M
Mark J. Howard
Researcher at University of Leeds
Publications - 16
Citations - 229
Mark J. Howard is an academic researcher from University of Leeds. The author has contributed to research in topics: Metabolome & Pyridine. The author has an hindex of 6, co-authored 16 publications receiving 128 citations. Previous affiliations of Mark J. Howard include University of Western Australia & University of Kent.
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Journal ArticleDOI
Ability of bone graft substitutes to support the osteoprogenitor cells: An in-vitro study.
Z. Dahabreh,Michalis Panteli,Ippokratis Pountos,Mark J. Howard,P. N. Campbell,Peter V. Giannoudis +5 more
TL;DR: Under the above experimental conditions, β-TCP was able to maintain better the viability of osteoprogenitor cells and allow proliferation and differentiation (P < 0.05).
Journal ArticleDOI
Identity and Activity of 2,4-Dichlorophenoxyacetic Acid Metabolites in Wild Radish ( Raphanus raphanistrum).
Danica E. Goggin,Gareth L. Nealon,Gregory R. Cawthray,Adrian Scaffidi,Mark J. Howard,Stephen B. Powles,Gavin R. Flematti +6 more
TL;DR: The lack of detectable 2, 4-D hydroxylation in wild radish and the lability of the glucose ester suggest that metabolic 2,4-D resistance is unlikely to develop in this species.
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Spin-States of Diastereomeric Iron(II) Complexes of 2,6-Bis(thiazolin-2-yl)pyridine (ThioPyBox) Ligands and a Comparison with the Corresponding PyBox Derivatives.
Namrah Shahid,Kay E. Burrows,Mark J. Howard,Christopher M. Pask,Oscar Cespedes,Patrick C. McGowan,Malcolm A. Halcrow +6 more
TL;DR: In this paper, homoleptic iron(II) complexes of thiazolinyl analogues of chiral PyBox tridentate ligands were investigated, and it was shown that the spin states of these compounds exhibit spin-crossover equilibria in CD3CN.
Journal ArticleDOI
The effect of tether groups on the spin states of iron(II)/bis[2,6-di(pyrazol-1-yl)pyridine] complexes
Izar Capel Berdiell,Víctor García-López,Mark J. Howard,Miguel Clemente-León,Malcolm A. Halcrow +4 more
TL;DR: In this paper, the synthesis of 6 2,6-di(pyrazol-1-yl)pyridine derivatives bearing dithiolane or carboxylic acid tether groups is described.
Posted ContentDOI
Metabolic changes of the host-pathogen environment in a Cryptosporidium infection
TL;DR: Using a 1H Nuclear Magnetic Resonance approach to metabolomics, the nature of the mouse gut metabolome is explored as well as providing the first insight into the metabolome of an infected cell line, revealing the potential contribution of host derived taurine to the diuretic aspects of the disease.