Russell, Nigel H., Thomas, Abin  ORCID: https://orcid.org/0000-0002-8283-6762, Hills, Robert K., Thomas, Ian, Gilkes, Amanda, Marquez Almuina, Nuria, Burns, Sarah, Marsh, Lucy, Vyas, Paresh, Metzner, Marlen, McCarthy, Nicholas, Andrew, Georgia, Byrne, Jennifer, Sellar, Rob S., Kelly, Richard, Cahalin, Paul, Malthe Overgaard, Ulrik, Mehta, Priyanka, Dennis, Mike, Knapper, Steven  ORCID: https://orcid.org/0000-0002-6405-4441 and Freeman, Sylvie D.
      2024.
      
      Treatment intensification with either fludarabine, AraC, G-CSF and idarubicin, or cladribine plus daunorubicin and AraC on the basis of residual disease status in older patients With AML: Results From the NCRI AML18 Trial.
      Journal of Clinical Oncology
      
      
      
      
      10.1200/JCO.24.00259
    
  
    
    
       
    
  
  
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      Freeman, Sylvie D, Thomas, Abin, Thomas, Ian, Vyas, Paresh, Gilkes, Amanda, Metzner, Marlen, Jakobsen, Niels Asger, Kennedy, Alison, Moore, Amy, Marquez Almuina, Nuria, Burns, Sarah, King, Sophie, Andrew, Georgia M., Gallagher, Kathleen M.E., Sellar, Rob, Cahalin, Paul, Weber, Duruta, Dennis, Mike, Mehta, Priyanka, Knapper, Steve  ORCID: https://orcid.org/0000-0002-6405-4441 and Russell, Nigel H.
      2022.
      
      A randomized comparison of the fractionated versus single dose schedule of Gemtuzumab Ozogamicin at induction with determinants of benefit for older AML patients: UK NCRI AML18 trial results.
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      10.1182/blood-2022-162245
    
  
  
       
       
     
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      Hole, Paul Spencer, Zabkiewicz, Joanna  ORCID: https://orcid.org/0000-0003-0951-3825, Munje, Chinmay, Newton, Zarabeth, Pearn, Lorna, White, Paul Charles  ORCID: https://orcid.org/0000-0002-6562-4696, Marquez, Nuria, Hills, Robert Kerrin  ORCID: https://orcid.org/0000-0003-0166-0062, Burnett, Alan Kenneth, Tonks, Alex  ORCID: https://orcid.org/0000-0002-6073-4976 and Darley, Richard Lawrence  ORCID: https://orcid.org/0000-0003-0879-0724
      2013.
      
      Overproduction of NOX-derived ROS in AML promotes proliferation and is associated with defective oxidative stress signaling.
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      10.1182/blood-2013-04-491944
    
  
  
       
       
     
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      Errington, Rachel Jane  ORCID: https://orcid.org/0000-0002-8016-4376, Chappell, Sally Claire, Khan, Imtiaz A., Marquez Almuina, Nuria, Wiltshire, Marie, Griesdoorn, Victoria D. and Smith, Paul James
      2013.
      
      Time-lapse microscopy approaches to track cell cycle and lineage progression at the single-cell level.
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      10.1002/0471142956.cy1204s64
    
  
  
       
       
     
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      Tiffen, P., Omidvar, Nader, Marquez, Nuria, Croston, D., Watson, C. and Clarkson, Richard W. E.  ORCID: https://orcid.org/0000-0001-7389-8673
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      A dual role for Oncostatin M signalling in the differentiation and death of mammary epithelial cells in vivo.
      Molecular Endocrinology
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      10.1210/me.2008-0097
    
  
  
       
       
     
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      Smith, Paul James, Marquez, Nuria, Wiltshire, Marie, Chappell, Sally Claire, Njoh, Kerenza, Campbell, Lee, Khan, Imtiaz Ali, Silvestre, Oscar and Errington, Rachel Jane  ORCID: https://orcid.org/0000-0002-8016-4376
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      Mitotic bypass via an occult cell cycle phase following DNA topoisomerase II inhibition in p53 functional human tumor cells.
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      10.4161/cc.6.16.4585
    
  
  
       
       
     
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      Marquez, Nuria, Chappell, Sally Claire, Sansom, Owen J.  ORCID: https://orcid.org/0000-0001-9540-3010, Clarke, Alan Richard  ORCID: https://orcid.org/0000-0002-4281-426X, Teesdale-Spittle, Paul, Errington, Rachel Jane  ORCID: https://orcid.org/0000-0002-8016-4376 and Smith, Paul James
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      Microtubule stress modifies intra-nuclear location of Msh2 in mouse embryonic fibroblasts.
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      Marquez, Nuria, Chappell, Sally Claire, Sansom, Owen J.  ORCID: https://orcid.org/0000-0001-9540-3010, Clarke, Alan Richard  ORCID: https://orcid.org/0000-0002-4281-426X, Errington, Rachel Jane  ORCID: https://orcid.org/0000-0002-8016-4376, Smith, Paul James and Court, Jonathan
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      Single cell tracking reveals that Msh2 is a key component of an early-acting DNA damage-activated G2 checkpoint.
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      10.1038/sj.onc.1206876
    
  
  
       
       
     
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