Zobrazeno 1 - 10
of 32
pro vyhledávání: '"N Martinez-Soria"'
Autor:
Paul Milne, Helen J. Blair, Cornelia Eckert, Zoya Kingsbury, Matthew Collin, Anetta Ptasinska, Alex Elder, Roderick Skinner, Janine Stutterheim, Jennifer Becq, Elena Zerkalenkova, Constanze Bonifer, Denis M. Schewe, Peter N. Cockerill, N Martinez-Soria, Oskar A. Haas, Peter Carey, Katarzyna Szoltysek, Deepali Pal, Hesta McNeill, Claus Meyer, Maria Rosaria Imperato, James C. Mulloy, Mark Wunderlich, Catherine Cargo, Paul Evans, Sarah E. Fordham, Shan Lin, Pierre Cauchy, Y Shi, Simon Bailey, Salam A. Assi, Rolf Marschalek, Josef Vormoor, Olaf Heidenreich, A Komkov, Michael J. Thirman, Simon Bomken, Ricky Tirtakusuma, Sirintra Nakjang, Fotini Vogiatzi, James M. Allan, Lisa J. Russell, Jayne Y. Hehir-Kwa, Muzlifah Haniffa, Yulia Olshanskaya, Vasily V. Grinev, Christine J. Harrison, Venetia Bigley, Daniel Williamson, Alex Smith, Natalia Miakova
Publikováno v:
Blood. 140:1875-1890
The fusion gene MLL-AF4 defines a high-risk subtype of pro-B acute lymphoblastic leukaemia. However, relapse can be associated with a switch from acute lymphoblastic to acute myeloid leukaemia. Here we show that these myeloid relapses share oncogene
Autor:
Salam A. Assi, Michael Seyani, Vasily V. Grinev, Mojgan Reza, N Martinez-Soria, Tatsiana V. Ramanouskaya, Anita van Oort, Hesta McNeill, Sirintra Nakjang, Job Smink, Constanze Bonifer, Olaf Heidenreich, Richard Clough, Ilya M. Ilyushonak, Farnaz Barneh
Publikováno v:
Nature Communications
Nature Communications, Vol 12, Iss 1, Pp 1-16 (2021)
Nature Communications, Vol 12, Iss 1, Pp 1-16 (2021)
The fusion oncogene RUNX1/RUNX1T1 encodes an aberrant transcription factor, which plays a key role in the initiation and maintenance of acute myeloid leukemia. Here we show that the RUNX1/RUNX1T1 oncogene is a regulator of alternative RNA splicing in
Autor:
Smink J, Constanze Bonifer, N Martinez-Soria, Tatsiana V. Ramanouskaya, Olaf Heidenreich, Grinev, Sirintra Nakjang, Clough R, Ilya M. Ilyushonak
SUMMARYThe fusion oncogene RUNX1/RUNX1T1 encodes an aberrant transcription factor, which plays a key role in the initiation and maintenance of the t(8;21)-positive acute myeloid leukemia. Here we show that this oncogene is a regulator of the alternat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0cee917d5c6b2e1edb787d3ab4136a57
Autor:
Simon Bomken, James C. Mulloy, Peter Carey, Zoya Kingsbury, Josef Vormoor, Paul Milne, Christine J. Harrison, Helen Blair, Jennifer Becq, Lisa J. Russell, Peter N. Cockerill, Jean-Baptiste Cazier, Constanze Bonifer, Daniel Williamson, James M Allan, Paul Evans, Anetta Ptasinska, Sirintra Nakjang, Maria Rosaria Imperato, Elena Zerkalenkova, Rolf Marschalek, Michael J. Thirman, Shan Lin, Alex Smith, Natalia Miakova, Muzlifa Haniffa, Ricky Tirtakusuma, Simon Bailey, Salam A. Assi, Catherine Cargo, Pierre Cauchy, Y Shi, Hesta McNeill, Yulia Olshanskaya, Fotini Vogiatzi, Claus Meyer, Sarah E. Fordham, Alex Elder, Matthew Collin, Roderick Skinner, Venetia Bigley, Olaf Heidenreich, A Komkov, Cornelia Eckert, Deepali Pal, Denis M. Schewe, N Martinez-Soria, Oskar A. Haas
Publikováno v:
SSRN Electronic Journal.
SummaryThe translocation MLL-AF4 defines a high-risk subtype of acute leukaemia which, uniquely amongst MLL translocations, is almost exclusively associated with a pro-B lymphoid phenotype. However, the ability to switch lineage at relapse allowed in
Autor:
N Martinez-Soria, C Bonifer, Helen J. Blair, H Issa, L McKenzie, A Isa, Olaf Heidenreich, Ricky Tirtakusuma
Publikováno v:
Klinische Pädiatrie.
Autor:
L McKenzie, N Martinez-Soria, S Luli, A Isa, Olaf Heidenreich, H Issa, Sirintra Nakjang, Helen J. Blair
Publikováno v:
Klinische Pädiatrie.
Autor:
Sirintra Nakjang, A Isa, N Martinez-Soria, Olaf Heidenreich, Victoria J. Forster, L McKenzie, Helen J. Blair
Publikováno v:
Klinische Pädiatrie.
Autor:
N Martinez-Soria, Victoria J. Forster, Helen J. Blair, Sirintra Nakjang, L McKenzie, Olaf Heidenreich
Publikováno v:
Klinische Pädiatrie. 228
Autor:
T H Brümmendorf, A Gessner, L Büchler, A Scholz, N Martinez Soria, Maria Thomas, Josef Vormoor, Olaf Heidenreich, Johann Greil, P Garrido Castro
Publikováno v:
Leukemia. 24:1751-1759
MLL/AF4 and AML/MTG8 represent two leukemic fusion genes, which are most frequently found in infant acute lymphoblastic leukemia (ALL) and acute myeloid leukemia (AML), respectively. We examined the influence of MLL/AF4 and AML1/MTG8 fusion genes on
Akademický článek
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