Nicholas C. Lea
Denmark Hill Campus
London, ENG, United Kingdom
London, ENG, United Kingdom
Last Updated: 09/26/2026
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Found 11 publications
Inhibitors of poly ADP-ribose polymerase (PARP) induce apoptosis of myeloid leukemic cells: potential for therapy of myeloid leukemia and myelodysplastic syndromes.
Journal: Haematologica
Published: August 01, 2021
Effect of low-level BCR-ABL1 kinase domain mutations identified by next-generation sequencing in patients with chronic myeloid leukaemia: a population-based study.
Journal: The Lancet. Haematology
Published: October 17, 2018
GATA2 monoallelic expression underlies reduced penetrance in inherited GATA2-mutated MDS/AML.
Journal: Leukemia
Published: December 21, 2017
Proteomic and genomic integration identifies kinase and differentiation determinants of kinase inhibitor sensitivity in leukemia cells.
Journal: Leukemia
Published: July 17, 2017
Heterozygous RTEL1 variants in bone marrow failure and myeloid neoplasms.
Journal: Blood advances
Published: May 02, 2017
Mixed T Cell Chimerism After Allogeneic Hematopoietic Stem Cell Transplantation for Severe Aplastic Anemia Using an Alemtuzumab-Containing Regimen Is Shaped by Persistence of Recipient CD8 T Cells.
Journal: Biology of blood and marrow transplantation : journal of the American Society for Blood and Marrow Transplantation
Published: September 04, 2016
Baseline cytokine profiling identifies novel risk factors for invasive fungal disease among haematology patients undergoing intensive chemotherapy or haematopoietic stem cell transplantation.
Journal: The Journal of infection
Published: February 13, 2016
Spliceosome mutations exhibit specific associations with epigenetic modifiers and proto-oncogenes mutated in myelodysplastic syndrome.
Journal: Haematologica
Published: January 10, 2013
TP53 mutations in myelodysplastic syndrome are strongly correlated with aberrations of chromosome 5, and correlate with adverse prognosis.
Journal: British journal of haematology
Published: September 25, 2012
Prevalence and clinical outcomes of the 46/1 haplotype, Janus kinase 2 mutations, and ten-eleven translocation 2 mutations in Budd-Chiari syndrome and their impact on thrombotic complications post liver transplantation.
Journal: Liver transplantation : official publication of the American Association for the Study of Liver Diseases and the International Liver Transplantation Society
Published: April 03, 2012
Showing 1-11 of 11
Last Updated: 09/26/2026