Kimberley Joanne Hatfield
Stilling
Gjesteforsker, Leukemia Research Group
Tilhørighet
Forskning
Prosjektet undersøker effekten av ulike medikamenter som blokkerer sentrale metabolske signalveier i akutt myeloid leukemi (AML). Prosjektet har som mål å karakterisere ulike metabolske signalveier i leukemiceller, samt autofagi, og studere hvordan dette bidrar til kjemoresistens i AML. Prosjektet er støttet av midler fra Bergens forskningsstiftelse.
Publikasjoner
2007
- Elisabeth Ersvær; Peter Hampson; Kimberley Joanne Hatfield et al. (2007). T cells remaining after intensive chemotherapy for acute myelogenous leukemia show a broad cytokine release profile including high levels of interferon-gamma that can be further increased by a novel protein kinase C agonist PEP005. (ekstern lenke)
- Camilla I Stapnes; Anne Paulus Døskeland; Kimberley Joanne Hatfield et al. (2007). The proteasome inhibitors bortezomib and PR-171 have antiproliferative and proapoptotic effects on primary human acute myeloid leukaemia cells. (ekstern lenke)
- Camilla I Stapnes; Anita Ryningen; Kimberley Joanne Hatfield et al. (2007). Functional characteristics and gene expression profiles of primary acute myeloid leukaemia cells identify patient subgroups that differ in the susceptibility to histone deacetylase inhibitors. (ekstern lenke)
2009
- Håkon Reikvam; Kimberley Joanne Hatfield; Astrid Marta Olsnes et al. (2009). PRIMARY HUMAN ACUTE MYELOGENOUS LEUKEMIA CELLS SHOW CONSTITUTIVE RELEASE OF SEVERAL MATRIX METALLOPROTEASES AND THEIR INHIBITORS. (ekstern lenke)
- Astrid Marta Olsnes; Kimberley Joanne Hatfield; Øystein Bruserud (2009). The chemokine system and its contribution to leukemogenesis and treatment responsiveness in patients with acute myeloid leukemia. (ekstern lenke)
- Kimberley Joanne Hatfield; Anne Margrete Øyan; Elisabeth Ersvær et al. (2009). Phase II study of subcutaneous alemtuzumab without dose escalation in patients with advanced-stage, relapsed chronic lymphocytic leukaemia. (ekstern lenke)
Prosjekter
2016-2020: Metabolic phenotypes of leukemia cells.