Wang, Ling, Moorman, Jonathan P, Yao, Zhi Q
Published in The Journal of immunology (1950) (01.05.2021)
Published in The Journal of immunology (1950) (01.05.2021)
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Runx1 is a central regulator of osteogenesis for bone homeostasis by orchestrating BMP and WNT signaling pathways
Tang, Chen-Yi, Wu, Mengrui, Zhao, Dongfeng, Edwards, Diep, McVicar, Abigail, Luo, Yuan, Zhu, Guochun, Wang, Yongjun, Zhou, Hou-De, Chen, Wei, Li, Yi-Ping
Published in PLoS genetics (21.01.2021)
Published in PLoS genetics (21.01.2021)
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Genetic variegation of clonal architecture and propagating cells in leukaemia
Anderson, Kristina, Lutz, Christoph, van Delft, Frederik W., Bateman, Caroline M., Guo, Yanping, Colman, Susan M., Kempski, Helena, Moorman, Anthony V., Titley, Ian, Swansbury, John, Kearney, Lyndal, Enver, Tariq, Greaves, Mel
Published in Nature (London) (20.01.2011)
Published in Nature (London) (20.01.2011)
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Clinical and pathogenic features of ETV6 -related thrombocytopenia with predisposition to acute lymphoblastic leukemia
Melazzini, Federica, Palombo, Flavia, Balduini, Alessandra, De Rocco, Daniela, Marconi, Caterina, Noris, Patrizia, Gnan, Chiara, Pippucci, Tommaso, Bozzi, Valeria, Faleschini, Michela, Barozzi, Serena, Doubek, Michael, Di Buduo, Christian A., Kozubik, Katerina Stano, Radova, Lenka, Loffredo, Giuseppe, Pospisilova, Sarka, Alfano, Caterina, Seri, Marco, Balduini, Carlo L., Pecci, Alessandro, Savoia, Anna
Published in Haematologica (Roma) (01.11.2016)
Published in Haematologica (Roma) (01.11.2016)
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RUNX1 C-terminal mutations impair blood cell differentiation by perturbing specific enhancer-promoter networks
Jayne, Nathan D., Liang, Zhengyu, Lim, Do-Hwan, Chen, Poshen B., Diaz, Cristina, Arimoto, Kei-Ichiro, Xia, Lingbo, Liu, Mengdan, Ren, Bing, Fu, Xiang-Dong, Zhang, Dong-Er
Published in Blood advances (28.05.2024)
Published in Blood advances (28.05.2024)
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Thrombocytopenia-associated mutations in the ANKRD26 regulatory region induce MAPK hyperactivation
Bluteau, Dominique, Balduini, Alessandra, Balayn, Nathalie, Currao, Manuela, Nurden, Paquita, Deswarte, Caroline, Leverger, Guy, Noris, Patrizia, Perrotta, Silverio, Solary, Eric, Vainchenker, William, Debili, Najet, Favier, Remi, Raslova, Hana
Published in The Journal of clinical investigation (01.02.2014)
Published in The Journal of clinical investigation (01.02.2014)
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Haematological spectrum and genotype-phenotype correlations in nine unrelated families with RUNX1 mutations from the French network on inherited platelet disorders
Latger-Cannard, Veronique, Philippe, Christophe, Bouquet, Alexandre, Baccini, Veronique, Alessi, Marie-Christine, Ankri, Annick, Bauters, Anne, Bayart, Sophie, Cornillet-Lefebvre, Pascale, Daliphard, Sylvie, Mozziconacci, Marie-Joelle, Renneville, Aline, Ballerini, Paola, Leverger, Guy, Sobol, Hagay, Jonveaux, Philippe, Preudhomme, Claude, Nurden, Paquita, Lecompte, Thomas, Favier, Remi
Published in Orphanet journal of rare diseases (26.04.2016)
Published in Orphanet journal of rare diseases (26.04.2016)
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A novel RUNX1 mutation with ANKRD26 dysregulation is related to thrombocytopenia in a sporadic form of myelodysplastic syndrome
