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British Journal of Hospital Medicine (London, England : 2005)|September 6, 2022
Optimising care for UK patients with acute myeloid leukaemiaAntonio Pagliuca, Asim Khwaja, Richard Dillon, et al.
Experimental Hematology|March 24, 2007
Shwachman-Diamond syndrome is not necessary for the terminal maturation of neutrophils but is important for maintaining viability of granulocyte precursorsMasafumi Yamaguchi, Kingo Fujimura, Hanae Toga, et al.
Proceedings of the National Academy of Sciences of the United States of America|June 11, 2010
Activity of any class IA PI3K isoform can sustain cell proliferation and survivalLazaros C Foukas, Inma M Berenjeno, Alexander Gray, et al.
British Journal of Haematology|November 20, 2002
The upregulation of CC chemokine receptor 7 and the increased migration of maturing dendritic cells to macrophage inflammatory protein 3beta and secondary lymphoid chemokine is mediated by the p38 stress-activated protein kinase pathwayKirit M Ardeshna, Arnold R Pizzey, Simon J Walker, et al.
Frontline Gastroenterology|August 26, 2017
Azathioprine-associated myelodysplastic syndrome in two patients with ulcerative colitisOmer F Ahmad, Margaret G Keane, Sara McCartney, et al.
Blood|May 24, 2014
Impact of FLT3(ITD) mutant allele level on relapse risk in intermediate-risk acute myeloid leukemiaDavid C Linch, Robert K Hills, Alan K Burnett, et al.
Proceedings of the National Academy of Sciences of the United States of America|June 6, 2006
Ultrasensitive and absolute quantification of the phosphoinositide 3-kinase/Akt signal transduction pathway by mass spectrometryPedro R Cutillas, Asim Khwaja, Mariona Graupera, et al.
Leukemia Research Reports|February 24, 2022
Gilteritinib monotherapy as a transplant bridging option for high risk <i>FLT3</i>-mutated AML with t(6;9)(p23;q34.1);DEK-NUP214 in morphological but not cytogenetic or molecular remission following standard induction chemotherapyJames W Day, Thomas A Fox, Rajeev Gupta, et al.
British Journal of Haematology|November 28, 2008
Homozygous HAX1 mutations in severe congenital neutropenia patients with sporadic disease: a novel mutation in two unrelated British kindredsBradley N Smith, Phil J Ancliff, Arnold Pizzey, et al.
British Journal of Haematology|March 18, 2008
Acute myeloid leukaemia blast cells with a tyrosine kinase domain mutation of FLT3 are less sensitive to lestaurtinib than those with a FLT3 internal tandem duplicationAdam J Mead, Rosemary E Gale, Panagiotis D Kottaridis, et al.
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