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Leukemia|April 1, 1996
Variable expression of p16 protein in patients with acute myeloid leukemia without gross rearrangements at the DNA levelR Jamal, N S Thomas, R E Gale, et al.British Journal of Haematology|May 12, 1998
Mutations of the granulocyte-colony stimulating factor receptor in patients with severe congenital neutropenia are not required for transformation to acute myeloid leukaemia and may be a bystander phenomenonT Bernard, R E Gale, J P Evans, et al.British Journal of Haematology|October 23, 1997
Acquired skewing of X-chromosome inactivation patterns in myeloid cells of the elderly suggests stochastic clonal loss with ageR E Gale, A K Fielding, C N Harrison, et al.Experimental Hematology|April 1, 1997
Analysis of the coding sequence for the GM-CSF receptor alpha and beta chains in patients with juvenile chronic myeloid leukemia (JCML)R W Freeburn, R E Gale, H M Wagner, et al.Blood|January 13, 1999
A large proportion of patients with a diagnosis of essential thrombocythemia do not have a clonal disorder and may be at lower risk of thrombotic complicationsC N Harrison, R E Gale, S J Machin, et al.Leukemia|January 1, 1996
The beta subunit common to the GM-CSF, IL-3 and IL-5 receptors is highly polymorphic but pathogenic point mutations in patients with acute myeloid leukaemia (AML) are rareR W Freeburn, R E Gale, H M Wagner, et al.Experimental Hematology|May 1, 1996
Expression of two alternatively spliced forms of the 5' untranslated region of the GM-CSF receptor alpha chain mRNAR Chopra, G Kendall, R E Gale, et al.Blood|February 7, 1998
A truncated isoform of the human beta chain common to the receptors for granulocyte-macrophage colony-stimulating factor, interleukin-3 (IL-3), and IL-5 with increased mRNA expression in some patients with acute leukemiaR E Gale, R W Freeburn, A Khwaja, et al.Leukemia|September 1, 1994
Analysis of mutations in the GM-CSF receptor alpha coding sequence in patients with acute myeloid leukaemia and haematologically normal individuals by RT-PCR-SSCPH M Wagner, R E Gale, R W Freeburn, et al.Blood|October 25, 2001
Mutations in the ELA2 gene encoding neutrophil elastase are present in most patients with sporadic severe congenital neutropenia but only in some patients with the familial form of the diseaseP J Ancliff, R E Gale, R Liesner, et al.Pageof 25