Ferrari, Silvia, Regazzo, Daniela, Omenetto, Elisabetta, Scaroni, Carla, Semenzato, Gianpietro, Fabris, Fabrizio, Vianello, Fabrizio
Published in Aging clinical and experimental research (01.07.2021)
Published in Aging clinical and experimental research (01.07.2021)
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Transcription Factor RUNX1 Regulates Platelet PCTP (Phosphatidylcholine Transfer Protein): Implications for Cardiovascular Events: Differential Effects of RUNX1 Variants
Mao, Guangfen, Songdej, Natthapol, Voora, Deepak, Goldfinger, Lawrence E., Del Carpio-Cano, Fabiola E., Myers, Rachel A., Rao, A. Koneti
Published in Circulation (New York, N.Y.) (05.09.2017)
Published in Circulation (New York, N.Y.) (05.09.2017)
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MEGSA: A Powerful and Flexible Framework for Analyzing Mutual Exclusivity of Tumor Mutations
Hua, Xing, Hyland, Paula L., Huang, Jing, Song, Lei, Zhu, Bin, Caporaso, Neil E., Landi, Maria Teresa, Chatterjee, Nilanjan, Shi, Jianxin
Published in American journal of human genetics (03.03.2016)
Published in American journal of human genetics (03.03.2016)
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Comparative genome-wide DNA methylation analysis in myocardial tissue from donors with and without Down syndrome
Cejas, Romina B., Wang, Jie, Hageman-Blair, Rachael, Liu, Song, Blanco, Javier G.
Published in Gene (05.01.2021)
Published in Gene (05.01.2021)
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Systems Pharmacogenomics Finds RUNX1 Is an Aspirin-Responsive Transcription Factor Linked to Cardiovascular Disease and Colon Cancer
Voora, Deepak, Rao, A. Koneti, Jalagadugula, Gauthami S., Myers, Rachel, Harris, Emily, Ortel, Thomas L., Ginsburg, Geoffrey S.
Published in EBioMedicine (01.09.2016)
Published in EBioMedicine (01.09.2016)
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Genetic modifiers of cardiorespiratory fitness response to lifestyle intervention
Peter, Inga, Papandonatos, George D, Belalcazar, L Maria, Yang, Yao, Erar, Bahar, Jakicic, John M, Unick, Jessica L, Balasubramanyam, Ashok, Lipkin, Edward W, Delahanty, Linda M, Wagenknecht, Lynne E, Wing, Rena R, McCaffery, Jeanne M, Huggins, Gordon S
Published in Medicine and science in sports and exercise (01.02.2014)
Published in Medicine and science in sports and exercise (01.02.2014)
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Replication of reported genetic associations of PADI4, FCRL3, SLC22A4 and RUNX1 genes with rheumatoid arthritis: results of an independent Japanese population and evidence from meta-analysis of East Asian studies
Takata, Yoichiro, Inoue, Hiroshi, Sato, Aya, Tsugawa, Kazue, Miyatake, Katsutoshi, Hamada, Daisuke, Shinomiya, Fumio, Nakano, Shunji, Yasui, Natsuo, Tanahashi, Toshihito, Itakura, Mitsuo
Published in Journal of human genetics (01.02.2008)
Published in Journal of human genetics (01.02.2008)
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Runx1 is required for zebrafish blood and vessel development and expression of a human RUNX1-CBF2T1 transgene advances a model for studies of leukemogenesis
Kalev-Zylinska, Maggie L., Horsfield, Julia A., Flores, Maria Vega C., Postlethwait, John H., Vitas, Maria R., Baas, Andrea M., Crosier, Philip S., Crosier, Kathryn E.
Published in Development (Cambridge) (15.04.2002)
Published in Development (Cambridge) (15.04.2002)
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