Zobrazeno 1 - 10
of 226
pro vyhledávání: '"Chaplin, Tracy"'
Autor:
Manodoro, Floriana, Marzec, Jacek, Chaplin, Tracy, Miraki-Moud, Farideh, Moravcsik, Eva, Jovanovic, Jelena V., Wang, Jun, Iqbal, Sameena, Taussig, David, Grimwade, David, Gribben, John G., Young, Bryan D., Debernardi, Silvana
Publikováno v:
In Blood 27 March 2014 123(13):2066-2074
Autor:
Paulsson, Kajsa, Cazier, Jean-Baptiste, MacDougall, Finlay, Stevens, Jane, Stasevich, Irina, Vrcelj, Nikoletta, Chaplin, Tracy, Lillington, Debra M., Lister, T. Andrew, Young, Bryan D.
Publikováno v:
Proceedings of the National Academy of Sciences of the United States of America, 2008 May 01. 105(18), 6708-6713.
Externí odkaz:
https://www.jstor.org/stable/25461858
Autor:
Bateman, Caroline M., Colman, Susan M., Chaplin, Tracy, Young, Bryan D., Eden, Tim O., Bhakta, Manoo, Gratias, Eric J., van Wering, Elisabeth R., Cazzaniga, Giovanni, Harrison, Christine J., Hain, Richard, Ancliff, Philip, Ford, Anthony M., Kearney, Lyndal, Greaves, Mel *
Publikováno v:
In Blood 29 April 2010 115(17):3553-3558
Publikováno v:
Proceedings of the National Academy of Sciences of the United States of America, 1995 Oct 01. 92(21), 9737-9741.
Externí odkaz:
https://www.jstor.org/stable/2368551
Segmental uniparental disomy is a commonly acquired genetic event in relapsed acute myeloid leukemia
Autor:
Raghavan, Manoj *, Smith, Lan-Lan, Lillington, Debra M., Chaplin, Tracy, Kakkas, Ioannis, Molloy, Gael, Chelala, Claude, Cazier, Jean-Baptiste, Cavenagh, James D., Fitzgibbon, Jude, Lister, T. Andrew, Young, Bryan D.
Publikováno v:
In Blood 1 August 2008 112(3):814-821
Publikováno v:
In Cancer Letters 2008 267(1):49-54
Autor:
Powles, Thomas, Poele, Robert te, Shamash, Jonathan, Chaplin, Tracy, Propper, David, Joel, Simon, Oliver, Tim, Liu, Wai Man
Publikováno v:
In Blood 1 February 2005 105(3):1214-1221
Autor:
Taanman Jan-Willem, Champion Michael P, Perrett David, Young Bryan D, Chaplin Tracy, Schulz Reiner, Arenas Hernandez Monica, Fensom Anthony, Marinaki Anthony M
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 5, Iss 1, p 34 (2010)
Abstract Background Inherited metabolic diseases (IMDs) comprise a diverse group of generally progressive genetic metabolic disorders of variable clinical presentations and severity. We have undertaken a study using microarray gene expression profili
Externí odkaz:
https://doaj.org/article/83dfb016925d47a0a0921359cabbcc18
Publikováno v:
Molecular Cancer, Vol 9, Iss 1, p 45 (2010)
Abstract Background The human cell cycle transcription factor FOXM1 is known to play a key role in regulating timely mitotic progression and accurate chromosomal segregation during cell division. Deregulation of FOXM1 has been linked to a majority of
Externí odkaz:
https://doaj.org/article/2c37ff178f7d4186bb746b2834495f7f
Autor:
Debernardi, Silvana, Bassini, Alessandra, Jones, Louise K., Chaplin, Tracy, Linder, Britta, de Bruijn, Diederik R.H., Meese, Eckart, Young, Bryan D.
Publikováno v:
In Blood 1 January 2002 99(1):275-281